Tallman M S, Appelbaum F R, Amos D, Goldberg R S, Livingston R B, Mortimer J, Weiden P L, Thomas E D
J Clin Oncol. 1987 Jun;5(6):918-26. doi: 10.1200/JCO.1987.5.6.918.
In order to test the toxicity and efficacy of intensive postremission therapy with high-dose cytosine arabinoside with L-asparaginase and amsacrine with etoposide in adults with acute nonlymphocytic leukemia (ANL), 100 adults (ages 19 to 75) with previously untreated ANL were entered into a study using six sequential cycles of chemotherapy. Cycles 1 (induction), 3, and 5 included conventional doses of daunomycin, cytosine arabinoside, 6-thioguanine, vincristine (VCR), and prednisone. Cycle 2 was cytosine arabinoside 3 g/m2 intravenously (IV) every 12 hours for four doses, followed by L-asparaginase 10,000 U intramuscularly (IM) at hour 42; this combination was repeated 1 week later. Cycle 4 included amsacrine 120 mg/m2/d and etoposide 100 mg/m2/d, both IV for five days, and cycle 6 was three monthly courses of VCR on day 1, and prednisone, mercaptopurine, and methotrexate each for five days. Seventy-four patients (74%) achieved complete remission (CR) (51 with cycle 1 and 23 after cycle 2). The overall disease-free survival (DFS) for patients achieving CR is 27% at 3 years by Kaplan-Meier analysis, while for patients achieving CR with cycle 1 it is 34%. The actuarial probability of being free from relapse at 3 years for patients achieving CR is 34%. Sixteen of the 74 CR patients (22%) died in CR while continuing to receive intensive chemotherapy, including 12 (18%) who succumbed to infection (nine bacterial, three fungal). After a median follow-up of 20 months, 36 patients have relapsed and 21 remain alive in CR. Intensive consolidation with high-dose cytosine arabinoside, amsacrine, and etoposide can modestly prolong DFS compared with historical controls. However, relapse continued to be a major problem and, in addition, with more aggressive consolidation therapy, infection during marrow aplasia resulted in a significant number of deaths.
为了测试大剂量阿糖胞苷联合L-天冬酰胺酶、安吖啶联合依托泊苷的强化缓解后治疗方案对成人急性非淋巴细胞白血病(ANL)的毒性和疗效,100名年龄在19至75岁、既往未经治疗的ANL成人患者进入一项采用六个连续化疗周期的研究。第1周期(诱导期)、第3周期和第5周期包括常规剂量的柔红霉素、阿糖胞苷、6-硫鸟嘌呤、长春新碱(VCR)和泼尼松。第2周期为阿糖胞苷3 g/m²静脉注射(IV),每12小时一次,共四剂,然后在第42小时肌肉注射(IM)L-天冬酰胺酶10000 U;1周后重复此联合用药。第4周期包括安吖啶120 mg/m²/d和依托泊苷100 mg/m²/d,均静脉注射五天,第6周期为第1天静脉注射VCR,为期三个月疗程,泼尼松、巯嘌呤和甲氨蝶呤各用五天。74名患者(74%)实现完全缓解(CR)(51名在第1周期后缓解,23名在第2周期后缓解)。通过Kaplan-Meier分析,实现CR的患者3年总无病生存率(DFS)为27%,而在第1周期实现CR的患者为34%。实现CR的患者3年无复发的精算概率为34%。74名CR患者中有16名(2