Hollard D, Sotto J J, Berthier R, Leger J, Michallet M
Cancer. 1980 Apr 1;45(7):1540-8. doi: 10.1002/1097-0142(19800401)45:7<1540::aid-cncr2820450705>3.0.co;2-#.
An unexpectedly high rate of long-term survivors in acute myeloid leukemia (AML) has been observed in a group of patients who achieved a first complete remission (CR) after induction of a therapeutic regimen including daunorubidomycine, vincristine, prednisone and stanozolol, and anabolizing steroid. The rate of CR was 52%. Maintenance therapy was very simple and the only association with stanozolol during this period suggested to us that an androgen, at low dosages, might be responsible for the unusual long-term survival time (45 months with a 95% confidence limit from 30 to 86 months). On the basis of our first observation, high dosages of the androgen were used during the induction phase of treatment but failed to demonstrate any advantage when associated with a drug regimen, including cytosine arabinoside (ARA-C). The reevaluation of each parameter for our group of patients did not allow selection of patients in terms of their age or the hematologic data obtained at presentation. Effects of androgen on the socalled normal hemopoietic cells and on the leukemic cells are discussed, particularly the possible antagonistic effect with ARA-C. A prospective statement is made concerning the possible condition of the prolongation of the complete remission in AML according to some experimental data which enforce the stimulative activity of androgen on the myeloid proliferation.
在一组接受包括柔红霉素、长春新碱、泼尼松和司坦唑醇(一种同化类固醇)的治疗方案诱导后首次实现完全缓解(CR)的急性髓系白血病(AML)患者中,观察到了出乎意料的高长期生存率。CR率为52%。维持治疗非常简单,在此期间唯一与司坦唑醇联合使用的情况让我们认为,低剂量的雄激素可能是导致异常长的长期生存时间(45个月,95%置信区间为30至86个月)的原因。基于我们的首次观察,在治疗诱导阶段使用了高剂量的雄激素,但与包括阿糖胞苷(ARA-C)在内的药物方案联合使用时未显示出任何优势。对我们这组患者的每个参数进行重新评估后,无法根据患者的年龄或就诊时获得的血液学数据对患者进行筛选。讨论了雄激素对所谓正常造血细胞和白血病细胞的影响,特别是与ARA-C可能存在的拮抗作用。根据一些实验数据,对雄激素对髓系增殖的刺激活性进行了前瞻性陈述,这些数据支持了雄激素对AML完全缓解期延长的可能情况。