Sève Pascal, Dumontet Charles
Université Claude Bernard Lyon, Lyon, France.
Lancet Oncol. 2008 Feb;9(2):168-75. doi: 10.1016/S1470-2045(08)70029-9.
On the basis of preclinical studies that show overexpression of class III beta-tubulin is associated with resistance to tubulin-binding agents, several investigators have addressed the relation between class III beta-tubulin and outcome in patients treated with such agents. High expression of class III beta-tubulin has been found to be correlated either with low response rates in patients treated with regimens containing taxanes or vinorelbine or with reduced survival in patients with non-small-cell lung cancer, in breast, ovarian, and gastric cancers, and in cancers of unknown primary site. Two studies have shown patients with advanced non-small-cell lung cancer receiving paclitaxel whose tumours expressed high levels of class III beta-tubulin had a lower response to paclitaxel and shorter survival, whereas this variable was not found to be predictive in patients receiving regimens without tubulin-binding agents. Conversely, analysis of samples from patients in the JBR-10 trial, which compared adjuvant chemotherapy to no further therapy in operable non-small-cell lung cancer, showed that chemotherapy seemed to overcome the negative prognostic effect of high levels of expression of class III beta-tubulin and the greatest benefit from cisplatin/vinorelbine was seen in patients with high levels of expression of class III beta-tubulin. Further analyses in operable and advanced non-small-cell lung cancer showed a relation between high expression of class III beta-tubulin and baseline factors such as age under 60 years, adenocarcinoma and large-cell carcinoma histologies, and advanced stage of disease. These results suggest that class III beta-tubulin could be both a prognostic and a predictive factor. Large randomised studies are warranted to determine the prognostic or predictive value of class III beta-tubulin in different settings and tumours.
临床前研究表明,III类β-微管蛋白的过表达与对微管蛋白结合剂的耐药性相关。基于此,一些研究人员探讨了III类β-微管蛋白与接受此类药物治疗的患者预后之间的关系。研究发现,III类β-微管蛋白的高表达要么与接受含紫杉烷或长春瑞滨方案治疗的患者低反应率相关,要么与非小细胞肺癌、乳腺癌、卵巢癌和胃癌以及原发部位不明的癌症患者的生存期缩短相关。两项研究表明,晚期非小细胞肺癌患者接受紫杉醇治疗,其肿瘤高表达III类β-微管蛋白时,对紫杉醇的反应较低且生存期较短,而在接受不含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性。相反,JBR-10试验对可手术的非小细胞肺癌患者进行辅助化疗与不进行进一步治疗的比较,对患者样本的分析表明,化疗似乎克服了III类β-微管蛋白高表达的负面预后影响,且III类β-微管蛋白高表达的患者从顺铂/长春瑞滨治疗中获益最大。对可手术和晚期非小细胞肺癌的进一步分析表明,III类β-微管蛋白的高表达与基线因素如60岁以下年龄、腺癌和大细胞癌组织学类型以及疾病晚期有关。这些结果表明,III类β-微管蛋白可能既是一个预后因素,也是一个预测因素。有必要进行大型随机研究,以确定III类β-微管蛋白在不同情况和肿瘤中的预后或预测价值。