Division of Medical Oncology, Giovanni Paolo II Oncology Institute, Bari, Italy.
Clin Lung Cancer. 2011 Nov;12(6):402-6. doi: 10.1016/j.cllc.2011.06.006. Epub 2011 Aug 10.
In advanced non-small-cell lung cancer (NSCLC), substantial similarities in terms of treatment efficacy and survival have emerged over the years between the different systemic chemotherapy regimens used. More recently, other topics such as histotype, maintenance therapy and quality of life have been explored to ameliorate this plateau. We present the treatment rationale and study design of the ERACLE (induction pEmetrexed and cisplatin followed by maintenance pemetRexed versus cArboplatin-paCLitaxel and bEvacizumab followed by maintenance bevacizumab) trial. Patients enrolled in the ERACLE trial are randomized between combination treatment arms: (A) cisplatin 75 mg/m(2) day 1 and pemetrexed 500 mg/m(2) day 1, every 3 weeks for six cycles followed (in responders or with stable disease) by pemetrexed 500 mg/m(2) day 1, every 3 weeks until progression; and (B) carboplatin AUC 6 day 1, plus paclitaxel 200 mg/m(2) day 1 and plus bevacizumab 15 mg/kg, every 3 weeks for six cycles followed (in responders or patients with stable disease) by bevacizumab 15 mg/kg every 3 weeks until progression. The primary objective of the study is to evaluate the difference in terms of quality of life between treatment arms. together with co-primary endpoints represented by the EuroQoL group (EQ-5D) questionnaire total score and the EQ-5D visual analog scale. Secondary endpoints are the evaluation of treatment activity and exploratory evaluation of treatment efficacy.
在晚期非小细胞肺癌(NSCLC)中,不同系统化疗方案在治疗效果和生存方面多年来出现了实质性的相似性。最近,人们还探讨了组织类型、维持治疗和生活质量等其他问题,以改善这种疗效平台。我们介绍了 ERACLE(诱导培美曲塞和顺铂,然后维持培美曲塞与卡铂-紫杉醇和贝伐珠单抗,然后维持贝伐珠单抗)试验的治疗原理和研究设计。入组 ERACLE 试验的患者在联合治疗组之间进行随机分组:(A)顺铂 75mg/m2,第 1 天,培美曲塞 500mg/m2,第 1 天,每 3 周为一个周期,共 6 个周期,然后(在应答者或疾病稳定者中)培美曲塞 500mg/m2,第 1 天,每 3 周为一个周期,直至进展;和(B)卡铂 AUC6,第 1 天,联合紫杉醇 200mg/m2,第 1 天,联合贝伐珠单抗 15mg/kg,每 3 周为一个周期,共 6 个周期,然后(在应答者或疾病稳定者中)贝伐珠单抗 15mg/kg,每 3 周为一个周期,直至进展。研究的主要目的是评估治疗组之间生活质量的差异。与共同主要终点一起评估,包括 EuroQoL 组(EQ-5D)问卷总分和 EQ-5D 视觉模拟量表。次要终点是评估治疗活性和治疗疗效的探索性评估。