Evidence map›Paper›PMID 27166398›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2016

Density, Distribution, and Composition of Immune Infiltrates Correlate with Survival in Merkel Cell Carcinoma.

Laurence Feldmeyer, Courtney W Hudgens, Genevieve Ray-Lyons, Priyadharsini Nagarajan, Phyu P Aung, Jonathan L Curry, Carlos A Torres-Cabala, Barbara Mino, Jaime Rodriguez-Canales, Alexandre Reuben and 9 more

Registry-linked trialAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. 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 64 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 2 pooled it
6.5field-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.

NCT03651271 phase2completednot on this mapstarted 2018, after this paper: background citation

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

64 citing papers in PubMed, 2 syntheses or guidelines pooled it, 106 citations in OpenAlex.

  1. Guideline
  2. Merkel Cell Carcinoma, Version 1.2018, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2018
    Guideline
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4 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 1 institution in 1 country.

Laurence FeldmeyerDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Courtney W HudgensDepartment of Translational and Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Genevieve Ray-LyonsDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Priyadharsini NagarajanDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Phyu P AungDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jonathan L CurryDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Carlos A Torres-CabalaDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Barbara MinoDepartment of Translational and Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jaime Rodriguez-CanalesDepartment of Translational and Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Alexandre ReubenDepartment of Surgical Oncology The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pei-Ling ChenDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jennifer S KoDepartment of Pathology, Cleveland Clinic, Cleveland, Ohio.
Steven D BillingsDepartment of Pathology, Cleveland Clinic, Cleveland, Ohio.
Roland L BassettDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ignacio I WistubaDepartment of Translational and Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zachary A CooperDepartment of Surgical Oncology The University of Texas MD Anderson Cancer Center, Houston, Texas.
Victor G PrietoDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jennifer A WargoDepartment of Surgical Oncology The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michael T TetzlaffDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas. mtetzlaff@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

Multidisciplinary Subspecialty Pathology Research Fellowship ProgramT32CA163185 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CZERNIAK, BOGDAN A, KEYOMARSI, KHANDAN · 2011 to 2015
$1.7M
NCI NIH HHS T32 CA163185
6 · The paper itself

Abstract

purposeMerkel cell carcinoma (MCC) is an aggressive cancer with frequent metastasis and death with few effective therapies. Because programmed death ligand-1 (PD-L1) is frequently expressed in MCC, immune checkpoint blockade has been leveraged as treatment for metastatic disease. There is therefore a critical need to understand the relationships between MCPyV status, immune profiles, and patient outcomes. EXPERIMENTAL

designIHC for CD3, CD8, PD-1, PD-L1, and MCPyV T-antigen (to determine MCPyV status) was performed on 62 primary MCCs with annotated clinical outcomes. Automated image analysis quantified immune cell density (positive cells/mm

resultsNo histopathologic variable associated with overall survival (OS) or disease-specific survival (DSS), whereas higher CD3

conclusionsThese findings establish the tumor-associated immune infiltrate at the tumor periphery as a robust prognostic indicator in MCC and provide a mechanistic rationale to further examine whether the immune infiltrate at the tumor periphery is relevant as a biomarker for response in ongoing and future checkpoint inhibitor trials in MCC. Clin Cancer Res; 22(22); 5553-63. ©2016 AACR.

Indexed as

AdultAgedAged, 80 and overAntigens, Viral, TumorBiomarkersCarcinoma, Merkel CellCD3 ComplexCD8-Positive T-LymphocytesFemaleHumansLymphocytes, Tumor-InfiltratingMaleMerkel cell polyomavirusMiddle AgedPrognosisReceptors, Antigen, T-CellAntigens, Viral, TumorBiomarkersCD3 ComplexReceptors, Antigen, T-Cell

Identifiers

PMID27166398
PMCPMC5857157
OpenAlexW2363164936

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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.