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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Class III beta-tubulin isotype predicts response in advanced breast cancer patients randomly treated either with single-agent doxorubicin or docetaxel.
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Class III beta-tubulin isotype predicts response in advanced breast cancer patients randomly treated either with single-agent doxorubicin or docetaxel.

机译:III类β-微管蛋白同种型可预测接受单药阿霉素或多西他赛治疗的晚期乳腺癌患者的反应。

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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 the TAX-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.
机译:目的:评估微管相关变量作为接受单药多西紫杉醇或阿霉素化疗的晚期乳腺癌患者反应和临床结局的潜在预测指标的作用。实验设计:对来自局部晚期或转移性乳腺癌患者的173份肿瘤样品进行了分析,这些患者参加了TAX-303 III期试验,其中患者被随机分配接受多西他赛或阿霉素。在原发性乳腺癌的福尔马林固定,石蜡包埋的肿瘤上,通过免疫组织化学评估了总的α-和β-微管蛋白,II至IV类β-微管蛋白同种型和tau蛋白的表达。结果:我们观察到,III类β-微管蛋白同种型“高”表达的患者对多西他赛的反应可能性比对阿霉素的治疗更高(赔率,1.9; 95%置信区间,1.01-3.7; P = 0.05)。在进展时间或总体存活率方面未观察到差异。结论:这项研究表明多西他赛相对于阿霉素的优越性似乎仅限于III类β-微管蛋白同型“高”表达的患者亚组。

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