Evidence map›Paper›PMID 37037616›Full record

ArticleCancer cell2023

Prior anti-CTLA-4 therapy impacts molecular characteristics associated with anti-PD-1 response in advanced melanoma.

Katie M Campbell, Meelad Amouzgar, Shannon M Pfeiffer, Timothy R Howes, Egmidio Medina, Michael Travers, Gabriela Steiner, Jeffrey S Weber, Jedd D Wolchok, James Larkin and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 2 pooled it
16.8field-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

69 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

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9 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

19 authors at 8 institutions in 2 countries.

Katie M CampbellDivision of Hematology/Oncology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA. Electronic address: katiecampbell@mednet.ucla.edu.
Meelad AmouzgarDepartment of Pathology, Stanford University, Stanford, CA 94305, USA; Parker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Shannon M PfeifferParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Timothy R HowesParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Egmidio MedinaDivision of Hematology/Oncology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Michael TraversParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Gabriela SteinerParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Jeffrey S WeberPerlmutter Cancer Center, NYU School of Medicine, New York, NY 10016, USA.
Jedd D WolchokParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Weill Cornell Medicine, New York, NY 10065, USA.
James LarkinDepartment of Medical Oncology, The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
F Stephen HodiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Silvia BoffoBristol Myers Squibb Corp., Princeton, NJ 08540, USA.
Lisa SalvadorBristol Myers Squibb Corp., Princeton, NJ 08540, USA.
Daniel TenneyBristol Myers Squibb Corp., Princeton, NJ 08540, USA.
Tracy TangBristol Myers Squibb Corp., Princeton, NJ 08540, USA.
Marshall A ThompsonParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Christine N SpencerParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Daniel K WellsParker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Antoni RibasDivision of Hematology/Oncology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA; Parker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA; Department of Molecular and Medical Pharmacology, University of California, Los Angeles, Los Angeles, CA 90095, USA; Division of Surgical Oncology, Department of Surgery, University of California, Los Angeles, Los Angeles, CA 90095, USA; Jonsson Comprehensive Cancer Center, University of California, Los Angeles, Los Angeles, CA 90024, USA. Electronic address: aribas@mednet.ucla.edu.
Parker Institute for Cancer Immunotherapy · USBristol-Myers Squibb (United States) · USUniversity of California, Los Angeles · USDana-Farber Cancer Institute · USNYU Langone’s Laura and Isaac Perlmutter Cancer CenterRoyal Marsden NHS Foundation Trust · GBStanford University · USWeill Cornell Medicine · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Project 3: Modeling and overcoming resistance to melanoma immunotherapyP01CA244118 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MORICEAU, GATIEN P · 2020 to 2024
$12.8M
Next Generation Cancer Immunotherapies to Defeat MelanomaR35CA197633 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTONI RIBAS · 2015 to 2026
$10.4M
T-cell intrinsic mechanisms of resistance to PD-1 checkpoint blockadeR01CA243486 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KROGSGAARD, MICHELLE, ZHU, CHENG · 2020 to 2024
$3.5M
(8) Genomic determinants of the T-cell regulome in immune checkpoint blockadeR01CA227505 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KIRCHHOFF, TOMAS, WEBER, JEFFREY S · 2018 to 2022
$3.0M
Correlative biomarkers of IL-6 blockade combined with checkpoint inhibitionR01CA244936 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MEHNERT, JANICE M. · 2020 to 2024
$2.9M
(PQ8) Predicting immune-related toxicity in the adjuvant melanoma setting with checkpoint inhibitionR01CA231295 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OSMAN, IMAN, WEBER, JEFFREY S · 2018 to 2022
$2.4M
NCI NIH HHS P01 CA244118NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA227505NCI NIH HHS R01 CA231295NCI NIH HHS R01 CA243486NCI NIH HHS R01 CA244936NCI NIH HHS R35 CA197633
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs), including CTLA-4- and PD-1-blocking antibodies, can have profound effects on tumor immune cell infiltration that have not been consistent in biopsy series reported to date. Here, we analyze seven molecular datasets of samples from patients with advanced melanoma (N = 514) treated with ICI agents to investigate clinical, genomic, and transcriptomic features of anti-PD-1 response in cutaneous melanoma. We find that prior anti-CTLA-4 therapy is associated with differences in genomic, individual gene, and gene signatures in anti-PD-1 responders. Anti-CTLA-4-experienced melanoma tumors that respond to PD-1 blockade exhibit increased tumor mutational burden, inflammatory signatures, and altered cell cycle processes compared with anti-CTLA-4-naive tumors or anti-CTLA-4-experienced, anti-PD-1-nonresponsive melanoma tumors. We report a harmonized, aggregate resource and suggest that prior CTLA-4 blockade therapy is associated with marked differences in the tumor microenvironment that impact the predictive features of PD-1 blockade therapy response.

Indexed as

MelanomaSkin NeoplasmsBiomarkers, TumorCTLA-4 AntigenHumansImmunotherapyTumor MicroenvironmentBiomarkers, TumorCTLA-4 Antigenimmune checkpoint blockadeimmunotherapymelanomameta-analysis

Identifiers

PMID37037616
PMCPMC10187051
OpenAlexW4363674478

What OpenQuestion holds

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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.