A modified EBMT risk score and the hematopoietic cell transplantation-specific comorbidity index for pre-transplant risk assessment in adult acute lymphoblastic leukemia

被引:48
作者
Terwey, Theis H. [1 ]
Hemmati, Philipp G. [1 ]
Martus, Peter [2 ]
Dietz, Ekkehart [2 ]
Vuong, Lam G. [1 ]
Massenkeil, Gero [1 ,3 ]
Doerken, Bernd [1 ]
Arnold, Renate [1 ]
机构
[1] Charite, Dept Hematol & Oncol, D-13353 Berlin, Germany
[2] Charite, Inst Biostat & Clin Epidemiol, D-13353 Berlin, Germany
[3] Stadt Klinikum Giitersloh, Dept Hematol Oncol & Gastroenterol, Gutersloh, Germany
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷 / 05期
关键词
hematopoietic stem cell transplantation; acute lymphoblastic leukemia; HCT recipients; ACUTE MYELOID-LEUKEMIA; REDUCED-INTENSITY; MYELODYSPLASTIC SYNDROMES; MARROW-TRANSPLANTATION; PERFORMANCE STATUS; PROGNOSTIC SCORE; HCT-CI; OUTCOMES; MORTALITY; LYMPHOMA;
D O I
10.3324/haematol.2009.011809
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Disease stage is the most important prognostic parameter in allogeneic hematopoietic cell transplantation (HCT) for acute lymphoblastic leukemia, but other factors such as donor/host histocompatibility and gender combination, recipient age, performance status and comorbidities need to be considered. Several scoring systems are available to predict outcome in HCT recipients; however, their prognostic relevance in acute lymphoblastic leukemia is not well defined. Design and Methods In the present study we evaluated a modified EBMT risk score (mEBMT) and the HCT-specific comorbidity index (HCT-CI) in 151 adult acute lymphoblastic leukemia patients who received allogeneic HCT from 1995 until 2007 at our center. Results Disease status was first complete remission (CR1) (47%), CR>1 (21%) or no CR (32%). Overall survival (OS) at one, two and five years was 62%, 51% and 40% and non-relapse mortality (NRM) was 21%, 24% and 32%. Median mEBMT was 3 (0-6). Higher mEBMT was associated with inferior OS (hazard ratio per score unit (HR): 1.50, P<0.001), higher NRM (HR: 1.36, P=0.042) and higher relapse mortality (HR: 1.68, P<0.001). Disease stage was the predominant prognostic factor in this score. Comorbidities were present in 71% of patients with mild hepatic disease (29%), moderate pulmonary disease (28%) and infections (23%) being the most common. Median HCT-CI was 1 (0-9). In univariate analysis a trend for inferior OS (HR: 1.08, P=0.20) and higher NRM (HR: 1.14, P=0.11) with increasing HCT-CI was observed but the level of significance was not reached. In additional analyses we found that reduced Karnofsky Performance Status (KPS) was associated with inferior OS (HR: 1.34, P=0.023) and higher relapse mortality (HR: 1.71, P=0.001) when analyzed univariately. However, KPS was associated with disease stage and significance was lost in multivariate analysis. Conclusions The mEBMT was prognostic in our patient cohort with predominant influence of disease stage, whereas a trend but no significant prognostic value was observed for the HCT-CI.
引用
收藏
页码:810 / 818
页数:9
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