Tabchi Samer, Blais Normand, Campeau Marie-Pierre, Tehfe Mustapha
Hematology - Oncology Division, Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, QC, Canada.
Radiation Oncology Department, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.
Cancer Chemother Pharmacol. 2017 Feb;79(2):381-387. doi: 10.1007/s00280-016-3226-0. Epub 2017 Jan 12.
To date, the best chemotherapy regimen to combine with concurrent radiotherapy in stage III non-small-cell lung cancer remains undetermined. We compared the survival outcomes and toxicities in patients who were treated with etoposide-cisplatin (EP), paclitaxel-carboplatin (PC), or vinblastine-cisplatin (VP) in one large cancer referral center.
We enrolled patients who received concurrent chemoradiotherapy at our university-affiliated hospital between January 1, 2009 and December 31, 2013. Demographic and clinical characteristics were identified. Progression-free survival (PFS) and overall survival (OS) between the different treatment groups were compared using Kaplan-Meier and Cox proportional hazards regression models. Treatment-related toxicities were also compared.
A total of 107 patients were treated with EP (31.8%), PC (32.7%) or VP (35.5%). Treatment with VP was significantly superior to PC, both in terms of median PFS [29.2 vs. 10.5 months; hazard ratio (HR) 0.43; 95% CI 0.21-0.85; p = 0.01] and in terms of median OS [40.7 vs. 17.8 months; (HR) 0.42; (0.21-0.84); p = 0.01]. However, there was no survival difference between EP and either one of the other regimens, but there was significantly more toxicities reported with the use of EP (73.5%) compared to PC (44.7%) or VP (37.1%); (p = 0.001). The most frequent non-hematologic toxicities for the entire cohort were esophagitis (28%), fatigue (22.4%), pneumonitis (14%), and nephrotoxicity (9.3%).
Although the present study is limited by its small cohort and its retrospective nature, the results suggest that VP might be superior to PC and is less toxic than EP.
迄今为止,III期非小细胞肺癌同步放化疗的最佳化疗方案仍未确定。我们在一家大型癌症转诊中心比较了接受依托泊苷-顺铂(EP)、紫杉醇-卡铂(PC)或长春碱-顺铂(VP)治疗的患者的生存结果和毒性。
我们纳入了2009年1月1日至2013年12月31日期间在我校附属医院接受同步放化疗的患者。确定了人口统计学和临床特征。使用Kaplan-Meier和Cox比例风险回归模型比较不同治疗组之间的无进展生存期(PFS)和总生存期(OS)。还比较了治疗相关毒性。
共有107例患者接受了EP(31.8%)、PC(32.7%)或VP(35.5%)治疗。在中位PFS方面[29.2对10.5个月;风险比(HR)0.43;95%置信区间0.21-0.85;p = 0.01]以及中位OS方面[40.7对17.8个月;(HR)0.42;(0.21-0.84);p = 0.01],VP治疗均显著优于PC。然而,EP与其他任何一种方案之间在生存方面没有差异,但与PC(44.7%)或VP(37.1%)相比,使用EP报告的毒性显著更多(73.5%);(p = 0.001)。整个队列中最常见的非血液学毒性是食管炎(28%)、疲劳(22.4%)、肺炎(14%)和肾毒性(9.3%)。
尽管本研究受样本量小和回顾性研究性质的限制,但结果表明VP可能优于PC且毒性低于EP。