Petti M C, Aloe Spiriti M A, Carella A M, Fioritoni G, Resegotti L, Rizzoli V, Tabilio A, Visani G, Vegna M L, Mandelli F
Haematologica. 1989 May-Jun;74(3):267-71.
In an attempt to reduce the risk of leukemic relapse, different post-remission intensifications based on high-dose Ara-C (HiDAC) and autologous bone marrow transplantation (ABMT) were evaluated in patients with acute non lymphocytic leukemia in first remission and compared as to response and toxicity. Between September, 1985 and May, 1987, 34 patients in complete remission were eligible for our study. Induction therapy consisted of one or two courses of daunorubicin (DNR) and Ara-C (schedule 3 + 7). Fourteen patients receiving intensive post-remission chemotherapy with DNR + Ara-C (schedule 2 + 5), HiDAC + DNR, and ABMT following pretransplant BAVC conditioning entered the first pilot study. A high toxicity was observed and only 5 of them completed the full treatment plan. Thus the second pilot study used a single post-remission intensive course with HiDAC + m-AMSA and ABMT following cyclophosphamide plus TBI or BAVC. This approach was more feasible. The preliminary results show the usefulness of intensive post-remission therapy: in fact, all patients but one who completed the treatment program are still in continuous complete remission. A large number of patients and a longer follow-up are required to draw final conclusions.
为降低白血病复发风险,对首次缓解的急性非淋巴细胞白血病患者评估了基于大剂量阿糖胞苷(HiDAC)和自体骨髓移植(ABMT)的不同缓解后强化治疗方案,并比较了其疗效和毒性。1985年9月至1987年5月,34例完全缓解的患者符合我们的研究条件。诱导治疗包括一或两个疗程的柔红霉素(DNR)和阿糖胞苷(3 + 7方案)。14例接受缓解后强化化疗(DNR + 阿糖胞苷,2 + 5方案、HiDAC + DNR)以及移植前BAVC预处理后进行ABMT的患者进入首个试点研究。观察到毒性较高,其中只有5例完成了完整治疗方案。因此,第二个试点研究采用单一的缓解后强化疗程,即HiDAC + m - AMSA以及环磷酰胺加全身照射(TBI)或BAVC预处理后进行ABMT。这种方法更可行。初步结果显示缓解后强化治疗是有效的:实际上,除一名完成治疗方案的患者外,所有患者仍处于持续完全缓解状态。需要大量患者和更长时间的随访才能得出最终结论。