Evidence map›Paper›PMID 21165163›Full record

ReviewOncotarget2010

EGFR-mutated lung cancer: a paradigm of molecular oncology.

Zhenfeng Zhang, Amy L Stiegler, Titus J Boggon, Susumu Kobayashi, Balazs Halmos

Abstract readReview
In one paragraph

Review in Oncotarget, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
–field-weighted citation impact
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

95 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Translational lung cancer research · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

35 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

5 authors.

Zhenfeng ZhangDivision of Hematology/Oncology, Herbert Irving Comprehensive Cancer Center, New York Presbyterian Hospital- Columbia University Medical Center, New York, NY, USA.
Amy L Stiegler
Titus J Boggon
Susumu Kobayashi
Balazs Halmos

Funding

BIOCHEMICAL ASPECTS OF CHEMOTHERAPYT32CA009085 · NCI · YALE UNIVERSITY · PI CHENG, YUNG-CHI · 1985 to 2009
$2.8M
Structural basis of Jak3-mediated interleukin-2 family signal transductionR01AI075133 · NIAID · YALE UNIVERSITY · PI BOGGON, TITUS JONATHON · 2007 to 2011
$2.2M
Structure and function of the integrin-linked kinase-PINCH-parvin complexR01GM088240 · NIGMS · YALE UNIVERSITY · PI BOGGON, TITUS JONATHON, CALDERWOOD, DAVID A · 2009 to 2012
$1.4M
Role of EGFR mutations and new therapeutics in lung cancerR00CA126026 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KOBAYASHI, SUSUMU · 2009 to 2011
$825k
NCI NIH HHS R00 CA126026NCI NIH HHS T32 CA009085NCI NIH HHS T32CA09085NIAID NIH HHS R00 AI075133NIAID NIH HHS R01 AI075133NIGMS NIH HHS R00 GM088240NIGMS NIH HHS R01 GM088240
6 · The paper itself

Abstract

The development of EGFR tyrosine kinase inhibitors for clinical use in non-small cell lung cancer and the subsequent discovery of activating EGFR mutations have led to an explosion of knowledge in the fields of EGFR biology, targeted therapeutics and lung cancer research. EGFR-mutated adenocarcinoma of the lung has clearly emerged as a unique clinical entity necessitating the routine introduction of molecular diagnostics into our current diagnostic algorithms and leading to the evidence-based preferential usage of EGFR-targeted agents for patients with EGFR-mutant lung cancers. This review will summarize our current understanding of the functional role of activating mutations, key downstream signaling pathways and regulatory mechanisms, pivotal primary and acquired resistance mechanisms, structure-function relationships and ultimately the incorporation of molecular diagnostics and small molecule EGFR tyrosine kinase inhibitors into our current treatment paradigms.

Indexed as

Molecular Diagnostic TechniquesAnimalsAntineoplastic AgentsCarcinomaErbB ReceptorsHumansLung NeoplasmsMedical OncologyModels, BiologicalMolecular Targeted TherapyMutant ProteinsProtein Kinase InhibitorsAntineoplastic AgentsEGFR protein, humanErbB ReceptorsMutant ProteinsProtein Kinase InhibitorsEGFRlung canceroncologytherapytyrosine kinase

Identifiers

PMID21165163
PMCPMC3001953

What OpenQuestion holds

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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.