Levin V A, Edwards M S, Wright D C, Seager M L, Schimberg T P, Townsend J J, Wilson C B
Cancer Treat Rep. 1980 Feb-Mar;64(2-3):237-44.
Fifty-eight patients harboring recurrent malignant brain tumors were evaluated. CCNU (110 mg/m2) was administered on Day 1, procarbazine (60 mg/m2) was administered daily for 14 days beginning on Day 8, and vincristine (1.4 mg/m2) was administered on Days 8 and 29 of each 6-week cycle of therapy. Therapy was continued until tumor progression was documented. Before each course, a neurologic examination was performed and radionuclide and computerized tomographic scans were obtained. Response and progression were defined as improvement or deterioration, respectively, in at least two of the three tests. Of the 46 patients harboring recurrent malignant gliomas, 12 (26%) responded to therapy, 18 (39%) had tumor progression, and 16 (35%) had disease stability. Nineteen of the 46 patients were not previously treated with another form of chemotherapy: eight (42%) responded to therapy, eight (42%) had disease stability, and only three (16%) had early tumor progression. The median time to tumor progression was 26 weeks for patients responding to therapy or having disease stability. Approximately 30% of the patients were alive without evidence of tumor progression at 1 year. Evaluated by time to tumor progression and rate of tumor response or stabilization, this combination was similar to the BCNU-5-fluorouracil combination used for patients harboring recurrent malignant glioma.
对58例复发性恶性脑肿瘤患者进行了评估。第1天给予洛莫司汀(110mg/m²),从第8天开始,丙卡巴肼(60mg/m²)每日给药,持续14天,每个6周治疗周期的第8天和第29天给予长春新碱(1.4mg/m²)。治疗持续至记录到肿瘤进展。每个疗程前进行神经系统检查,并进行放射性核素和计算机断层扫描。缓解和进展分别定义为三项检查中至少两项有改善或恶化。在46例复发性恶性胶质瘤患者中,12例(26%)对治疗有反应,18例(39%)肿瘤进展,16例(35%)病情稳定。46例患者中有19例此前未接受过其他形式的化疗:8例(42%)对治疗有反应,8例(42%)病情稳定,只有3例(16%)早期肿瘤进展。对治疗有反应或病情稳定的患者,肿瘤进展的中位时间为26周。约30%的患者在1年时存活且无肿瘤进展迹象。根据肿瘤进展时间和肿瘤反应或稳定率评估,该联合方案与用于复发性恶性胶质瘤患者的卡氮芥-5-氟尿嘧啶联合方案相似。