Immune checkpoint blockers in solid organ transplant recipients and cancer: the INNOVATED cohort.

allograft rejection cancer immune checkpoint inhibitors lung cancer solid-organ transplant

Journal

ESMO open
ISSN: 2059-7029
Titre abrégé: ESMO Open
Pays: England
ID NLM: 101690685

Informations de publication

Date de publication:
22 Apr 2024
Historique:
received: 27 01 2024
revised: 08 03 2024
accepted: 18 03 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 23 4 2024
Statut: aheadofprint

Résumé

Patients with solid organ transplant (SOT) and solid tumors are usually excluded from clinical trials testing immune checkpoint blockers (ICB). As transplant rates are increasing, we aimed to evaluate ICB outcomes in this population, with a special focus on lung cancer. We conducted a multicenter retrospective cohort study collecting real data of ICB use in patients with SOT and solid tumors. Clinical data and treatment outcomes were assessed by using retrospective medical chart reviews in every participating center. Study endpoints were: overall response rate (ORR), 6-month progression-free survival (PFS), and grade ≥3 immune-related adverse events. From August 2016 to October 2022, 31 patients with SOT (98% kidney) and solid tumors were identified (36.0% lung cancer, 19.4% melanoma, 13.0% genitourinary cancer, 6.5% gastrointestinal cancer). Programmed death-ligand 1 expression was positive in 29% of tumors. Median age was 61 years, 69% were males, and 71% received ICB as first-line treatment. In the whole cohort the ORR was 45.2%, with a 6-month PFS of 56.8%. In the lung cancer cohort, the ORR was 45.5%, with a 6-month PFS of 32.7%, and median overall survival of 4.6 months. The grade 3 immune-related adverse events rate leading to ICB discontinuation was 12.9%. Allograft rejection rate was 25.8%, and risk of rejection was similar regardless of the type of ICB strategy (monotherapy or combination, 28% versus 33%, P = 1.0) or response to ICB treatment. ICB could be considered a feasible option for SOT recipients with some advanced solid malignancies and no alternative therapeutic options. Due to the risk of allograft rejection, multidisciplinary teams should be involved before ICB therapy.

Sections du résumé

BACKGROUND BACKGROUND
Patients with solid organ transplant (SOT) and solid tumors are usually excluded from clinical trials testing immune checkpoint blockers (ICB). As transplant rates are increasing, we aimed to evaluate ICB outcomes in this population, with a special focus on lung cancer.
METHODS METHODS
We conducted a multicenter retrospective cohort study collecting real data of ICB use in patients with SOT and solid tumors. Clinical data and treatment outcomes were assessed by using retrospective medical chart reviews in every participating center. Study endpoints were: overall response rate (ORR), 6-month progression-free survival (PFS), and grade ≥3 immune-related adverse events.
RESULTS RESULTS
From August 2016 to October 2022, 31 patients with SOT (98% kidney) and solid tumors were identified (36.0% lung cancer, 19.4% melanoma, 13.0% genitourinary cancer, 6.5% gastrointestinal cancer). Programmed death-ligand 1 expression was positive in 29% of tumors. Median age was 61 years, 69% were males, and 71% received ICB as first-line treatment. In the whole cohort the ORR was 45.2%, with a 6-month PFS of 56.8%. In the lung cancer cohort, the ORR was 45.5%, with a 6-month PFS of 32.7%, and median overall survival of 4.6 months. The grade 3 immune-related adverse events rate leading to ICB discontinuation was 12.9%. Allograft rejection rate was 25.8%, and risk of rejection was similar regardless of the type of ICB strategy (monotherapy or combination, 28% versus 33%, P = 1.0) or response to ICB treatment.
CONCLUSIONS CONCLUSIONS
ICB could be considered a feasible option for SOT recipients with some advanced solid malignancies and no alternative therapeutic options. Due to the risk of allograft rejection, multidisciplinary teams should be involved before ICB therapy.

Identifiants

pubmed: 38653155
pii: S2059-7029(24)00772-5
doi: 10.1016/j.esmoop.2024.103004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103004

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

J Remon (J)

Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif. Electronic address: JORDI.REMON-MASIP@gustaveroussy.fr.

E Auclin (E)

Department of Cancer Medicine, Hôpital Européen Georges-Pompidou, Paris, France.

L Zubiri (L)

Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, USA.

S Schneider (S)

Department Pneumology, Hôpital de Bayonne, Bayonne, France.

D Rodriguez-Abreu (D)

Medical Oncology Department, Complejo Hospitalario Universitario Insular-Materno Infantil de Gran Canaria, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain.

N Minatta (N)

Department of Oncology Hospital Italiano Buenos Aires, Buenos Aires, Argentina.

O Gautschi (O)

Department of Cancer Medicine, University of Berne and Cantonal Hospital of Lucerne, Lucerne, Switzerland.

F Aboubakar (F)

Department of Pneumology, Cliniques Universitaires Saint Luc, Brussels, Belgium.

E Muñoz-Couselo (E)

Department of Oncology, Hospital Vall d'Hebron de Barcelona, VHIO Vall d'Hebron Institute of Oncology, Barcelona, Spain.

T Pierret (T)

Department of Pneumology, CHU Grenoble Alpes, Grenoble, France.

S I Rothschild (SI)

Medical Oncology Department, University Hospital Basel, Basel; Division Oncology/Hematology, Department of Medicine, Cantonal Hospital Baden, Baden, Switzerland.

F Cortiula (F)

Department of Oncology, University Hospital of Udine, Udine, Italy.

K L Reynolds (KL)

Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, USA.

C Thibault (C)

Department of Cancer Medicine, Hôpital Européen Georges-Pompidou, Paris, France.

A Gavralidis (A)

Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, USA; Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston; Salem Hospital, Salem, USA.

N Blais (N)

Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.

F Barlesi (F)

Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.

D Planchard (D)

Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.

B M D Besse (BMD)

Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.

Classifications MeSH