Evidence map›Paper›PMID 26169963›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2015

Emerging Agents and New Mutations in EGFR-Mutant Lung Cancer.

Deborah Ayeni, Katerina Politi, Sarah B Goldberg

Open access · bronzeAbstract readComment
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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
4.1field-weighted citation impact, top 6% 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, 39 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Renal biopsy-driven molecular target identification in glomerular disease.Pflugers Archiv : European journal of physiology · 2017
    Review
  13. Management ofCurrent oncology (Toronto, Ont.) · 2017
    Review
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Deborah AyeniDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Katerina PolitiDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut. Department of Medicine (Section of Medical Oncology), Yale University School of Medicine, New Haven, Connecticut. Yale Cancer Center, Yale University School of Medicine, New Haven, Connecticut. katerina.politi@yale.edu sarah.goldberg@yale.edu.
Sarah B GoldbergDepartment of Medicine (Section of Medical Oncology), Yale University School of Medicine, New Haven, Connecticut. Yale Cancer Center, Yale University School of Medicine, New Haven, Connecticut. katerina.politi@yale.edu sarah.goldberg@yale.edu.
Yale Cancer Center · USYale University · US

Funding

Yale SPORE in Lung Cancer (YSILC): The Biology and Personalized Treatment of Lung CancerP50CA196530 · NCI · YALE UNIVERSITY · PI Shuangge Ma · 2015 to 2026
$31.1M
Mutant EGF Receptor-Dependent Lung Cancer in Human Cell Lines and Transgenic MiceR01CA120247 · NCI · YALE UNIVERSITY · PI POLITI, KATERINA ABIGAIL · 2006 to 2014
$3.8M
Overcoming acquired resistance to EGFR inhibitors in lung cancerR01CA121210 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI LOVLY, CHRISTINE M. · 2007 to 2016
$2.9M
Targeting the Immune System in Mouse Models of Lung AdenocarcinomaR01CA195720 · NCI · YALE UNIVERSITY · PI KAECH, SUSAN M, POLITI, KATERINA ABIGAIL · 2015 to 2017
$1.8M
NCI NIH HHS P50 CA196530NCI NIH HHS R01 CA120247NCI NIH HHS R01CA120247NCI NIH HHS R01 CA121210NCI NIH HHS R01 CA195720NCI NIH HHS R01CA195720
6 · The paper itself

Abstract

Third-generation mutant-specific EGFR tyrosine kinase inhibitors are showing robust clinical activity, particularly in lung cancers harboring the EGFR(T790M) mutation, yet acquired resistance to these agents emerges. Additional mutations in EGFR can confer resistance that, depending on their genomic context, could determine new drug sensitivities of the cancer cells.

Indexed as

AllelesMutationAcrylamidesAnimalsAntineoplastic AgentsDrug Resistance, NeoplasmErbB ReceptorsHumansProtein Kinase InhibitorsPyrimidinesAcrylamidesAntineoplastic AgentsErbB ReceptorsProtein Kinase InhibitorsPyrimidines

Identifiers

PMID26169963
PMCPMC4720502
OpenAlexW1840856333

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.