Evidence map›Paper›PMID 27859938›Full record

ReviewHead & neck2017

Head and neck squamous cell carcinoma: Ambiguous human papillomavirus status, elevated p16, and deleted retinoblastoma 1.

Tim N Beck, Chad H Smith, Douglas B Flieder, Thomas J Galloway, John A Ridge, Erica A Golemis, Ranee Mehra

Abstract readCase ReportsReview
In one paragraph

Review in Head & neck, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 16 citations in OpenAlex.

  1. [Expert consensus on artificial intelligence-assisted data acquisition and clinical application in electronic nasopharyngolaryngoscopy].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2026
    Article
  2. Article
  3. Article
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

7 authors at 1 institution in 1 country.

Tim N BeckProgram in Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Chad H SmithProgram in Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Douglas B FliederDepartment of Pathology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Thomas J GallowayDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
John A RidgeProgram in Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Erica A GolemisProgram in Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Ranee MehraProgram in Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Fox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
Therapeutic Micro RNA Strategies for Ovarian CancerP50CA083638 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI DALY, MARY BERYL, REBBECK, TIMOTHY R · 1999 to 2013
$33.6M
Novel Targets in Endocrine ResponsivenessU54CA149147 · NCI · GEORGETOWN UNIVERSITY · PI MADHAVAN, SUBHA · 2010 to 2014
$6.9M
Msi2 regulates the aggressiveness of Non-Small Cell Lung Cancer (NSCLC)R21CA191425 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GOLEMIS, ERICA A. · 2016 to 2017
$427k
A Role for AMH Autocrine Signaling in NSCLCR21CA181287 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GOLEMIS, ERICA A. · 2014 to 2015
$421k
Characterization of AMH as part of a novel TGF-beta signaling loopF30CA180607 · NCI · DREXEL UNIVERSITY · PI BECK, TIM NICO · 2014 to 2017
$163k
NCI NIH HHS F30 CA180607NCI NIH HHS P30 CA006927NCI NIH HHS P50 CA083638NCI NIH HHS R21 CA181287NCI NIH HHS R21 CA191425NCI NIH HHS U54 CA149147
6 · The paper itself

Abstract

backgroundHead and neck squamous cell carcinoma (HNSCC) is potentially curable, but treatment planning remains a challenge. Oncogenic human papillomavirus (HPV)-positive disease is often associated with a good prognosis compared with HPV-negative disease. However, some HPV-positive HNSCC recurs, often with distant metastases and significant treatment resistance. METHODS AND

resultsWe performed p16 immunohistochemistry (IHC), in situ hybridization (ISH) for high-risk HPV, and comprehensive genomic profiling on oropharyngeal HNSCC with basaloid features and particularly aggressive disease course, noting a rare genetic event: a deleting mutation (exons 5-17) of the tumor suppressor and dominant cell cycle regulator retinoblastoma 1 (RB1). Genomic and transcriptomic data available through FoundationOne and The Cancer Genome Atlas (TCGA) were reviewed for additional HNSCC cases with RB1 alterations.

conclusionRB1 alterations may have important prognostic implications, particularly in the context of high p16 expression, in both HPV-positive and HPV-negative HNSCC. © 2016 Wiley Periodicals, Inc. Head Neck 39: E34-E39, 2017.

Indexed as

AgedBiopsy, NeedleCarcinoma, Squamous CellChemoradiotherapyCyclin-Dependent Kinase Inhibitor p16E2F1 Transcription FactorFollow-Up StudiesGene DeletionHead and Neck NeoplasmsHumansImmunohistochemistryIn Situ HybridizationMalePapillomaviridaeSquamous Cell Carcinoma of Head and NeckTongue NeoplasmsCyclin-Dependent Kinase Inhibitor p16E2F1 Transcription Factorhead and neck squamous cell carcinomahuman papillomavirusp16retinoblastoma 1 (RB1)The Cancer Genome Atlas (TCGA)

Identifiers

PMID27859938
PMCPMC5439525
OpenAlexW2557386463

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.