Efficacy of First-Line Nivolumab Plus Ipilimumab in Unresectable Pleural Mesothelioma: A Multicenter Real-World Study (ImmunoMeso LATAM).

Checkpoint inhibition Immunotherapy Malignant pleural mesothelioma Nivolumab+Ipilimumab Real-world

Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
21 Sep 2024
Historique:
received: 29 06 2024
revised: 21 08 2024
accepted: 18 09 2024
medline: 19 10 2024
pubmed: 19 10 2024
entrez: 18 10 2024
Statut: aheadofprint

Résumé

The phase 3 CheckMate-743 trial demonstrated a prolonged overall survival (OS) benefit with nivolumab plus ipilimumab over chemotherapy as first-line treatment in patients with unresectable pleural mesothelioma (PM). However, given that Latin American (LATAM) patients were notably underrepresented in this trial, we retrospectively assessed the effectiveness and safety of this regimen in this population. This retrospective study included patients from 15 centers in LATAM with unresectable or metastatic PM treated with first-line nivolumab plus ipilimumab in a real-world data (RWD) scenario. Demographic, clinicopathological characteristics, and safety data were collected from medical charts. Progression-free survival (PFS), and OS were calculated using the Kaplan-Meier method. From June 2017, and January 2024 96 patients were included: epithelioid 78% (n = 75), 81% were ECOG 0-1 (n = 78). With a median follow-up of 24.1 months, median PFS and OS were 8 months (95% CI, 6.6-9.4), and 22 months (95% CI, 18.9-25), respectively. No statistical difference in OS was observed between epithelioid versus nonepithelioid histology (median 23 months vs. 19 months, respectively; P = .29). Treatment efficacy was also consistent among different clinical subgroups. Any and grade 3-4 adverse events were found in 43.1% (n = 28), and 18.5% (n = 12) of patients, respectively. Remarkably, no OS impact was observed in patients who had dose delay or treatment discontinuation due to immune-related adverse events, and those who experienced any adverse event. This multicenter RWD study demonstrated the clinically meaningful benefit of first-line ipilimumab and nivolumab in LATAM patients with unresectable or metastatic PM, and data is consistent with previous trial findings.

Sections du résumé

BACKGROUND BACKGROUND
The phase 3 CheckMate-743 trial demonstrated a prolonged overall survival (OS) benefit with nivolumab plus ipilimumab over chemotherapy as first-line treatment in patients with unresectable pleural mesothelioma (PM). However, given that Latin American (LATAM) patients were notably underrepresented in this trial, we retrospectively assessed the effectiveness and safety of this regimen in this population.
METHODS METHODS
This retrospective study included patients from 15 centers in LATAM with unresectable or metastatic PM treated with first-line nivolumab plus ipilimumab in a real-world data (RWD) scenario. Demographic, clinicopathological characteristics, and safety data were collected from medical charts. Progression-free survival (PFS), and OS were calculated using the Kaplan-Meier method.
RESULTS RESULTS
From June 2017, and January 2024 96 patients were included: epithelioid 78% (n = 75), 81% were ECOG 0-1 (n = 78). With a median follow-up of 24.1 months, median PFS and OS were 8 months (95% CI, 6.6-9.4), and 22 months (95% CI, 18.9-25), respectively. No statistical difference in OS was observed between epithelioid versus nonepithelioid histology (median 23 months vs. 19 months, respectively; P = .29). Treatment efficacy was also consistent among different clinical subgroups. Any and grade 3-4 adverse events were found in 43.1% (n = 28), and 18.5% (n = 12) of patients, respectively. Remarkably, no OS impact was observed in patients who had dose delay or treatment discontinuation due to immune-related adverse events, and those who experienced any adverse event.
CONCLUSIONS CONCLUSIONS
This multicenter RWD study demonstrated the clinically meaningful benefit of first-line ipilimumab and nivolumab in LATAM patients with unresectable or metastatic PM, and data is consistent with previous trial findings.

Identifiants

pubmed: 39424512
pii: S1525-7304(24)00200-6
doi: 10.1016/j.cllc.2024.09.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Diego Enrico (D)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina. Electronic address: denrico@alexanderfleming.org.

