Evidence map›Paper›PMID 36860910›Full record

ArticleCancer research communications2021

Comprehensive Immunoprofiling of High-Risk Oral Proliferative and Localized Leukoplakia.

Glenn J Hanna, Alessandro Villa, Nikhil Mistry, Yonghui Jia, Charles T Quinn, Madison M Turner, Kristen D Felt, Kathleen Pfaff, Robert I Haddad, Ravindra Uppaluri and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Glenn J HannaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-9969-2523
Alessandro VillaOral Medicine Clinic, University of California San Francisco School of Dentistry, San Francisco, California.ORCID 0000-0002-1966-6000
Nikhil MistryDivision of Oral Medicine and Dentistry, Harvard School of Dental Medicine, Boston, Massachusetts.
Yonghui JiaDepartment of Pathology, Brigham & Women's Hospital, Boston, Massachusetts.
Charles T QuinnDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Madison M TurnerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Kristen D FeltImmunoProfile, Brigham & Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts.
Kathleen PfaffDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Robert I HaddadDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Ravindra UppaluriDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Scott J RodigDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Sook-Bin WooDivision of Oral Medicine and Dentistry, Harvard School of Dental Medicine, Boston, Massachusetts.
Ann Marie EgloffDepartment of Pathology, Brigham & Women's Hospital, Boston, Massachusetts.
F Stephen HodiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Dana-Farber Cancer Institute · USBrigham and Women's Hospital · USHarvard University · USDana-Farber Brigham Cancer Center · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral leukoplakia is common and may, in some cases, progress to carcinoma. Proliferative leukoplakia is a progressive, often multifocal subtype with a high rate of malignant transformation compared with the more common localized leukoplakia. We hypothesized that the immune microenvironment and gene expression patterns would be distinct for proliferative leukoplakia compared with localized leukoplakia. We summarize key clinicopathologic features among proliferative leukoplakia and localized leukoplakia and compare cancer-free survival (CFS) between subgroups. We analyze immunologic gene expression profiling in proliferative leukoplakia and localized leukoplakia tissue samples (NanoString PanCancer Immune Oncology Profiling). We integrate immune cell activation and spatial distribution patterns in tissue samples using multiplexed immunofluorescence and digital image capture to further define proliferative leukoplakia and localized leukoplakia. Among Significance: This is the first in-depth profiling effort to immunologically characterize high-risk proliferative leukoplakia as compared with the more common localized leukoplakia. We observed a notable cytotoxic T-cell and Treg signature with relative overexpression of PD-L1 in high-risk proliferative leukoplakia providing a strong preclinical rationale for investigating PD-1/PD-L1 axis blockade in this disease as preventative immunotherapy.

Indexed as

B7-H1 AntigenCD8-Positive T-LymphocytesGene Expression ProfilingHumansLeukoplakia, OralProgrammed Cell Death 1 ReceptorTumor MicroenvironmentB7-H1 AntigenProgrammed Cell Death 1 Receptor

Identifiers

PMID36860910
PMCPMC9973379
OpenAlexW3206049324

What OpenQuestion holds

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LicenceCC BY
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.