Schold S C, Herndon J E, Burger P C, Halperin E C, Vick N A, Cairncross J G, Macdonald D R, Dropcho E J, Morawetz R, Bigner D D
Duke University, Durham, NC.
J Clin Oncol. 1993 Jan;11(1):77-83. doi: 10.1200/JCO.1993.11.1.77.
We conducted a phase III trial comparing intravenous (IV) diaziquone (AZQ) and carmustine (BCNU) as single agents in patients with cerebral anaplastic gliomas who had received surgery and radiotherapy. Its purpose was to compare the efficacy of AZQ with that of BCNU, the standard agent for brain tumor chemotherapy.
Randomization between the two regimens occurred 8 weeks after completion of radiotherapy. A total of 251 patients were randomized to receive either AZQ or BCNU, and there were no significant differences between the two treatment arms in any of the known prognostic variables, including age, histologic grade, and Karnofsky performance status (KPS).
There was no significant difference in either time to tumor progression or survival between the two treatment arms. Age and histology were strong predictors of outcome, whereas KPS had relatively less effect. Three groups of patients with distinctly different outcomes could be identified: (1) older age (45+) and glioblastoma/gliosarcoma (GBM/GS) patients had a median survival of 37 weeks after randomization; (2) patients with either older age or GBM/GS had a median survival of 61 weeks; and (3) younger age (< 45) and non-GBM/GS (usually anaplastic astrocytoma) patients had a median survival of 147 weeks. Toxicity was primarily hematologic, although acute gastrointestinal toxicity and chronic pulmonary toxicity were more common with BCNU. Patients randomized to AZQ who had significant hematologic toxicity that required dose reduction after the first treatment cycle had significantly longer time to tumor progression and survival than those who did not require dose reduction (P = .011 and .016, respectively).
There was no significant difference in efficacy between AZQ and BCNU in patients with anaplastic gliomas as tested in this study, although AZQ was somewhat better tolerated.
我们开展了一项III期试验,比较静脉注射二氮喹酮(AZQ)和卡莫司汀(BCNU)作为单一药物用于接受过手术和放疗的间变性脑胶质瘤患者的疗效。其目的是比较AZQ与脑肿瘤化疗的标准药物BCNU的疗效。
放疗结束8周后对两种治疗方案进行随机分组。共有251例患者被随机分配接受AZQ或BCNU治疗,在包括年龄、组织学分级和卡氏功能状态(KPS)在内的任何已知预后变量方面,两个治疗组之间均无显著差异。
两个治疗组在肿瘤进展时间或生存期方面均无显著差异。年龄和组织学是预后的有力预测因素,而KPS的影响相对较小。可以识别出三组预后明显不同的患者:(1)年龄较大(45岁以上)且为胶质母细胞瘤/胶质肉瘤(GBM/GS)的患者随机分组后的中位生存期为37周;(2)年龄较大或为GBM/GS的患者中位生存期为61周;(3)年龄较小(<45岁)且非GBM/GS(通常为间变性星形细胞瘤)的患者中位生存期为147周。毒性主要为血液学毒性,尽管急性胃肠道毒性和慢性肺部毒性在BCNU治疗时更为常见。在第一个治疗周期后因严重血液学毒性需要降低剂量的随机接受AZQ治疗的患者,其肿瘤进展时间和生存期明显长于那些不需要降低剂量的患者(分别为P = 0.011和0.016)。
在本研究中测试的间变性胶质瘤患者中,AZQ和BCNU的疗效无显著差异,尽管AZQ的耐受性稍好。