Juan Elias Gomez (JE)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Danilo Aguirre (D)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Natalia Soledad Tissera (NS)

Department of Medical Oncology, Upper Gastrointestinal and Endocrine Tumor Group, Vall´d Hebron Institute of Oncology (VHIO), Barcelona, Spain.

Florencia Tsou (F)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Carmen Pupareli (C)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Delfina Peralta Tanco (DP)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Federico Waisberg (F)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Andrés Rodríguez (A)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Manglio Rizzo (M)

Clinical Oncology Unit, Hospital Universitario Austral, Pilar Buenos Aires, Argentina; Laboratorio de Inmuno-biología del Cáncer, Instituto de Investigaciones en Medicina Traslacional, Universidad Austral-Consejo Nacional de Investigaciones Científicas y Tecnologicas (CONICET), Buenos Aires, Argentina.

Nicolás Minatta (N)

Clinical Oncology Unit, Hospital Universitario Austral, Pilar Buenos Aires, Argentina.

Picon Rafael (P)

Clinical Oncology Unit, Hospital Universitario Austral, Pilar Buenos Aires, Argentina.

Luis Basbus (L)

Departamento de Oncología, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

Lorena Lupinacci (L)

Departamento de Oncología, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

Diego Kaen (D)

Departamento de Oncología, Hospital de Clínicas Virgen María de Fátima, National University of La Rioja, La Rioja, Argentina.

Mauro Ramos (M)

Departamento de Oncología, Hospital Alemán, Buenos Aires, Argentina.

Virginia Bluthgen (V)

Departamento de Oncología, Hospital Alemán, Buenos Aires, Argentina.

Nicolas Castagneris (N)

Medical Oncology Unit, Reina Fabiola University Clinic, Universidad Católica de Córdoba, Córdoba, Argentina.

María Pía Coppola (MP)

Departamento de Oncología, Hospital Zonal Especializado en Agudos y Crónicos Dr. Antonio Cetrangolo, Buenos Aires, Argentina.

Alejandra Scocimarro (A)

Departamento de Oncología, Hospital Zonal Especializado en Agudos y Crónicos Dr. Antonio Cetrangolo, Buenos Aires, Argentina.

María Florencia Guerra (MF)

Departamento de Oncología, Angel Roffo Oncology Institute, Universtiy of Buenos Aires, Buenos Aires, Argentina.

Aldo Perfetti (A)

Department of Medical Oncology, Center for Medical Education and Clinical Research Norberto Quirno (CEMIC), Buenos Aires, Argentina.

Patricio Levit (P)

Department of Medical Oncology, Unión Personal-Accord Salud, Buenos Aires, Argentina.

Marco Galvez-Nino (M)

Clinical Research Unit, Auna Ideas, Lima, Perú.

Luis Mas (L)

Department of Medical Oncology, Oncosalud - Auna, Lima, Perú; Latin American Cansortium for Lung Cancer Research.

Leonardo Rojas (L)

Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center - CTIC, Direction of Research and Education/Thoracic Oncology Functional Unit, Bogotá, Colombia.

Jairo Zuluaga (J)

Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center - CTIC, Direction of Research and Education/Thoracic Oncology Functional Unit, Bogotá, Colombia.

Matías Chacón (M)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina.

Luis Corrales (L)

Departamento de Oncología, Centro de Investigación y Manejo del Cáncer (CIMCA), San José, Costa Rica; Latin American Cansortium for Lung Cancer Research.

Suraj Samtani (S)

Departamento de Oncología, Clínica Las Condes Santiago, Las Condes, Chile.

Oscar Arrieta (O)

Departamento de Oncología, Instituto Nacional de Cancerología (INCan), México City, México; Latin American Cansortium for Lung Cancer Research.

Andrés Cardona (A)

Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center - CTIC, Direction of Research and Education/Thoracic Oncology Functional Unit, Bogotá, Colombia; Latin American Cansortium for Lung Cancer Research.

Jordi Remon (J)

Department of Cancer Medicine, Gustave Roussy, Villejuif, France.

Claudio Martín (C)

Department of Medical Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina; Latin American Cansortium for Lung Cancer Research.

Classifications MeSH