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Efficacy and Safety of Nivolumab Plus Ipilimumab versus Sunitinib in First-line Treatment of Patients with Advanced Sarcomatoid Renal Cell Carcinoma.
Tannir, Nizar M; Signoretti, Sabina; Choueiri, Toni K; McDermott, David F; Motzer, Robert J; Flaifel, Abdallah; Pignon, Jean-Christophe; Ficial, Miriam; Frontera, Osvaldo Arén; George, Saby; Powles, Thomas; Donskov, Frede; Harrison, Michael R; Barthélémy, Philippe; Tykodi, Scott S; Kocsis, Judit; Ravaud, Alain; Rodriguez-Cid, Jeronimo R; Pal, Sumanta K; Murad, Andre M; Ishii, Yuko; Saggi, Shruti Shally; McHenry, M Brent; Rini, Brian I.
Afiliação
  • Tannir NM; Department of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas. ntannir@mdanderson.org.
  • Signoretti S; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Choueiri TK; Department of Oncologic Pathology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • McDermott DF; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Motzer RJ; Division of Medical Oncology, Beth Israel Deaconess Medical Center, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.
  • Flaifel A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Pignon JC; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Ficial M; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Frontera OA; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • George S; Centro de Investigación Clínica Bradford Hill, Recoleta, Chile.
  • Powles T; Department of Medicine, Roswell Park Cancer Institute, Buffalo, New York.
  • Donskov F; Department of Urology, Barts Cancer Institute, Queen Mary University of London, Royal Free NHS Trust, London, United Kingdom.
  • Harrison MR; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Barthélémy P; Department of Medicine, Duke Cancer Institute, Durham, North Carolina.
  • Tykodi SS; Medical Oncology Unit, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Kocsis J; Department of Medicine, University of Washington and Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Ravaud A; Oncology Department, Debrecen University Clinical Center, Debrecen, Hungary.
  • Rodriguez-Cid JR; Department of Oncoradiology, Bács-kiskun County Teaching Hospital (BKMK) Centre of Oncoradiology, Kecskemét, Hungary.
  • Pal SK; Department of Medical Oncology, Bordeaux University Hospital, Bordeaux, France.
  • Murad AM; Centro Oncológico, Hospital Médica Sur, Mexico City, Mexico.
  • Ishii Y; Department of Medical Oncology and Therapeutics Research, City of Hope, Duarte, California.
  • Saggi SS; CENANTRON-PERSONAL-Precision Oncology, Belo Horizonte, Minas Gerais, Brazil.
  • McHenry MB; Department of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.
  • Rini BI; Department of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.
Clin Cancer Res ; 27(1): 78-86, 2021 01 01.
Article em En | MEDLINE | ID: mdl-32873572
ABSTRACT

PURPOSE:

Patients with advanced renal cell carcinoma with sarcomatoid features (sRCC) have poor prognoses and suboptimal outcomes with targeted therapy. This post hoc analysis of the phase III CheckMate 214 trial analyzed the efficacy of nivolumab plus ipilimumab (NIVO+IPI) versus sunitinib in patients with sRCC. PATIENTS AND

METHODS:

Patients with sRCC were identified via independent central pathology review of archival tumor tissue or histologic classification per local pathology report. Patients were randomized 11 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.

RESULTS:

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]); n = 74] versus sunitinib [14.2 months (9.3-22.9); n = 65; HR, 0.45 (95% CI, 0.3-0.7; P = 0.0004)]; PFS benefits with NIVO+IPI were similarly observed [median 26.5 vs. 5.1 months; HR, 0.54 (95% CI, 0.33-0.86; P = 0.0093)]. Confirmed ORR was 60.8% with NIVO+IPI versus 23.1% with sunitinib, with complete response rates of 18.9% versus 3.1%, respectively. No new safety signals emerged.

CONCLUSIONS:

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.See related commentary by Hwang et al., p. 5.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Neoplasias Renais Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Neoplasias Renais Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article