Boehm A, Sperr W R, Leitner G, Worel N, Oehler L, Jaeger E, Mitterbauer M, Haas O A, Valent P, Kalhs P, Rabitsch W
Department of Internal Medicine I, Bone Marrow Transplantation Unit, Medical University of Vienna, Austria.
Eur J Clin Invest. 2008 Dec;38(12):945-52. doi: 10.1111/j.1365-2362.2008.02041.x.
Recent data suggest that, among other factors, comorbidity may be an important prognostic variable in patients with myelodysplastic syndromes (MDS) who are eligible for haematopoietic stem cell transplantation (SCT).
We examined the overall survival (OS) and underlying risk factors in 45 adult patients with MDS (n = 38), chronic myelomonocytic leukaemia (n = 1), or secondary acute myeloid leukaemia (AML) arising from MDS (n = 6), who underwent allogeneic SCT at our Institution.
With a median follow-up of 37 months, OS for all patients was 23%, post-transplant relapse occurred in 11 patients, and 10 patients died from treatment-related complications. The overall outcome and survival was independent of cytogenetic abnormalities and International Prognostic Scoring System (IPSS). However, we identified comorbidity as defined by the haematopoietic cell transplantation specific comorbidity index (HCT-CI), as a significant adverse prognostic variable in our MDS patients.
Based on these data and similar published data we recommend selecting patients with MDS or secondary AML for SCT according to the presence of comorbidities.
近期数据表明,在诸多因素中,合并症可能是适合进行造血干细胞移植(SCT)的骨髓增生异常综合征(MDS)患者的一个重要预后变量。
我们研究了45例成年患者的总生存期(OS)及潜在风险因素,这些患者包括MDS患者(n = 38)、慢性粒单核细胞白血病患者(n = 1)或由MDS引发的继发性急性髓系白血病(AML)患者(n = 6),他们均在我们机构接受了异基因SCT。
中位随访37个月,所有患者的OS为23%,11例患者发生移植后复发,10例患者死于治疗相关并发症。总体结局和生存与细胞遗传学异常及国际预后评分系统(IPSS)无关。然而,我们将造血细胞移植特异性合并症指数(HCT-CI)所定义的合并症确定为我们MDS患者的一个显著不良预后变量。
基于这些数据及类似的已发表数据,我们建议根据合并症的存在情况来选择MDS或继发性AML患者进行SCT。