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Experiencia de un centro" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1084 "Ancho" => 3402 "Tamanyo" => 170488 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Univariate survival analysis by risk factor.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Tumours of the central nervous system (CNS) are the most frequent solid tumours and the leading cause of cancer-related death in children.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Embryonal tumours account for approximately 25% of all primary CNS tumours in individuals aged less than 18 years.<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">2</span></a> According to WHO classification, they can be categorized into three groups: medulloblastoma, CNS supratentorial primitive neuroectodermal tumor (sPNET) and atypical teratoid/rhabdoid tumour (AT/RT).<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">3</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Medulloblastoma is the most frequent brain tumour in children and accounts for 15–20% of all CNS tumours. It has a neuroectodermal origin and an infratentorial location. Approximately 75% arise in the cerebellar vermis and grow towards the fourth ventricle. It is more frequent in males (≈65%) and the median age of onset is approximately 7 years.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">3</span></a> Historically, medulloblastoma has been classified based on histology: classical, desmoplastic/nodular, with extensive nodularity, anaplastic or large cell, with the worst prognosis corresponding to the anaplastic and large cell category, and a favourable prognosis in desmoplastic medulloblastoma.</p><p id="par0020" class="elsevierStylePara elsevierViewall">The most common clinical presentation consists of symptoms caused by raised intracranial pressure, such as headache, nausea and vomiting or irritability, lasting weeks or even months, although other symptoms may also manifest depending on tumour location, such as changes in balance, ataxia, dysmetria, sixth cranial nerve palsy, etc.<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The initial diagnosis is made by computed tomography (CT) and magnetic resonance imaging (MRI). Computed tomography allows for the urgent evaluation of the tumour and its complications, but MRI is the gold standard.<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">6</span></a> Up to 30% of patients may have dissemination through the subarachnoid space at the time of diagnosis, so diagnostic staging is completed by MRI of the spine and histological assessment of cerebrospinal fluid (CSF).<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">7</span></a> Extra-axial metastases are very rare.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">8</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The differential diagnosis must include other tumours of the posterior fossa, such as pilocytic astrocytoma, ependymoma or AT/RT.<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">6,9</span></a> Thus, the diagnosis must be confirmed by histological assessment.</p><p id="par0035" class="elsevierStylePara elsevierViewall">The clinical prognostication of medulloblastoma is intimately associated to three key factors: patient age, the presence of metastasis at the time of diagnosis, and the degree of residual disease after surgery, with a poorer prognosis in patients aged less than 3–5 years, with disseminated disease, or with more than 1.5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleSup">2</span> of residual tumour.<a class="elsevierStyleCrossRefs" href="#bib0195"><span class="elsevierStyleSup">10,11</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Advances in research in recent years have led to a new classification scheme for medulloblastoma that divides it into four molecular subgroups: Wnt/βcatenin group, Sonic Hedgehog group, group 3 and group 4, each of which has different biological and clinical characteristics.<a class="elsevierStyleCrossRefs" href="#bib0205"><span class="elsevierStyleSup">12,13</span></a> For example, group 3 has the poorest prognosis and is frequently associated with <span class="elsevierStyleItalic">MYC</span> amplification.<a class="elsevierStyleCrossRefs" href="#bib0205"><span class="elsevierStyleSup">12,14,15</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The cornerstones of treatment are surgery, radiotherapy and chemotherapy, with different treatment schemes based on the aforementioned risk factors. The first line of treatment is tumour resection, as extensive as possible. This is followed in all cases, save in very young children, by craniospinal irradiation with posterior fossa boost treatment at varying doses based on risk. Chemotherapy (platinum derivatives, lomustine, methotrexate, etc.) has proven useful as an adjuvant therapy since the 1990s, and its intensification is a decisive factor in high-risk cases or in patients that cannot undergo radiotherapy due to their significant sequelae, such as children aged less than 5 years.</p><p id="par0050" class="elsevierStylePara elsevierViewall">In this review, we will analyse the clinical factors involved in the prognostication of medulloblastoma and the changes in the management of medulloblastoma in recent decades along with their impact on survival.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Patients and methods</span><p id="par0055" class="elsevierStylePara elsevierViewall">We conducted a retrospective review of all patients aged 14 years or less with a histopathological diagnosis of medulloblastoma treated in the Paediatric Oncology Unit of the Hospital La Fe between January 1990 and December 2013. A pathologist specialised in paediatric tumours confirmed all cases by histological assessment. We excluded patients referred by other hospitals for hematopoietic stem cell transplantation or radiotherapy. Staging was investigated by craniospinal MRI (except in one patient in 1990, in which staging was determined by cranial CT) and CSF cytology. The extent of disease was established using the Chang system,<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">16</span></a> and we defined metastatic disease as any medulloblastoma with detection of tumour cells in CSF cytology and/or with dissemination in the infra- or supratentorial subarachnoid space diagnosed by means of imaging tests. All patients were treated based on their risk factors following consecutive protocols of the International Society of Paediatric Oncology (SIOP). In the 1990s, trial protocols for average-risk medulloblastoma evaluated the efficacy of adding adjuvant chemotherapy in randomly assigned patients.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">17–20</span></a> Thus, following surgery, some patients were treated exclusively with radiotherapy and others with a combination of chemotherapy and radiotherapy. Children aged less than 3–5 years were treated with chemotherapy alone following surgical resection. High-risk medulloblastomas were treated with surgery, radiotherapy and high-dose chemotherapy<a class="elsevierStyleCrossRefs" href="#bib0240"><span class="elsevierStyleSup">19,21</span></a> (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). In this review, we defined high-risk patients as those with metastatic medulloblastoma and/or more than 1.5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleSup">2</span> of residual tumour, and average-risk patients as those in whom total or near-total (residual tumour <1.5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleSup">2</span>) resection was achieved and without metastatic disease.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">We collected data for the following variables: dates of birth, diagnosis, relapse, death and last followup; sex; clinical manifestations at diagnosis, radiologic location, extent of disease (MRI/CSL cytology), histological variant, treatment protocol used, presence of residual disease after surgery, degree of response to treatment, and outcome.