Literature DB >> 28818704

Orphan Drug Regulation: A missed opportunity for children and adolescents with cancer.

Gilles Vassal1, Pam Kearns2, Patricia Blanc3, Nicole Scobie4, Delphine Heenen5, Andy Pearson6.   

Abstract

BACKGROUND: Oncology represents a major sector in the field of orphan drug development in Europe. The objective was to evaluate whether children and adolescents with cancer benefited from the Orphan Drug Regulation.
METHODS: Data on orphan drug designations (ODDs) and registered orphan drugs from 8th August 2000 to 10th September 2016 were collected from the Community Register of medicinal products for human use. Assessment history, product information and existence of paediatric investigation plans were searched and retrieved from the European Medicine Agency website.
RESULTS: Over 16 years, 272 of 657 oncology ODDs (41%) concerned a malignant condition occurring both in adults and children. The five most common were acute myeloid leukaemia, high-grade glioma, acute lymphoblastic leukaemia, graft-versus-host disease and soft-tissue sarcomas. 74% of 31 marketing authorisations (MAs) for an indication both in adults and children (26 medicines) had no information for paediatric use in their Summary of Product Characteristics (SmPC) at the time of the first MA. Furthermore, 68% still have no paediatric information in their most recently updated SmPC, at a median of 7 years after. Only 15 ODDs (2%) pertained to a malignancy occurring specifically in children and only two drugs received an MA: Unituxin for high-risk neuroblastoma and Votubia for sub-ependymal giant-cell astrocytoma.
CONCLUSION: The Orphan Drug Regulation failed to promote the development of innovative therapies for malignancies occurring in children. Major delays and waivers occurred through the application of the Paediatric Medicines Regulation. The European regulatory environment needs to be improved to accelerate innovation for children and adolescents dying of cancer.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Childhood cancer; New drugs; Orphan

Mesh:

Substances:

Year:  2017        PMID: 28818704     DOI: 10.1016/j.ejca.2017.07.021

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  3 in total

1.  Updated clinical and biological information from the two-stage phase II study of imatinib mesylate in subjects with relapsed/refractory neuroblastoma.

Authors:  Fabio Morandi; Loredana Amoroso; Alessandra Dondero; Roberta Castriconi; Stefano Parodi; Roberto Luksch; Fiorina Casale; Aurora Castellano; Alberto Garaventa; Alessandro Moretta; Cristina Bottino; Mirco Ponzoni; Maria Valeria Corrias
Journal:  Oncoimmunology       Date:  2018-07-30       Impact factor: 8.110

2.  Health technology assessment and reimbursement policy for oncology orphan drugs in Central and Eastern Europe.

Authors:  Krzysztof Piotr Malinowski; Paweł Kawalec; Wojciech Trąbka; Christoph Sowada; Guenka Petrova; Manoela Manova; Alexandra Savova; Pero Draganić; Juraj Slabý; Agnes Männik; Kristóf Márky; Zinta Rugaja; Jolanta Gulbinovic; Tomas Tesar; Marian Sorin Paveliu
Journal:  Orphanet J Rare Dis       Date:  2020-10-08       Impact factor: 4.123

3.  Rationale of the rare cancer list: a consensus paper from the Joint Action on Rare Cancers (JARC) of the European Union (EU).

Authors:  Paolo G Casali; Annalisa Trama
Journal:  ESMO Open       Date:  2020-03
  3 in total

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