Sposto R, Ertel I J, Jenkin R D, Boesel C P, Venes J L, Ortega J A, Evans A E, Wara W, Hammond D
University of Southern California School of Medicine, Los Angeles.
J Neurooncol. 1989 Jul;7(2):165-77. doi: 10.1007/BF00165101.
Fifty-eight patients with high-grade astrocytoma were treated by members of the Childrens Cancer Study Group in a prospective randomized trial designed to study the effectiveness of chemotherapy as an adjuvant to standard surgical treatment and radiotherapy. Following surgical therapy, patients were assigned randomly to radiotherapy with or without chemotherapy consisting of chloroethyl-cyclohexyl nitrosourea, vincristine, and prednisone. Treatment with chemotherapy prolonged survival and event-free survival. Five-year event-free survival was 46% for patients in the radiotherapy and chemotherapy group, and 18% for patients in the radiotherapy-alone group. Five-year survival was similarly improved. The differences in outcome due to treatment were statistically significant after correcting for imbalances in important prognostic factors (event-free survival, p = 0.026; survival, p = 0.067). The presence of mitoses or necrosis in the tumor specimen was associated with poorer outcome. Patients whose initial surgery was limited to biopsy, and patients with basal ganglia lesions, also had significantly worse outcome. Chemotherapy administered at the time of recurrence in a small number of patients did not produce any long-term survivors. This study is to our knowledge the only randomized trial to investigate effectiveness of chemotherapy in the treatment of high-grade astrocytoma in children.
儿童癌症研究组的成员对58例高级别星形细胞瘤患者进行了一项前瞻性随机试验,旨在研究化疗作为标准手术治疗和放疗辅助手段的有效性。手术治疗后,患者被随机分配接受放疗,放疗组部分患者同时接受由氯乙环己亚硝脲、长春新碱和泼尼松组成的化疗。化疗延长了患者的生存期和无事件生存期。放疗联合化疗组患者的5年无事件生存率为46%,单纯放疗组为18%。5年生存率也有类似改善。在校正重要预后因素的不平衡后,治疗导致的结果差异具有统计学意义(无事件生存期,p = 0.026;生存期,p = 0.067)。肿瘤标本中存在有丝分裂或坏死与较差的预后相关。初始手术仅限于活检的患者以及基底节区病变患者的预后也明显较差。少数患者复发时进行化疗未产生长期存活者。据我们所知,这项研究是唯一一项调查化疗治疗儿童高级别星形细胞瘤有效性的随机试验。