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Renal toxicities associated with pembrolizumab

Authors :
David Malka
Alexis Mathian
Olivier Lambotte
Hassan Izzedine
Zahir Amoura
Andrea Varga
Sihem Kaaki
Christine Mateus
Alexandra Leary
Jean-Charles Soria
Isabelle Brocheriou
Aurélien Marabelle
Stéphane Champiat
Jean-Michel Goujon
Emilie Routier
Cécile Picard
Nathalie Quellard
Judith Michels
Jean-Marie Michot
Université Paris-Est Créteil Val-de-Marne - Faculté de médecine (UPEC Médecine)
Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Institut Mondor de Recherche Biomédicale (IMRB)
Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Service de médecine interne [CHU Pitié-Salpétrière]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Pitié-Salpêtrière [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)
Département d’Innovation Thérapeutique et essais précoces [Gustave Roussy] (DITEP)
Institut Gustave Roussy (IGR)
Service d'Anatomie et cytologie pathologiques = Service de Pathologie [CHU Pitié-Salpêtrière] (ACP)
CHU Pitié-Salpêtrière [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Département Interdisciplinaire de Soins de Support aux Patients en Onco-hématologie [Gustave Roussy] (DISSPO)
Oncologie dermatologique
Département de médecine oncologique [Gustave Roussy]
Institut Gustave Roussy (IGR)-Institut Gustave Roussy (IGR)
Oncologie digestive
Oncologie gynécologique
AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre)
Centre hospitalier universitaire de Poitiers (CHU Poitiers)
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Service de pathologie [CHU Pitié-Salpêtrière]
Source :
Clinical Kidney Journal, Clinical Kidney Journal, 2019, 12 (1), pp.81-88. ⟨10.1093/ckj/sfy100⟩, Clinical Kidney Journal, Oxford University Press, 2019, 12 (1), pp.81-88. ⟨10.1093/ckj/sfy100⟩
Publication Year :
2018
Publisher :
Oxford University Press (OUP), 2018.

Abstract

International audience; Objective : Expanded clinical experience with patients treated by pembrolizumab has accumulated. However, renal toxicities associated with this anti-programmed cell death 1 agent are poorly described because kidney histology is rarely sought. As a nephrology referral centre, we aimed to describe the clinic-biological and histopathological characteristics of pembrolizumab-related nephropathy and its response to treatment.Methods : We conducted a monocentric large case series study, including all pembrolizumab-treated cancer patients presenting a renal toxicity addressed to our centre from 2015 to 2017.Results : A total of 12 patients (7 men) out of 676 pembrolizumab-treated patients (incidence 1.77%) were included (median age 69.75 years). Patients were referred for acute kidney injury (n = 10) and/or proteinuria (n = 2). A kidney biopsy was performed in all patients, with a median duration of use of 9 months (range 1-24 months) after the beginning of treatment. Biopsy showed that four patients had acute interstitial nephritis (AIN), whereas five had acute tubular injury (ATI) alone, one had minimal change disease (MCD) and ATI, and one had MCD alone. Pembrolizumab withdrawal coupled with corticosteroid therapy was the most effective treatment for kidney function recovery. Drug reintroduction resulted in a more severe recurrence of AIN in one patient who required maintenance of pembrolizumab. Two patients died of cancer progression with one of them developing severe renal failure requiring dialysis.Conclusion : In our series, ATI, AIN and MCD are the most frequent forms of kidney involvement under pembrolizumab therapy. Kidney dysfunction is usually isolated but can be severe. Use of corticosteroids in case of AIN improves the glomerular filtration rate.

Details

ISSN :
20488513 and 20488505
Volume :
12
Database :
OpenAIRE
Journal :
Clinical Kidney Journal
Accession number :
edsair.doi.dedup.....739d954e8a2373b75a44dd1dcf20c321
Full Text :
https://doi.org/10.1093/ckj/sfy100