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a foreign drug and later on an orphan drug for treatment of multiple myeloma authorised by the European Medicines Agency &#40;EMA&#41; since 2001&#46; Its exceptional and controlled use has also been authorised for other diseases&#44; such as erythema nodosum or actinic prurigo&#44; when there are no other treatment options&#46; In multiple myeloma in particular&#44; one of its derivatives&#44; lenalidomide&#44; which is authorised for use in Spain&#44; has been replacing thalidomide in many cases&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Contrary to its initial marketing authorisation&#44; the prescription and dispensation of thalidomide are now restricted to a single authorised indication &#40;first-line treatment&#44; in combination with melphalan and prednisone&#44; in patients with untreated multiple myeloma&#44; aged &#8805;65 years or ineligible for high-dose chemotherapy&#41; and subject to a strict pregnancy prevention programme &#40;PPE&#41; and controlled access system &#40;AEMPS&#41;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a>&#58; the same surveillance and control system established for thalidomide analogues with more recent marketing authorisations&#44; such as lenalidomide and pomalidomide&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In fact&#44; the system calls for strict safety requirements&#44; and it is similar to the one established by the Food and Drug Administration &#40;FDA&#41; to prevent teratogenicity&#44; the System for Thalidomide Education and Prescribing Safety &#40;STEPS&#41;&#44; which was implemented in 1998 with the initial approval in the United States of thalidomide as an orphan drug for treatment of erythema nodosum&#44; which was then extended to multiple myeloma&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> It is worth mentioning that&#44; paradoxically&#44; in the 1960s the United States had rejected the initial application submitted by Chemie Gr&#252;nenthal for the marketing of thalidomide for symptomatic treatment of nausea and vomiting during pregnancy due to a lack of safety data&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">We ought to remember that the teratogenic effects that affected more than 10&#44;000 newborns worldwide marked a turning point in the process of authorization and marketing of drugs for human use&#44; setting the foundations of the current system for monitoring the safety of drugs pre and post marketing &#40;drug surveillance&#41; and specifically recommendations concerning use during pregnancy and&#47;breastfeeding &#40;international classification of pregnancy categories for drugs based on foetal risk&#41;&#46; These are indispensable principles today for conducting preclinical and clinical research on new drugs&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Still&#44; what has happened in the past 10 years to the individuals affected by thalidomide in Spain&#63;</p><p id="par0035" class="elsevierStylePara elsevierViewall">At present&#44; in our country&#44; contrary to Germany&#44; the Netherlands or Portugal&#44; where all thalidomide victims have been awarded compensation&#44; the Association of Victims of Thalidomide of Spain &#40;AVITE&#41; is still fighting to gain recognition for affected survivors &#40;more than 300&#41; and compensation for individuals born with malformations known to result from thalidomide exposure between the 1950s and 1985 &#40;Royal Decree of 2018&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Financial support payments should have been effected in 2019&#44; but the benefits were never paid due to noncompliance with Law 6&#47;2018 on the General State Budget&#46; In response to this&#44; AVITE filed a suit against the government and the state&#44; but since the cassation appeal was dismissed by the Supreme Court of Spain&#44; it has announced future demonstrations once the political campaigns for the upcoming elections start to claim the payment of due compensations&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The story goes on&#8230;</p></span>"
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Letter to the Editor
Thalidomide, the story goes on
Talidomida, la historia continúa
Esther Papaseita,b, Magí Farréa,b, Óscar Garcia-Algarc,d,
Corresponding author
ogarciaa@clinic.cat

Corresponding author.
