Atezolizumab plus Bevacizumab Versus Sunitinib for Patients with Untreated Metastatic Renal Cell Carcinoma and Sarcomatoid Features: A Prespecified Subgroup Analysis of the IMmotion151 Clinical Trial.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
05 2021
Historique:
received: 25 02 2020
accepted: 10 06 2020
pubmed: 14 7 2020
medline: 10 2 2022
entrez: 14 7 2020
Statut: ppublish

Résumé

Patients with metastatic renal cell carcinoma with sarcomatoid features (sRCC) have a poor prognosis and have shown limited responsiveness to inhibition of the VEGF pathway. We conducted a prespecified analysis of the randomised, phase 3 IMmotion151 trial in previously untreated patients with advanced or metastatic RCC to assess the effectiveness of atezolizumab + bevacizumab versus sunitinib in a subgroup of patients with sarcomatoid features. Patients whose tumour had any component of sarcomatoid features were included and received atezolizumab + bevacizumab (n = 68) or sunitinib (n = 74). Baseline characteristics were similar between the groups. Median progression-free survival was significantly longer in the group receiving atezolizumab + bevacizumab overall (8.3 vs 5.3 mo; hazard ratio [HR] 0.52 95% confidence interval [CI] 0.34-0.79) and in the subset of patients with PD-L1-positive tumours (8.6 vs 5.6 mo; HR 0.45, 95% CI 0.26-0.77). More patients receiving atezolizumab + bevacizumab achieved an objective response (49% vs 14%), including complete responses (10% vs 3%), and reported greater symptom improvements versus sunitinib. Safety was consistent with the known profiles of each drug and with that reported in the overall safety-evaluable population of IMmotion151. This analysis supports enhanced activity of atezolizumab + bevacizumab in patients with sRCC. PATIENT SUMMARY: In this report, we looked at patients with a specific type of kidney cancer (tumours with sarcomatoid features) that has been hard to treat. A treatment with two drugs (atezolizumab and bevacizumab) appeared to help patients live longer without the disease getting worse than another drug (sunitinib) that is often used. Patients who took the two drugs also said they were better able to carry out their everyday activities than patients who took sunitinib. The combination of these two drugs may work better in patients with this type of advanced kidney cancer.

Identifiants

pubmed: 32654802
pii: S0302-2838(20)30450-4
doi: 10.1016/j.eururo.2020.06.021
pmc: PMC9376009
mid: NIHMS1819590
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Pharmaceutical Preparations 0
Bevacizumab 2S9ZZM9Q9V
atezolizumab 52CMI0WC3Y
Sunitinib V99T50803M

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

659-662

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 European Association of Urology. Published by Elsevier B.V. All rights reserved.

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Auteurs

Brian I Rini (BI)

Vanderbilt University Medical Center, Nashville, TN, USA. Electronic address: brian.rini@vumc.org.

Robert J Motzer (RJ)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Thomas Powles (T)

Barts Cancer Institute and the Royal Free Hospital, Queen Mary University of London, London, UK.

David F McDermott (DF)

Beth Israel Deaconess Medical Center, Boston, MA, USA.

Bernard Escudier (B)

Gustave Roussy, Villejuif, France.

Frede Donskov (F)

Aarhus University Hospital, Aarhus, Denmark.

Robert Hawkins (R)

The Christie NHS Foundation Trust, Manchester, UK.

Sergio Bracarda (S)

Azienda Ospedaliera S. Maria, Terni, Italy.

Jens Bedke (J)

University of Tübingen, Tübingen, Germany.

Ugo De Giorgi (U)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, IRCCS, Meldola, Italy.

Camillo Porta (C)

IRCCS San Matteo University Hospital Foundation, Pavia, Italy.

Alain Ravaud (A)

CHU Hopitaux de Bordeaux - Hôpital Saint-André, Bordeaux, France.

Francis Parnis (F)

Ashford Cancer Centre Research, Kurralta Park, SA, Australia.

Enrique Grande (E)

MD Anderson Cancer Center Madrid, Madrid, Spain.

Wei Zhang (W)

Genentech Inc., South San Francisco, CA, USA.

Mahrukh Huseni (M)

Genentech Inc., South San Francisco, CA, USA.

Susheela Carroll (S)

Genentech Inc., South San Francisco, CA, USA.

Roxana Sufan (R)

Genentech Inc., South San Francisco, CA, USA.

Christina Schiff (C)

Genentech Inc., South San Francisco, CA, USA.

Michael B Atkins (MB)

Georgetown Lombardi Comprehensive Cancer Center, Washington, DC, USA.

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Classifications MeSH