</p><p id="par0065" class="elsevierStylePara elsevierViewall">We have expressed categorical variables as absolute frequencies and percentages, and continuous variables as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>standard deviation (SD) if they followed a normal distribution (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>.05 in the Kolmogorov–Smirnov test) or as median and range if the distribution was not normal. We estimated survival curves using the Kaplan–Meier method, performed univariate contrasts by means of the log-rank test, and used Cox regression for the multivariate analysis. The factors included in the multivariate analysis were those that had shown significant differences in the univariate analysis as well as clinical factors that have been traditionally considered as indicators of a poor prognosis. We defined statistical significance as <span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>.05. We performed the statistical analysis with the statistical package SPSS version 20.0, and generated the graphs with R version 3.0.2.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Results</span><p id="par0070" class="elsevierStylePara elsevierViewall">In the period under study, 86 CNS embryonal tumours were diagnosed in patients aged less than 14 years. Of all these tumours, 74.4% were medulloblastomas (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>63), 24.4% sPNETs (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>22), and one was an AT/RT (1.1%).</p><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Patients</span><p id="par0075" class="elsevierStylePara elsevierViewall">The median age at diagnosis was 7 years (range, 7 months–14 years). Forty-two patients were male (66.7%) and 21 female (33.3%). The most frequent clinical presentation consisted of symptoms caused by raised intracranial pressure: 50 patients had vomiting (79.4%) and 45 had headache (71.4%) at the time of diagnosis. Other neurologic symptoms that were associated with tumour location included gait changes and ataxia (36.5%), ocular misalignment or diplopia due to sixth cranial nerve involvement (12.7%) or symptoms consistent with involvement of other cranial nerves (25.4%) such as facial paralysis, hearing loss, and others. Less frequent symptoms included convulsions, somnolence, irritability or psychomotor regression. Two of these patients presented with motor skill deficits; one with dysphagia, and one with learning impairments of abrupt onset. Seventeen patients (27%) required placement of a ventriculoperitoneal shunt prior to surgical resection for the management of hydrocephalus secondary to the tumour. <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a> summarises the characteristics of the patients.</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Tumour location:</span> the most frequent tumour location was the cerebellar vermis (75%), followed by the cerebellar hemispheres (24% left, 16% right) and 9.5% in other cerebellar structures, such as the peduncles. Fifty-seven percent of the medulloblastomas occupied the fourth ventricle. Twenty-one patients (32%)had dissemination at the time of diagnosis, which was detected by radiology.</p><p id="par0085" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Surgery:</span> total or near-total resection was achieved with a single surgery in 50 patients (82.5%). Seven patients underwent a second surgery, and total resection was achieved in three.</p><p id="par0090" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Histological subtypes:</span> the most frequent subtype was classic medulloblastoma (71%), followed by desmoplastic medulloblastoma (25.4%) and, last of all, there were only two cases of anaplastic and large cell medulloblastoma.</p><p id="par0095" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Staging:</span> 24 patients were considered high-risk due to the detection of disseminated disease by imaging tests at the time of diagnosis (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>21), presence of tumour cells in CSF (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>7) and/or presence of residual disease (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>10). The other 39 patients were classified as average-risk.</p><p id="par0100" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Adjuvant therapy:</span> 53 patients (84.2%) received postsurgical radiotherapy, which was the sole adjuvant therapy in 12. The remaining 41 patients received radiotherapy and chemotherapy following different treatment protocols (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>), and 13 of them underwent megatherapy with autologous stem cell rescue at least once. Ten patients, all of them aged less than 4 years, were treated with chemotherapy alone following surgery.</p><p id="par0105" class="elsevierStylePara elsevierViewall">Treatment was completed by 87.3% of patients. In six patients (9.5%), treatment was discontinued due to disease progression or recurrence. In the remaining patients (3.2%), treatment was discontinued for other reasons (choice of the family, change of medical facility, etc.).</p><p id="par0110" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Survival analysis:</span> at present, 35 patients are not receiving treatment, with a median duration of followup of 5.1 years (range, 0.65–21.7 years). At 3 and 5 years from diagnosis, the overall survival (OS) was 66<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>13% and 55<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>14% (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>), and the event-free survival was 48<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>13% and 43<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>14%, respectively.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0115" class="elsevierStylePara elsevierViewall">During the followup, half of the patients (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>32) experienced a recurrence or disease progression. Of these patients, seven are still alive and are currently not receiving any treatment. Recurrences and disease progression happened in the first five years of followup in all patients, except in one patient that experienced a local recurrence at seven years and died after undergoing different lines of treatment.</p><p id="par0120" class="elsevierStylePara elsevierViewall">Four patients (6.3%) died of toxicity, all of them before year 2000. Two died during initial treatment due to transplant-related complications, and another two during relapse treatment—one due to transplant complications and the other due to polymicrobial sepsis and invasive fungal infection.</p><p id="par0125" class="elsevierStylePara elsevierViewall">The <span class="elsevierStyleItalic">univariate analysis</span> by risk groups found a 5-year OS of 48<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>22% in patients with high-risk medulloblastoma and 61<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>17% in patients with average-risk medulloblastoma (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.11). In the analysis by risk factor, staging at the time of diagnosis (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.018) and adjuvant chemotherapy (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.039) were significantly associated with survival. We want to highlight the improvement in the 5-year overall survival, which increased from 44% in the 1990–2000 period to 70% between 2000 and 2013 (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.032) (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>).</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0130" class="elsevierStylePara elsevierViewall">We did not find statistically significant differences based on the extent of surgical resection (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.348) or histological subtype (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.923).