[Reporting data of patients receiving CAR T cell therapy into the EBMT registry: Guidelines of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)].
Saisie des données des patients faisant l’objet d’un traitement par cellules CAR-T : recommandations de la Société Francophone de Greffe de Moelle et de Thérapie Cellulaire (SFGM-TC).
Antigens, CD19
/ therapeutic use
Biological Products
Bone Marrow Transplantation
Congresses as Topic
Data Collection
/ methods
Databases, Factual
Europe
Follow-Up Studies
Humans
Immunotherapy, Adoptive
/ statistics & numerical data
Receptors, Antigen, T-Cell
/ therapeutic use
Registries
Societies, Medical
Time Factors
Car-T
Date entry
MACRO
ProMISe
Saisie de données
Journal
Bulletin du cancer
ISSN: 1769-6917
Titre abrégé: Bull Cancer
Pays: France
ID NLM: 0072416
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
07
10
2019
accepted:
19
10
2019
pubmed:
14
12
2019
medline:
29
12
2020
entrez:
14
12
2019
Statut:
ppublish
Résumé
Tisagenlecleucel (Kymriah™) and axicabtagene ciloleucel (Yescarta™) are the first two approved drug products that belong to of a new class of therapies manufactured through an industrial process that includes the ex vivo genetic modification of human autologous T lymphocytes with viral vectors. Since CAR-T Cells qualify as gene therapy medicinal products, there is a requirement for long-term (15 years) follow-up of treated patients. As part of a global initiative aiming at a better use of continental registries to study the outcome of homogeneous groups of patients, EMA issued a positive opinion on the use of the EBMT registry to capture LTFU of patients treated with CAR-T Cell in EU Member states. The use of a European registry will provide a global view of this new field across EU countries and across diverse indications, and bears advantages over the use of registries dedicated to specific categories of diseases, or national registries. This is an important asset to fully measure the medical value of these innovative therapies in real-life conditions, and assess whether pricing is fully justified. To fulfill EMA requirements, as well as requirements from Pharma companies, EBMT has designed a new Cellular Therapy Med-A form that allows to capture the essential information on the administered drug product, disease and patient. Registering patients and capturing follow-up data is already possible in Promise, and will be made easier when the full migration of the EBMT database from Promise to MACRO is completed in the forthcoming weeks. Negotiations are ongoing with all interested parties including patients to define in which conditions data will be accessed and analyzed; the underlying principle is to favor rather than restrict the use of data, with a view to build cooperative projects involving relevant cooperative groups and professional associations. Here, we present practical recommendations issued by SFGM-TC to help data managers capture information related to patients treated with CAR-T Cells.
Identifiants
pubmed: 31831153
pii: S0007-4551(19)30375-3
doi: 10.1016/j.bulcan.2019.10.003
pii:
doi:
Substances chimiques
Antigens, CD19
0
Biological Products
0
Receptors, Antigen, T-Cell
0
tisagenlecleucel
Q6C9WHR03O
axicabtagene ciloleucel
U2I8T43Y7R
Types de publication
Journal Article
Practice Guideline
Langues
fre
Sous-ensembles de citation
IM
Pagination
S178-S184Informations de copyright
Copyright © 2019. Published by Elsevier Masson SAS.