Efficacy and Safety of Nivolumab Plus Ipilimumab versus Sunitinib in First-line Treatment of Patients with Advanced Sarcomatoid Renal Cell 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:
01 01 2021
Historique:
received: 29 05 2020
revised: 30 07 2020
accepted: 27 08 2020
pubmed: 3 9 2020
medline: 14 8 2021
entrez: 3 9 2020
Statut: ppublish

Résumé

Patients with advanced renal cell carcinoma with sarcomatoid features (sRCC) have poor prognoses and suboptimal outcomes with targeted therapy. This Patients with sRCC were identified via independent central pathology review of archival tumor tissue or histologic classification per local pathology report. Patients were randomized 1:1 to receive nivolumab (3 mg/kg) plus ipilimumab (1 mg/kg) every 3 weeks (four doses) then nivolumab 3 mg/kg every 2 weeks, or sunitinib 50 mg orally every day (4 weeks; 6-week cycles). Outcomes in patients with sRCC were not prespecified. Endpoints in patients with sRCC and International Metastatic Renal Cell Carcinoma Database Consortium intermediate/poor-risk disease included overall survival (OS), progression-free survival (PFS) per independent radiology review, and objective response rate (ORR) per RECIST v1.1. Safety outcomes used descriptive statistics. Of 1,096 randomized patients in CheckMate 214, 139 patients with sRCC and intermediate/poor-risk disease and six with favorable-risk disease were identified. With 42 months' minimum follow-up in patients with sRCC and intermediate/poor-risk disease, median OS [95% confidence interval (CI)] favored NIVO+IPI [not reached (NR) (25.2-not estimable [NE]); NIVO+IPI showed unprecedented long-term survival, response, and complete response benefits versus sunitinib in previously untreated patients with sRCC and intermediate/poor-risk disease, supporting the use of first-line NIVO+IPI for this population.

Identifiants

pubmed: 32873572
pii: 1078-0432.CCR-20-2063
doi: 10.1158/1078-0432.CCR-20-2063
pmc: PMC8589223
mid: NIHMS1625995
doi:

Substances chimiques

Ipilimumab 0
Nivolumab 31YO63LBSN
Protein Serine-Threonine Kinases EC 2.7.11.1
Sunitinib V99T50803M

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

78-86

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentOn
Type : CommentIn
Type : CommentIn

Informations de copyright

©2020 American Association for Cancer Research.

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Auteurs

Nizar M Tannir (NM)

Department of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas. ntannir@mdanderson.org.

Sabina Signoretti (S)

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Oncologic Pathology, Dana-Farber Cancer Institute, Boston, Massachusetts.

Toni K Choueiri (TK)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.

David F McDermott (DF)

Division of Medical Oncology, Beth Israel Deaconess Medical Center, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.

Robert J Motzer (RJ)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Abdallah Flaifel (A)

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Jean-Christophe Pignon (JC)

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Miriam Ficial (M)

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Osvaldo Arén Frontera (OA)

Centro de Investigación Clínica Bradford Hill, Recoleta, Chile.

Saby George (S)

Department of Medicine, Roswell Park Cancer Institute, Buffalo, New York.

Thomas Powles (T)

Department of Urology, Barts Cancer Institute, Queen Mary University of London, Royal Free NHS Trust, London, United Kingdom.

Frede Donskov (F)

Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

Michael R Harrison (MR)

Department of Medicine, Duke Cancer Institute, Durham, North Carolina.

Philippe Barthélémy (P)

Medical Oncology Unit, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Scott S Tykodi (SS)

Department of Medicine, University of Washington and Fred Hutchinson Cancer Research Center, Seattle, Washington.

Judit Kocsis (J)

Oncology Department, Debrecen University Clinical Center, Debrecen, Hungary.
Department of Oncoradiology, Bács-kiskun County Teaching Hospital (BKMK) Centre of Oncoradiology, Kecskemét, Hungary.

Alain Ravaud (A)

Department of Medical Oncology, Bordeaux University Hospital, Bordeaux, France.

Jeronimo R Rodriguez-Cid (JR)

Centro Oncológico, Hospital Médica Sur, Mexico City, Mexico.

Sumanta K Pal (SK)

Department of Medical Oncology and Therapeutics Research, City of Hope, Duarte, California.

Andre M Murad (AM)

CENANTRON-PERSONAL-Precision Oncology, Belo Horizonte, Minas Gerais, Brazil.

Yuko Ishii (Y)

Department of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.

Shruti Shally Saggi (SS)

Department of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.

M Brent McHenry (MB)

Department of Biostatistics, Bristol Myers Squibb, Princeton, New Jersey.

Brian I Rini (BI)

Division of Hematology/Oncology, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee.

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