</p><p id="par0135" class="elsevierStylePara elsevierViewall">In the <span class="elsevierStyleItalic">multivariate analysis</span>, patient age (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.008) along with the presence of disseminated disease at the time of diagnosis and/or of more than 1.5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleSup">2</span> of residual tumour (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.007) and the use of adjuvant chemotherapy (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.008) were significantly correlated to survival, while the period of treatment was not (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.467) (<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>).</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Discussion</span><p id="par0140" class="elsevierStylePara elsevierViewall">Medulloblastoma is the most frequent paediatric brain tumour. Its survival has improved in recent decades thanks to the addition of chemotherapy to the standard treatment with surgery and radiotherapy,<a class="elsevierStyleCrossRefs" href="#bib0240"><span class="elsevierStyleSup">19,20,22</span></a> intensification treatment in high-risk medulloblastoma,<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">21,23–25</span></a> and advances in supportive care.</p><p id="par0145" class="elsevierStylePara elsevierViewall">This study analyses the experience in our hospital in the diagnosis and management of medulloblastoma in paediatric patients. To do so, we did a retrospective review of all the cases of medulloblastoma diagnosed and treated in our unit since 1990.</p><p id="par0150" class="elsevierStylePara elsevierViewall">Patient characteristics (age at the time of diagnosis, sex, clinical manifestations, tumour location and presence of metastases) were similar to those described in the literature.<a class="elsevierStyleCrossRefs" href="#bib0160"><span class="elsevierStyleSup">3,5</span></a> The median age at diagnosis was 7 years, and the prevalence was higher in males. The most frequent presenting symptoms are derived from the increased intracranial pressure caused by the tumour. Usually, these are accompanied by other neurologic symptoms and signs, but it is not rare for these patients to present exclusively nausea/vomiting or headache. Seventeen of our patients presented with vomiting and headache, five with only headache, and another five with only vomiting. Therefore, in patients with nonspecific presentations involving vomiting or headache, and especially combining both, we must contemplate the possibility of an intracranial tumour. The most frequent tumour location was the cerebellar vermis. One third of the patients had disseminated disease at the time of diagnosis, and the proportion of patients in whom total or near total resection was achieved in our series is the same as the proportion reported in the literature.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">20</span></a> The most frequent histological subtype, consistent with other published series, was classic medulloblastoma, followed by desmoplastic medulloblastoma.<a class="elsevierStyleCrossRefs" href="#bib0165"><span class="elsevierStyleSup">4,26</span></a></p><p id="par0155" class="elsevierStylePara elsevierViewall">The 3-year OS of medulloblastoma patients in our series was 66<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>13%, which is consistent with the OS for this type of tumour in Spain based on data from the National Registry of Paediatric Tumours (65<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>17%).<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">27</span></a></p><p id="par0160" class="elsevierStylePara elsevierViewall">In patients classified as average-risk, the 3-year OS was 68<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>16%, somewhat lower than that reported by other international groups, which may be due to the small sample size and the long period under study. The latter involves changes in risk classifications and treatment approaches, which would lead to small deviations in small samples from the results obtained by other groups.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">17–20,22,28</span></a></p><p id="par0165" class="elsevierStylePara elsevierViewall">In high-risk patients, the 3-year OS was 64<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>20%, consistent with other studies that reported a survival for this group of 60–70%.<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">23,24</span></a></p><p id="par0170" class="elsevierStylePara elsevierViewall">The univariate analysis did not find statistically significant differences between both risk groups, as there were confounding factors such as age and variability in adjuvant therapy that need to be taken into account.</p><p id="par0175" class="elsevierStylePara elsevierViewall">When we analysed clinical risk factors separately, we confirmed that the prognosis was poorer in patients with disseminated disease at the time of diagnosis (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.017). Survival was higher in patients with total tumour resection compared to those with more than 1.5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleSup">2</span> of residual disease, but these differences were not statistically significant (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.348), probably due to the small number of patients with residual tumours. We did not observe statistically significant differences between the different histological groups, as only two patients received a diagnosis of anaplastic/large cell medulloblastoma, which precluded the study of this factor.</p><p id="par0180" class="elsevierStylePara elsevierViewall">In the period under study there was a clear improvement in survival in the last decade, with the 5-year OS increasing from 44<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>25% to 70<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>23% in patients that received their diagnosis starting at year 2000 (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.032), similar to the survival reported in other case series.<a class="elsevierStyleCrossRefs" href="#bib0245"><span class="elsevierStyleSup">20,22</span></a> This improvement in survival is mostly due to the systematic use of chemotherapy in the standard treatment of medulloblastoma (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.000), with no significant differences in survival between the two periods associated to any of the other clinical risk factors (age, residual disease and dissemination at the time of diagnosis).</p><p id="par0185" class="elsevierStylePara elsevierViewall">The results of the multivariate analysis of changes in survival between these two decades stopped being statistically significant when chemotherapy was added to the model. However, we did find statistically significant differences for all other clinical risk factors: age, presence of residual disease and/or dissemination at the time of diagnosis, which had a negative impact on survival (<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>).</p><p id="par0190" class="elsevierStylePara elsevierViewall">Therefore, we can conclude that the key factors that have led to improved survival in recent decades were the incorporation of chemotherapy to treatment schemes, which has been clearly demonstrated by all collaborative research groups (SIOP, COG) in the 1990s, and the intensification of treatment. However, we cannot underestimate the influence of advances in radiotherapy and imaging techniques, as the stage of disease and the extent of tumour resection can be determined more accurately today.</p><p id="par0195" class="elsevierStylePara elsevierViewall">Future efforts must focus on adjusting the intensity of treatment to clinical as well as biological risk factors to minimise adverse effects. Until a few years ago, the biology of medulloblastoma was poorly understood, but biological tests are increasingly included in the diagnosis of medulloblastoma that allow a better characterisation of the tumour.