Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Unit 431, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Neuro Oncol. 2010 Nov;12(11):1167-72. doi: 10.1093/neuonc/noq100. Epub 2010 Aug 20.
External beam radiation therapy (XRT) with concomitant temozolomide and 6 cycles of adjuvant temozolomide (5/28-day schedule) improves survival in patients with newly diagnosed glioblastoma compared with XRT alone. Studies suggest that dose-dense temozolomide schedules and addition of cytostatic agents may further improve efficacy. This factorial design phase I/II protocol tested dose-dense temozolomide alone and combined with cytostatic agents. Patients with newly diagnosed glioblastoma received fractionated XRT to 60 Gy concomitant with temozolomide (75 mg/m²)/day for 42 days). In the phase I portion, patients with stable disease or radiologic response 1 month after chemoradiation were randomized to adjuvant temozolomide alone (150 mg/m²/day, 7/14-day schedule) or with doublet combinations of thalidomide (400 mg/day), isotretinoin (100 mg/m²/day), and/or celecoxib (400 mg twice daily), or all 3 agents. Toxicity was assessed after 4 weeks. Among 54 patients enrolled (median age, 52 years; median Karnofsky performance status, 90), adjuvant treatment was not administered to 12 (22%), primarily because of disease progression (n = 10). All combinations were well tolerated. Grade 3/4 lymphopenia developed in 63% of patients, but no related infections occurred. One patient treated with temozolomide plus isotretinoin plus thalidomide had dose-limiting grade 3 fatigue and rash, and 1 patient receiving all 4 agents had dose-limiting grade 4 neutropenia. Venous thrombosis occurred in 7 patients, 4 of whom received thalidomide. From study entry, median survival was 20 months and the 2-year survival rate was 40%. Multiple cytostatic agents can be safely combined with dose-dense temozolomide. The factorial-based phase II portion of this study is currently ongoing.
与单纯外照射放疗(XRT)相比,XRT 联合替莫唑胺治疗并同时给予 6 个周期的辅助替莫唑胺(5/28 天方案)可改善新诊断胶质母细胞瘤患者的生存。研究表明,密集剂量替莫唑胺方案和添加细胞抑制剂可能进一步提高疗效。本两阶段设计的 I/II 期研究方案检测了密集剂量替莫唑胺单独应用及与细胞抑制剂联合应用的疗效。新诊断的胶质母细胞瘤患者接受分割 XRT 至 60Gy 同步替莫唑胺(75mg/m2/天)治疗 42 天)。在 I 期部分,放化疗后 1 个月疾病稳定或影像学反应的患者随机接受辅助替莫唑胺单药治疗(150mg/m2/天,7/14 天方案)或替莫唑胺联合细胞抑制剂的双药治疗(沙利度胺 400mg/天、异维 A 酸 100mg/m2/天和/或塞来昔布 400mg 每天 2 次),或三联治疗。在 4 周时评估毒性。在入组的 54 例患者中(中位年龄 52 岁,中位 Karnofsky 表现状态 90),12 例(22%)未给予辅助治疗,主要是因为疾病进展(n=10)。所有联合用药均耐受良好。63%的患者发生 3/4 级淋巴细胞减少症,但无相关感染发生。1 例接受替莫唑胺+异维 A 酸+沙利度胺治疗的患者出现剂量限制性 3 级疲劳和皮疹,1 例接受所有 4 种药物治疗的患者出现剂量限制性 4 级中性粒细胞减少症。7 例患者发生静脉血栓形成,其中 4 例接受沙利度胺治疗。从入组开始,中位生存时间为 20 个月,2 年生存率为 40%。多种细胞抑制剂可与密集剂量替莫唑胺安全联合应用。本研究基于该方案的 II 期部分目前正在进行中。