Association of Tumor Mutational Burden and PD-L1 with the Efficacy of Pembrolizumab with or without Chemotherapy versus Chemotherapy in Advanced Urothelial Carcinoma.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
30 Oct 2024
Historique:
received: 13 11 2023
revised: 26 02 2024
accepted: 18 09 2024
medline: 30 10 2024
pubmed: 30 10 2024
entrez: 30 10 2024
Statut: aheadofprint

Résumé

The three-arm, phase III KEYNOTE-361 study did not meet its dual primary endpoints of progression-free survival (PFS) or overall survival (OS) with first-line pembrolizumab plus chemotherapy versus chemotherapy in advanced urothelial carcinoma. This prespecified exploratory analysis assessed the association of tumor mutational burden (TMB) and PD-L1 combined positive score (CPS) with clinical outcomes. TMB and PD-L1 CPS were determined via whole-exome sequencing and PD-L1 IHC 22C3 pharmDx, respectively. The association was evaluated in each treatment arm using logistic regression [objective response rate (ORR)] and Cox proportional hazards regression models (PFS and OS); one-sided (pembrolizumab monotherapy; pembrolizumab plus chemotherapy) and two-sided (chemotherapy) nominal P values were calculated. Significance was prespecified at α = 0.05 without multiplicity adjustment. Efficacy was evaluated by prespecified cutoffs of 175 mutations/exome (TMB) and CPS 10 (PD-L1). Of the 993 treated patients, 820 (82.6%) and 993 (100%) had evaluable TMB and CPS data, respectively. Continuous TMB was positively associated with ORR, PFS, and OS for pembrolizumab monotherapy (one-sided P < 0.001, P < 0.001, and P = 0.007, respectively); PFS and OS for pembrolizumab plus chemotherapy (one-sided P = 0.007 and P = 0.010, respectively); and OS for chemotherapy alone (two-sided P = 0.040). Continuous PD-L1 CPS showed evidence of anticipated association with ORR and PFS for pembrolizumab monotherapy. The subgroup with TMB ≥175 mutations/exome and PD-L1 CPS ≥10 had the highest PFS and OS improvements with pembrolizumab alone or with chemotherapy versus chemotherapy alone. These data suggest that TMB may be predictive of the response to pembrolizumab alone or with chemotherapy in advanced urothelial carcinoma.

Identifiants

pubmed: 39475359
pii: 749557
doi: 10.1158/1078-0432.CCR-23-3518
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

OF1-OF12

Informations de copyright

©2024 The Authors; Published by the American Association for Cancer Research.

Auteurs

Aude Fléchon (A)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Rafael Morales-Barrera (R)

Vall d'Hebron Institute of Oncology, Vall d´Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.

Thomas Powles (T)

Barts Cancer Centre, St Bartholomew's Hospital, London, United Kingdom.
Barts Cancer Institute, Barts Health NHS Trust, Queen Mary University of London, London, United Kingdom.

Ajjai Alva (A)

University of Michigan Health System, Ann Arbor, Michigan.

Mustafa Özgüroğlu (M)

Division of Medical Oncology, Department of Internal Medicine, Cerrahpaşa School of Medicine, Istanbul University-Cerrahpaşa, Istanbul, Turkey.

Tibor Csöszi (T)

County Oncology Centre, Hetényi Géza Hospital, Szolnok, Hungary.

Yohann Loriot (Y)

Institut Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Alejo Rodriguez-Vida (A)

Medical Oncology Department, Hospital del Mar Research Institute, Barcelona, Spain.

Lajos Géczi (L)

Medical Oncology Center and the National Tumor Biology Laboratory, National Institute of Oncology, Budapest, Hungary.

Susanna Y Cheng (SY)

Sunnybrook Health Sciences Centre, Odette Cancer Centre, Toronto, Canada.

Yves Fradet (Y)

CHU de Québec-Université Laval, Quebec City, Canada.

Stéphane Oudard (S)

Georges Pompidou European Hospital, University Paris Cité, Paris, France.

Christof Vulsteke (C)

Department of Medical Oncology, Maria Middelares Hospital, Gent, Belgium.
Center for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.

Seyda Gunduz (S)

Istinye University Liv Hospital, Istanbul, Turkey.
Minimally Invasive Therapeutics Laboratory, Mayo Clinic, Scottsdale, Arizona.

Ronac Mamtani (R)

Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.

Evan Y Yu (EY)

Division of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, Washington.
Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Alvaro Montesa Pino (A)

UGC Medical Oncology, Hospital Regional Universitario de Málaga, Hospital Universitario Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga, Málaga, Spain.

Urbano Anido (U)

Department of Medical Oncology, Complejo Hospitalario Universitario de Santiago, Santiago de Compostela, Spain.

Mehmet A N Sendur (MAN)

Department of Medical Oncology, Ankara Yıldırım Beyazıt University Faculty of Medicine, Ankara Bilkent City Hospital, Ankara, Turkey.

Gwenaelle Gravis (G)

Department of Medical Oncology, Paoli-Calmettes Institute, Marseille, France.

János Révész (J)

Institute of Radiotherapy and Clinical Oncology, Borsod-Abaúj-Zemplén County Hospital and University Teaching Hospital, Miskolc, Hungary.

Vladimir Kostorov (V)

Leningrad Regional Oncology Dispensary, Ulitsa Savushkina, Saint Petersburg, Russia.

Olivier Huillard (O)

Department of Medical Oncology, Hôpital Cochin, Institut du Cancer Paris, Cancer Research for Personalized Medicine (CARPEM), AP-HP Centre, Université de Paris Cité, Paris, France.

Junshui Ma (J)

Merck & Co., Inc., Rahway, New Jersey.

Mohini Rajasagi (M)

Merck & Co., Inc., Rahway, New Jersey.

Amir Vajdi (A)

Merck & Co., Inc., Rahway, New Jersey.

Jared Lunceford (J)

Merck & Co., Inc., Rahway, New Jersey.

Razvan Cristescu (R)

Merck & Co., Inc., Rahway, New Jersey.

Kentaro Imai (K)

Merck & Co., Inc., Rahway, New Jersey.

Blanca Homet Moreno (B)

Merck & Co., Inc., Rahway, New Jersey.

Nobuaki Matsubara (N)

National Cancer Center Hospital East, Chiba, Japan.

Classifications MeSH