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Pembrolizumab plus chemotherapy versus chemotherapy in untreated advanced pleural mesothelioma in Canada, Italy, and France: a phase 3, open-label, randomised controlled trial.
Chu, Quincy; Perrone, Francesco; Greillier, Laurent; Tu, Wei; Piccirillo, Maria Carmela; Grosso, Federica; Lo Russo, Giuseppe; Florescu, Marie; Mencoboni, Manlio; Morabito, Alessandro; Cecere, Fabiana Letizia; Ceresoli, Giovanni Luca; Dawe, David E; Zucali, Paolo Andrea; Pagano, Maria; Goffin, John R; Sanchez, Myriam Locatelli; Gridelli, Cesare; Zalcman, Gerard; Quantin, Xavier; Westeel, Virginie; Gargiulo, Piera; Delfanti, Sara; Tu, Dongsheng; Lee, Christopher W; Leighl, Natasha; Sederias, Joana; Brown-Walker, Pamela; Luo, Yiwen; Lantuejoul, Sylvie; Tsao, Ming-Sound; Scherpereel, Arnaud; Bradbury, Penelope; Laurie, Scott A; Seymour, Lesley.
Affiliation
  • Chu Q; Cross Cancer Institute, Edmonton, AB, Canada.
  • Perrone F; Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G Pascale, Napoli, Italy.
  • Greillier L; Aix Marseille Univ, Marseille, France; Assistance publique - Hôpitaux de Marseille, Marseille, France; L'Institut National de la Santé et de la Recherche Médicale, Marseille, France; Centre National de la Recherche Scientifique, Marseille, France; Cancer Research Centre of Marseille, Marseille, Fran
  • Tu W; Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.
  • Piccirillo MC; Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G Pascale, Napoli, Italy.
  • Grosso F; Mesothelioma and Rare Cancer Unit, Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
  • Lo Russo G; Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
  • Florescu M; Centre Hospitalier de l'Université de Montreal, Montreal, QC, Canada.
  • Mencoboni M; Unit di Oncologia Ospedale Villa Scassi, Genova Sampierdarena, Italy.
  • Morabito A; Oncologia Clinica e Sperimentale Toraco-polmonare, Istituto Nazionale Tumori IRCCS Fondazione G Pascale, Napoli, Italy.
  • Cecere FL; IRCCS Regina Elena National Cancer Institute Rome, Italy.
  • Ceresoli GL; Oncologia Medica Humanitas Gavazzeni Bergamo, Bergamo, Italy.
  • Dawe DE; CancerCare Manitoba, Winnipeg, MB, Canada.
  • Zucali PA; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Department of Oncology, IRCCS Humanitas Research Hospital, Milan, Italy.
  • Pagano M; Oncologia Medica IRCCS Arcispedale Maria Nuova Reggio Emilia, Reggio Emilia, Italy.
  • Goffin JR; Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton, ON, Canada.
  • Sanchez ML; Service de Pneumologie, Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre Bénite, France.
  • Gridelli C; Azienda Ospedaliera San Giuseppe Moscati Dipartimento di Oncologia Medica, Avellino, Italy.
  • Zalcman G; Université Paris Cité, Hôpital Bichat-Claude Bernard, Thoracic Oncology Department, Assistance publique-Hôpitaux de Paris Nord, Paris, France.
  • Quantin X; Montpellier Cancer Institute and Montpellier Cancer Research Institute, INSERM U1194, University of Montpellier, Montpellier, France.
  • Westeel V; Hôpital Jean Minjoz, Besancon Cedex, France.
  • Gargiulo P; Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G Pascale, Napoli, Italy.
  • Delfanti S; Mesothelioma and Rare Cancer Unit, Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
  • Tu D; Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.
  • Lee CW; BC Cancer - Surrey, BC, Canada.
  • Leighl N; Princess Margaret Cancer Centre, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.
  • Sederias J; Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.
  • Brown-Walker P; Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.
  • Luo Y; Merck & Co, Rahway, NJ, USA.
  • Lantuejoul S; Grenoble Alpes University and Department of Biopathology, Centre Léon Bérard and Netmeso Mesopath Network, Lyon, France.
  • Tsao MS; Princess Margaret Cancer Centre, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.
  • Scherpereel A; University of Lille, CHU Lille, INSERM U1189, OncoThAI, Lille, France.
  • Bradbury P; Princess Margaret Cancer Centre, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.
  • Laurie SA; Ottawa Hospital Research Institute, Ottawa, ON, Canada; University of Ottawa, Ottawa, ON, Canada.
  • Seymour L; Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada. Electronic address: lseymour@ctg.queensu.ca.
Lancet ; 402(10419): 2295-2306, 2023 12 16.
Article in En | MEDLINE | ID: mdl-37931632
ABSTRACT

