Evidence map›Paper›PMID 28866730›Full record

ReviewCancer metastasis reviews2017

EGFR-targeted therapies in the post-genomic era.

Mary Jue Xu, Daniel E Johnson, Jennifer R Grandis

Open access · greenAbstract readReview
In one paragraph

Review in Cancer metastasis reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed, 4 pooled it
11.2field-weighted citation impact, top 1% 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

139 citing papers in PubMed, 4 syntheses or guidelines pooled it, 240 citations in OpenAlex.

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79 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

3 authors at 1 institution in 1 country.

Mary Jue XuDepartment of Otolaryngology, University of California San Francisco, 2380 Sutter Street, San Francisco, CA, 94113, USA.
Daniel E JohnsonDepartment of Otolaryngology, University of California San Francisco, 2380 Sutter Street, San Francisco, CA, 94113, USA.
Jennifer R GrandisDepartment of Otolaryngology, University of California San Francisco, 2380 Sutter Street, San Francisco, CA, 94113, USA. Jennifer.Grandis@ucsf.edu.
University of California, San Francisco · US

Funding

WILD TYPE P53-BASED ADJUVANT IMMUNOTHERAPY FOR SCCHNP50CA097190 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 2004 to 2026
$49.6M
PI3K Pathway Mutations in Head and Neck CancerR01DE023685 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GRANDIS, JENNIFER RUBIN, JOHNSON, DANIEL E · 2014 to 2023
$5.1M
Implications of Procaspase-8 Mutations in Oral Squamous Cell CarcinomaR01DE024728 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHNSON, DANIEL E · 2016 to 2020
$2.0M
NCI NIH HHS P50 CA097190NIDCR NIH HHS R01 DE023685NIDCR NIH HHS R01 DE024728
6 · The paper itself

Abstract

Over 90% of head and neck cancers overexpress the epidermal growth factor receptor (EGFR). In diverse tumor types, EGFR overexpression has been associated with poorer prognosis and outcomes. Therapies targeting EGFR include monoclonal antibodies, tyrosine kinase inhibitors, phosphatidylinositol 3-kinase (PI3K) inhibitors, and antisense gene therapy. Few EGFR-targeted therapeutics are approved for clinical use. The monoclonal antibody cetuximab is a Food and Drug Administration (FDA)-approved EGFR-targeted therapy, yet has exhibited modest benefit in clinical trials. The humanized monoclonal antibody nimotuzumab is also approved for head and neck cancers in Cuba, Argentina, Colombia, Peru, India, Ukraine, Ivory Coast, and Gabon in addition to nasopharyngeal cancers in China. Few other EGFR-targeted therapeutics for head and neck cancers have led to as significant responses as seen in lung carcinomas, for instance. Recent genome sequencing of head and neck tumors has helped identify patient subgroups with improved response to EGFR inhibitors, for example, cetuximab in patients with the KRAS-variant and the tyrosine kinase inhibitor erlotinib for tumors harboring MAPK1

Indexed as

AnimalsCarcinoma, Squamous CellErbB ReceptorsGenetic TherapyHead and Neck NeoplasmsHumansMolecular Targeted TherapyProtein Kinase InhibitorsRandomized Controlled Trials as TopicSquamous Cell Carcinoma of Head and NeckEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsCetuximabEGFRGenomicsHead and neck SCC

Identifiers

PMID28866730
PMCPMC5693744
OpenAlexW2751381819

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.