Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
J Neurooncol. 2012 Feb;106(3):643-9. doi: 10.1007/s11060-011-0709-z. Epub 2011 Oct 4.
To estimate the sustained (≥8 weeks) objective response rate in pediatric patients with recurrent or progressive high-grade gliomas (HGG, Stratum A) or brainstem gliomas (BSG, Stratum B) treated with the combination of O6-benzylguanine (O6BG) and temozolomide(®) (TMZ). Patients received O6BG 120 mg/m(2)/d IV followed by TMZ 75 mg/m(2)/d orally daily for 5 consecutive days of each 28-day course. The target objective response rate to consider the combination active was 17%. A two-stage design was employed. Forty-three patients were enrolled; 41 were evaluable for response, including 25 patients with HGG and 16 patients with BSG. The combination of O6BG and TMZ was tolerable, and the primary toxicities were myelosuppression and gastrointestinal symptoms. One sustained (≥8 weeks) partial response was observed in the HGG cohort; no sustained objective responses were observed in the BSG cohort. Long-term (≥6 courses) stable disease (SD) was observed in 4 patients in Stratum A and 1 patient in Stratum B. Of the 5 patients with objective response or long-term SD, 3 underwent central review with 2 reclassified as low-grade gliomas. The combination of O6BG and TMZ did not achieve the target response rate for activity in pediatric patients with recurrent or progressive HGG and BSG.
评估 O6-苯甲基鸟嘌呤(O6BG)联合替莫唑胺(TMZ)治疗复发性或进行性高级别脑胶质瘤(HGG,A 层)或脑干胶质瘤(BSG,B 层)患儿的持续(≥8 周)客观缓解率。患者接受 O6BG 120mg/m2/d 静脉滴注,随后 TMZ 75mg/m2/d 口服,每天 1 次,连续 5 天,每 28 天为 1 个疗程。考虑组合有效的目标客观缓解率为 17%。采用两阶段设计。共入组 43 例患者;41 例患者可评估疗效,包括 25 例 HGG 患者和 16 例 BSG 患者。O6BG 和 TMZ 联合治疗耐受良好,主要毒性为骨髓抑制和胃肠道症状。在 HGG 队列中观察到 1 例持续(≥8 周)部分缓解;BSG 队列中未观察到持续的客观缓解。A 层中有 4 例患者和 B 层中有 1 例患者观察到长期(≥6 个疗程)稳定疾病(SD)。在 5 例客观缓解或长期 SD 的患者中,3 例经中心复查,2 例重新分类为低级别胶质瘤。O6BG 和 TMZ 的联合治疗未能达到复发性或进行性 HGG 和 BSG 患儿的治疗活性目标缓解率。