Department of Medical Oncology, General Hospital of CPLA, No.28 FuXing Road, Beijing, China.
BMC Cancer. 2010 Nov 10;10:621. doi: 10.1186/1471-2407-10-621.
Adjuvant chemotherapy has been shown to improve survival rates of postoperative patients with non-small cell lung cancer (NSCLC). Biomarkers could help select an appropriate chemotherapy for NSCLC patients or predict the efficacy of chemotherapy. The objective of this study was to explore the possible prognostic and predictive role of topoisomerase II alpha (TopIIα) expression level in postoperative NSCLC patients who received adjuvant chemotherapy.
Patients with stage I-III NSCLC, who underwent surgery in our hospital from January 2004 to December 2007 and who also received adjuvant chemotherapy after surgery, were analyzed in this study. Expression of TopIIα and Ki67 in paraffin-embedded tissues was detected by immunohistochemistry (IHC). The relationships between clinicopathological characteristics, chemotherapy regimens, the expression of biomarkers and disease free survival (DFS) were analyzed.
TopIIα and Ki67 were highly expressed in 22.5% and 36.4% of the 151 patients, respectively. Univariate survival analysis showed that male sex (P = 0.036), non-adenocarcinoma (P = 0.004), earlier pathological TNM stage (P = 0.001) or pathological N stage (P < 0.001), and high expression of TopIIα (P = 0.012) were correlated with better DFS, whereas age, smoking history, different chemotherapy regimens, T stage and expression level of Ki67 were of no prognostic significance. Further stratified analysis showed that vinorelbine (NVB)-containing adjuvant regimens were generally associated with better DFS than regimens without NVB in patients with low TopIIα expression, though the difference was not statistically significant (P = 0.065). Pairwise comparisons for patients with low TopIIα expression indicated that the NVB-containing regimen was associated with better DFS than the docetaxel (TXT)-containing regimen (P = 0.047). COX multivariate analysis showed that pathological TNM stage, histological subtype and expression level of TopIIα to be independent of risk factors affecting DFS in postoperative NSCLC patients who received chemotherapy.
High TopIIα expression was discovered to be correlated with better DFS for postoperative NSCLC patients who received adjuvant chemotherapy. The NVB-containing chemotherapy regimen was more effective than the TXT-containing regimen in improving DFS in patients with low TopIIα expression. TopIIα could be considered to be an independent prognostic biomarker of DFS in postoperative NSCLC patients who received adjuvant chemotherapy.
辅助化疗已被证明可以提高非小细胞肺癌(NSCLC)术后患者的生存率。生物标志物可以帮助选择合适的 NSCLC 患者化疗或预测化疗的疗效。本研究的目的是探讨拓扑异构酶 II 阿尔法(TopIIα)表达水平在接受辅助化疗的 NSCLC 术后患者中的可能预后和预测作用。
本研究分析了 2004 年 1 月至 2007 年 12 月在我院接受手术治疗且术后接受辅助化疗的 I-III 期 NSCLC 患者。通过免疫组织化学(IHC)检测石蜡包埋组织中 TopIIα和 Ki67 的表达。分析了临床病理特征、化疗方案、生物标志物的表达与无病生存期(DFS)的关系。
在 151 例患者中,TopIIα和 Ki67 的高表达率分别为 22.5%和 36.4%。单因素生存分析显示,男性(P=0.036)、非腺癌(P=0.004)、较早的病理 TNM 分期(P=0.001)或病理 N 分期(P<0.001)、高 TopIIα 表达(P=0.012)与较好的 DFS 相关,而年龄、吸烟史、不同的化疗方案、T 分期和 Ki67 的表达水平与预后无关。进一步分层分析显示,在低 TopIIα 表达的患者中,含长春瑞滨(NVB)的辅助方案通常与更好的 DFS 相关,尽管差异无统计学意义(P=0.065)。对于低 TopIIα 表达的患者进行两两比较,结果表明含 NVB 的方案与含多西紫杉醇(TXT)的方案相比,DFS 更好(P=0.047)。COX 多因素分析显示,病理 TNM 分期、组织学亚型和 TopIIα 的表达水平是影响接受化疗的 NSCLC 术后患者 DFS 的独立危险因素。
高 TopIIα 表达与接受辅助化疗的 NSCLC 术后患者的 DFS 相关。在低 TopIIα 表达的患者中,含 NVB 的化疗方案比含 TXT 的方案更能改善 DFS。TopIIα 可作为接受辅助化疗的 NSCLC 术后患者 DFS 的独立预后生物标志物。