H. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA.
J Thorac Oncol. 2010 Mar;5(3):369-75. doi: 10.1097/JTO.0b013e3181cee24f.
We examined the efficacy of enzastaurin plus pemetrexed as second-line therapy in patients with advanced (stage IIIA/B or IV) non-small cell lung cancer in a double-blinded, randomized, phase II study.
Patients received pemetrexed 500 mg/m intravenously on day 1 of 21-day cycles (day 8 in cycle 1) plus oral enzastaurin (250 mg two times per day; combination arm) or placebo (pemetrexed arm). Both arms received supplementation with vitamin B12, folic acid, and dexamethasone. An interim analysis was conducted to determine whether efficacy would warrant a phase III study.
The interim analysis showed no evidence of improved progression-free survival with enzastaurin. At final analysis (N = 160, 80 in each arm), baseline characteristics were well balanced. There was no significant difference in progression-free survival (3.0 months, p = 0.544) or overall survival (9.6 months in combination arm and 7.4 months in pemetrexed arm, p = 0.171). Drug-related serious adverse events included cerebrovascular accident, palpitations, and renal failure (n = 1, each) in combination arm and neutropenic sepsis, thrombocytopenia, and panniculitis (n = 1, each) in pemetrexed arm. Nonhematologic drug-related grade 3/4 toxicities were similar in both arms. Grade 3/4 hematologic toxicities were higher with the combination, specifically leukopenia (6.3% versus 0%), neutropenia (15.2% versus 5.0%), and thrombocytopenia (8.9% versus 1.3%). Of the 26 deaths reported on-study or within 30 days of discontinuation (10 in combination arm and 16 in pemetrexed arm), none were drug related.
The combination regimen of enzastaurin and pemetrexed is well tolerated but does not improve efficacy over pemetrexed and placebo as second-line treatment of unselected patients with advanced non-small cell lung cancer.
我们在一项双盲、随机、二期研究中,检查了恩杂鲁胺联合培美曲塞作为晚期(III 期 A/B 或 IV 期)非小细胞肺癌二线治疗的疗效。
患者接受培美曲塞 500 mg/m 静脉滴注,每 21 天周期(第 1 周期第 8 天),联合口服恩杂鲁胺(每天两次,每次 250 mg;联合组)或安慰剂(培美曲塞组)。两组均接受维生素 B12、叶酸和地塞米松补充治疗。中期分析旨在确定疗效是否需要进行三期研究。
中期分析显示,恩杂鲁胺组无改善无进展生存期的证据。最终分析(N=160,每组 80 例)时,基线特征均衡。无进展生存期(3.0 个月,p=0.544)或总生存期(联合组 9.6 个月,培美曲塞组 7.4 个月,p=0.171)无显著差异。药物相关严重不良事件包括联合组的脑血管意外、心悸和肾衰竭(各 1 例),以及培美曲塞组的中性粒细胞败血症、血小板减少和脂膜炎(各 1 例)。非血液学药物相关 3/4 级毒性在两组中相似。联合组的 3/4 级血液学毒性更高,具体为白细胞减少(6.3%对 0%)、中性粒细胞减少(15.2%对 5.0%)和血小板减少(8.9%对 1.3%)。研究期间或停药后 30 天内报告的 26 例死亡中(联合组 10 例,培美曲塞组 16 例),均与药物无关。
恩杂鲁胺联合培美曲塞方案耐受良好,但与培美曲塞和安慰剂相比,作为未经选择的晚期非小细胞肺癌二线治疗并不能提高疗效。