Socinski Mark A, Smit Egbert F, Lorigan Paul, Konduri Kartik, Reck Martin, Szczesna Aleksandra, Blakely Johnetta, Serwatowski Piotr, Karaseva Nina A, Ciuleanu Tudor, Jassem Jacek, Dediu Mircea, Hong Shengyan, Visseren-Grul Carla, Hanauske Axel-Rainer, Obasaju Coleman K, Guba Susan C, Thatcher Nick
Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, USA.
J Clin Oncol. 2009 Oct 1;27(28):4787-92. doi: 10.1200/JCO.2009.23.1548. Epub 2009 Aug 31.
Following a phase II trial in which pemetrexed-platinum demonstrated similar activity to that of historical etoposide-platinum controls, a phase III study was conducted to compare pemetrexed-carboplatin with etoposide-carboplatin for the treatment of extensive-stage small-cell lung cancer (ES-SCLC).
Chemotherapy-naive patients with ES-SCLC and an Eastern Cooperative Oncology Group performance status of zero to 2 were randomly assigned to receive pemetrexed-carboplatin (pemetrexed 500 mg/m(2) on day 1; carboplatin at area under the serum concentration-time curve [AUC] 5 on day 1) or etoposide-carboplatin (etoposide 100 mg/m(2) on days 1 through 3; carboplatin AUC 5 on day 1) every 3 weeks for up to six cycles. The primary objective of the study was noninferiority of pemetrexed-carboplatin overall survival with a 15% margin.
Accrual was terminated with 908 of 1,820 patients enrolled after results of a planned interim analysis. In the final analysis, pemetrexed-carboplatin was inferior to etoposide-carboplatin for overall survival (median, 8.1 v 10.6 months; hazard ratio [HR],1.56; 95% CI, 1.27 to 1.92; log-rank P < .01) and progression-free survival (median, 3.8 v 5.4 months; HR, 1.85; 95% CI, 1.58 to 2.17; log-rank P < .01). Objective response rates were also significantly lower for pemetrexed-carboplatin (31% v 52%; P < .001). Pemetrexed-carboplatin had lower grade 3 to 4 neutropenia, febrile neutropenia, and leukopenia than etoposide-carboplatin; grade 3 to 4 thrombocytopenia was comparable between arms and anemia was higher in the pemetrexed-carboplatin arm.
Pemetrexed-carboplatin is inferior for the treatment of ES-SCLC. Planned translational research and pharmacogenomic analyses of tumor and blood samples may help explain the study results and provide insight into new treatment strategies.
在一项II期试验中,培美曲塞-铂类方案显示出与既往依托泊苷-铂类对照方案相似的活性,随后开展了一项III期研究,比较培美曲塞-卡铂与依托泊苷-卡铂治疗广泛期小细胞肺癌(ES-SCLC)的疗效。
既往未接受过化疗、东部肿瘤协作组体能状态为0至2的ES-SCLC患者被随机分配接受培美曲塞-卡铂方案(第1天给予培美曲塞500 mg/m²;第1天给予卡铂,血清浓度-时间曲线下面积[AUC]为5)或依托泊苷-卡铂方案(第1至3天给予依托泊苷100 mg/m²;第1天给予卡铂AUC 5),每3周进行1次,最多6个周期。该研究的主要目的是培美曲塞-卡铂方案的总生存期非劣效于对照方案,非劣效边际为15%。
在计划的中期分析结果出来后,1820名入组患者中有908名患者入组,随后研究入组终止。在最终分析中,培美曲塞-卡铂方案在总生存期方面劣于依托泊苷-卡铂方案(中位生存期分别为8.1个月和10.6个月;风险比[HR]为1.56;95%置信区间[CI]为1.27至1.92;对数秩检验P <.01),无进展生存期方面也劣于依托泊苷-卡铂方案(中位生存期分别为3.8个月和5.4个月;HR为1.85;95% CI为1.58至2.17;对数秩检验P <.01)。培美曲塞-卡铂方案的客观缓解率也显著低于依托泊苷-卡铂方案(31%对52%;P <.001)。培美曲塞-卡铂方案3至4级中性粒细胞减少、发热性中性粒细胞减少和白细胞减少的发生率低于依托泊苷-卡铂方案;3至4级血小板减少在两组之间相当,培美曲塞-卡铂组贫血发生率更高。
培美曲塞-卡铂方案治疗ES-SCLC疗效较差。计划开展的针对肿瘤和血液样本的转化研究及药物基因组学分析可能有助于解释研究结果,并为新的治疗策略提供见解。