Evidence map›Paper›PMID 30934880›Full record

ArticleCancers2019

Genetic Factors Associated with a Poor Outcome in Head and Neck Cancer Patients Receiving Definitive Chemoradiotherapy.

David M Vossen, Caroline V M Verhagen, Martijn van der Heijden, Paul B M Essers, Harry Bartelink, Marcel Verheij, Lodewyk F A Wessels, Michiel W M van den Brekel, Conchita Vens

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 2 institutions in 1 country.

David M VossenDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. d.vossen@nki.nl.
Caroline V M VerhagenDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. cverhagen@rijnstate.nl.
Martijn van der HeijdenDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. ma.vd.heijden@nki.nl.
Paul B M EssersDepartment of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. p.essers@nki.nl.
Harry BartelinkDepartment of Radiation Oncology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. h.bartelink@nki.nl.
Marcel VerheijDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. m.verheij@nki.nl.
Lodewyk F A WesselsDivision of Molecular Carcinogenesis, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. l.wessels@nki.nl.
Michiel W M van den BrekelDepartment of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. m.vd.brekel@nki.nl.ORCID 0000-0002-6338-6743
Conchita VensDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. c.vens@nki.nl.
The Netherlands Cancer Institute · NLAmsterdam UMC Location University of Amsterdam · NL

Funding

KWF Kankerbestrijding DESIGNVerwelius n/a
6 · The paper itself

Abstract

About half of advanced stage head and neck squamous cell carcinoma (HNSCC) patients can be cured by chemoradiotherapy. Patient outcome may be partially determined by the genetic alterations in HNSCC, rendering these alterations promising candidate prognostic factors and/or therapeutic targets. However, their relevance in patient outcome prognosis remains to be assessed in patients that receive standard-of-care chemoradiotherapy. We therefore tested whether frequent genetic alterations were associated with progression free survival (PFS) in advanced stage HNSCC patients who were uniformly treated with definitive platinum-based chemoradiotherapy. To this end, we performed targeted DNA sequencing on frozen pre-treatment tumor biopsy material from 77 patients with advanced stage oro- and hypopharyngeal carcinoma. This provided somatic point mutation and copy number aberration data of 556 genes. The most frequently mutated genes,

Indexed as

chemoradiotherapyDNA sequence analysisgenomicshead and neck squamous cell carcinomamutationpharyngeal neoplasmsprognosis

Identifiers

PMID30934880
PMCPMC6521057
OpenAlexW2933167929

What OpenQuestion holds

Textmetadata
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.