Shi Yan, Chen Li, Li Jie, Lü Ya-li, Jiao Shun-chang
Department of Medical Oncology, PLA General Hospital, Beijing 100853, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2010 Aug;32(4):375-82. doi: 10.3881/j.issn.1000-503X.2010.04.004.
To determine the predictive value of excision repair cross complementation group 1 (ERCC1),ribonucleotide reductase subunit M1 (RRM1), and β-tubulin 3 expressions in postoperative patients with stage 1- 3 non-small cell lung cancer (NSCLC) receiving adjuvant chemotherapy.
All NSCLC patients received surgery therapy followed by at least one cycle of adjuvant chemotherapy in our hospital from January 2004 to December 2007. The expressions of ERCC1, RRM1, and β-tubulin 3 were detected by immunohistochemical methods. The relationships among clinicopathologic characteristics, chemotherapy regimens,biomarkers' expressions and disease-free survival (DFS) were analyzed.
The high-expression rates of ERCC1, RRM1, and β-tubulin 3 were 36.4%,43.7%,and 38.4%,respectively. The expressions of these three biomarkers were not correlated. After a median follow-up of 35.8 months, 80 patients experienced metastatic or recurrent tumors and 40 patients died. The median overall survival was not reached and the median DFS was 24.1 months. Univariate survival analysis showed that sex, clinical stage,and adenocarcinoma or not were related to DFS, while age, smoke history, chemotherapy regimens, and expression levels of ERCC1, RRM1, and β-tubulin 3 has no prognostic significance in these surgically resected NSCLC patients who were receiving adjuvant chemotherapy. Male (P=0.036), earlier clinical stage (P=0.001), and non-adenocarcinoma (P=0.004) predicted better DFS. Stratified analysis indicated that in RRM1 high-expression strata,the regimens with gemcitabine had curtailed DFS compared with other regimens (P=0.054); in β-tubulin 3 high-expression strata,the regimens containing taxane (including paclitaxel and docetaxel subgroups) had curtailed DFS compared with other regimens (P=0.076), although there was no statistical significance. However,there were no similar predictive significance in RRM1 and β-tubulin 3 low-expression strata or in ERCC1 strata with different expression levels. COX proportional regression analysis showed that adenocarcinoma or not and clinical stage were independent risk factors of DFS in this population.
In postoperative NSCLC patients who are receiving adjuvant chemotherapy, patients with high expression of RRM1 tends to be resistant to gemcitabine and patients with high expression of β-tubulin 3 tends to be resistant to taxane drugs. ERCC1, RRM1, and β-tubulin 3 detected by immunohistochemistry can be biomarkers to help to choose better chemotherapy regimen and predict the effectiveness of adjuvant chemotherapy.
确定切除修复交叉互补基因1(ERCC1)、核糖核苷酸还原酶亚基M1(RRM1)和β微管蛋白3表达对接受辅助化疗的Ⅰ-Ⅲ期非小细胞肺癌(NSCLC)术后患者的预测价值。
2004年1月至2007年12月期间,我院所有NSCLC患者均接受手术治疗,并至少接受一个周期的辅助化疗。采用免疫组化方法检测ERCC1、RRM1和β微管蛋白3的表达。分析临床病理特征、化疗方案、生物标志物表达与无病生存期(DFS)之间的关系。
ERCC1、RRM1和β微管蛋白3的高表达率分别为36.4%、43.7%和38.4%。这三种生物标志物的表达无相关性。中位随访35.8个月后,80例患者出现肿瘤转移或复发,40例患者死亡。总生存期未达到中位值,中位DFS为24.1个月。单因素生存分析显示,性别、临床分期以及是否为腺癌与DFS相关,而年龄、吸烟史、化疗方案以及ERCC1、RRM1和β微管蛋白3的表达水平在这些接受辅助化疗的手术切除NSCLC患者中无预后意义。男性(P=0.036)、临床分期较早(P=0.001)和非腺癌(P=0.004)预示着更好的DFS。分层分析表明,在RRM1高表达组中,与其他方案相比,含吉西他滨的方案DFS缩短(P=0.054);在β微管蛋白3高表达组中,含紫杉烷的方案(包括紫杉醇和多西他赛亚组)与其他方案相比DFS缩短(P=0.076),尽管无统计学意义。然而,在RRM1和β微管蛋白3低表达组或不同表达水平的ERCC1组中无类似的预测意义。COX比例回归分析显示,是否为腺癌和临床分期是该人群DFS的独立危险因素。
在接受辅助化疗的NSCLC术后患者中,RRM1高表达患者可能对吉西他滨耐药,β微管蛋白3高表达患者可能对紫杉烷类药物耐药。免疫组化检测的ERCC1、RRM1和β微管蛋白3可作为生物标志物,有助于选择更好的化疗方案并预测辅助化疗的疗效。