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">29</span></a> This review did not include biological tests, as it is only recently that they have been incorporated in everyday clinical practice. Future studies should take all of these aspects into account to make a comprehensive analysis of the behaviour of medulloblastoma.</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Funding</span><p id="par0200" class="elsevierStylePara elsevierViewall">Instituto de Investigación Sanitaria La Fe. Asociación Pablo Ugarte.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Conflict of interests</span><p id="par0205" class="elsevierStylePara elsevierViewall">The authors have no conflict of interests to declare.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:11 [ 0 => array:3 [ "identificador" => "xres782726" "titulo" => "Abstract" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0005" "titulo" => "Objective" ] 1 => array:2 [ "identificador" => "abst0010" "titulo" => "Patients and methods" ] 2 => array:2 [ "identificador" => "abst0015" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abst0020" "titulo" => "Conclusion" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec781689" "titulo" => "Keywords" ] 2 => array:3 [ "identificador" => "xres782727" "titulo" => "Resumen" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0025" "titulo" => "Objetivo" ] 1 => array:2 [ "identificador" => "abst0030" "titulo" => "Pacientes y métodos" ] 2 => array:2 [ "identificador" => "abst0035" "titulo" => "Resultados" ] 3 => array:2 [ "identificador" => "abst0040" "titulo" => "Conclusión" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec781688" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Patients and methods" ] 6 => array:3 [ "identificador" => "sec0015" "titulo" => "Results" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0020" "titulo" => "Patients" ] ] ] 7 => array:2 [ "identificador" => "sec0025" "titulo" => "Discussion" ] 8 => array:2 [ "identificador" => "sec0030" "titulo" => "Funding" ] 9 => array:2 [ "identificador" => "sec0035" "titulo" => "Conflict of interests" ] 10 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2016-01-25" "fechaAceptado" => "2016-03-01" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec781689" "palabras" => array:4 [ 0 => "Embryonal tumours" 1 => "Medulloblastoma" 2 => "Survival analysis" 3 => "Prognostic factors" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec781688" "palabras" => array:4 [ 0 => "Tumores embrionarios" 1 => "Meduloblastoma" 2 => "Análisis de supervivencia" 3 => "Factores pronóstico" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:3 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Objective</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">The aim of the study is to analyse variations in the treatment of medulloblastoma, the most common childhood brain tumour, and its impact on survival over the past two decades, as well as its clinical and pathological features.</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Patients and methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Survival analysis of all patients under 14 years old diagnosed with medulloblastoma between January 1990 and December 2013 in a Paediatric Oncology Unit.</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Sixty-three patients were diagnosed and treated for medulloblastoma, with a median follow-up of 5.1 years (range 0.65–21.7 years). The overall survival (OS) at 3 and 5 years was 66<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>13% and 55<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>14%, respectively.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">The OS at 5 years was 44<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>25% in patients diagnosed in the 1990s, showing an increase to 70<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>23% (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.032) since 2000. Clinical prognosis factors were included in the logistic regression model: age (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.008), presence of metastases and/or residual tumour (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.007), and receiving chemotherapy with radiotherapy after surgery (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>.008). Statistically significant differences were observed for all of them.</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusion</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">In our institution there has been a significant increase in medulloblastoma survival in the last decades. Multivariate analysis showed that this improvement was not related to the date of diagnosis, but with the introduction of chemotherapy in adjuvant treatment. This study confirmed that clinical factors significantly associated with worse outcome were age and presence of metastases at diagnosis.</p></span>" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0005" "titulo" => "Objective" ] 1 => array:2 [ "identificador" => "abst0010" "titulo" => "Patients and methods" ] 2 => array:2 [ "identificador" => "abst0015" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abst0020" "titulo" => "Conclusion" ] ] ] "es" => array:3 [ "titulo" => "Resumen" "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Objetivo</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Analizar las variaciones en el tratamiento del meduloblastoma, el tumor cerebral más frecuente en la infancia, y su repercusión en la supervivencia durante las 2 últimas décadas, así como sus características clínicas y anatomopatológicas.</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Pacientes y métodos</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Análisis de supervivencia de todos los casos de meduloblastoma diagnosticados en menores de 14 años desde enero de 1990 hasta diciembre del 2013 en una Unidad de Oncología Pediátrica.</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Sesenta y tres pacientes fueron diagnosticados y tratados de meduloblastoma. La mediana de seguimiento fue 5,1 años (rango 0,65-21,7 años). La supervivencia global (SG) a los 3 y 5 años fue 66<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>13% y 55<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>14%, respectivamente. En los pacientes diagnosticados en la década de los 90, la SG a los 5 años fue 44%<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>25%, observándose un ascenso hasta 70<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>23% (p = 0,032) a partir del año 2000. En el modelo de regresión logística se incluyeron los factores clínicos implicados en el pronóstico: edad (p = 0,008), presencia de metástasis y/o resto tumoral (p = 0,007) y haber recibido quimioterapia, junto a radioterapia, tras la cirugía (p = 0,008), observándose diferencias estadísticamente significativas para todos ellos.</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclusión</span><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">En la última década se ha producido un importante aumento de la supervivencia del meduloblastoma en nuestro centro. En el análisis multivariante se observó que esta mejoría no estaba relacionada con la fecha de diagnóstico, sino con la introducción de la quimioterapia en el tratamiento adyuvante. Se confirmó que los factores clínicos relacionados significativamente con un peor pronóstico son la edad y la presencia de metástasis al diagnóstico.</p></span>" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0025" "titulo" => "Objetivo" ] 1 => array:2 [ "identificador" => "abst0030" "titulo" => "Pacientes y métodos" ] 2 => array:2 [ "identificador" => "abst0035" "titulo" => "Resultados" ] 3 => array:2 [ "identificador" => "abst0040" "titulo" => "Conclusión" ] ] ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Igual Estellés L, Berlanga Charriel P, Cañete Nieto A. Meduloblastoma: mejoría de la supervivencia en las últimas décadas. Experiencia de un centro. An Pediatr (Barc). 2017;86:4–10.