Evidence map›Paper›PMID 32873572›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Efficacy and Safety of Nivolumab Plus Ipilimumab versus Sunitinib in First-line Treatment of Patients with Advanced Sarcomatoid Renal Cell Carcinoma.

Nizar M Tannir, Sabina Signoretti, Toni K Choueiri, David F McDermott, Robert J Motzer, Abdallah Flaifel, Jean-Christophe Pignon, Miriam Ficial, Osvaldo Arén Frontera, Saby George and 14 more

Open access · hybridAbstract readComment
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 136 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
136citing papers in PubMed, 5 pooled it
20.9field-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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

136 citing papers in PubMed, 5 syntheses or guidelines pooled it, 229 citations in OpenAlex.

  1. Guideline
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  5. New developments in existing WHO entities and evolving molecular concepts: The Genitourinary Pathology Society (GUPS) update on renal neoplasia.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Guideline
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  7. Triplet Strategies in Metastatic Clear Cell Renal Cell Carcinoma: A Worthy Option in the First-Line Setting?American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting · 2023
    Trial
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  19. Sarcomatoid Renal Cell Carcinoma: A Clinical Review.Diagnostics (Basel, Switzerland) · 2026
    Review
  20. Review

76 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 19 institutions in 9 countries.

Nizar M TannirDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas. ntannir@mdanderson.org.
Sabina SignorettiDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-5000-9105
Toni K ChoueiriDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
David F McDermottDivision of Medical Oncology, Beth Israel Deaconess Medical Center, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.
Robert J MotzerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-6925-2327
Abdallah FlaifelDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-6705-018X
Jean-Christophe PignonDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Miriam FicialDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-2005-9267
Osvaldo Arén FronteraCentro de Investigación Clínica Bradford Hill, Recoleta, Chile.
Saby GeorgeDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, New York.ORCID 0000-0002-0444-5870
Thomas PowlesDepartment of Urology, Barts Cancer Institute, Queen Mary University of London, Royal Free NHS Trust, London, United Kingdom.
Frede DonskovDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0002-8449-863X
Michael R HarrisonDepartment of Medicine, Duke Cancer Institute, Durham, North Carolina.
Philippe BarthélémyMedical Oncology Unit, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Scott S TykodiDepartment of Medicine, University of Washington and Fred Hutchinson Cancer Research Center, Seattle, Washington.
Judit KocsisOncology Department, Debrecen University Clinical Center, Debrecen, Hungary.ORCID 0000-0002-6110-9750
Alain RavaudDepartment of Medical Oncology, Bordeaux University Hospital, Bordeaux, France.
Jeronimo R Rodriguez-CidCentro Oncológico, Hospital Médica Sur, Mexico City, Mexico.
Sumanta K PalDepartment of Medical Oncology and Therapeutics Research, City of Hope, Duarte, California.
Andre M MuradCENANTRON-PERSONAL-Precision Oncology, Belo Horizonte, Minas Gerais, Brazil.
Yuko IshiiDepartment of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.
Shruti Shally SaggiDepartment of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.
M Brent McHenryDepartment of Biostatistics, Bristol Myers Squibb, Princeton, New Jersey.
Brian I RiniDivision of Hematology/Oncology, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee.
Brigham and Women's Hospital · USBristol-Myers Squibb (Sweden) · SEAarhus University Hospital · DKBeth Israel Deaconess Medical Center · USCity Of Hope National Medical Center · USClínica Alemana · CLDana-Farber Cancer Institute · USDuke Medical Center · USFred Hutch Cancer Center · USHôpitaux Universitaires de Strasbourg · FRHospital Médica Sur · MXMemorial Sloan Kettering Cancer Center · USQueen Mary University of London · GBRoswell Park Comprehensive Cancer Center · USThe University of Texas MD Anderson Cancer Center · USUniversidade Federal de Minas Gerais · BRUniversité de Bordeaux · FRUniversity of Debrecen · HUVanderbilt University · US

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
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposePatients with advanced renal cell carcinoma with sarcomatoid features (sRCC) have poor prognoses and suboptimal outcomes with targeted therapy. This PATIENTS AND

methodsPatients 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.

resultsOf 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]);

conclusionsNIVO+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.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsHippo Signaling PathwayHumansImmunotherapyIpilimumabNivolumabProtein Serine-Threonine KinasesSunitinibIpilimumabNivolumabProtein Serine-Threonine KinasesSunitinib

Identifiers

PMID32873572
PMCPMC8589223
OpenAlexW3081958456

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.