Evidence map›Paper›PMID 39671533›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2025

Three-Year Overall Survival With Nivolumab Plus Relatlimab in Advanced Melanoma From RELATIVITY-047.

Hussein A Tawbi, F Stephen Hodi, Evan J Lipson, Dirk Schadendorf, Paolo A Ascierto, Luis Matamala, Erika Castillo Gutiérrez, Piotr Rutkowski, Helen Gogas, Christopher D Lao and 9 more

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03470922 (A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined With Nivolumab Versus Nivolumab in Participants With Previously Untreated Metastatic or Unresectable Melanoma), which is not on this map. Cited by 53 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT03470922 phase2 / phase3active not recruitingnot on this map

A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined With Nivolumab Versus Nivolumab in Participants With Previously Untreated Metastatic or Unresectable Melanoma

TypeinterventionalSponsorBristol-Myers SquibbRan2018 to 2030Enrolled714ConditionsMelanomaArmsRelatlimab, Nivolumab
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
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  7. Next-generation therapeutics for glioblastoma: Challenges and future directions.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
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  13. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
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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

19 authors.

Hussein A TawbiThe University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0003-1942-851X
F Stephen HodiDana-Farber Cancer Institute, Boston, MA.
Evan J LipsonBloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine, The Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD.ORCID 0000-0003-2976-0911
Dirk SchadendorfUniversity of Essen and the German Cancer Consortium, Essen, Germany.ORCID 0000-0003-3524-7858
Paolo A AsciertoIstituto Nazionale dei Tumori IRCCS "Fondazione G. Pascale," Naples, Italy.ORCID 0000-0002-8322-475X
Luis MatamalaInstituto Oncológico Fundación Arturo López Pérez and Department of Oncology, Instituto Nacional dfoel Cáncer, Santiago, Chile.
Erika Castillo GutiérrezFAICIC Clinical Research, Veracruz, Mexico.
Piotr RutkowskiMaria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID 0000-0002-8920-5429
Helen GogasNational and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-0451-2885
Christopher D LaoMichigan Medicine, Rogel Cancer Center, University of Michigan, Ann Arbor, MI.
Juliana Janoski De MenezesHospital Nossa Senhora da Conceição, Porto Alegre, Brazil.ORCID 0000-0002-5981-2324
Stéphane DalleHospices Civils de Lyon, Cancer Research Center of Lyon, Pierre-Bénite, France.
Ana Maria AranceHospital Clinic Barcelona and IDIBAPS, Barcelona, Spain.
Jean-Jacques GrobAix-Marseille University, CHU Timone, Marseille, France.ORCID 0000-0002-0667-153X
Barbara RattoBristol Myers Squibb, Princeton, NJ.
Saima RodriguezBristol Myers Squibb, Princeton, NJ.
Antonella MazzeiBristol Myers Squibb, Princeton, NJ.
Sonia DolfiBristol Myers Squibb, Princeton, NJ.
Georgina V LongMelanoma Institute Australia, The University of Sydney, Royal North Shore and Mater Hospitals, Sydney, NSW, Australia.ORCID 0000-0001-8894-3545

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nivolumab plus relatlimab demonstrated a statistically significant improvement in progression-free survival (PFS), along with a clinically meaningful, but not statistically significant improvement in overall survival (OS) and a numerically higher objective response rate (ORR) compared with nivolumab in the RELATIVITY-047 trial (ClinicalTrials.gov identifier: NCT03470922). We report updated descriptive efficacy and safety results from RELATIVITY-047 with a median follow-up of 33.8 months. Median PFS was 10.2 months (95% CI, 6.5 to 15.4) with nivolumab plus relatlimab and 4.6 months (95% CI, 3.5 to 6.5) with nivolumab (hazard ratio [HR], 0.79 [95% CI, 0.66 to 0.95]); median OS was 51.0 months (95% CI, 34.0 to not reached) and 34.1 (95% CI, 25.2 to 44.7) months, respectively (HR, 0.80 [95% CI, 0.66 to 0.99]). ORR was 43.7% (95% CI, 38.4 to 49.0) with nivolumab plus relatlimab and 33.7% (95% CI, 28.8 to 38.9) with nivolumab. Efficacy across the majority of prespecified subgroups favored the combination. No new or unexpected safety signals were identified. Overall, at 3-year follow-up, the benefit observed with nivolumab plus relatlimab compared with nivolumab in patients with advanced melanoma was sustained, with the OS HR 95% CI upper bound now <1. This benefit is accompanied by a safety profile consistent with previous reports.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsMelanomaNivolumabSkin NeoplasmsAdultAgedAntibodies, Monoclonal, HumanizedFemaleHumansMaleMiddle AgedProgression-Free SurvivalAntibodies, Monoclonal, HumanizedNivolumabrelatlimab

Identifiers

PMID39671533
PMCPMC12054981

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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.