[Acceptability and effectiveness of immunotherapy in patients with melanoma].
Acceptabilité et efficacité des immunothérapies dans le traitement du mélanome.
Adult
Aged
Aged, 80 and over
Antibodies, Monoclonal, Humanized
/ administration & dosage
Antineoplastic Agents, Immunological
/ administration & dosage
Female
Humans
Immunotherapy
/ adverse effects
Ipilimumab
/ administration & dosage
Male
Melanoma
/ drug therapy
Middle Aged
Retrospective Studies
Skin Neoplasms
/ drug therapy
Survival Rate
Time Factors
Advanced melanoma
Adverse effects
Drug safety
Effets indésirables
Immunotherapy
Immunothérapie
Mélanome avancé
Overall survival
Survie globale
Sécurité
Journal
Therapie
ISSN: 1958-5578
Titre abrégé: Therapie
Pays: France
ID NLM: 0420544
Informations de publication
Date de publication:
Jun 2019
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
355-367Informations de copyright
Copyright © 2018 Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS. All rights reserved.