Evidence map›Paper›PMID 17375033›Full record

Trial reportThe pharmacogenomics journal2008

Epidermal growth factor receptor polymorphisms and clinical outcomes in non-small-cell lung cancer patients treated with gefitinib.

G Liu, S Gurubhagavatula, W Zhou, Z Wang, B Y Yeap, K Asomaning, L Su, R Heist, T J Lynch, D C Christiani

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in The pharmacogenomics journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
–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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Journal of oncology · 2020
    Review
  11. Article
  12. Review
  13. Article
  14. Frequencies of EGFR single nucleotide polymorphisms in non-small cell lung cancer patients and healthy individuals in the Republic of Serbia: a preliminary study.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  15. Skin problems and EGFR-tyrosine kinase inhibitor.Japanese journal of clinical oncology · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

10 authors.

G LiuDepartment of Medicine, Harvard Medical School, Massachusetts General Hospital Cancer Center and Hematology-Oncology Division, Massachusetts General Hospital, Boston, MA, USA. Geoffrey.Liu@uhn.on.ca
S Gurubhagavatula
W Zhou
Z Wang
B Y Yeap
K Asomaning
L Su
R Heist
T J Lynch
D C Christiani

Funding

Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI SUSAN A KORRICK · 1985 to 2026
$44.6M
GENETIC SUSCEPTIBILITY TO LUNG CANCERR01CA074386 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI CHRISTIANI, DAVID C · 1997 to 2008
$4.8M
Molecular Epidemiology of Esophageal Cancer PrognosisR01CA109193 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LIU, GEOFFREY · 2004 to 2008
$1.9M
H.pylori, genes and esophageal adenocarcinomaR03CA110822 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LIU, GEOFFREY · 2004 to 2005
$175k
NCI NIH HHS CA109193NCI NIH HHS CA110822NCI NIH HHS CA74386NCI NIH HHS ES/CA 06409NIEHS NIH HHS ES00002
6 · The paper itself

Abstract

The-216G/T, -191C/A, intron 1 and Arg497Lys epidermal growth factor receptor (EGFR) polymorphisms were evaluated in 92 advanced non-small-cell lung cancer patients treated with gefitinib, an EGFR tyrosine-kinase inhibitor. Improved progression free survival (PFS) was found in patients homozygous for the shorter lengths of intron 1 polymorphism (S/S; S=16 or fewer CA repeats; log-rank test (LRT) P=0.03) and for patients carrying any T allele of the -216G/T polymorphism (LRT, P=0.005). When considered together, patients with intron 1 S/S genotype and at least one T allele of -216G/T had improved PFS (LRT P=0.0006; adjusted hazard ratio (AHR), 0.60 (95% confidence interval, 0.36-0.98)) and overall survival (LRT P=0.02; AHR, 0.60 (0.36-1.00)) when compared with all others. The T allele of -216G/T was also associated with significantly higher rates of stable disease/partial response (P=0.01) and a significantly higher risk of treatment-related rash/diarrhea (P=0.004, multivariate model). EGFR intron 1 and -216G/T polymorphisms influence clinical outcomes in gefitinib-treated non-small-cell lung cancer patients.

Indexed as

Gene Expression Regulation, NeoplasticPolymorphism, GeneticAdultAgedAged, 80 and overAntineoplastic AgentsCarcinoma, Non-Small-Cell LungCase-Control StudiesDiarrheaDisease-Free SurvivalErbB ReceptorsExanthemaFemaleGefitinibHomozygoteHumansAntineoplastic AgentsEGFR protein, humanErbB ReceptorsGefitinibProtein Kinase InhibitorsQuinazolines

Identifiers

PMID17375033

What OpenQuestion holds

Textmetadata
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.