Miura Nami, Kamita Masahiro, Kakuya Takanori, Fujiwara Yutaka, Tsuta Koji, Shiraishi Hideaki, Takeshita Fumitaka, Ochiya Takahiro, Shoji Hirokazu, Huang Wilber, Ohe Yuichiro, Yamada Tesshi, Honda Kazufumi
Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan.
Oncotarget. 2016 May 31;7(22):33165-78. doi: 10.18632/oncotarget.8890.
Although several clinical trials have demonstrated the benefits of platinum-combined adjuvant chemotherapy for resected non-small cell lung cancer (NSCLC), predictive biomarkers for the efficacy of such therapy have not yet been identified. Selection of patients with high metastatic ability in the early stage of non-small cell lung cancer (NSCLC) has the potential to predict clinical benefit of adjuvant chemotherapy (ADJ).In order to develop a predictive biomarker for efficacy of ADJ, we reanalyzed patient data using a public database enrolled by JBR.10, which was a clinical trial to probe the clinical benefits of ADJ in stage-IB/II patients with NSCLC. The patients who were enrolled by JBR.10 were classified into 2 subgroups according to expression of the ACTN4 transcript: ACTN4 positive (ACTN4 (+)) and ACTN4 negative (ACTN4 (-)). In the ACTN4 (+) group, overall survival (OS) was significantly higher in the ADJ subgroup compared with the observation subgroup (OBS), indicating a significant survival benefit of ADJ. However, no difference in OS was found between ADJ and OBS groups in ACTN4 (-). Although ACTN4 expression level did not correlate with the chemosensitivity of cancer cell lines for cytotoxic drugs, the metastatic potential of A549 lung adenocarcinoma cells was significantly reduced by ACTN4 shRNA in in vitro assays and in an animal transplantation model. The clinical and preclinical data suggested that ACTN4 is a potential predictive biomarker for efficacy of ADJ in stage-IB/II patients with NSCLC, by reflecting the metastatic potential of tumor cells.
尽管多项临床试验已证明铂类联合辅助化疗对可切除的非小细胞肺癌(NSCLC)有益,但尚未确定此类治疗疗效的预测生物标志物。选择非小细胞肺癌(NSCLC)早期具有高转移能力的患者有可能预测辅助化疗(ADJ)的临床获益。为了开发一种预测ADJ疗效的生物标志物,我们使用JBR.10登记的公共数据库重新分析了患者数据,JBR.10是一项探究ADJ对IB/II期NSCLC患者临床获益的临床试验。根据ACTN4转录本的表达情况,将JBR.10纳入的患者分为2个亚组:ACTN4阳性(ACTN4(+))和ACTN4阴性(ACTN4(-))。在ACTN4(+)组中,与观察亚组(OBS)相比,ADJ亚组的总生存期(OS)显著更高,表明ADJ具有显著的生存获益。然而,在ACTN4(-)组中,ADJ组和OBS组之间的OS没有差异。尽管ACTN4表达水平与癌细胞系对细胞毒性药物的化疗敏感性无关,但在体外试验和动物移植模型中,ACTN4 shRNA可显著降低A549肺腺癌细胞的转移潜能。临床和临床前数据表明,ACTN4可能是IB/II期NSCLC患者ADJ疗效的预测生物标志物,因为它反映了肿瘤细胞的转移潜能。