Blume K G, Forman S J, O'Donnell M R, Doroshow J H, Krance R A, Nademanee A P, Snyder D S, Schmidt G M, Fahey J L, Metter G E
Blood. 1987 Apr;69(4):1015-20.
In a phase I/II study, 47 patients (median age, 24 years) with hematologic malignancies (33 patients with acute leukemia not in first remission and 14 patients with other advanced malignant hematologic disorders) were treated with total body irradiation and high doses of etoposide (VP16-213) followed by bone marrow transplantation. At the time of analysis, 21 patients were alive, and 19 of them were in continued complete remission for 101 days to greater than 40 months (median, 12 months). The actuarial disease-free survival rate of the 33 acute leukemia patients is 43% (2 SEM, 18%) and the actuarial relapse rate is 32% (2 SEM, 20%). Five of the 14 patients with the other hematologic malignancies are alive, and four of them continue to be free of disease for 8 to 27 months. Pharmacokinetic studies established a strong correlation between the administered drug doses and their plasma levels and also demonstrated complete drug clearance prior to marrow grafting. An etoposide dose of 60 mg/kg body weight was found to be the maximum tolerated dose. This new preparatory regimen was well tolerated and was not associated with specific acute or long-term regimen-related toxicities. Our data suggest that total body irradiation with high-dose etoposide presents a viable alternative to other preparatory regimens. The role of this novel combination remains to be defined by future prospective randomized trials.
在一项I/II期研究中,47例血液系统恶性肿瘤患者(中位年龄24岁)(33例急性白血病患者处于非首次缓解期,14例患有其他晚期恶性血液系统疾病)接受了全身照射和大剂量依托泊苷(VP16 - 213)治疗,随后进行骨髓移植。在分析时,21例患者存活,其中19例持续完全缓解101天至超过40个月(中位时间为12个月)。33例急性白血病患者的无病生存率精算值为43%(2个标准误,18%),复发率精算值为32%(2个标准误,20%)。14例患有其他血液系统恶性肿瘤的患者中有5例存活,其中4例持续无病8至27个月。药代动力学研究表明给药剂量与其血浆水平之间存在强相关性,并且还证明在骨髓移植前药物已完全清除。发现依托泊苷的最大耐受剂量为60 mg/kg体重。这种新的预处理方案耐受性良好,且与特定的急性或长期方案相关毒性无关。我们的数据表明,全身照射联合大剂量依托泊苷是其他预处理方案的可行替代方案。这种新型联合方案的作用仍有待未来前瞻性随机试验来确定。