a Servicio de Farmacología Clínica, Hospital Universitari Germans Trias i Pujol i Institut de Recerca Germans Trias i Pujol (HUGTiP-IGTP), Badalona, Barcelona, Spain
b Universitat Autònoma de Barcelona (UAB), Cerdanyola del Vallès, Barcelona, Spain
c Servicio de Neonatología, ICGON, Hospital Clínic-Maternitat, IDIBAPS, Barcelona, Spain
d Universidad de Barcelona, Barcelona, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">It has been almost 10 years since we published an editorial in <span class="elsevierStyleItalic">Anales de Pediatr&#237;a</span> under the title &#8220;Thalidomide&#58; an unfinished history&#8221;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> After this time interval&#44; recently there have been news about the reauthorisation for the marketing of thalidomide in Spain&#44; and&#44; as regards those affected by it&#44; the story remains unfinished 10 years later&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Sixty years after the discovery of the severe teratogenic effects of thalidomide&#44; the drug is once again being marketed in Spain since February 2&#44; 2023 &#40;Spanish Agency of Medicines and Medical Devices&#44; AEMPS&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> To date it had only been available as a drug subject to special medical control since 1985&#44; a foreign drug and later on an orphan drug for treatment of multiple myeloma authorised by the European Medicines Agency &#40;EMA&#41; since 2001&#46; Its exceptional and controlled use has also been authorised for other diseases&#44; such as erythema nodosum or actinic prurigo&#44; when there are no other treatment options&#46; In multiple myeloma in particular&#44; one of its derivatives&#44; lenalidomide&#44; which is authorised for use in Spain&#44; has been replacing thalidomide in many cases&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Contrary to its initial marketing authorisation&#44; the prescription and dispensation of thalidomide are now restricted to a single authorised indication &#40;first-line treatment&#44; in combination with melphalan and prednisone&#44; in patients with untreated multiple myeloma&#44; aged &#8805;65 years or ineligible for high-dose chemotherapy&#41; and subject to a strict pregnancy prevention programme &#40;PPE&#41; and controlled access system &#40;AEMPS&#41;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a>&#58; the same surveillance and control system established for thalidomide analogues with more recent marketing authorisations&#44; such as lenalidomide and pomalidomide&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In fact&#44; the system calls for strict safety requirements&#44; and it is similar to the one established by the Food and Drug Administration &#40;FDA&#41; to prevent teratogenicity&#44; the System for Thalidomide Education and Prescribing Safety &#40;STEPS&#41;&#44; which was implemented in 1998 with the initial approval in the United States of thalidomide as an orphan drug for treatment of erythema nodosum&#44; which was then extended to multiple myeloma&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> It is worth mentioning that&#44; paradoxically&#44; in the 1960s the United States had rejected the initial application submitted by Chemie Gr&#252;nenthal for the marketing of thalidomide for symptomatic treatment of nausea and vomiting during pregnancy due to a lack of safety data&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">We ought to remember that the teratogenic effects that affected more than 10&#44;000 newborns worldwide marked a turning point in the process of authorization and marketing of drugs for human use&#44; setting the foundations of the current system for monitoring the safety of drugs pre and post marketing &#40;drug surveillance&#41; and specifically recommendations concerning use during pregnancy and&#47;breastfeeding &#40;international classification of pregnancy categories for drugs based on foetal risk&#41;&#46; These are indispensable principles today for conducting preclinical and clinical research on new drugs&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Still&#44; what has happened in the past 10 years to the individuals affected by thalidomide in Spain&#63;</p><p id="par0035" class="elsevierStylePara elsevierViewall">At present&#44; in our country&#44; contrary to Germany&#44; the Netherlands or Portugal&#44; where all thalidomide victims have been awarded compensation&#44; the Association of Victims of Thalidomide of Spain &#40;AVITE&#41; is still fighting to gain recognition for affected survivors &#40;more than 300&#41; and compensation for individuals born with malformations known to result from thalidomide exposure between the 1950s and 1985 &#40;Royal Decree of 2018&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Financial support payments should have been effected in 2019&#44; but the benefits were never paid due to noncompliance with Law 6&#47;2018 on the General State Budget&#46; In response to this&#44; AVITE filed a suit against the government and the state&#44; but since the cassation appeal was dismissed by the Supreme Court of Spain&#44; it has announced future demonstrations once the political campaigns for the upcoming elections start to claim the payment of due compensations&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The story goes on&#8230;</p></span>"
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ISSN: 23412879
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Idiomas
Anales de Pediatría (English Edition)