Predictors of long-term outcome following high-dose chemotherapy in high-risk primary breast cancer

被引:20
作者
Somlo, G
Simpson, JF
Frankel, P
Chow, W
Leong, L
Margolin, K
Morgan, R
Raschko, J
Shibata, S
Forman, S
Kogut, N
McNamara, M
Molina, A
Somlo, E
Doroshow, JH
机构
[1] City Hope Natl Med Ctr, Dept Med Oncol & Therapeut Res, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Dept Biostat, Duarte, CA 91010 USA
[3] City Hope Natl Med Ctr, Dept Hematol & Bone Marrow Transplantat, Duarte, CA 91010 USA
[4] Vanderbilt Univ, Med Ctr, Div Anat Pathol, Nashville, TN USA
关键词
high-risk breast cancer; high-dose therapy; risk factors;
D O I
10.1038/sj.bjc.6600450
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report on a predictive model of long-term outcome in 1 14 high-risk breast cancer patients treated with high-dose chemotherapy between 1989 and 1994. Paraffin-blocks from 90 of the 1 14 primaries were assessed for the presence of five risk factors: grade, mitotic index, protein expression of p53, HER2/neu, and oestrogen/progesterone receptor status; we could analyse the effect of risk factors in 84 of these 90 tumours. Seven-year relapse-free and overall survival was 58% (95% confidence interval 44-74%) and 82% (95% confidence interval 71-94%) vs 33% (95% confidence interval 21-52%) and 41% (95% confidence interval 28-60%) for patients whose primary tumours displayed greater than or equal to 3 risk factors vs patients with less than or equal to 2 risk factors. For the entire group of 168 high-risk breast cancer patients, inflammatory stage IIIB disease and involved post-mastectomy margins were associated with decreased relapse-free survival and overall survival; patients treated with non-doxorubicin containing standard adjuvant therapy experienced worse overall survival (RR, 2,08; 95% confidence interval 1.04 to 4.16; P=0.04), while adjuvant tamoxifen improved overall survival (RR, 0.65; 95% confidence interval 0.41-1.01; P=0.054). Future trial designs and patient selection for studies specific for high-risk breast cancer patients should include appropriate prognostic models. Validation of such models could come from recently completed randomised, prospective trials. (C) 2002 Cancer Research UK.
引用
收藏
页码:281 / 288
页数:8
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