Evidence map›Paper›PMID 19451690›Full record

ArticleThe Journal of clinical investigation2009

Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions.

Martin L Sos, Kathrin Michel, Thomas Zander, Jonathan Weiss, Peter Frommolt, Martin Peifer, Danan Li, Roland Ullrich, Mirjam Koker, Florian Fischer and 33 more

Registry-linked trialAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02577341 (A Prospective Randomized Phase Ⅱ Study of Nimotuzumab Combined With Chemoradiotherapy for Unresectable, Locally Advanced Squamous Cell Lung Cancer), which is not on this map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing 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.

NCT02577341 phase2completednot on this mapstarted 2015, after this paper: background citation

A Prospective Randomized Phase Ⅱ Study of Nimotuzumab Combined With Chemoradiotherapy for Unresectable, Locally Advanced Squamous Cell Lung Cancer

TypeinterventionalSponsorSun Yat-sen UniversityRan2015 to 2020Enrolled122ConditionsNon-small-cell Lung CancerArmsNimotuzumab, docetaxel and cisplatin, daily RT to the chest
3 · Its place in the literature

Who cites it

138 citing papers in PubMed.

  1. Trial
  2. Dual Inhibition of EGFR and c-Src by Cetuximab and Dasatinib Combined with FOLFOX Chemotherapy in Patients with Metastatic Colorectal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Trial
  3. Trial
  4. A multicenter phase II study of ganetespib monotherapy in patients with genotypically defined advanced non-small cell lung cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Trial
  5. Phase II study of dasatinib in patients with advanced non-small-cell lung cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2010
    Trial
  6. Phase I/II study of the Src inhibitor dasatinib in combination with erlotinib in advanced non-small-cell lung cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2010
    Trial
  7. Article
  8. Review
  9. May EPH/Ephrin Targeting Revolutionize Lung Cancer Treatment?International journal of molecular sciences · 2022
    Review
  10. Review
  11. Patient-Derived In Vitro and In Vivo Models of Cancer.Advances in experimental medicine and biology · 2022
    Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

78 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

43 authors.

Martin L SosMax Planck Institute for Neurological Research, Klaus-Joachim-Zülch Laboratories of Max Planck Society, and University of Köln Medical Faculty, University of Köln, Cologne, Germany.
Kathrin Michel
Thomas Zander
Jonathan Weiss
Peter Frommolt
Martin Peifer
Danan Li
Roland Ullrich
Mirjam Koker
Florian Fischer
Takeshi Shimamura
Daniel Rauh
Craig Mermel
Stefanie Fischer
Isabel Stückrath
Stefanie Heynck
Rameen Beroukhim
William Lin
Wendy Winckler
Kinjal Shah
Thomas LaFramboise
Whei F Moriarty
Megan Hanna
Laura Tolosi
Jörg Rahnenführer
Roel Verhaak
Derek Chiang
Gad Getz
Martin Hellmich
Jürgen Wolf
Luc Girard
Michael Peyton
Barbara A Weir
Tzu-Hsiu Chen
Heidi Greulich
Jordi Barretina
Geoffrey I Shapiro
Levi A Garraway
Adi F Gazdar
John D Minna
Matthew Meyerson
Kwok-Kin Wong
Roman K Thomas

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Translational studies of Hsp90 inhibitors in NSCLCP50CA090578 · NCI · DANA-FARBER CANCER INST · PI JOHNSON, BRUCE D · 2008 to 2012
$11.4M
In vivo analysis of EGFR mutant driven lung cancers responses to radiation therapR01CA122794 · NCI · DANA-FARBER CANCER INST · PI WONG, KWOK KIN · 2006 to 2015
$2.8M
NCI NIH HHS P50 CA070907NCI NIH HHS P50 CA090578NCI NIH HHS P50CA70907NCI NIH HHS R01 CA122794NIA NIH HHS R01 AG2400401NIGMS NIH HHS T32 GM007753
6 · The paper itself

Abstract

Somatic genetic alterations in cancers have been linked with response to targeted therapeutics by creation of specific dependency on activated oncogenic signaling pathways. However, no tools currently exist to systematically connect such genetic lesions to therapeutic vulnerability. We have therefore developed a genomics approach to identify lesions associated with therapeutically relevant oncogene dependency. Using integrated genomic profiling, we have demonstrated that the genomes of a large panel of human non-small cell lung cancer (NSCLC) cell lines are highly representative of those of primary NSCLC tumors. Using cell-based compound screening coupled with diverse computational approaches to integrate orthogonal genomic and biochemical data sets, we identified molecular and genomic predictors of therapeutic response to clinically relevant compounds. Using this approach, we showed that v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS) mutations confer enhanced Hsp90 dependency and validated this finding in mice with KRAS-driven lung adenocarcinoma, as these mice exhibited dramatic tumor regression when treated with an Hsp90 inhibitor. In addition, we found that cells with copy number enhancement of v-abl Abelson murine leukemia viral oncogene homolog 2 (ABL2) and ephrin receptor kinase and v-src sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog (avian) (SRC) kinase family genes were exquisitely sensitive to treatment with the SRC/ABL inhibitor dasatinib, both in vitro and when it xenografted into mice. Thus, genomically annotated cell-line collections may help translate cancer genomics information into clinical practice by defining critical pathway dependencies amenable to therapeutic inhibition.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Non-Small-Cell LungCell Line, TumorDrug Evaluation, PreclinicalErbB ReceptorsGene Expression ProfilingHumansMagnetic Resonance ImagingMiceModels, MolecularMutationPhenotypeProtein Structure, TertiarySubstrate SpecificityAntineoplastic AgentsErbB Receptors

Identifiers

PMID19451690
PMCPMC2689116

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.