针对成人急性髓性白血病,采用大剂量阿糖胞苷或自体骨髓移植进行特定年龄组(±50岁)缓解后巩固治疗的疗效评估。
Outcome assessment of age group-specific (+/- 50 years) post-remission consolidation with high-dose cytarabine or bone marrow autograft for adult acute myelogenous leukemia.
作者信息
Bassan R, Raimondi R, Lerede T, D'emilio A, Buelli M, Borleri G, Personeni A, Bellavita P, Rodeghiero F, Barbui T
机构信息
Division of Hematology, Ospedali Riuniti, Bergamo, Italy.
出版信息
Haematologica. 1998 Jul;83(7):627-35.
BACKGROUND AND OBJECTIVE
To assess outcome of an age-adapted post-remission strategy for adult patients with acute myelogenous leukemia (AML, FAB-M3 excluded), including autologous bone marrow transplantation (ABMT) or high-dose cytarabine (HIDAC) consolidation.
DESIGN AND METHODS
AML patients in first complete remission (CR) after doxorubicin-cytarabine-thioguanine (DoxAT) chemotherapy were scheduled to receive two identical early consolidation courses followed by HIDAC (1 g/m2/bd for 6 days), if aged > 50 years, or HiDAC plus total body irradiation (TBI) plus ABMT if aged < 50 years, the bone marrow being harvested prior to the HiDAC/TBI regimen and unpurged. Results were examined by treatment intention and in actual treatment groups, by selected pretreatment and therapy-related variables, and compared with age and disease matched historical patients treated with DoxAT consolidation without additional HIDAC or ABMT.
RESULTS
One-hundred and eight (70%) of 153 patients achieved a response and were evaluable after a follow-up of 3.3-8.8 years. According to treatment intention, long-term relapse-free survival (RFS) was significantly improved in both age groups compared with controls (< 50 years: 41% vs 15%, p < 0.05; > 50 years: 33% vs 22%, p < 0.005). Actually, 41 patients proceeded to ABMT and 24 to the HIDAC cycle (including 5 aged < 50 years), 23 had early consolidation only (1: refusal; 1: inadequate marrow harvest; 21: complications), 10 relapsed and 2 died very early into remission, 7 were submitted to an allogeneic BMT, and one denied any post-remission therapy. The long-term RFS rates for ABMT and HIDAC groups were 53% and 54% (47% for 19 patients aged > 50), respectively, significantly better than for historical patients or those unable to go beyond early consolidation (p < 0.005, adjusted for early adverse events). Overall 5-year survival rate was 40% (p < 0.0001), 54% for CR patients, 60% after ABMT, and 65% after HIDAC. Relative to the ABMT and HIDAC intensive treatment groups, only the presence of hepatosplenomegaly at diagnosis was associated with a significantly worse outcome like that of the control study.
INTERPRETATION AND CONCLUSIONS
This age-adapted double post-remission consolidation strategy with ABMT (allo-BMT) or HIDAC was applicable to only about two thirds of responders and was effective in about half these cases, regardless of patient age or specific treatment modality. While the loss of CR patients from treatment realization was unrelated to the study design and depended mainly on recurrence of AML and toxic complication, the exact place of ABMT vs HIDAC consolidation remains unsettled, calling for a new study in comparable patient and risk groups.
背景与目的
评估针对成年急性髓系白血病(AML,不包括FAB-M3)患者的年龄适应性缓解后治疗策略的疗效,该策略包括自体骨髓移植(ABMT)或大剂量阿糖胞苷(HIDAC)巩固治疗。
设计与方法
接受阿霉素-阿糖胞苷-硫鸟嘌呤(DoxAT)化疗后首次完全缓解(CR)的AML患者,若年龄>50岁,计划接受两个相同的早期巩固疗程,随后接受HIDAC(1 g/m²/每日两次,共6天);若年龄<50岁,则接受HIDAC加全身照射(TBI)加ABMT,骨髓在HIDAC/TBI方案之前采集且未进行净化处理。通过治疗意向和实际治疗组,根据选定的预处理和治疗相关变量对结果进行检查,并与年龄和疾病匹配的接受DoxAT巩固治疗且未进行额外HIDAC或ABMT的历史患者进行比较。
结果
153例患者中有108例(70%)获得缓解,在3.3 - 8.8年的随访后可进行评估。根据治疗意向,与对照组相比,两个年龄组的长期无复发生存(RFS)均显著改善(<50岁:41%对15%,p<0.05;>50岁:33%对22%,p<0.005)。实际上,41例患者进行了ABMT,24例进入HIDAC周期(包括5例年龄<50岁),23例仅接受了早期巩固治疗(1例:拒绝;1例:骨髓采集不足;21例:并发症),10例复发,2例在缓解早期死亡,7例接受了异基因骨髓移植,1例拒绝任何缓解后治疗。ABMT组和HIDAC组的长期RFS率分别为53%和54%(19例年龄>50岁患者为47%),显著优于历史患者或无法完成早期巩固治疗的患者(p<0.005,针对早期不良事件进行调整)。总体5年生存率为40%(p<0.0001),CR患者为54%,ABMT后为60%,HIDAC后为65%。相对于ABMT和HIDAC强化治疗组,仅诊断时存在肝脾肿大与对照研究结果相似,预后显著较差。
解读与结论
这种采用ABMT(异基因BMT)或HIDAC的年龄适应性双缓解后巩固策略仅适用于约三分之二的缓解者,且在约一半的此类病例中有效,无论患者年龄或具体治疗方式如何。虽然因治疗实施导致CR患者流失与研究设计无关,主要取决于AML复发和毒性并发症,但ABMT与HIDAC巩固治疗的确切地位仍未确定,需要在可比的患者和风险组中进行新的研究。