Su ShengFa, Liu LingFeng, Geng YiChao, OuYang WeiWei, Ma Zhu, Li QingSong, Zhao ChaoFen, Li Mei, Wang Yu, Luo DaXian, Yang WenGang, He ZhiXu, Lu Bing
Department of Thoracic Oncology, Affiliated Hospital of Guizhou Medical University, Guizhou Cancer Hospital.
Teaching and Research Section of Oncology, Guizhou Medical University.
Anticancer Drugs. 2019 Mar;30(3):295-301. doi: 10.1097/CAD.0000000000000729.
The aim of this study was to compare the clinical efficacy of pemetrexed+cisplatin (PP) versus docetaxel+cisplatin (DP) for the treatment of stage IV lung adenocarcinoma. We retrospectively analyzed the clinical data of 147 patients with stage IV lung adenocarcinoma treated between January 2011 and December 2015, 100 of which were in the DP group whereas 47 were in the DP group. Main inclusion criteria were treatment-naive patients, first-line treatment with PP or DP with no molecular targeted therapy during treatment, 2-6 cycles of first-line chemotherapy with unknown status of epidermal growth factor receptor (EGFR) mutation, 18-75 years of age, and Karnofsky performance status score of at least 70. Prognostic factors for survival were identified by using univariate and multivariate analyses. Propensity score matching was performed to further adjust for confounding. A total of 47 pairs were successfully matched between the two groups. The median overall survival was 9.0 months in the DP group and 17.0 months in the PP group; the 1-year survival rate was 29.8 and 59.6%, respectively; the 2-year survival rate was 12.8 and 21.1%, respectively (χ=4.128, P=0.042); and median progression-free survival was 6.0 and 8.0 months, respectively (χ=4.839, P=0.028). Cox multivariate analysis showed that chemotherapy regimen and number of metastatic organs were independent factors for OS. The effect of the radiotherapy dose on the primary tumor on OS was close to statistically significant. The incidence of grade 3-4 neutropenia was more significantly reduced in the DP group than in the PP group after matching (61.7 vs. 27.7%, P=0.002), with no between-group difference for adverse effects on platelets or hemoglobin. For patients with stage IV lung adenocarcinoma and unknown EGFR mutation status, PP was more effective than DP in prolonging survival and had a less adverse effect on neutrophils.
本研究旨在比较培美曲塞+顺铂(PP)与多西他赛+顺铂(DP)治疗IV期肺腺癌的临床疗效。我们回顾性分析了2011年1月至2015年12月期间接受治疗的147例IV期肺腺癌患者的临床资料,其中100例在DP组,47例在PP组。主要纳入标准为初治患者、一线使用PP或DP治疗且治疗期间未进行分子靶向治疗、一线化疗2 - 6周期、表皮生长因子受体(EGFR)突变状态未知、年龄18 - 75岁以及卡诺夫斯基功能状态评分至少为70分。通过单因素和多因素分析确定生存的预后因素。进行倾向评分匹配以进一步调整混杂因素。两组之间成功匹配了47对。DP组的中位总生存期为9.0个月,PP组为17.0个月;1年生存率分别为29.8%和59.6%;2年生存率分别为12.8%和21.1%(χ=4.128,P = 0.042);中位无进展生存期分别为6.0个月和8.0个月(χ=4.839,P = 0.028)。Cox多因素分析显示化疗方案和转移器官数量是总生存期的独立因素。原发肿瘤放疗剂量对总生存期的影响接近具有统计学意义。匹配后,DP组3 - 4级中性粒细胞减少的发生率比PP组显著降低(61.7%对27.7%,P = 0.002),两组在对血小板或血红蛋白的不良反应方面无差异。对于IV期肺腺癌且EGFR突变状态未知的患者,PP在延长生存期方面比DP更有效,且对中性粒细胞的不良反应更小。