Evidence map›Paper›PMID 41107054›Full record

ArticleHead & neck2026

A Practical Method for Detecting Prognostic CD57+ T Cells in Head and Neck Cancer.

Brianna Brammer, Brendan L C Kinney, Vikash Kansal, Nicole C Schmitt

Abstract read
In one paragraph

Article in Head & neck, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Brianna BrammerDepartment of Otolaryngology-Head and Neck Surgery, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-3042-7326
Brendan L C KinneyDepartment of Otolaryngology-Head and Neck Surgery, Emory University, Atlanta, Georgia, USA.
Vikash KansalDepartment of Otolaryngology-Head and Neck Surgery, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-8240-2112
Nicole C SchmittDepartment of Otolaryngology-Head and Neck Surgery, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-0571-3531

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
Emory Integrated Genomics CoreEmory Pediatrics/Winship Flow Cytometry CoreEmory Woodruff Health Sciences Center for Health in AgingNCI NIH HHS P30 CA138292NIH/NCI P30CA138292Winship Cancer InstituteWinship Cancer Tissue and Pathology Resource
6 · The paper itself

Abstract

backgroundRecurrence of head and neck squamous cell carcinoma (HNSCC) affects nearly half of patients and greatly reduces survival. There are currently no well-established mechanisms to predict which HNSCC patients will experience disease recurrence. We have previously shown that an elevated proportion of highly differentiated, CD57+ effector memory T (HD TEMRA) cells in circulation is associated with early recurrence and poor locoregional disease control in HNSCC patients.

methodsHere, we present refined flow cytometry panels utilizing fewer fluorescent antibodies that retain the prognostic value of HD TEMRA cells in predicting HNSCC recurrence.

resultsIn our cohort of surgically treated HNSCC patients, identifying HD TEMRA cells via flow cytometry as live CD8+ CD28- CD57+ cells effectively predicted disease recurrence. When assessing this cohort by disease subsite, we found that for patients with oral squamous cell carcinoma, identifying HD TEMRA cells by CD8+ CD57+ alone was sufficient for predicting locoregional disease recurrence.

conclusionsThese refined panels enhance the clinical utility of HD TEMRA proportion as a biomarker due to their technical and analytic ease. Implementation of HD TEMRA cell proportion as a clinical biomarker could aid in personalized HNSCC treatment planning.

Indexed as

CD57 AntigensHead and Neck NeoplasmsMemory T CellsNeoplasm Recurrence, LocalSquamous Cell Carcinoma of Head and NeckAgedCD8-Positive T-LymphocytesCohort StudiesFemaleFlow CytometryHumansMaleMiddle AgedPrognosisCD57 AntigensbiomarkerCD57flow cytometryhead and neck cancerrecurrenceTEMRA cells

Identifiers

PMID41107054
PMCPMC12824510

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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.