Park Sojung, Kim Hyun Jung, Choi Chang-Min, Lee Dae Ho, Kim Sang-We, Lee Jung-Shin, Kim Woo Sung, Choi Se Hoon, Rho Jin Kyung, Lee Jae Cheol
Department of Pulmonary and Critical Care Medicine, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Department of Internal Medicine, Kyungpook National University Hospital, Kyungpook National University School of Medicine, 130 Dongdeok-ro, Jung-gu, Daegu, 41944, South Korea.
BMC Cancer. 2016 Jul 7;16:417. doi: 10.1186/s12885-016-2457-0.
Pemetrexed is widely used for the treatment of advanced non-squamous non-small-cell lung cancer (NSCLC). However, factors that can predict the benefits of pemetrexed therapy have not yet been defined.
We compared the clinical and molecule pathological characteristics of good and poor responders among a cohort of 1,848 non-squamous NSCLC patients who had received at least two cycles of pemetrexed therapy between November 2006 and February 2015. Among these cases, 92 good responders who were the top 5 % in terms of progression-free survival (PFS) and 222 poor responders who had progressive disease after only 2 cycles of therapy were selected for the analysis.
The median PFS of the good responders was 29.9 months (range; 20.9-90.0) and the median number of cycle was 37 (range; 18-129). Although 53.5 % of patients showed stable disease (SD), this response was sustained (median PFS in SD, 29.6 months). A never-smoking status was related to better survival outcome, whereas EGFR mutation, two or more metastatic sites, and intra-abdominal metastasis were each associated with a poor PFS. ALK translocation showed a tendency for a positive impact on response to pemetrexed, whereas metastatic lesion to liver, adrenal gland or bone showed a tendency for a negative impact despite not reaching our threshold for statistical significance.
Predictive factors, such as smoking status, the status of genetic alteration and tumor burden, should be considered when administering pemetrexed therapy for non-squamous NSCLC.
培美曲塞广泛用于治疗晚期非鳞状非小细胞肺癌(NSCLC)。然而,尚未明确可预测培美曲塞治疗获益的因素。
我们比较了2006年11月至2015年2月期间接受至少两个周期培美曲塞治疗的1848例非鳞状NSCLC患者中,疗效良好和疗效不佳者的临床及分子病理特征。在这些病例中,选取无进展生存期(PFS)处于前5%的92例疗效良好者和仅接受2个周期治疗后即出现疾病进展的222例疗效不佳者进行分析。
疗效良好者的中位PFS为29.9个月(范围:20.9 - 90.0),中位周期数为37个(范围:18 - 129)。虽然53.5%的患者疾病稳定(SD),但这种反应持续存在(SD患者的中位PFS为29.6个月)。从不吸烟状态与更好的生存结果相关,而表皮生长因子受体(EGFR)突变、两个或更多转移部位以及腹腔转移均与较差的PFS相关。间变性淋巴瘤激酶(ALK)易位对培美曲塞反应有积极影响的趋势,而肝、肾上腺或骨转移灶对反应有消极影响的趋势,尽管未达到我们的统计学意义阈值。
在对非鳞状NSCLC患者进行培美曲塞治疗时,应考虑吸烟状态、基因改变状态和肿瘤负荷等预测因素。