Class III β-tubulin isotype predicts response in advanced breast cancer patients randomly treated either with single-agent doxorubicin or docetaxel

被引:58
作者
Galmarini, Carlos M. [1 ]
Treilleux, Isabelle [2 ]
Cardoso, Fatima [3 ]
Bernard-Marty, Chantal [3 ]
Durbecq, Virginie [3 ]
Gancberg, David [4 ]
Bissery, Marie-Christine [5 ]
Paesmans, Marianne [3 ]
Larsimont, Denis [3 ]
Piccart, Martine J. [3 ]
Di Leo, Angelo [6 ]
Dumontet, Charles [1 ]
机构
[1] Univ Lyon 1, F-69365 Lyon, France
[2] Ctr Leon Berard, F-69373 Lyon, France
[3] Inst Jules Bordet, B-1000 Brussels, Belgium
[4] Commiss European Communities, Joint Res Ctr, Inst Reference Mat & Measurements, Geel, Belgium
[5] Aventis Oncol, Vitry Sur Seine, France
[6] Hosp Prato, Med Oncol Unit, Prato, Italy
关键词
D O I
10.1158/1078-0432.CCR-07-4741
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the role of microtubule-associated variables as potential predictors of response and clinical outcome in patients with advanced breast cancer receiving single-agent docetaxel or doxorubicin chemotherapy. Experimental Design: The analysis was done on 173 tumor samples from patients with locally advanced or metastatic breast cancer who have participated in theTAX-303 phase III trial in which patients were randomly assigned to receive docetaxel or doxorubicin. Expression of total alpha- and beta-tubulin, classes II to IV beta-tubulin isotypes, and tau protein was evaluated by immunohistochemistry on formalin-fixed, paraffin-embedded tumors from the primary breast cancer. Results: We observed that patients with "high" expression of class III beta-tubulin isotype had a higher probability of response to docetaxel than to doxorubicin treatment (odds ratio, 1.9; 95% confidence interval, 1.01-3.7; P = 0.05). No difference was observed in terms of time to progression or in terms of overall survival. Conclusions: This study suggests that the superiority of docetaxel over doxorubicin seems to be confined to the subgroup of patients with "high" expression of class III beta-tubulin isotype.
引用
收藏
页码:4511 / 4516
页数:6
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