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III 类β-微管蛋白作为预测可切除非小细胞肺癌辅助化疗获益的标志物的交叉验证研究:四项随机试验的分析。

Cross-validation study of class III beta-tubulin as a predictive marker for benefit from adjuvant chemotherapy in resected non-small-cell lung cancer: analysis of four randomized trials.

机构信息

Department of Medicine, Dalhousie University and Department of Oncology, Saint John Regional Hospital, Saint John.

Department of Laboratory Medicine and Pathology, Cross Cancer Institute and University of Alberta, Edmonton, Canada; Departments of.

出版信息

Ann Oncol. 2012 Jan;23(1):86-93. doi: 10.1093/annonc/mdr033. Epub 2011 Apr 6.

Abstract

BACKGROUND

The IALT, JBR.10, ANITA and Cancer and Leukemia Group B 9633 trials compared adjuvant chemotherapy with observation for patients with resected non-small-cell lung cancer (R-NSCLC). Data from the metastatic setting suggest high tumor class III beta-tubulin (TUBB3) expression is a determinant of insensitivity to tubulin-targeting agents (e.g. vinorelbine, paclitaxel). In 265 patients from JBR.10 (vinorelbine-cisplatin versus observation), high TUBB3 was an adverse prognostic factor and was associated (nonsignificantly) with 'greater' survival benefit from chemotherapy. We explored this further in additional patients from JBR.10 and the other three trials.

PATIENTS AND METHODS

TUBB3 immunohistochemical staining was scored for 1149 patients on the four trials. The original JBR.10 cut-off scores were used to classify tumors as TUBB3 high or low. The prognostic and predictive value of TUBB3 on disease-free survival (DFS) and overall survival (OS) was assessed by Cox models stratified by trial and adjusted for clinical factors.

RESULTS

High TUBB3 expression was prognostic for OS [hazard ratio (HR)=1.27 (1.07-1.51), P=0.008) and DFS [HR=1.30 (1.11-1.53), P=0.001). TUBB3 was not predictive of a differential treatment effect [interaction P=0.20 (OS), P=0.23 (DFS)]. Subset analysis (n=420) on vinorelbine-cisplatin gave similar results.

CONCLUSIONS

The prognostic effect of high TUBB3 expression in patients with R-NSCLC has been validated. We were unable to confirm a predictive effect for TUBB3.

摘要

背景

IALT、JBR.10、ANITA 和癌症与白血病组 B9633 试验比较了辅助化疗与观察治疗对接受手术治疗的非小细胞肺癌(R-NSCLC)患者的效果。转移性疾病数据表明,高肿瘤 III 类β-微管蛋白(TUBB3)表达是对微管靶向药物(如长春瑞滨、紫杉醇)不敏感的决定因素。在 JBR.10 试验(长春瑞滨-顺铂与观察治疗)的 265 名患者中,高 TUBB3 是一个不利的预后因素,且与化疗的“更大”生存获益相关(无统计学意义)。我们在 JBR.10 试验和其他三项试验的其他患者中进一步探讨了这一点。

患者和方法

对四项试验的 1149 名患者进行 TUBB3 免疫组织化学染色评分。采用原始 JBR.10 截断评分将肿瘤分为 TUBB3 高表达或低表达。通过按试验分层的 Cox 模型评估 TUBB3 对无病生存(DFS)和总生存(OS)的预后和预测价值,并根据临床因素进行调整。

结果

高 TUBB3 表达与 OS [风险比(HR)=1.27(1.07-1.51),P=0.008]和 DFS [HR=1.30(1.11-1.53),P=0.001]相关。TUBB3 对治疗效果的差异无预测作用[交互 P=0.20(OS),P=0.23(DFS)]。长春瑞滨-顺铂亚组分析(n=420)得出了相似的结果。

结论

R-NSCLC 患者中高 TUBB3 表达的预后作用已得到验证。我们未能证实 TUBB3 的预测作用。

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