Evidence map›Paper›PMID 41053075›Full record

Trial reportNature communications2025

Inflammation and mutational burden differentially associated with nivolumab or ipilimumab combination efficacy in colorectal cancer.

Ming Lei, Michael J Overman, Jin Yao, Thierry André, Sara Lonardi, Heinz-Josef Lenz, Massimo Aglietta, Fabio Gelsomino, Ray McDermott, Ka Yeung Mark Wong and 14 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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.

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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
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

24 authors.

Ming Lei *Department of Translational Medicine, Bristol Myers Squibb, Princeton, NJ, USA. Ming.Lei1@bms.com.ORCID http://orcid.org/0000-0002-1292-5911
Michael J Overman *Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jin YaoDepartment of Translational Bioinformatics, Informatics & Predictive Sciences, Bristol Myers Squibb, Princeton, NJ, USA.
Thierry AndréSorbonne Université and Department of Medical Oncology, Hôpital Saint Antoine, Assistance Publique Hôpitaux de Paris and INSERM, Unité Mixte de Recherche Scientifique 938, and SIRIC CURAMUS, Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0002-5103-7095
Sara LonardiDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.ORCID http://orcid.org/0000-0002-7593-8138
Heinz-Josef LenzDepartment of Medicine, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-2178-9568
Massimo AgliettaMedical Oncology Department, Candiolo Cancer Institute, FPO-IRCCS, Candiolo (TO), Italy.
Fabio GelsominoDepartment of Oncology and Hematology, Division of Oncology, University Hospital of Modena, Modena, Italy.ORCID http://orcid.org/0000-0001-7979-4795
Ray McDermottDepartment of Medical Oncology, St Vincent's University Hospital and Cancer Trials Ireland, Dublin, Ireland.
Ka Yeung Mark WongDepartment of Medical Oncology, Crown Princess Mary Cancer Centre, Westmead Hospital, Sydney, Australia.
Michael A MorseDepartment of Medicine, Duke University Medical Center, Durham, NC, USA.
Eric Van CutsemDepartment of Digestive Oncology, University Hospitals Gasthuisberg/Leuven and KU Leuven, Leuven, Belgium.
Alain HendliszDepartment of Medical Oncology, Institut Jules Bordet, Brussels, Belgium.
Dana B CardinDepartment of Medicine, Division of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-0269-9615
Bart NeynsDepartment of Medical Oncology, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Andrew HillTasman Oncology Research Ltd., Southport, Qld, Australia.
Anuradha KrishnamurthyDepartment of Medicine, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
Franklin ChenDepartment of Cellular Therapy and Developmental Therapeutics, Novant Health Cancer Institute, Winston-Salem, NC, USA.
Samith KochuparambilDepartment of Medical Oncology, Minnesota Oncology, Minneapolis, MN, USA.
Robert R JenqDepartment of Genomic Medicine and Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-5434-439X
Sandzhar AbdullaevDepartment of Clinical Development, Bristol Myers Squibb, Princeton, NJ, USA.
Beilei HeDepartment of Global Biostatistics and Data Science, Bristol Myers Squibb, Princeton, NJ, USA.
Ruslan NovosiadlyDepartment of Translational Medicine, Bristol Myers Squibb, Princeton, NJ, USA.
Scott KopetzDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA. skopetz@mdanderson.org.ORCID http://orcid.org/0000-0001-9647-3416

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Nivolumab alone and in combination with ipilimumab demonstrated durable clinical benefit in patients with previously treated microsatellite instability-high/mismatch repair-deficient metastatic colorectal cancer in the phase 2 CheckMate 142 study. Here, we report exploratory biomarker analyses from CheckMate 142 evaluating associations between various tissue biomarkers and the efficacy of nivolumab monotherapy and nivolumab plus ipilimumab combination in these patients. Higher expression of inflammation-related gene expression signatures is associated with improved response per investigator assessment and survival benefit with nivolumab monotherapy. In contrast, higher tumor mutational burden, tumor indel burden, and degrees of microsatellite instability are associated with improved response per investigator assessment and survival benefit with nivolumab plus ipilimumab. While interpretation is limited by the exploratory nature of these analyses, they suggest that tumor antigenicity rather than baseline tumor inflammation might be important for the combinatorial efficacy. Validation of these findings in larger, randomized studies is necessary.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsColorectal NeoplasmsInflammationIpilimumabNivolumabAntineoplastic Agents, ImmunologicalBiomarkers, TumorFemaleHumansMaleMicrosatellite InstabilityMutationTreatment OutcomeAntineoplastic Agents, ImmunologicalBiomarkers, TumorIpilimumabNivolumab

Identifiers

PMID41053075
PMCPMC12501054

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.