Locasciulli Anna, Oneto Rosi, Bacigalupo Andrea, Socié Gerard, Korthof Elisabeth, Bekassy Albert, Schrezenmeier Hubert, Passweg Jakob, Führer MoniKa
Ematologia e Trapianto di Midollo, Ospedale San Camillo, Circonvallazione Gianicolense 87, 00152 Roma Italy.
Haematologica. 2007 Jan;92(1):11-8. doi: 10.3324/haematol.10075.
The treatment of acquired aplastic anemia (AA) is based on allogeneic bone marrow transplantation (BMT) and immunosuppressive therapy. The aim of this study was to assess the outcome of children and adults with AA treated in the last decade, and to determine whether results have improved in two sequential time periods,1991-1996 and 1997-2002.
Two-thousands and seventy-nine consecutive patients with AA, classified according to first-line treatment: BMT (n=1567) or immunosuppressive therapy (n= 912), the patients for the two sequential time periods were studied. Analyses included variables related to patients, disease and transplant.
The actuarial 10-year survival was 73% and 68% for BMT or immunosuppressive treatment, respectively (p=0.002). BMT outcome improved significantly with time (69% and 77%, p=001) for both matched sibling donor (MSD) (74% and 80%; p=0.003 ), alternative donor (38% and 65% p=0.0001), and was better in children (79% versus 68%, p<0.0001). Multivariate analysis: favorable predictors (p<0.001) were younger age, transplant beyond 1996, MSD, a short interval diagnosis-transplant , no irradiation. IS: no significant improvement over time (69% and 73% p=0.29). Survival was significantly better in children (81% versus 70%, p=0.001), especially in vSAA(83% versus 62%, p=0.0002). Combined IS was superior to single drug treatment (77% versus 62%, p=0.002). Multivariate analysis: significant predictors of survival: age > or =16 years (p=0.0009), longer interval between diagnosis -treatment (p=0.04), single drug versus combined IS (p=0.02).
Outcome has improved in subsets of AA patients: those receiving first- line BMT and children with vSAA treated with IS. Age remains a major predictor for both treatments. Early intervention is associated with a significantly better outcome and is strongly recommended, whatever the first-line therapy.
获得性再生障碍性贫血(AA)的治疗基于异基因骨髓移植(BMT)和免疫抑制治疗。本研究的目的是评估过去十年中接受治疗的儿童和成人AA患者的治疗结果,并确定在1991 - 1996年和1997 - 2002年这两个连续时间段内结果是否有所改善。
连续纳入2079例AA患者,根据一线治疗方法分类:BMT(n = 1567)或免疫抑制治疗(n = 912),对这两个连续时间段的患者进行研究。分析包括与患者、疾病和移植相关的变量。
BMT组和免疫抑制治疗组的10年精算生存率分别为73%和68%(p = 0.002)。BMT的治疗结果随时间显著改善(69%和77%,p = 0.01),无论是匹配同胞供者(MSD)(74%和80%;p = 0.003)、替代供者(38%和65%,p = 0.0001),且在儿童中效果更好(79%对68%,p < 0.0001)。多因素分析:有利的预测因素(p < 0.001)为年龄较小、1996年后进行移植、MSD、诊断 - 移植间隔时间短、未接受放疗。免疫抑制治疗(IS):随时间无显著改善(69%和73%,p = 0.29)。儿童的生存率显著更高(81%对70%,p = 0.001),尤其是非常严重再生障碍性贫血(vSAA)(83%对62%,p = 0.0002)。联合免疫抑制治疗优于单一药物治疗(77%对62%,p = 0.002)。多因素分析:生存的显著预测因素:年龄≥16岁(p = 0.0009)、诊断 - 治疗间隔时间长(p = 0.04)、单一药物与联合免疫抑制治疗(p = 0.02)。
AA患者亚组的治疗结果有所改善:接受一线BMT的患者以及接受免疫抑制治疗的vSAA儿童。年龄仍然是两种治疗的主要预测因素。早期干预与显著更好的结果相关,无论一线治疗方法如何,均强烈推荐早期干预。