Liu Jingjing, Li Shuang, Zhang Shuang, Yang Changliang, Zhang Liang, Zhang Bin, Cheng Ying, Wang Changli
Department of Lung Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin Lung Cancer Center, Tianjin, China.
Department of Thoracic Oncology, Jilin Provincial Cancer Hospital, Changchun, China.
J Thorac Dis. 2020 Oct;12(10):5765-5773. doi: 10.21037/jtd-20-755.
Anlotinib is a multi-targeted tyrosine kinase inhibitor that inhibits tumor angiogenesis which has shown activity in several malignancies and approved for the treatment of small cell lung cancer (SCLC) in China. However, there are no markers can predict the clinical outcomes of anlotinib. We aimed to evaluate the efficacy of anlotinib in extensive stage SCLC (ES-SCLC) patients who failed at least two regimens treatment and to explore potential factors related to its survival benefit.
Patients with ES-SCLC treated with anlotinib monotherapy were screened between March 2017 and May 2019, prognostic nutritional index (PNI) before treatment were collected. Progression free survival (PFS) and overall survival (OS) were calculated and compared using the Kaplan-Meier method and the log-rank test. The prognostic values of each variable were evaluated with univariate and multivariate Cox proportional hazard regression (PHR) analyses.
A total of 41 patients with ES-SCLC were received anlotinib treatment, the median age was 57 (range, 33-76). Median OS was significantly longer in the PNI high arm compared with the low arm [8.4 months (95% CI, 5.1-9.6 months) 4.7 months (95% CI, 2.1-6.3 months); hazard ratio (HR) 0.42 (95% CI, 0.21-0.85); P=0.01]. The median PFS of two arms were 4.1 months (95% CI, 2.1-8.2 months) and 2.6 months (95% CI, 0.7-3.9 months), respectively (HR =0.53, 95% CI, 0.27-1.02, P=0.05). Multivariate analysis confirmed that PNI (P<0.01) and LDH (P<0.01) were significant independent biomarkers for OS.
The present study demonstrated that pretreatment PNI can be used as a novel and convenient biomarker to predict the prognosis in ES-SCLC patients treated with anlotinib.
安罗替尼是一种多靶点酪氨酸激酶抑制剂,可抑制肿瘤血管生成,已在多种恶性肿瘤中显示出活性,并在中国被批准用于治疗小细胞肺癌(SCLC)。然而,尚无标志物可预测安罗替尼的临床疗效。我们旨在评估安罗替尼在至少经过两种方案治疗失败的广泛期小细胞肺癌(ES-SCLC)患者中的疗效,并探索与其生存获益相关的潜在因素。
筛选2017年3月至2019年5月期间接受安罗替尼单药治疗的ES-SCLC患者,收集治疗前的预后营养指数(PNI)。采用Kaplan-Meier法和对数秩检验计算并比较无进展生存期(PFS)和总生存期(OS)。通过单因素和多因素Cox比例风险回归(PHR)分析评估各变量的预后价值。
共有41例ES-SCLC患者接受了安罗替尼治疗,中位年龄为57岁(范围33-76岁)。PNI高分组的中位OS显著长于低分组[8.4个月(95%CI,5.1-9.6个月)对4.7个月(95%CI,2.1-6.3个月);风险比(HR)0.42(95%CI,0.21-0.85);P=0.01]。两组的中位PFS分别为4.1个月(95%CI,2.1-8.2个月)和2.6个月(95%CI,0.7-3.9个月)(HR=0.53,95%CI,0.27-1.02,P=0.05)。多因素分析证实PNI(P<0.01)和乳酸脱氢酶(LDH)(P<0.01)是OS的显著独立生物标志物。
本研究表明,治疗前PNI可作为预测接受安罗替尼治疗的ES-SCLC患者预后的一种新型且便捷的生物标志物。