BACKGROUND:

Pleural mesothelioma usually presents at an advanced, incurable stage. Chemotherapy with platinum-pemetrexed is a standard treatment. We hypothesised that the addition of pembrolizumab to platinum-pemetrexed would improve overall survival in patients with pleural mesothelioma.

METHODS:

We did this open-label, international, randomised phase 3 trial at 51 hospitals in Canada, Italy, and France. Eligible participants were aged 18 years or older, with previously untreated advanced pleural mesothelioma, with an Eastern Cooperative Oncology Group performance status score of 0 or 1. Patients were randomly assigned (11) to intravenous chemotherapy (cisplatin [75 mg/m2] or carboplatin [area under the concentration-time curve 5-6 mg/mL per min] with pemetrexed 500 mg/m2, every 3 weeks for up to 6 cycles), with or without intravenous pembrolizumab 200 mg every 3 weeks (up to 2 years). The primary endpoint was overall survival in all randomly assigned patients; safety was assessed in all randomly assigned patients who received at least one dose of study therapy. This trial is registered with ClinicalTrials.gov, NCT02784171, and is closed to accrual.

FINDINGS:

Between Jan 31, 2017, and Sept 4, 2020, 440 patients were enrolled and randomly assigned to chemotherapy alone (n=218) or chemotherapy with pembrolizumab (n=222). 333 (76 %) of patients were male, 347 (79%) were White, and median age was 71 years (IQR 66-75). At final analysis (database lock Dec 15, 2022), with a median follow-up of 16·2 months (IQR 8·3-27·8), overall survival was significantly longer with pembrolizumab (median overall survival 17·3 months [95% CI 14·4-21·3] with pembrolizumab vs 16·1 months [13·1-18·2] with chemotherapy alone, hazard ratio for death 0·79; 95% CI 0·64-0·98, two-sided p=0·0324). 3-year overall survival rate was 25% (95% CI 20-33%) with pembrolizumab and 17% (13-24%) with chemotherapy alone. Adverse events related to study treatment of grade 3 or 4 occurred in 60 (27%) of 222 patients in the pembrolizumab group and 32 (15%) of 211 patients in the chemotherapy alone group. Hospital admissions for serious adverse events related to one or more study drugs were reported in 40 (18%) of 222 patients in the pembrolizumab group and 12 (6%) of 211 patients in the chemotherapy alone group. Grade 5 adverse events related to one or more drugs occurred in two patients on the pembrolizumab group and one patient in the chemotherapy alone group.

INTERPRETATION:

In patients with advanced pleural mesothelioma, the addition of pembrolizumab to standard platinum-pemetrexed chemotherapy was tolerable and resulted in a significant improvement in overall survival. This regimen is a new treatment option for previously untreated advanced pleural mesothelioma.

FUNDING:

The Canadian Cancer Society and Merck & Co.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mesothelioma, Malignant / Mesothelioma Limits: Aged / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: Lancet Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mesothelioma, Malignant / Mesothelioma Limits: Aged / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: Lancet Year: 2023 Document type: Article Affiliation country: