Pavlovsky S, Gonzalez Llaven J, Garcia Martinez M A, Sobrevilla P, Eppinger-Helft M, Marin A, López-Hernández M, Fernandez I, Rubio M E, Ibarra S
Centro de Internación e Investigación Clinica, Angelica Ocampo, Buenos Aires, Argentina.
Ann Hematol. 1994 Jul;69(1):11-5. doi: 10.1007/BF01757342.
Between May 1985 and November 1988, 143 adult patients with previously untreated acute nonlymphocytic leukemia were randomized to receive mitoxantrone and cytarabine (MTT+Ara-C) or daunomycin and cytarabine (DNM+Ara-C) in order to compare the efficacy and acute and chronic toxicities. Therapy consisted of 3 days of MTT 12 mg/m2/i.v. or DNM 45 mg/m2/i.v.; both groups received Ara-C 100 mg/m2 daily by continuous infusion (CI) for 7 days. Those who failed to achieve a complete remission after one induction course received a second induction course for 2 and 5 days at the same doses. All the patients who achieved complete remission received two consolidations of 2 days of MTT or DNM and 5 days of Ara-C in CI at the same dose as for induction. Of the 72 patients on MTT+Ara-C, 38 (53%) achieved complete remission, compared with 29 (43%) of 67 treated with DNM+Ara-C. Three and 5 patients had partial remission, 7 and 18 failed to respond, 24 and 15 died in the first 21 days of induction, of those treated with MTT+Ara-C or DNM+Ara-C, respectively (p = 0.34). Median duration of complete remission and survival was 185 and 103 days or 165 and 160 days, respectively (p = 0.85). More early deaths were observed with MTT+Ara-C due to greater myelosuppression, and a higher incidence of failure with DNM+Ara-C. No significant differences between treatment groups were observed in 21 categories of adverse events. The results demonstrate similar incidence of complete response, length of duration of complete remission, overall survival, and toxicity with MTT+Ara-C and DNM+Ara-C.
1985年5月至1988年11月期间,143例既往未接受过治疗的成年急性非淋巴细胞白血病患者被随机分组,分别接受米托蒽醌和阿糖胞苷(MTT+Ara-C)或柔红霉素和阿糖胞苷(DNM+Ara-C)治疗,以比较两者的疗效及急慢性毒性。治疗方案为MTT 12 mg/m²静脉注射3天或DNM 45 mg/m²静脉注射3天;两组均连续7天每日持续静脉输注(CI)阿糖胞苷100 mg/m²。那些在一个诱导疗程后未达到完全缓解的患者,以相同剂量接受第二个2天或5天的诱导疗程。所有达到完全缓解的患者接受两个巩固疗程,即MTT或DNM 2天及CI阿糖胞苷5天,剂量与诱导疗程相同。接受MTT+Ara-C治疗的72例患者中,38例(53%)达到完全缓解,而接受DNM+Ara-C治疗的67例患者中有29例(43%)达到完全缓解。MTT+Ara-C组和DNM+Ara-C组分别有3例和5例部分缓解,7例和18例无反应,24例和15例在诱导治疗的前21天死亡(p = 0.34)。完全缓解和生存的中位持续时间分别为185天和103天或165天和160天(p = 0.85)。由于MTT+Ara-C导致的骨髓抑制更强,观察到更多早期死亡病例,而DNM+Ara-C组失败发生率更高。在21类不良事件中,治疗组之间未观察到显著差异。结果表明,MTT+Ara-C和DNM+Ara-C的完全缓解发生率、完全缓解持续时间、总生存期及毒性相似。