</p>" ] ] "multimedia" => array:5 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1418 "Ancho" => 1583 "Tamanyo" => 59482 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Overall survival in medulloblastoma patients in our series (95% CI).</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1084 "Ancho" => 3402 "Tamanyo" => 170488 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Univariate survival analysis by risk factor.</p>" ] ] 2 => array:8 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at1" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">AR MB, average risk medulloblastoma; CTX, chemotherapy; HR MB, high-risk medulloblastoma; RTX,radiotherapy.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Protocol \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Treatment scheme \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">SIOP 1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Surgery<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>RTX<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>CTX <span class="elsevierStyleItalic">(lomustine, vincristine)</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">SIOP PNET 3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">AR MB: Surgery<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>CTX <span class="elsevierStyleItalic">(vincristine, carboplatin, etoposide, cyclophosphamide)</span><span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>RTX<br>MB AR: Surgery<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>CTX <span class="elsevierStyleItalic">(vincristine, carboplatin, etoposide, cyclophosphamide)</span><span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>RTX \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">HIT-SIOP PNET 4 for AR MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Surgery<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>RTX<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>8 cycles of CTX (cisplatin, lomustine, vincristine) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">HART for HR MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">High-dose CTX <span class="elsevierStyleItalic">(methotrexate, vincristine, etoposide, cyclophosphamide, carboplatin)</span><span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>hyperfractionated and accelerated RTX (HART)<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>double megatherapy <span class="elsevierStyleItalic">(thiotepa)</span> autologous haematopoietic stem cell transplantation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">SEHOP<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>3 years \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Surgery<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>CTX <span class="elsevierStyleItalic">(cisplatin, etoposide, vincristine, cyclophosphamide, methotrexate, carboplatin)</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Head Start<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>3 years \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">3 cycles of CTX <span class="elsevierStyleItalic">(vincristine, etoposide, cyclophosphamide, cisplatin</span><span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">methotrexate)</span><span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>3 cycles megatherapy <span class="elsevierStyleItalic">(thiotepa, carboplatin)</span> with autologous transplant \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab1300512.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Protocols applied during the reviewed periods (1990–2013).</p>" ] ] 3 => array:8 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at2" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Characteristics \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">n</span> (%) \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleItalic">Sex</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Male \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">42 (66.7) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Female \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">21 (33.3) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleItalic">Symptoms at time of diagnosis</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Vomiting \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">50 (79.4) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Headache \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">45 (71.4) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Ataxia/gait changes \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">23 (36.5) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Hydrocephalus<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>VP shunting \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">17 (26.9) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Cranial nerve involvement \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">14 (22.2) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Sixth cranial nerve palsy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">8 (12.7) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Other \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">16 (25.3) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleItalic">Location</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Vermis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">47 (74.6) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Left cerebellar hemisphere \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">15 (23.8) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Right cerebellar hemisphere \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">10 (15.8) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Fourth ventricle \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">36 (57.1) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Other (cerebellar peduncles…) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">6 (9.5) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleItalic">Staging</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Localised \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">40 (63.4) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>M1 (localised, CSF+) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">3 (4.8) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Metastatic (M2–M4) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">20 (31.7) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleItalic">Histology</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Classic MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">46 (71.4) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Desmoplastic/nodular MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">15 (25.4) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Anaplastic MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">1 (1.6) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Large cell MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">1 (1.6) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="table-entry " colspan="2" align="left" valign="top"><span class="elsevierStyleItalic">Treatment protocol</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>SIOP 1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">7 (11.1) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>SIOP 3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">19 (30.2) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>SIOP PNET 4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">16 (25.3) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>SEHOP<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>3 years \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">7 (11.1) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>HEAD START<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>3 years \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">3 (4.8) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>HART MILAN HR-MB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">9 (14.3) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Other \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">2 (3.2) \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab1300513.