Archimbaud E, Leblond V, Fenaux P, Dombret H, Cordonnier C, Dreyfus F, Cony-Makhoul P, Tilly H, Troussard X, Auzanneau G, Thomas X, Ffrench M, Marie J P
Service d'Hématologie, Hôpital Edouard Herriot, Lyon, France.
Hematol Cell Ther. 1996 Apr;38(2):161-7. doi: 10.1007/s00282-996-0161-2.
Timed sequential chemotherapy (TSC) combining mitoxantrone on days 1-3, etoposide on days 8-10 and cytarabine on days 1-3 and 8-10, was administered to 240 patients with advanced acute myelogenous leukemia (AML). Sixty one percent of patients, with a 95% confidence interval (CI) ranging from 54 to 67%, achieved complete remission (CR), including 47% (CI: 38-55%) of refractory patients and 78% (CI: 70-86%) of late first relapse patients (p < 0.0001). Thirty percent of patients did not respond to therapy and 9% died from toxicity. Median duration of neutropenia was 32 days and of thrombocytopenia 29 days. Severe non hematologic toxicity included sepsis in 45% of patients and mucositis in 27%. Post-remission therapy varied but included maintenance chemotherapy in most patients, a second course of TSC in 27, autologous stem cell transplantation in 17 and allogeneic transplantation in 20. Median survival of patients who were not transplanted was 7 months with 13% (CI: 7-19%) survival at 5 years. Median disease-free survival (DFS) was 9 months with 13% (CI: 6-20%) DFS at 5 years. Previous refractoriness was the main factor associated with poor prognosis for achieving CR, DFS and survival in a multivariate analysis. There was no difference in DFS between patients receiving the different modalities of intensive post-remission therapy. These results confirm initial reports on TSC and show that some patients with first relapse off therapy can enjoy prolonged DFS using chemotherapy only.
对240例晚期急性髓系白血病(AML)患者实施了序贯定时化疗(TSC),即第1 - 3天使用米托蒽醌,第8 - 10天使用依托泊苷,第1 - 3天和第8 - 10天使用阿糖胞苷。61%的患者实现完全缓解(CR),95%置信区间(CI)为54%至67%,其中难治性患者为47%(CI:38% - 55%),首次复发晚期患者为78%(CI:70% - 86%)(p < 0.0001)。30%的患者对治疗无反应,9%死于毒性反应。中性粒细胞减少的中位持续时间为32天,血小板减少为29天。严重非血液学毒性包括45%的患者发生败血症和27%的患者发生粘膜炎。缓解后治疗方式各异,但大多数患者接受维持化疗,27例患者接受第二个疗程的TSC,17例患者接受自体干细胞移植,20例患者接受异基因移植。未接受移植患者的中位生存期为7个月,5年生存率为13%(CI:7% - 19%)。无病生存期(DFS)的中位时间为9个月,5年DFS率为13%(CI:6% - 20%)。在多变量分析中,既往难治性是影响实现CR、DFS和生存预后不良的主要因素。接受不同强化缓解后治疗方式的患者DFS无差异。这些结果证实了关于TSC的初步报告,并表明一些首次复发后停止治疗的患者仅通过化疗即可获得延长的DFS。