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Title: Survivin is an independent prognostic marker for risk stratification of breast cancer patients.
Author(s): Span, P.N. (14500435X)
Sweep, C.G.J. (074620967)
Wiegerinck, E.T.G. (321454529)
Tjan-Heijnen, V.C. (298975777)
Manders, P. (265602726)
Beex, L.V.A.M. (068435223)
Kok, J.B. de (203248937)
Publication year: 2004
Document type: Article / Letter to editor
Journal: Clinical Chemistry
ISSN: 0009-9147
Volume: vol. 50
Issue: iss. 11
Start page: p. 1986
End page: p. 1993
Abstract: BACKGROUND: Results in previous qualitative studies of the association of the apoptosis inhibitor survivin with prognosis of breast cancer patients have been contradictory. METHODS: Survivin mRNA was measured by quantitative TaqMan reverse transcription-PCR in 275 breast cancer tissues from patients with operable tumors and was correlated with established clinicopathologic factors, relapse-free survival [(RFS); 102 events], and overall survival [(OS); 81 events]. RESULTS: High survivin mRNA concentrations were found mainly in tissues from younger patients and in high-grade cancer tissues. High survivin concentrations were most strongly associated with estrogen receptor- or progesterone receptor-negative tumors. In univariate Cox regression analysis for RFS, survivin concentrations were significantly associated with poor prognosis with a hazard ratio (HR) of 1.99 (95% confidence interval, 1.31-3.02; P = 0.001) for every 10-fold increase in expression. For OS, a significant contribution of survivin to poor prognosis was found with a HR of 2.76 (1.67-4.55; P <0.001). Multivariate analyses were performed including established clinicopathologic factors. For RFS, age (P = 0.027), nodal category (P <0.001), and survivin [HR = 1.78 (1.18-2.68); P = 0.006] contributed significantly to the model. For OS, only nodal category (P <0.001) and survivin [HR = 3.05 (1.83-5.10); P <0.001] were significant. CONCLUSION: Survivin demonstrates a strong, independent, association with poor prognosis. Survivin might be used as a new marker to stratify breast cancer patients for more optimal treatment modalities, or it could be a promising new target for therapy.
Subject: UMCN 1.2: Molecular diagnosis, prognosis and monitoring
UMCN 5.2: Endocrinology and reproduction
Organization: Chemical Endocrinology
UMCN Extern
Medical Oncology
Clinical Chemistry
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/57695

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