Evidence map›Paper›PMID 39190534›Full record

Trial reportThe Journal of experimental medicine2024

Immunologic signatures of response and resistance to nivolumab with ipilimumab in advanced metastatic cancer.

Apostolia M Tsimberidou, Farah A Alayli, Kwame Okrah, Alexandra Drakaki, Danny N Khalil, Shivaani Kummar, Saad A Khan, F Stephen Hodi, David Y Oh, Christopher R Cabanski and 30 more

Registry-linked trialAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03651271 (An Exploratory Study of Nivolumab With or Without Ipilimumab According to the Percentage of Tumoral CD8 Cells in Participants With Advanced Metastatic Cancer), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

NCT03651271 phase2completednot on this map

An Exploratory Study of Nivolumab With or Without Ipilimumab According to the Percentage of Tumoral CD8 Cells in Participants With Advanced Metastatic Cancer

TypeinterventionalSponsorParker Institute for Cancer ImmunotherapyRan2018 to 2023Enrolled100ConditionsAdvanced Metastatic Cancer, Advanced Prostate CancerArmsNivolumab Monotherapy, Nivolumab and Ipilimumab and Combination for Metastatic Cancer, Nivolumab and Ipilimumab (3 mg/kg) Combination for Prostate Cancer, Nivolumab and Ipilimumab (5 mg/kg) Combination for Prostate Cancer
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Identifying a Csmd3Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Programmed cell death in triple-negative breast cancer.Cellular & molecular biology letters · 2025
    Review
  8. 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

40 authors.

Apostolia M Tsimberidou *Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0003-2713-233X
Farah A Alayli *Parker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0003-1155-1756
Kwame Okrah *Parker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0003-7210-5741
Alexandra DrakakiUniversity of California, Los Angeles , Los Angeles, CA, USA.ORCID 0000-0001-8865-3548
Danny N KhalilMemorial Sloan Kettering Cancer Center , New York, NY, USA.ORCID 0000-0003-4688-0958
Shivaani KummarStanford University , Stanford, CA, USA.ORCID 0000-0001-6906-1627
Saad A KhanStanford University , Stanford, CA, USA.ORCID 0000-0002-3440-9774
F Stephen HodiDana-Farber Cancer Institute , Boston, MA, USA.ORCID 0000-0001-6825-091X
David Y OhUniversity of California, San Francisco , San Francisco, CA, USA.ORCID 0000-0002-3310-0994
Christopher R CabanskiParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0007-9938-1331
Shikha GautamParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0003-4885-7823
Stefanie L MeierParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-2709-8429
Meelad AmouzgarParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0003-0521-9223
Shannon M PfeifferParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-4291-9483
Robin KageyamaParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-2865-4976
EnJun YangParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0003-1511-7511
Marko SpasicParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0005-5693-312X
Michael T TetzlaffDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-7899-4138
Wai Chin FooDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-0471-4911
Travis J HollmannMemorial Sloan Kettering Cancer Center , New York, NY, USA.ORCID 0000-0003-1599-0433
Yanyun LiMemorial Sloan Kettering Cancer Center , New York, NY, USA.ORCID 0009-0004-6250-5562
Matthew AdamowMemorial Sloan Kettering Cancer Center , New York, NY, USA.ORCID 0000-0002-7709-0126
Phillip WongMemorial Sloan Kettering Cancer Center , New York, NY, USA.ORCID 0000-0002-6360-849X
Jonni S MooreUniversity of Pennsylvania , Philadelphia, PA, USA.ORCID 0000-0002-2975-336X
Sharlene VelichkoNatera Inc. , Austin, TX, USA.ORCID 0000-0002-0133-100X
Richard O ChenPersonalis Inc. , Fremont, CA, USA.ORCID 0000-0002-2842-4476
Dinesh KumarParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0003-2699-5827
Samantha BucktroutParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0000-7531-0255
Ramy IbrahimParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-4988-5693
Ute DuganParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0006-3558-4503
Lisa SalvadorBristol Myers Squibb , New York, NY, USA.ORCID 0009-0001-7932-9639
Vanessa M Hubbard-LuceyCancer Research Institute , New York, NY, USA.ORCID 0000-0002-1235-9737
Jill O'Donnell-TormeyCancer Research Institute , New York, NY, USA.ORCID 0009-0007-1843-3671
Sandra Santulli-MarottoParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0009-0004-5307-9223
Lisa H ButterfieldParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-3439-9844
Diane M Da SilvaParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0001-7317-4886
Justin FairchildParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-4478-7146
Theresa M LaValleeParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0002-1769-3195
Lacey J PadrónParker Institute for Cancer Immunotherapy , San Francisco, CA, USA.ORCID 0000-0003-0064-5565
Padmanee SharmaDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0003-4658-055X

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Bristol Myers SquibbCancer Research InstituteNCI NIH HHS P30 CA008748Parker Institute for Cancer Immunotherapy
6 · The paper itself

Abstract

Identifying pan-tumor biomarkers that predict responses to immune checkpoint inhibitors (ICI) is critically needed. In the AMADEUS clinical trial (NCT03651271), patients with various advanced solid tumors were assessed for changes in intratumoral CD8 percentages and their response to ICI. Patients were grouped based on tumoral CD8 levels: those with CD8 <15% (CD8-low) received nivolumab (anti-PD-1) plus ipilimumab (anti-CTLA4) and those with CD8 ≥15% (CD8-high) received nivolumab monotherapy. 79 patients (72 CD8-low and 7 CD8-high) were treated. The disease control rate was 25.0% (18/72; 95% CI: 15.8-35.2) in CD8-low and 14.3% (1/7; 95% CI: 1.1-43.8) in CD8-high. Tumors from 35.9% (14/39; 95% CI: 21.8-51.4) of patients converted from CD8 <15% pretreatment to ≥15% after treatment. Multiomic analyses showed that CD8-low responders had an inflammatory tumor microenvironment pretreatment, enhanced by an influx of CD8 T cells, CD4 T cells, B cells, and macrophages upon treatment. These findings reveal crucial pan-cancer immunological features for ICI response in patients with metastatic disease.

Indexed as

CD8-Positive T-LymphocytesDrug Resistance, NeoplasmIpilimumabNivolumabAdultAgedFemaleHumansImmune Checkpoint InhibitorsMaleMiddle AgedNeoplasm MetastasisNeoplasmsTumor MicroenvironmentImmune Checkpoint InhibitorsIpilimumabNivolumab

Identifiers

PMID39190534
PMCPMC11349049

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.