Warrell R P, Straus D J, Young C W
Cancer Treat Rep. 1982 May;66(5):1121-5.
We treated 45 patients with advanced malignant lymphoma, using a combination of methyl-GAG and teniposide (VM-26). All patients had received extensive prior treatment with combination chemotherapy with or without irradiation. Both methyl-GAG (600 mg/m2) and VM-26 (100 mg/m2) were administered on Days 1 and 8 of the treatment protocol and, in responding patients, every 2 weeks thereafter. Partial responses occurred in six of 12 patients with Hodgkin's disease and in ten of 31 patients with non-Hodgkin's lymphoma. The median duration of response for all patients was 3 1/2 months (range, 1 1/2-11). There were moderate toxic effects, including nausea, myalgia, weakness, and myelosuppression. Relative to our recent experience with methyl-GAG as a single agent, the addition of VM-26 to methyl-GAG did not produce a superior rate or duration of response in similar, heavily pretreated patient populations with malignant lymphoma; however, the combination caused considerably more myelotoxicity. We conclude that the use of VM-26 with methyl-GAG in this dose schedule offers no advantage over single-agent therapy. Methyl-GAG, when administered on a biweekly schedule, is effective and well-tolerated. This agent should be considered for incorporation into chemotherapy protocols for the therapy of previously untreated patients with malignant lymphoma.
我们采用甲基甘氨酸二乙酯(methyl-GAG)和替尼泊苷(VM-26)联合治疗了45例晚期恶性淋巴瘤患者。所有患者此前均接受过含或不含放疗的联合化疗。在治疗方案的第1天和第8天给予甲基甘氨酸二乙酯(600mg/m²)和VM-26(100mg/m²),对于有反应的患者,此后每2周给药一次。12例霍奇金病患者中有6例出现部分缓解,31例非霍奇金淋巴瘤患者中有10例出现部分缓解。所有患者的中位缓解持续时间为3.5个月(范围为1.5 - 11个月)。有中度毒性反应,包括恶心、肌痛、虚弱和骨髓抑制。相对于我们近期使用甲基甘氨酸二乙酯单药治疗的经验,在类似的、接受过大量预处理的恶性淋巴瘤患者群体中,将VM-26添加到甲基甘氨酸二乙酯中并未产生更高的缓解率或更长的缓解持续时间;然而,联合用药导致的骨髓毒性要大得多。我们得出结论,按此剂量方案使用VM-26与甲基甘氨酸二乙酯联合治疗并不比单药治疗更具优势。甲基甘氨酸二乙酯按每两周一次的方案给药时有效且耐受性良好。对于此前未接受治疗的恶性淋巴瘤患者的化疗方案,应考虑纳入该药物。