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Patient characteristics (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>63).</p>" ] ] 4 => array:8 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at3" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Variable \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Hazard ratio \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">95% CI \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">P</span> \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">0.821 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">0.710–0.949 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">.008 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">High-risk (metastasis and or residual tumour<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>1.5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleSup">2</span>) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">0.323 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">0.143–0.730 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">.007 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Chemotherapy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">4.688 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">1.510–14.556 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">.008 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Treatment period \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">1.375 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">0.583–3.242 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="char" valign="top">.467 \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab1300514.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Multivariate analysis of clinical prognostic factors.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:29 [ 0 => array:3 [ "identificador" => "bib0150" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Childhood cancer incidence and survival in Spain" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "R. Peris-Bonet" 1 => "D. Salmerón" 2 => "M.A. Martínez-Beneito" 3 => "J. Galceran" 4 => "R. Marcos-Gragera" 5 => "S. Felipe" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Ann Oncol" "fecha" => "2010" "volumen" => "21" "paginaInicial" => "103" "paginaFinal" => "110" "itemHostRev" => array:3 [ "pii" => "S0009739X13001358" "estado" => "S300" "issn" => "0009739X" ] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0155" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "The incidence of medulloblastomas and primitive neurectodermal tumours in adults and children" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "N.R. Smoll" 1 => "K.J. Drummond" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.jocn.2012.04.009" "Revista" => array:6 [ "tituloSerie" => "J Clin Neurosci" "fecha" => "2012" "volumen" => "19" "paginaInicial" => "1541" "paginaFinal" => "1544" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/22981874" "web" => "Medline" ] ] ] ] ] ] ] ] 2 => array:3 [ "identificador" => "bib0160" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "WHO classification of tumours of the central nervous system" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "N. Louis David" 1 => "M.D. Hiroko Ohgaki" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Libro" => array:2 [ "fecha" => "2007" "editorial" => "International Agency for Research on Cancer" ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0165" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Large cell/anaplastic medulloblastomas. A pediatric oncology group study" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "H.G. Brown" 1 => "J.L. Kepner" 2 => "E.J. Perlman" 3 => "H.S. Friedman" 4 => "D.R. Strother" 5 => "P.K. Duffner" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "J Neuropathol Exp Neurol" "fecha" => "2000" "volumen" => "59" "paginaInicial" => "857" "paginaFinal" => "865" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/11079775" "web" => "Medline" ] ] ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0170" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Medulloblastoma" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ 0 => "G. Dahll" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1177/0883073809341668" "Revista" => array:6 [ "tituloSerie" => "J Child Neurol" "fecha" => "2009" "volumen" => "24" "paginaInicial" => "1418" "paginaFinal" => "1430" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19841429" "web" => "Medline" ] ] ] ] ] ] ] ] 5 => array:3 [ "identificador" => "bib0175" "etiqueta" => "6" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Meduloblastoma pediátrico, revisión y puesta al día" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ 0 => "M.I. Martínez León" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Radiología" "fecha" => "2011" "volumen" => "53" "paginaInicial" => "134" "paginaFinal" => "145" ] ] ] ] ] ] 6 => array:3 [ "identificador" => "bib0180" "etiqueta" => "7" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Evaluation of intracranial cerebrospinal fluid cytology in staging pediatric medulloblastomas, supratentorial primitive neuroectodermal tumors, and ependymomas" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "S. Terterov" 1 => "M.D. Krieger" 2 => "I. Bowen" 3 => "J.G. McComb" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.3171/2010.5.PEDS09333" "Revista" => array:6 [ "tituloSerie" => "J Neurosurg Pediatr" "fecha" => "2010" "volumen" => "6" "paginaInicial" => "131" "paginaFinal" => "136" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/20672933" "web" => "Medline" ] ] ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0185" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Extracranial metastases of medulloblastoma in adults: literature review" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "S. Rochkind" 1 => "I. Blatt" 2 => "M. Sadeh" 3 => "Y. Goldhammer" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "J Neurol Neurosurg Psychiatry" "fecha" => "1991" "volumen" => "54" "paginaInicial" => "70" "paginaFinal" => "86" ] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0190" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Neuroimaging of pediatric posterior fossa tumors including review of the literature" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "A. Poretti" 1 => "A. Meoded" 2 => "T.A. Huisman" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1002/jmri.22722" "Revista" => array:5 [ "tituloSerie" => "J Magn Reson Imaging" "fecha" => "2012" "volumen" => "35" "paginaInicial" => "32" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/21989968" "web" => "Medline" ] ] ] ] ] ] ] ] 9 => array:3 [ "identificador" => "bib0195" "etiqueta" => "10" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Medulloblastoma: present concepts of stratification into risk groups" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "R.J. Packer" 1 => "B.R. Rood" 2 => "T.G. McDonald" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "71316" "Revista" => array:6 [ "tituloSerie" => "Pediatr Neurosurg" "fecha" => "2003" "volumen" => "39" "paginaInicial" => "60" "paginaFinal" => "67" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/12845195" "web" => "Medline" ] ] ] ] ] ] ] ] 10 => array:3 [ "identificador" => "bib0200" "etiqueta" => "11" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Long term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomized multicenter trial HIT91" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "K. Von Hoff" 1 => "B. Hinkes" 2 => "N.U. Gerber" 3 => "F. Deinlein" 4 => "U. Mittler" 5 => "C. Urban" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.ejca.2009.01.015" "Revista" => array:6 [ "tituloSerie" => "Eur J Cancer" "fecha" => "2009" "volumen" => "45" "paginaInicial" => "1209" "paginaFinal" => "1217" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19250820" "web" => "Medline" ] ] ] ] ] ] ] ] 