Evidence map›Paper›PMID 19513067›Full record

ArticleBritish journal of cancer2009

Quantitative immunohistochemical expression of c Kit in breast carcinomas is predictive of patients' outcome.

C Charpin, S Giusiano, S Charfi, V Secq, S Carpentier, L Andrac, M-N Lavaut, C Allasia, P Bonnier, S Garcia

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Article in British journal of cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

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0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Trial
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  6. Nanotechniques Inactivate Cancer Stem Cells.Nanoscale research letters · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Biofunctional characteristics of in situ and invasive breast carcinoma.Cellular oncology (Dordrecht, Netherlands) · 2013
    Article
  11. Article
  12. Article
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

C CharpinDepartment of Pathology, Hôpital Nord and Université de la Méditerranée (Aix Marseille II), Marseille, France. colette.charpin@ap-hm.fr
S Giusiano
S Charfi
V Secq
S Carpentier
L Andrac
M-N Lavaut
C Allasia
P Bonnier
S Garcia

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundc Kit (CD117) expression in tissues has been reported as a relevant target for specific therapy in some human malignancies, but has been poorly documented in breast carcinomas.

methodsThe prognostic significance of c Kit in a series of 924 breast carcinomas (mean follow-up, 79 months) was investigated using standardised high-throughput quantitative densitometry of immunohistochemical precipitates in tissue microarrays.

resultsc Kit was expressed in 14.7% breast carcinomas (and in 42 out of 586 node-negative tumours). In univariate analysis, (log-rank test) the score of c Kit expression correlated with poor patient outcome P=0.02 and particularly in node-negative cases (P=0.002). In multivariate Cox analysis, c Kit was an indicator of metastasis independent of 25 other concomitantly evaluated markers of prognosis. Logistic regression showed that c Kit ranked 10 out of 25 (P=0.041), and was included in a 10-marker signature that allowed 79.2% of the patients to be correctly classified in the metastatic or metastasis-free categories independently of hormone receptors and HER-2 status. Interestingly, c Kit was also a significant predictor of metastasis in node-negative tumours (2 out of 25 ranking, P<0.0001) and included in a six-marker signature of prognosis, correctly classifying 88.6% of the patients (P<0.0001).

conclusionWe concluded that, as assessed by quantitative immunohistochemistry, c Kit is an independent prognostic indicator that could also potentially serve as a target for specific therapy in breast carcinomas.

Indexed as

Biomarkers, TumorBreast NeoplasmsDensitometryFemaleHumansImmunohistochemistryLogistic ModelsLymphatic MetastasisMicroarray AnalysisMultivariate AnalysisNeoplasm InvasivenessPredictive Value of TestsPrognosisProto-Oncogene Proteins c-kitROC CurveBiomarkers, TumorProto-Oncogene Proteins c-kit

Identifiers

PMID19513067
PMCPMC2713691

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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.