Prognostic utility of HOXB13: IL17BR and molecular grade index in early-stage breast cancer patients from the Stockholm trial

被引:144
|
作者
Jerevall, P-L [1 ]
Ma, X-J [2 ]
Li, H. [2 ]
Salunga, R. [2 ]
Kesty, N. C. [2 ]
Erlander, M. G. [2 ]
Sgroi, D. C. [3 ]
Holmlund, B. [1 ]
Skoog, L. [4 ]
Fornander, T. [5 ]
Nordenskjold, B. [1 ]
Stal, O. [1 ]
机构
[1] Linkoping Univ, Dept Clin & Expt Med, Div Oncol, Fac Hlth Sci, SE-58185 Linkoping, Sweden
[2] BioTheranostics, San Diego, CA 92121 USA
[3] Massachusetts Gen Hosp, Dept Pathol, Mol Pathol Res Unit, Boston, MA 02129 USA
[4] Stockholm S Gen Hosp, Dept Oncol, Karolinska Univ Hosp, SE-11883 Stockholm, Sweden
[5] Karolinska Univ Hosp, Dept Pathol & Cytol, SE-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Breast Cancer Index; recurrence; risk assessment; gene expression profiling; prognosis; 2-GENE EXPRESSION RATIO; ADJUVANT TAMOXIFEN; SURVIVAL; RECEPTOR; ASSAY; RECURRENCE; PREDICTION; THERAPY; WOMEN;
D O I
10.1038/bjc.2011.145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: A dichotomous index combining two gene expression assays, HOXB13:IL17BR (H : I) and molecular grade index (MGI), was developed to assess risk of recurrence in breast cancer patients. The study objective was to demonstrate the prognostic utility of the combined index in early-stage breast cancer. METHODS: In a blinded retrospective analysis of 588 ER-positive tamoxifen-treated and untreated breast cancer patients from the randomised prospective Stockholm trial, H: I and MGI were measured using real-time RT-PCR. Association with patient outcome was evaluated by Kaplan-Meier analysis and Cox proportional hazard regression. A continuous risk index was developed using Cox modelling. RESULTS: The dichotomous H:I+MGI was significantly associated with distant recurrence and breast cancer death. The >50% of tamoxifen-treated patients categorised as low-risk had <3% 10-year distant recurrence risk. A continuous risk model (Breast Cancer Index (BCI)) was developed with the tamoxifen-treated group and the prognostic performance tested in the untreated group was 53% of patients categorised as low risk with an 8.3% 10-year distant recurrence risk. CONCLUSION: Retrospective analysis of this randomised, prospective trial cohort validated the prognostic utility of H:I+MGI and was used to develop and test a continuous risk model that enables prediction of distant recurrence risk at the patient level. British Journal of Cancer (2011) 104, 1762-1769. doi:10.1038/bjc.2011.145 www.bjcancer.com Published online 10 May 2011 (C) 2011 Cancer Research UK
引用
收藏
页码:1762 / 1769
页数:8
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