11 => array:3 [ "identificador" => "bib0205" "etiqueta" => "12" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Molecular subgroups of medulloblastoma: the current consensus" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "M.D. Taylor" 1 => "P.A. Northcott" 2 => "A. Korshunov" 3 => "M. Remke" 4 => "Y.J. Cho" 5 => "S.C. Clifford" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1007/s00401-011-0922-z" "Revista" => array:6 [ "tituloSerie" => "Acta Neuropathol" "fecha" => "2012" "volumen" => "123" "paginaInicial" => "465" "paginaFinal" => "472" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/22134537" "web" => "Medline" ] ] ] ] ] ] ] ] 12 => array:3 [ "identificador" => "bib0210" "etiqueta" => "13" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Beta-catenin status predicts a favorable outcome in childhood medulloblastoma: The United Kingdom Children's Cancer Study Group Brain Tumour Committee" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "D.W. Ellison" 1 => "O.E. Onilude" 2 => "J.C. Lindsey" 3 => "M.E. Lusher" 4 => "C.L. Weston" 5 => "R.E. Taylor" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1200/JCO.2005.01.5479" "Revista" => array:6 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2005" "volumen" => "23" "paginaInicial" => "7951" "paginaFinal" => "7957" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/16258095" "web" => "Medline" ] ] ] ] ] ] ] ] 13 => array:3 [ "identificador" => "bib0215" "etiqueta" => "14" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Outcome prediction in pediatric medulloblastoma based on DNA copy-number aberrations of chromosomes 6q and 17q and the MYC and MYCN loci" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "S. Pfister" 1 => "M. Remke" 2 => "A. Benner" 3 => "F. Mendrzyk" 4 => "G. Toedt" 5 => "J. Felsberg" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1200/JCO.2008.17.9432" "Revista" => array:6 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2009" "volumen" => "27" "paginaInicial" => "1627" "paginaFinal" => "1636" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19255330" "web" => "Medline" ] ] ] ] ] ] ] ] 14 => array:3 [ "identificador" => "bib0220" "etiqueta" => "15" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "MYCN amplification predicts poor outcome for patients with supratentorial primitive neuroectodermal tumors of the central nervous system" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "M. Gessi" 1 => "A.O. von Bueren" 2 => "A. Treszl" 3 => "A.Z. Mühlen" 4 => "W. Hartmann" 5 => "M. Warmuth-Metz" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1093/neuonc/not302" "Revista" => array:6 [ "tituloSerie" => "Neuro-Oncology" "fecha" => "2014" "volumen" => "16" "paginaInicial" => "924" "paginaFinal" => "932" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/24470553" "web" => "Medline" ] ] ] ] ] ] ] ] 15 => array:3 [ "identificador" => "bib0225" "etiqueta" => "16" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Metastatic medulloblastoma in childhood: Chang's classification revisited" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "C. Dufour" 1 => "A. Beaugrand" 2 => "B. Pizer" 3 => "J. Micheli" 4 => "M.S. Aubelle" 5 => "A. Fourcade" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:4 [ "tituloSerie" => "J Surg Oncol" "fecha" => "2012" "volumen" => "2012" "paginaInicial" => "245385" ] ] ] ] ] ] 16 => array:3 [ "identificador" => "bib0230" "etiqueta" => "17" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Adjuvant chemotherapy for medulloblastoma: the first multi-centre control trial of the International Society of Paediatric Oncology (SIOP I)" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:5 [ 0 => "D.M. Tait" 1 => "H. Thornton-Jones" 2 => "H.J. Bloom" 3 => "J. Lemerle" 4 => "P. Morris-Jones" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Eur J Cancer" "fecha" => "1990" "volumen" => "26" "paginaInicial" => "464" "paginaFinal" => "469" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/2141512" "web" => "Medline" ] ] ] ] ] ] ] ] 17 => array:3 [ "identificador" => "bib0235" "etiqueta" => "18" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Prospective randomised trial of chemotherapy given before radiotherapy in childhood medulloblastoma. International Society of Paediatric Oncology (SIOP) and the (German) Society of Paediatric Oncology (GPO): SIOP II" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "C.C. Bailey" 1 => "A. Gnekow" 2 => "S. Wellek" 3 => "M. Jones" 4 => "C. Round" 5 => "J. Brown" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Med Pediatr Oncol" "fecha" => "1995" "volumen" => "25" "paginaInicial" => "166" "paginaFinal" => "178" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7623725" "web" => "Medline" ] ] ] ] ] ] ] ] 18 => array:3 [ "identificador" => "bib0240" "etiqueta" => "19" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Results of a randomized Study of preradiation chemotherapy versus radiotherapy alone for nonmetastatic medulloblastoma: the international Society of Paediatric Onoclogy/United Kingdom Children's Cancer Study group-Pnet 3 Study" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "R.E. Taylor" 1 => "C.C. Bailey" 2 => "K. Robinson" 3 => "C.L. Weston" 4 => "D. Ellison" 5 => "J. Ironside" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1200/JCO.2003.05.116" "Revista" => array:6 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2003" "volumen" => "21" "paginaInicial" => "1581" "paginaFinal" => "1591" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/12697884" "web" => "Medline" ] ] ] ] ] ] ] ] 19 => array:3 [ "identificador" => "bib0245" "etiqueta" => "20" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Hyperfractionated versus conventional radiotherapy followed by chemotherapy in standard-risk medulloblastoma: results from the randomized multicenter HIT-SIOP PNET 4 trial" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "B. Lannering" 1 => "S. Rutkowski" 2 => "F. Doz" 3 => "B. Pizer" 4 => "G. Gustafsson" 5 => "A. Navajas" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1200/JCO.2011.39.8719" "Revista" => array:6 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2012" "volumen" => "30" "paginaInicial" => "3187" "paginaFinal" => "3193" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/22851561" "web" => "Medline" ] ] ] ] ] ] ] ] 20 => array:3 [ "identificador" => "bib0250" "etiqueta" => "21" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Hyperfractionated accelerated radiotherapy in the Milan strategy for metastatic medulloblastoma" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "L. Gandola" 1 => "M. Massimino" 2 => "G. Cefalo" 3 => "C. Solero" 4 => "F. Spreafico" 5 => "E. Pecori" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2009" "volumen" => "27" "paginaInicial" => "566" "paginaFinal" => "571" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/27960724" "web" => "Medline" ] ] ] ] ] ] ] ] 21 => array:3 [ "identificador" => "bib0255" "etiqueta" => "22" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Phase III study of craniospinal radiation therapy followed by adjuvant chemotherapy for newly diagnosed average-risk medulloblastoma" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "R.J. Packer" 1 => "A. Gajjar" 2 => "G. Vezina" 3 => "L. Rorke-Adams" 4 => "P.C. Burger" 5 => "P.L. Robertson" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1200/JCO.2006.06.4980" "Revista" => array:6 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2006" "volumen" => "24" "paginaInicial" => "4202" "paginaFinal" => "4208" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/16943538" "web" => "Medline" ] ] ] ] ] ] ] ] 22 => array:3 [ "identificador" => "bib0260" "etiqueta" => "23" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Outcome of children with metastatic medulloblastoma treated with carboplatin during craniospinal radiotherapy: a children oncology group phase I/II study" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "R.I. Jakacki" 1 => "P.C. Burger" 2 => "T. Zhou" 3 => "E.J. Holmes" 4 => "M. Kocak" 