Keskin A, Tombuloğlu M, Atamer M A, Büyükkeçeci F
Department of Hematology, Faculty of Medicine, University of Ege, Bornova-Izmir, Turkey.
Acta Haematol. 1994;92(1):14-7. doi: 10.1159/000204130.
Thirty adult patients with relapsing or refractory acute leukemia were treated with mitoxantrone 10 mg/m2 daily by 20-min intravenous infusion for 5 days and cytosine arabinoside (Ara-C) 200 mg/m2 daily by continuous infusion for 5 days. Complete remission was obtained in 9 of 15 patients (60%) with acute myeloblastic leukemia (AML), with a mean duration of 6 months (range 2-12 months). Among 15 patients with acute lymphoblastic leukemia (ALL), complete remission was obtained in 5 patients (33.3%), with a mean duration of 2 months. Partial remission was achieved in 2 patients with AML and 1 patient with ALL. Myelosuppression developed in all patients following chemotherapy. Nonhematologic side effects consisted of nausea, vomiting, mild alopecia, stomatitis and transient hepatic dysfunction. No cardiopulmonary toxicity or neurotoxicity was observed. Our therapeutic responses are similar to those obtained with high-dose Ara-C and mitoxantrone but with less toxicity.
30例复发或难治性急性白血病成年患者接受了米托蒽醌治疗,剂量为10mg/m²,每日静脉输注20分钟,共5天;阿糖胞苷(Ara-C)剂量为200mg/m²,持续输注5天。15例急性髓细胞白血病(AML)患者中有9例(60%)获得完全缓解,平均缓解持续时间为6个月(范围2 - 12个月)。15例急性淋巴细胞白血病(ALL)患者中,5例(33.3%)获得完全缓解,平均缓解持续时间为2个月。2例AML患者和1例ALL患者获得部分缓解。所有患者化疗后均出现骨髓抑制。非血液学副作用包括恶心、呕吐、轻度脱发、口腔炎和短暂性肝功能障碍。未观察到心肺毒性或神经毒性。我们的治疗反应与高剂量Ara-C和米托蒽醌相似,但毒性较小。