Sève Pascal, Mackey John, Isaac Sylvie, Trédan Olivier, Souquet Pierre-Jean, Pérol Maurice, Lai Raymond, Voloch Alain, Dumontet Charles
Service de Médecine Interne, Hospices Civils de Lyon, France.
Mol Cancer Ther. 2005 Dec;4(12):2001-7. doi: 10.1158/1535-7163.MCT-05-0244.
Both fundamental and clinical studies suggest that class III beta-tubulin expression is associated with resistance to taxanes and constitutes a prognostic factor in several solid tumors. In this study, we assessed the prognostic and predictive value of class III beta-tubulin in tumors of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) treated with paclitaxel-based or other regimens that did not include tubulin-binding agents. Expression of class III beta-tubulin was examined immunohistochemically in 91 tumor samples obtained before treatment from patients with stage III and IV NSCLC, including 47 who received paclitaxel-based regimens and 44 who received regimens without tubulin-binding agents. Response to chemotherapy, progression-free survival, and overall survival were correlated with the expression of class III beta-tubulin protein. The response rate was 37.5% (16 responses among 45 evaluable patients) among patients receiving paclitaxel. Patients whose tumors expressed low levels of class III beta-tubulin isotype had a better response rate, longer progression-free survival, and overall survival (P < 0.001, 0.004, and 0.002, respectively), whereas this variable was not found to be predictive in patients receiving regimens without tubulin-binding agents. A multivariate analysis taking into account sex, age, histology, stage, and class III beta-tubulin confirmed that low-level class III beta-tubulin expression was independently correlated with progression-free survival (P = 0.003) and overall survival (P = 0.003). These findings suggest that the expression levels of class III beta-tubulin in tumor cells is predictive of response to therapy and patient outcome in patients with NSCLC receiving paclitaxel-based chemotherapy but is not a general prognostic factor in this patient population.
基础研究和临床研究均表明,Ⅲ类β-微管蛋白的表达与对紫杉烷类药物的耐药性相关,并且是多种实体瘤的一个预后因素。在本研究中,我们评估了Ⅲ类β-微管蛋白在接受以紫杉醇为基础或其他不包括微管蛋白结合剂方案治疗的局部晚期或转移性非小细胞肺癌(NSCLC)患者肿瘤中的预后和预测价值。采用免疫组织化学方法检测了91例Ⅲ期和Ⅳ期NSCLC患者治疗前获取的肿瘤样本中Ⅲ类β-微管蛋白的表达,其中47例接受以紫杉醇为基础的方案,44例接受不包括微管蛋白结合剂的方案。化疗反应、无进展生存期和总生存期与Ⅲ类β-微管蛋白的表达相关。接受紫杉醇治疗的患者中,缓解率为37.5%(45例可评估患者中有16例缓解)。肿瘤表达低水平Ⅲ类β-微管蛋白亚型的患者缓解率更高、无进展生存期和总生存期更长(分别为P<0.001、0.004和0.002),而在接受不包括微管蛋白结合剂方案治疗的患者中未发现该变量具有预测价值。一项纳入性别、年龄、组织学类型、分期和Ⅲ类β-微管蛋白的多因素分析证实,低水平Ⅲ类β-微管蛋白表达与无进展生存期(P=0.003)和总生存期(P=0.003)独立相关。这些发现表明,肿瘤细胞中Ⅲ类β-微管蛋白的表达水平可预测接受以紫杉醇为基础化疗的NSCLC患者的治疗反应和患者预后,但并非该患者群体的一个普遍预后因素。