Evidence map›Paper›PMID 32997575›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2020

Five-Year Outcomes With Nivolumab in Patients With Wild-Type

Caroline Robert, Georgina V Long, Benjamin Brady, Caroline Dutriaux, Anna Maria Di Giacomo, Laurent Mortier, Piotr Rutkowski, Jessica C Hassel, Catriona M McNeil, Ewa Anna Kalinka and 17 more

Open access · hybridAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed, 7 pooled it
9.8field-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

135 citing papers in PubMed, 7 syntheses or guidelines pooled it, 219 citations in OpenAlex.

  1. Pooled it
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  12. Article
  13. A baseline systemic inflammatory signature predicts anti-PD-1 response in advanced melanoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  14. Anti-PD-1 Combinations: Triplets and Beyond.Current oncology reports · 2026
    Review
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  18. Prognostic value of TMTV and Dmax calculated fromEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
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  20. Review

75 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

27 authors at 20 institutions in 12 countries.

Caroline RobertGustave Roussy, Villejuif, France.ORCID 0000-0002-9493-0238
Georgina V LongMelanoma Institute Australia, University of Sydney, and Royal North Shore and Mater Hospitals, Sydney, New South Wales, Australia.ORCID 0000-0001-8894-3545
Benjamin BradyCabrini Health, Melbourne, Victoria, Australia.
Caroline DutriauxHôpital Saint André Centre Hospitalier Universitaire, Bordeaux, France.
Anna Maria Di GiacomoCenter for Immuno-Oncology, University Hospital of Siena, Siena, Italy.
Laurent MortierUniversity of Lille, INSERM U1189, Service de Dermatologie, Chu Lille, Lille, France.
Piotr RutkowskiMaria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Jessica C HasselNational Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany.ORCID 0000-0001-7575-6230
Catriona M McNeilChris O'Brien Lifehouse, Melanoma Institute Australia, and Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Ewa Anna KalinkaPolish Mother's Memorial Hospital-Research Institute, Lodz, Poland.ORCID 0000-0003-4791-8372
Céleste LebbéUniversité de Paris, INSERM U976, and Dermatology and CIC, AP-HP, Saint Louis Hospital, Paris, France.ORCID 0000-0002-5854-7290
Julie CharlesGrenoble Alpes University Hospital, INSERM U1209, Grenoble Alpes University, Grenoble, France.
Micaela M HernbergHelsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-0139-4596
Kerry J SavageBritish Columbia Cancer Agency, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-5835-9863
Vanna Chiarion-SileniOncology Institute of Veneto Istituto di Ricovero e Cura a Carattere Scientifico, Padua, Italy.ORCID 0000-0001-9191-9124
Catalin MihalcioiuRoyal Victoria Hospital, McGill University, Montreal, Quebec, Canada.
Cornelia MauchUniversity Hospital Cologne and Centrum für Integrierte Onkologie Köln, Bonn, Germany.
Ana AranceHospital Clínic Barcelona, Barcelona, Spain.
Francesco CognettiRegina Elena Institute, Rome, Italy.ORCID 0000-0003-2022-9446
Lars NyDepartment of Oncology, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID 0000-0003-3864-5958
Henrik SchmidtAarhus University Hospital, Aarhus, Denmark.
Dirk SchadendorfDepartment of Dermatology, Comprehensive Cancer Center, University Hospital Essen, Essen, Germany.ORCID 0000-0003-3524-7858
Helen GogasNational and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-0451-2885
Jesús ZocoSyneos Health, Braine l'Alleud, Belgium.ORCID 0000-0003-1164-4306
Sandra ReBristol Myers Squibb, Princeton, NJ.
Paolo A AsciertoIstituto Nazionale Tumori IRCCS Fondazione Pascale, Naples, Italy.ORCID 0000-0002-8322-475X
Victoria AtkinsonPrincess Alexandra Hospital, Woolloongabba, and Gallipoli Medical Research Foundation, Greenslopes Private Hospital, Greenslopes, Queensland, Australia.
Inserm · FRAarhus University Hospital · DKBC Cancer Agency · CABristol-Myers Squibb (United States) · USCabrini Hospital · AUCentrum für Integrierte Onkologie · DEDeutsches Historisches Institut Rom · ITGerman Cancer Research Center · DEGreenslopes Private Hospital · AUHeidelberg University · DEHelsinki University Hospital · FIHôpital Saint-André · FRHospital Clínic de Barcelona · ESIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITNational and Kapodistrian University of Athens · GRPolish Mother’s Memorial Hospital Research Institute · PLRoyal Prince Alfred Hospital · AURoyal Victoria Hospital · CASahlgrenska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe CheckMate 066 trial investigated nivolumab monotherapy as first-line treatment for patients with previously untreated PATIENTS AND

methodsIn this multicenter, double-blind, phase III study, 418 patients with previously untreated, unresectable, stage III/IV, wild-type

resultsPatients were followed for a minimum of 60 months from the last patient randomly assigned (median follow-up, 32.0 months for nivolumab and 10.9 months for dacarbazine). Five-year OS rates were 39% with nivolumab and 17% with dacarbazine; PFS rates were 28% and 3%, respectively. Five-year OS was 38% in patients randomly assigned to dacarbazine who had subsequent therapy, including nivolumab (n = 37). ORR was 42% with nivolumab and 14% with dacarbazine; among patients alive at 5 years, ORR was 81% and 39%, respectively. Of 42 patients treated with nivolumab who had a complete response (20%), 88% (37 of 42) were alive as of the 5-year analysis. Among 75 nivolumab-treated patients alive and evaluable at the 5-year analysis, 83% had not received subsequent therapy; 23% were still on study treatment, and 60% were treatment free. Safety analyses were similar to the 3-year report.

conclusionResults from this 5-year analysis confirm the significant benefit of nivolumab over dacarbazine for all end points and add to the growing body of evidence supporting long-term survival with nivolumab mono-therapy. Survival is strongly associated with achieving a durable response, which can be maintained after treatment discontinuation, even without subsequent systemic therapies.

Indexed as

Antineoplastic Agents, AlkylatingAntineoplastic Agents, ImmunologicalDacarbazineHumansMelanomaNivolumabProgression-Free SurvivalProto-Oncogene Proteins B-rafSurvival RateAntineoplastic Agents, AlkylatingAntineoplastic Agents, ImmunologicalBRAF protein, humanDacarbazineNivolumabProto-Oncogene Proteins B-raf

Identifiers

PMID32997575
PMCPMC7676881
OpenAlexW3090469545

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.