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Immune Checkpoint Inhibitor Rechallenge After Immune-Related Adverse Events in Patients With Cancer

Authors :
Franck Thuny
Sophie Fedrizzi
Véronique Lelong-Boulouard
Charles Dolladille
Jennifer Cautela
Marion Sassier
Angélique Da-Silva
Damien Legallois
Paul Milliez
Stéphane Ederhy
Anne-Flore Plane
Basile Chrétien
Joachim Alexandre
Ariel Cohen
CHU Caen
Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Département de Pharmacologie [CHU Caen]
Université de Caen Normandie (UNICAEN)
Normandie Université (NU)-Normandie Université (NU)-CHU Caen
Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN)
Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN)
Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Normandie Université (NU)
Source :
JAMA oncology, JAMA oncology, American Medical Association, 2020, 6 (6), pp.865. ⟨10.1001/jamaoncol.2020.0726⟩, JAMA oncology, 2020, 6 (6), pp.865. ⟨10.1001/jamaoncol.2020.0726⟩, JAMA Oncol
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

International audience; Importance Limited information is available on the safety of a rechallenge with an immune checkpoint inhibitor (ICI) after an immune-related adverse event (irAE). Objective To identify the recurrence rate of the same irAE that prompted discontinuation of ICI therapy after an ICI rechallenge in patients with cancer and to identify the clinical features associated with such recurrences. Design, Setting, and Participants This observational, cross-sectional, pharmacovigilance cohort study examined individual case safety reports from the World Health Organization database VigiBase, which contains case reports from more than 130 countries. Case reports were extracted from database inception (1967) to September 1, 2019. All consecutive ICI cases with at least 1 associated irAE were included. Main Outcomes and Measures The primary outcome was the rate of recurrence of the initial irAE after an ICI rechallenge. Secondary outcomes included the factors associated with the recurrence after a rechallenge among informative rechallenges, the recurrence rate according to the ICI regimen (anti-programmed cell death 1 or anti-programmed cell death ligand 1 monotherapy, anti-cytotoxic T-lymphocyte antigen-4 monotherapy, or combination therapy), and the rate of occurrence of a different irAE after a rechallenge. Results A total of 24 079 irAE cases associated with at least 1 ICI were identified. Among the irAEs, 452 of 6123 irAEs associated with ICI rechallenges (7.4%) were informative rechallenges. One hundred thirty recurrences (28.8%; 95% CI, 24.8-33.1) of the initial irAE were observed. In a rechallenge, colitis (reporting odds ratio [OR], 1.77; 95% CI, 1.14-2.75; P = .01), hepatitis (reporting OR, 3.38; 95% CI, 1.31-8.74; P = .01), and pneumonitis (reporting OR, 2.26; 95% CI, 1.18-4.32; P = .01) were associated with a higher recurrence rate, whereas adrenal events were associated with a lower recurrence rate (reporting OR, 0.33; 95% CI, 0.13-0.86; P = .03) compared with other irAEs. Conclusions and Relevance This cohort study found a 28.8% recurrence rate of the same irAE associated with the discontinuation of ICI therapy after a rechallenge with the same ICI. Resuming ICI therapy could be considered for select patients, with appropriate monitoring and use of standard treatment algorithms to identify and treat toxic effects.

Details

Language :
English
ISSN :
23742437
Database :
OpenAIRE
Journal :
JAMA oncology, JAMA oncology, American Medical Association, 2020, 6 (6), pp.865. ⟨10.1001/jamaoncol.2020.0726⟩, JAMA oncology, 2020, 6 (6), pp.865. ⟨10.1001/jamaoncol.2020.0726⟩, JAMA Oncol
Accession number :
edsair.doi.dedup.....3bed097e6d0d18b235d0bb13fa69ed48
Full Text :
https://doi.org/10.1001/jamaoncol.2020.0726⟩