Evidence map›Paper›PMID 38340723›Full record

ArticleCell reports. Medicine2024

Circulating cancer-specific CD8 T cell frequency is associated with response to PD-1 blockade in Merkel cell carcinoma.

Thomas Pulliam, Saumya Jani, Lichen Jing, Heeju Ryu, Ana Jojic, Carolyn Shasha, Jiajia Zhang, Rima Kulikauskas, Candice Church, Charlie Garnett-Benson and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cell reports. 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 NCT02488759 (Non-Comparative, Open-Label, Multiple Cohort, Phase 1/2 Study of Nivolumab Monotherapy and Nivolumab Combination Therapy in Subjects With Virus-Positive and Virus-Negative Solid Tumors), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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.

NCT02488759 phase1 / phase2completednot on this map

Non-Comparative, Open-Label, Multiple Cohort, Phase 1/2 Study of Nivolumab Monotherapy and Nivolumab Combination Therapy in Subjects With Virus-Positive and Virus-Negative Solid Tumors

TypeinterventionalSponsorBristol-Myers SquibbRan2015 to 2022Enrolled578ConditionsVarious Advanced CancerArmsNivolumab, Ipilimumab, Relatlimab, Daratumumab
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  17. Merkel cell polyomavirus-specific and CD39Cell reports. Medicine · 2024
    Article
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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 at 6 institutions in 1 country.

Thomas PulliamDivision of Dermatology, Department of Medicine, University of Washington, Seattle, WA 98109, USA.
Saumya JaniDivision of Dermatology, Department of Medicine, University of Washington, Seattle, WA 98109, USA; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98109, USA.
Lichen JingDepartment of Medicine, University of Washington, Seattle, WA 98109, USA.
Heeju RyuVaccine and Infectious Disease Department, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Ana JojicVaccine and Infectious Disease Department, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Carolyn ShashaVaccine and Infectious Disease Department, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Jiajia ZhangDepartment of Oncology, Johns Hopkins University, Baltimore, MD 21827, USA; The Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University, Baltimore, MD 21287, USA.
Rima KulikauskasDivision of Dermatology, Department of Medicine, University of Washington, Seattle, WA 98109, USA.
Candice ChurchDivision of Dermatology, Department of Medicine, University of Washington, Seattle, WA 98109, USA.
Charlie Garnett-BensonBristol Myers Squibb, Princeton, NJ 08540, USA.
Ted GooleyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Aude ChapuisDepartment of Medicine, University of Washington, Seattle, WA 98109, USA; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Kelly PaulsonPaul G. Allen Research Center, Providence-Swedish Cancer Institute, Seattle, WA 98104, USA; Elson S. Floyd College of Medicine, Washington State University, Spokane, WA 99202, USA.
Kellie N SmithDepartment of Oncology, Johns Hopkins University, Baltimore, MD 21827, USA; The Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University, Baltimore, MD 21287, USA.
Drew M PardollDepartment of Oncology, Johns Hopkins University, Baltimore, MD 21827, USA; The Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University, Baltimore, MD 21287, USA.
Evan W NewellDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98109, USA; Vaccine and Infectious Disease Department, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
David M KoelleDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98109, USA; Department of Medicine, University of Washington, Seattle, WA 98109, USA; Vaccine and Infectious Disease Department, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA; Department of Global Health, University of Washington, Seattle, WA 98109, USA; Benaroya Research Institute, Seattle, WA 98101, USA.
Suzanne L TopalianThe Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University, Baltimore, MD 21287, USA; Department of Surgery, Johns Hopkins University, Baltimore, MD 21287, USA.
Paul NghiemDivision of Dermatology, Department of Medicine, University of Washington, Seattle, WA 98109, USA. Electronic address: pnghiem@uw.edu.
Fred Hutch Cancer Center · USUniversity of Washington · USBloomberg (United States) · USJohns Hopkins University · USBristol-Myers Squibb (United States) · USGeorgia Highlands College · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Understand & overcome resistance to PD-1P01CA225517 · NCI · UNIVERSITY OF WASHINGTON · PI Cecilia C Yeung · 2019 to 2026
$22.7M
Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
PD-1/PD-L1 modulation in cancer therapyR01CA142779 · NCI · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M., TAUBE, JANIS M · 2010 to 2025
$8.2M
Immunogenomic determinants of response and resistance to neoadjuvant anti-PD-1 in resectable NSCLCR37CA251447 · NCI · JOHNS HOPKINS UNIVERSITY · PI Kellie Nicole Smith · 2021 to 2026
$2.2M
Exhaustion mechanisms in Merkel cell polyomavirus-specific T cellsF30CA254168 · NCI · UNIVERSITY OF WASHINGTON · PI PULLIAM, THOMAS · 2020 to 2023
$168k
NCI NIH HHS F30 CA254168NCI NIH HHS P01 CA225517NCI NIH HHS P30 CA015704NCI NIH HHS R01 CA142779NCI NIH HHS R37 CA251447NCI NIH HHS T32 CA080416
6 · The paper itself

Abstract

Understanding cancer immunobiology has been hampered by difficulty identifying cancer-specific T cells. Merkel cell polyomavirus (MCPyV) causes most Merkel cell carcinomas (MCCs). All patients with virus-driven MCC express MCPyV oncoproteins, facilitating identification of virus (cancer)-specific T cells. We studied MCPyV-specific T cells from 27 patients with MCC using MCPyV peptide-HLA-I multimers, 26-color flow cytometry, single-cell transcriptomics, and T cell receptor (TCR) sequencing. In a prospective clinical trial, higher circulating MCPyV-specific CD8 T cell frequency before anti-PD-1 treatment was strongly associated with 2-year recurrence-free survival (75% if detectable, 0% if undetectable, p = 0.0018; ClinicalTrial.gov: NCT02488759). Intratumorally, such T cells were typically present, but their frequency did not significantly associate with response. Circulating MCPyV-specific CD8 T cells had increased stem/memory and decreased exhaustion signatures relative to their intratumoral counterparts. These results suggest that cancer-specific CD8 T cells in the blood may play a role in anti-PD-1 responses. Thus, strategies that augment their number or mobilize them into tumors could improve outcomes.

Indexed as

Carcinoma, Merkel CellSkin NeoplasmsCD8-Positive T-LymphocytesClinical Trials as TopicHumansProgrammed Cell Death 1 ReceptorProspective StudiesProgrammed Cell Death 1 Receptoracquired resistanceanti-PD-1cancer-specific T cellsHLA-IMerkel cell carcinomaMerkel cell polyomavirusnivolumabprimary resistanceskin cancer

Identifiers

PMID38340723
PMCPMC10897614
OpenAlexW4391722966

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.