Evidence map›Paper›PMID 32673417›Full record

Trial reportCancer2020

Nivolumab versus everolimus in patients with advanced renal cell carcinoma: Updated results with long-term follow-up of the randomized, open-label, phase 3 CheckMate 025 trial.

Robert J Motzer, Bernard Escudier, Saby George, Hans J Hammers, Sandhya Srinivas, Scott S Tykodi, Jeffrey A Sosman, Elizabeth R Plimack, Giuseppe Procopio, David F McDermott and 21 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 195 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
195citing papers in PubMed, 10 pooled it
17.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01668784 phase3completednot on this map

A Randomized, Open-Label, Phase 3 Study of Nivolumab (BMS-936558) vs. Everolimus in Subjects With Advanced or Metastatic Clear-Cell Renal Cell Carcinoma Who Have Received Prior Anti-Angiogenic Therapy

TypeinterventionalSponsorBristol-Myers SquibbRan2012 to 2021Enrolled821ConditionsAdvanced or Metastatic (Medically or Surgically Unresectable) Clear-cell Renal Cell CarcinomaArmsNivolumab, Everolimus
NCT07686744 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Phase I Clinical Trial of Personalized Neoantigen Peptide Vaccine in Combination With Pembrolizumab for the Safety and Efficacy in Patients With Advanced, Recurrent or Refractory Renal Cell Carcinoma

TypeinterventionalSponsorJian LinRan2026 to 2029Enrolled8ConditionsRenal Cell Carcinoma, Advanced, Recurrent, RefractoryArmsPersonalized Neoantigen Polyepitope Peptide Vaccine
3 · Its place in the literature

Who cites it

195 citing papers in PubMed, 10 syntheses or guidelines pooled it, 331 citations in OpenAlex.

  1. Guideline
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  3. Treatments for renal cell carcinoma: NICE Pilot Treatment Pathways Appraisal.Health technology assessment (Winchester, England) · 2026
    Pooled it
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  7. SEOM SOGUG clinical guideline for treatment of kidney cancer (2022).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Guideline
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135 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors at 20 institutions in 13 countries.

Robert J MotzerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-6925-2327
Bernard EscudierDepartment of Medical Oncology, Gustave Roussy, Villejuif, France.
Saby GeorgeDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, New York.
Hans J HammersDivision of Hematology and Oncology, UT Southwestern Kidney Cancer Program, Dallas, Texas.
Sandhya SrinivasStanford Cancer Institute, Stanford University Medical Center, Stanford, California.
Scott S TykodiDepartment of Medicine, University of Washington and Fred Hutchinson Cancer Research Center, Seattle, Washington.
Jeffrey A SosmanDepartment of Hematology/Oncology, Northwestern University Medical Center, Chicago, Illinois.
Elizabeth R PlimackDepartment of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Giuseppe ProcopioFondazione Istituto Nazionale Tumori, Milan, Italy.ORCID 0000-0002-2498-402X
David F McDermottBeth Israel Deaconess Medical Center, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.
Daniel CastellanoOncologia Medica, Hospital Universitario 12 De Octubre, Madrid, Spain.
Toni K ChoueiriLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-9201-3217
Frede DonskovDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Howard GurneyDepartment of Medical Oncology, Westmead Hospital and Macquarie University, Westmead, New South Wales, Australia.
Stéphane OudardService de Cancérologie Médicale, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France.
Martin RichardetFundacion Richardet Longo, Instituto Oncologico de Cordoba, Cordoba, Argentina.
Katriina PeltolaComprehensive Cancer Center, Helsinki University Hospital, Helsinki, Finland.
Ajjai S AlvaDivision of Hematology and Oncology, University of Michigan, Ann Arbor, Michigan.
Michael CarducciSidney Kimmel Comprehensive Cancer Center, Johns Hopkins Medicine, Baltimore, Maryland.
John WagstaffSouth West Wales Cancer Institute and Swansea University College of Medicine, Swansea, United Kingdom.ORCID 0000-0002-1140-5981
Christine ChevreauInstitut Claudius Regaud, Institut Universitaire du Cancer de Toulouse - Oncopole, Toulouse, France.ORCID 0000-0001-9866-913X
Satoshi FukasawaProstate Center and Division of Urology, Chiba Cancer Center, Chiba, Japan.
Yoshihiko TomitaDepartment of Urology, Department of Molecular Oncology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Thomas C GaulerDepartment of Medicine, University Hospital Essen, University of Duisburg-Essen, Duisburg, Germany.
Christian K KollmannsbergerDivision of Medical Oncology, BC Cancer-Vancouver Cancer Centre, Vancouver, British Columbia, Canada.
Fabio A SchutzBeneficencia Portuguesa de São Paulo, São Paulo, Brazil.
James LarkinRoyal Marsden Hospital NHS Foundation Trust, London, United Kingdom.
David CellaRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
M Brent McHenryDepartment of Biostatistics, Bristol Myers Squibb, Princeton, New Jersey.
Shruti Shally SaggiDepartment of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.
Nizar M TannirDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Bristol-Myers Squibb (United States) · USNorthwestern University · USAarhus University Hospital · DKAssistance Publique – Hôpitaux de Paris · FRBC Cancer Agency · CABeneficência Portuguesa de São Paulo · BRBeth Israel Deaconess Medical Center · USChiba Cancer Center · JPDana-Farber Cancer Institute · USFondazione IRCCS Istituto Nazionale dei Tumori · ITFox Chase Cancer Center · USGower College Swansea · GBHelsinki University Hospital · FIHospital Universitario 12 De Octubre · ESInstitut Claudius Regaud · FRInstitut Gustave Roussy · FRInstituto Oncológico de Córdoba · ARJohns Hopkins University · USMemorial Sloan Kettering Cancer Center · USNiigata University · JP

