Hassler Marco Ronald, Pfeifer Wolfgang, Knocke-Abulesz Thomas Hendrik, Geissler Klaus, Altorjai Gabriele, Dieckmann Karin, Marosi Christine
Department of Internal Medicine I, Clinical Division of Oncology, Medical University of Vienna, Austria.
Wien Klin Wochenschr. 2013 Aug;125(15-16):481-6. doi: 10.1007/s00508-013-0402-7. Epub 2013 Aug 2.
This multicentric randomized phase II study investigated the feasibility and toxicity of temozolomide (TMZ) added to whole brain radiotherapy (WBRT) followed by adjuvant TMZ in patients with multiple brain metastases of non-small-cell lung cancer (NSCLC).
Patients with multiple brain metastases from NSCLC aged ≥ 18 years, classified according to recursive partitioning analysis class I or II and with adequate organ functions were eligible. Treatment consisted of WBRT + TMZ 75 mg/m² for 2 weeks followed at day 28 by TMZ 100 mg/m²/day 2 weeks on/2 weeks off for up to 6 months (radiochemotherapy, RCT) or WBRT alone (radiotherapy, RT).
The study enrolled only 35 patients (22 patients in RCT and 13 in RT) and had to be closed prematurely due to poor accrual. The toxicity was mainly due to TMZ with WHO grade 3 and 4 thrombocytopenia in 3/22 versus 0/13, leucocytopenia in 1/22 versus 0/13 and lymphocytopenia in 7/22 versus 12/13 patients in RCT and RT respectively. Thirteen patients in RCT and six in RT progressed systemically and dropped out before first restaging of the response in brain. Median time to progression (TTP) was 2.4 months (95 % CI: 2-2.6 months) and 2.0 months (95 % CI: 0.5-3.5 months), median overall survival (OAS) was 3 months (95% CI: 1.7-3.1 months) and 6.3.months (95 % CI: 0.2-7.6 months) in RCT and RT, respectively.
Like other studies before on patients with brain metastases, insufficient number of recruited patients does not allow conclusions on efficacy and toxicity as the study closed prematurely.
这项多中心随机II期研究调查了替莫唑胺(TMZ)联合全脑放疗(WBRT),随后辅助使用TMZ治疗非小细胞肺癌(NSCLC)多发脑转移患者的可行性和毒性。
年龄≥18岁、根据递归分割分析分为I或II类且器官功能良好的NSCLC多发脑转移患者符合条件。治疗方案为WBRT + TMZ 75 mg/m²,持续2周,然后在第28天给予TMZ 100 mg/m²/天,2周用药/2周停药,持续6个月(放化疗,RCT)或单纯WBRT(放疗,RT)。
该研究仅招募了35名患者(RCT组22例,RT组13例),由于入组情况不佳,不得不提前结束。毒性主要归因于TMZ,RCT组和RT组3/22与0/13的患者出现WHO 3级和4级血小板减少,1/22与0/13的患者出现白细胞减少,7/22与12/13的患者出现淋巴细胞减少。RCT组13例患者和RT组6例患者出现全身进展,在首次脑部反应重新分期前退出。RCT组和RT组的中位进展时间(TTP)分别为2.4个月(95%CI:2 - 2.6个月)和2.0个月(95%CI:0.5 - 3.5个月),中位总生存期(OAS)分别为3个月(95%CI:1.7 - 3.1个月)和6.3个月(95%CI:0.2 - 7.6个月)。
与之前其他关于脑转移患者的研究一样,由于研究提前结束,招募患者数量不足,无法得出关于疗效和毒性的结论。