Evidence map›Paper›PMID 31605795›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2019

Quantitative Assessment of CMTM6 in the Tumor Microenvironment and Association with Response to PD-1 Pathway Blockade in Advanced-Stage Non-Small Cell Lung Cancer.

Jon Zugazagoitia, Yuting Liu, Maria Toki, John McGuire, Fahad Shabbir Ahmed, Brian S Henick, Richa Gupta, Scott N Gettinger, Roy S Herbst, Kurt A Schalper and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. A CMTM6 Nanobody Overcomes EGFR-TKI Resistance in Non-Small Cell Lung Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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  15. [Advances in the Study of Chemokine-like Factor Superfamily Members in Tumors].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. CMTM6 as a master regulator of PD-L1.Cancer immunology, immunotherapy : CII · 2022
    Review
  20. The clinical and prognostic significance of CMTM6/PD-L1 in oncology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
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

11 authors at 2 institutions in 2 countries.

Jon ZugazagoitiaDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Yuting LiuDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Maria TokiDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut; Department of Medicine, Sotiria General Hospital, Athens School of Medicine, Athens, Greece.
John McGuireDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Fahad Shabbir AhmedDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Brian S HenickDepartment of Medicine (Oncology), Columbia University Medical Center, New York, New York.
Richa GuptaDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Scott N GettingerDepartment of Medicine (Oncology), Yale University School of Medicine, New Haven, Connecticut.
Roy S HerbstDepartment of Medicine (Oncology), Yale University School of Medicine, New Haven, Connecticut.
Kurt A SchalperDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut; Department of Medicine (Oncology), Yale University School of Medicine, New Haven, Connecticut.
David L RimmDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut; Department of Medicine (Oncology), Yale University School of Medicine, New Haven, Connecticut. Electronic address: david.rimm@yale.edu.
Yale University · USColumbia University Irving Medical Center · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
Yale SPORE in Lung Cancer (YSILC): The Biology and Personalized Treatment of Lung CancerP50CA196530 · NCI · YALE UNIVERSITY · PI Shuangge Ma · 2015 to 2026
$31.1M
NCATS NIH HHS UL1 TR001863NCI NIH HHS P30 CA016359NCI NIH HHS P50 CA196530
6 · The paper itself

Abstract

introductionCKLF like MARVEL transmembrane domain containing 6 (CMTM6) has been described as a programmed death ligand 1 (PD-L1) regulator at the protein level by modulating stability through ubiquitination. In this study, we describe the patterns of CMTM6 expression and assess its association with response to programmed cell death 1 pathway blockade in NSCLC.

methodsWe used multiplexed quantitative immunofluorescence to determine the expression of CMTM6 and PD-L1 in 438 NSCLCs represented in tissue microarrays, including in two independent retrospective cohorts of immunotherapy-treated (n = 69) and non-immunotherapy-treated (n = 258) patients and a third collection of EGFR- and KRAS-genotyped tumors (n = 111).

resultsTumor and stromal CMTM6 expression was detected in approximately 70% of NSCLCs. CMTM6 expression was not associated with clinical features or EGFR/KRAS mutational status and showed a modest correlation with T-cell infiltration (R

conclusionThis study supports the mechanistic role for CMTM6 in stabilization of PD-L1 in patient tumors and suggests that high coexpression of CMTM6 and PD-L1, particularly in stromal immune cells (macrophages), might identify the greatest benefit from programmed cell death 1 axis blockade in NSCLC.

Indexed as

AgedB7-H1 AntigenCarcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsMaleMARVEL Domain-Containing ProteinsMembrane ProteinsMyelin ProteinsNeoplasm StagingRetrospective StudiesTissue Array AnalysisTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanCMTM6 protein, humanMARVEL Domain-Containing ProteinsMembrane ProteinsMyelin ProteinsCMTM6Immune checkpoint blockadeMacrophagesNSCLCPD-L1

Identifiers

PMID31605795
PMCPMC6951804
OpenAlexW2979775607

What OpenQuestion holds

Textmetadata
LicenceTDM
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.