[Acceptability and effectiveness of immunotherapy in patients with melanoma].

Acceptabilité et efficacité des immunothérapies dans le traitement du mélanome.

Journal

Therapie
ISSN: 1958-5578
Titre abrégé: Therapie
Pays: France
ID NLM: 0420544

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 03 04 2018
revised: 18 05 2018
accepted: 22 05 2018
pubmed: 9 9 2018
medline: 28 12 2019
entrez: 9 9 2018
Statut: ppublish

Résumé

The immunotherapies known as "inhibitors of checkpoint" (ICP) are monoclonal antibodies used since 2010 and have dramatically modified the management of the advanced or metastatic melanomas. By reactivating the anti-tumoral immune response, these antibodies can activate the immune system in all the tissues with a risk to induce immune related adverse events (IrAE). Thus, the adverse effect's profile of ICP is considered as very different from that usually associated with conventional chemotherapies. The objectives of our retrospective monocentric study were the evaluation of the real life's safety and efficiency of the ipilimumab and the pembrolizumab in patients with an advanced melanoma. Seventy-two patients treated by ipilimumab and\or pembrolizumab between August 1st, 2008 and December 31st, 2016 were investigated. The main IrAE occurring involved the gastro- intestinal, skin, and the endocrine systems. The average onset time of IrAE was 39, 104 and 68 days, respectively and their respective duration was of 67, 50 and 111 days. There were 13 events of grade III and IV along with one death. The overall survival was 5 months for the patients treated in monotherapy with ipilimumab, and 14 months for those treated by pembrolizumab. Our real life's study tends to confirm the current safety profile of ICP treatment. Moreover and according to our analyses, the drug sequence seems to have a global survival impact.

Identifiants

pubmed: 30193804
pii: S0040-5957(18)30123-9
doi: 10.1016/j.therap.2018.05.003
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
Ipilimumab 0
pembrolizumab DPT0O3T46P

Types de publication

Journal Article

Langues

fre

Sous-ensembles de citation

IM

Pagination

355-367

Informations de copyright

Copyright © 2018 Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Marie-Blanche Valnet-Rabier (MB)

Centre régional de pharmacovigilance, CHU de Besançon, 25030 Besançon, France. Electronic address: mbrabier@chu-besancon.fr.

Charles Marcucci (C)

Pôle pharmaceutique, CHU de Besançon, 25030 Besançon, France.

Samuel Limat (S)

Pôle pharmaceutique, CHU de Besançon, 25030 Besançon, France; Inserm, EFS BFC, UMR1098, interactions hôte-greffon-tumeur/ingénierie cellulaire et génique, université Bourgogne Franche-Comté, 25000 Besançon, France.

Siamak Davani (S)

Centre régional de pharmacovigilance, CHU de Besançon, 25030 Besançon, France.

François Aubin (F)

Service de dermatologie, CHU de Besançon, 25030 Besançon, France.

Virginie Nerich (V)

Pôle pharmaceutique, CHU de Besançon, 25030 Besançon, France; Inserm, EFS BFC, UMR1098, interactions hôte-greffon-tumeur/ingénierie cellulaire et génique, université Bourgogne Franche-Comté, 25000 Besançon, France.

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Classifications MeSH