5 => "A. Onar" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "J Clin Oncol" "fecha" => "2012" "volumen" => "20" "paginaInicial" => "2648" "paginaFinal" => "2653" ] ] ] ] ] ] 23 => array:3 [ "identificador" => "bib0265" "etiqueta" => "24" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "A phase <span class="elsevierStyleSmallCaps">ii</span> study of preradiotherapy chemotherapy followed by hyperfractionated radiotherapy for newly diagnosed high-risk medulloblastoma/primitive neuroectodermal tumor: a report from the Children's Oncology Group (CCG 9931)" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "J. Allen" 1 => "B. Donahue" 2 => "M. Mehta" 3 => "D.C. Miller" 4 => "L.B. Rorke" 5 => "R. Jakacki" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.ijrobp.2008.09.019" "Revista" => array:6 [ "tituloSerie" => "Int J Radiat Oncol Biol Phys" "fecha" => "2009" "volumen" => "74" "paginaInicial" => "1006" "paginaFinal" => "1011" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19356859" "web" => "Medline" ] ] ] ] ] ] ] ] 24 => array:3 [ "identificador" => "bib0270" "etiqueta" => "25" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Risk-adapted craniospinal radiotherapy followed by high-dose chemotherapy and stem-cell rescue in children with newly diagnosed medulloblastoma (St Jude Medulloblastoma-96): long-term results from a prospective, multicentre trial" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "A. Gajjar" 1 => "M. Chintagumpala" 2 => "D. Ashley" 3 => "S. Kellie" 4 => "L.E. Kun" 5 => "T.E. Merchant" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/S1470-2045(06)70867-1" "Revista" => array:6 [ "tituloSerie" => "Lancet Oncol" "fecha" => "2006" "volumen" => "7" "paginaInicial" => "813" "paginaFinal" => "820" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/17012043" "web" => "Medline" ] ] ] ] ] ] ] ] 25 => array:3 [ "identificador" => "bib0275" "etiqueta" => "26" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Medulloblastoma variants: age-dependent occurrence and relation to Gorlin síndrome—a new clinical perspective" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "M.L. Garrè" 1 => "A. Cama" 2 => "F. Bagnasco" 3 => "G. Morana" 4 => "F. Giangaspero" 5 => "M. Brisigotti" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1158/1078-0432.CCR-08-2023" "Revista" => array:6 [ "tituloSerie" => "Clin Cancer Res" "fecha" => "2009" "volumen" => "15" "paginaInicial" => "2463" "paginaFinal" => "2471" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19276247" "web" => "Medline" ] ] ] ] ] ] ] ] 26 => array:3 [ "identificador" => "bib0280" "etiqueta" => "27" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Cáncer Infantil en España. Informe preliminar estadísticas 1980–2013. Registro Nacional de Tumores Infantiles, Sociedad Española de Hematología y Oncología Pediátrica (RNTI-SEHOP)" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:5 [ 0 => "R. Peris Bonet" 1 => "S. Felipe García" 2 => "N. Martínez Ruiz" 3 => "E. Pardo Romaguera" 4 => "S. Valero Poveda" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Libro" => array:3 [ "fecha" => "2014" "editorial" => "Universitat de València" "editorialLocalizacion" => "Valencia, España" ] ] ] ] ] ] 27 => array:3 [ "identificador" => "bib0285" "etiqueta" => "28" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT’91" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "K. Von Hoff" 1 => "B. Hinkes" 2 => "N.U. Gerber" 3 => "F. Deinlein" 4 => "U. Mittler" 5 => "C. Urban" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.ejca.2009.01.015" "Revista" => array:6 [ "tituloSerie" => "Eur J Cancer" "fecha" => "2009" "volumen" => "45" "paginaInicial" => "1209" "paginaFinal" => "1217" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19250820" "web" => "Medline" ] ] ] ] ] ] ] ] 28 => array:3 [ "identificador" => "bib0290" "etiqueta" => "29" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Prognostic significance of clinical, histopathological, and molecular characteristics of medulloblastomas in the prospective HIT2000 multicenter clinical trial cohort" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "T. Pietsch" 1 => "R. Schmidt" 2 => "M. Remke" 3 => "A. Korshunov" 4 => "V. Hovestadt" 5 => "D.T. Jones" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1007/s00401-014-1276-0" "Revista" => array:6 [ "tituloSerie" => "Acta Neuropathol" "fecha" => "2014" "volumen" => "128" "paginaInicial" => "137" "paginaFinal" => "149" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/24791927" "web" => "Medline" ] ] ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/23412879/0000008600000001/v1_201612270102/S2341287916301417/v1_201612270102/en/main.assets" "Apartado" => array:4 [ "identificador" => "26005" "tipo" => "SECCION" "en" => array:2 [ "titulo" => "Original Articles" "idiomaDefecto" => true ] "idiomaDefecto" => "en" ] "PDF" => "https://static.elsevier.es/multimedia/23412879/0000008600000001/v1_201612270102/S2341287916301417/v1_201612270102/en/main.pdf?idApp=UINPBA00005H&text.app=https://analesdepediatria.org/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2341287916301417?idApp=UINPBA00005H" ]
Year/Month | Html | Total | |
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2024 November | 19 | 9 | 28 |
2024 October | 117 | 50 | 167 |
2024 September | 101 | 30 | 131 |
2024 August | 124 | 69 | 193 |
2024 July | 145 | 40 | 185 |
2024 June | 278 | 39 | 317 |
2024 May | 100 | 47 | 147 |
2024 April | 81 | 35 | 116 |
2024 March | 107 | 27 | 134 |
2024 February | 97 | 38 | 135 |
2024 January | 122 | 34 | 156 |
2023 December | 177 | 23 | 200 |
2023 November | 108 | 25 | 133 |
2023 October | 90 | 27 | 117 |
2023 September | 89 | 25 | 114 |
2023 August | 67 | 21 | 88 |
2023 July | 75 | 25 | 100 |
2023 June | 79 | 34 | 113 |
2023 May | 127 | 28 | 155 |
2023 April | 62 | 23 | 85 |
2023 March | 113 | 26 | 139 |
2023 February | 88 | 21 | 109 |
2023 January | 68 | 21 | 89 |
2022 December | 92 | 34 | 126 |
2022 November | 89 | 36 | 125 |
2022 October | 74 | 39 | 113 |
2022 September | 61 | 39 | 100 |
2022 August | 56 | 42 | 98 |
2022 July | 42 | 31 | 73 |
2022 June | 66 | 31 | 97 |
2022 May | 58 | 46 | 104 |
2022 April | 73 | 43 | 116 |
2022 March | 126 | 58 | 184 |
2022 February | 76 | 36 | 112 |
2022 January | 74 | 55 | 129 |
2021 December | 68 | 54 | 122 |
2021 November | 72 | 66 | 138 |
2021 October | 82 | 73 | 155 |
2021 September | 70 | 36 | 106 |
2021 August | 82 | 49 | 131 |
2021 July | 104 | 48 | 152 |
2021 June | 89 | 56 | 145 |
2021 May | 109 | 55 | 164 |
2021 April | 252 | 98 | 350 |
2021 March | 135 | 53 | 188 |
2021 February | 83 | 28 | 111 |
2021 January | 103 | 33 | 136 |
2020 December | 107 | 36 | 143 |
2020 November | 71 | 21 | 92 |
2020 October | 69 | 25 | 94 |
2020 September | 80 | 29 | 109 |
2020 August | 161 | 18 | 179 |
2020 July | 130 | 16 | 146 |
2020 June | 136 | 28 | 164 |
2020 May | 125 | 27 | 152 |
2020 April | 43 | 21 | 64 |
2020 March | 39 | 18 | 57 |
2020 February | 40 | 22 | 62 |
2020 January | 41 | 16 | 57 |
2019 December | 68 | 32 | 100 |
2019 November | 36 | 14 | 50 |
2019 October | 51 | 15 | 66 |
2019 September | 62 | 16 | 78 |
2019 August | 76 | 15 | 91 |
2019 July | 69 | 40 | 109 |
2019 June | 66 | 45 | 111 |
2019 May | 73 | 35 | 108 |
2019 April | 101 | 40 | 141 |
2019 March | 58 | 22 | 80 |
2019 February | 65 | 19 | 84 |
2019 January | 63 | 19 | 82 |
2018 December | 70 | 28 | 98 |
2018 November | 113 | 27 | 140 |
2018 October | 114 | 30 | 144 |
2018 September | 55 | 11 | 66 |
2018 August | 2 | 0 | 2 |
2018 July | 2 | 0 | 2 |
2018 June | 2 | 0 | 2 |
2018 May | 3 | 0 | 3 |
2018 April | 29 | 0 | 29 |
2018 March | 29 | 0 | 29 |
2018 February | 11 | 0 | 11 |
2018 January | 25 | 0 | 25 |
2017 December | 14 | 0 | 14 |
2017 November | 17 | 0 | 17 |
2017 October | 18 | 0 | 18 |
2017 September | 23 | 0 | 23 |
2017 August | 12 | 0 | 12 |
2017 July | 22 | 1 | 23 |
2017 June | 43 | 17 | 60 |
2017 May | 41 | 13 | 54 |
2017 April | 93 | 77 | 170 |
2017 March | 23 | 26 | 49 |
2017 February | 14 | 9 | 23 |
2017 January | 37 | 18 | 55 |
2016 December | 2 | 9 | 11 |