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
Bristol-Myers Squibb and ONO Pharmaceutical Company LtdNCI NIH HHS P30 CA006927NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016672NIH HHS P30 CA016672
6 · The paper itself

Abstract

backgroundCheckMate 025 has shown superior efficacy for nivolumab over everolimus in patients with advanced renal cell carcinoma (aRCC) along with improved safety and tolerability. This analysis assesses the long-term clinical benefits of nivolumab versus everolimus.

methodsThe randomized, open-label, phase 3 CheckMate 025 trial (NCT01668784) included patients with clear cell aRCC previously treated with 1 or 2 antiangiogenic regimens. Patients were randomized to nivolumab (3 mg/kg every 2 weeks) or everolimus (10 mg once a day) until progression or unacceptable toxicity. The primary endpoint was overall survival (OS). The secondary endpoints were the confirmed objective response rate (ORR), progression-free survival (PFS), safety, and health-related quality of life (HRQOL).

resultsEight hundred twenty-one patients were randomized to nivolumab (n = 410) or everolimus (n = 411); 803 patients were treated (406 with nivolumab and 397 with everolimus). With a minimum follow-up of 64 months (median, 72 months), nivolumab maintained an OS benefit in comparison with everolimus (median, 25.8 months [95% CI, 22.2-29.8 months] vs 19.7 months [95% CI, 17.6-22.1 months]; hazard ratio [HR], 0.73; 95% CI, 0.62-0.85) with 5-year OS probabilities of 26% and 18%, respectively. ORR was higher with nivolumab (94 of 410 [23%] vs 17 of 411 [4%]; P < .001). PFS also favored nivolumab (HR, 0.84; 95% CI, 0.72-0.99; P = .0331). The most common treatment-related adverse events of any grade were fatigue (34.7%) and pruritus (15.5%) with nivolumab and fatigue (34.5%) and stomatitis (29.5%) with everolimus. HRQOL improved from baseline with nivolumab but remained the same or deteriorated with everolimus.

conclusionsThe superior efficacy of nivolumab over everolimus is maintained after extended follow-up with no new safety signals, and this supports the long-term benefits of nivolumab monotherapy in patients with previously treated aRCC. LAY SUMMARY: CheckMate 025 compared the effects of nivolumab (a novel immunotherapy) with those of everolimus (an older standard-of-care therapy) for the treatment of advanced kidney cancer in patients who had progressed on antiangiogenic therapy. After 5 years of study, nivolumab continues to be better than everolimus in extending the lives of patients, providing a long-lasting response to treatment, and improving quality of life with a manageable safety profile. The results demonstrate that the clinical benefits of nivolumab versus everolimus in previously treated patients with advanced kidney cancer continue in the long term.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Renal CellEverolimusFemaleFollow-Up StudiesHumansKidney NeoplasmsMaleNivolumabTreatment OutcomeEverolimusNivolumabadvanced renal cell carcinoma (aRCC)CheckMate 025everolimusimmune checkpoint inhibitornivolumabpreviously treated

Identifiers

PMID32673417
PMCPMC8415096
OpenAlexW3042347895

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.