Comorbidity as prognostic variable in MDS: comparative evaluation of the HCT-CI and CCI in a core dataset of 419 patients of the Austrian MDS Study Group

被引:88
作者
Sperr, W. R. [1 ]
Wimazal, F. [1 ]
Kundi, M. [2 ]
Baumgartner, C. [1 ]
Noesslinger, T. [3 ]
Makrai, A. [3 ]
Stauder, R. [4 ]
Krieger, O. [5 ]
Pfeilstoecker, M. [1 ,6 ]
Valent, P. [1 ,6 ]
机构
[1] Med Univ Vienna, Div Hematol & Hemostaseol, Dept Internal Med 1, A-1090 Vienna, Austria
[2] Med Univ Vienna, Inst Environm Hlth, A-1090 Vienna, Austria
[3] Hanusch Hosp, Med Dept Hematol & Oncol 3, Vienna, Austria
[4] Med Univ Innsbruck, Dept Internal Med 5, Innsbruck, Austria
[5] Hosp Elisabethinen, Dept Internal Med 1, Linz, Austria
[6] Ludwig Boltzmann Cluster Oncol, Vienna, Austria
关键词
comorbidity; MDS; prognostication; survival; PRIMARY MYELODYSPLASTIC SYNDROMES; SCORING SYSTEM; ELDERLY-PATIENTS; PREDICTING SURVIVAL; CLASSIFICATION; PROPOSALS; DIAGNOSIS; CANCER; LEUKEMIA; IMPACT;
D O I
10.1093/annonc/mdp258
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients and methods: In the present study, the influence of comorbidity on survival and acute myeloid leukemia (AML) evolution was analyzed retrospectively in 419 patients with de novo myelodysplastic syndromes (MDS) (observation period: 1985-2007). The median age was 71 years (range 24-91 years). Two different scoring systems, the hematopoietic stem-cell transplantation-specific comorbidity index (HCT-CI) and the Charlson comorbidity index (CCI) were applied. Results: The HCT-CI was found to be a significant prognostic factor for overall survival (OS, P < 0.05) as well as event-free survival (EFS, P < 0.05) in our patients, whereas the CCI was of prognostic significance for OS (P < 0.05), but not for EFS. For AML-free survival, neither the HCT-CI nor the CCI were of predictive value. A multivariate analysis including age, lactate dehydrogenase, ferritin, karyotype, number of cytopenias, French-American-British groups, and comorbidity was applied. Comorbidity was found to be an independent prognostic factor in patients with low- or int-1-risk MDS (P < 0.05) regarding OS and EFS. Conclusions: Together, our data show that comorbidity is an important risk factor for OS and EFS in patients with MDS.
引用
收藏
页码:114 / 119
页数:6
相关论文
共 40 条
[1]   Impact of Acquired Comorbidities on All-Cause Mortality Rates Among Older Breast Cancer Survivors [J].
Ahern, Thomas P. ;
Lash, Timothy L. ;
Thwin, Soe Soe ;
Silliman, Rebecca A. .
MEDICAL CARE, 2009, 47 (01) :73-79
[2]  
AUL C, 1994, LEUKEMIA, V8, P1906
[3]  
AUL C, 1992, LEUKEMIA, V6, P52
[4]   The myelodysplastic syndromes: Diagnosis, molecular biology and risk assessment [J].
Bennett, JM ;
Komrokji, RS .
HEMATOLOGY, 2005, 10 :258-269
[5]   A comparative review of classification systems in myelodysplastic syndromes (MDS) [J].
Bennett, JM .
SEMINARS IN ONCOLOGY, 2005, 32 (04) :S3-S10
[6]   THE CHRONIC MYELOID LEUKEMIAS - GUIDELINES FOR DISTINGUISHING CHRONIC GRANULOCYTIC, ATYPICAL CHRONIC MYELOID, AND CHRONIC MYELOMONOCYTIC LEUKEMIA - PROPOSALS BY THE FRENCH-AMERICAN-BRITISH-COOPERATIVE-LEUKEMIA-GROUP [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, H ;
SULTAN, C ;
COX, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 87 (04) :746-754
[7]  
BENNETT JM, 1982, BRIT J HAEMATOL, V51, P189, DOI 10.1111/j.1365-2141.1982.tb08475.x
[8]   Treatment and prognostic factors in myelodysplastic syndromes [J].
Boogaerts, MA ;
Verhoef, GEG ;
Demuynck, H .
BAILLIERES CLINICAL HAEMATOLOGY, 1996, 9 (01) :161-183
[9]  
Brunning RD, 2001, WHO CLASSIFICATION T, P62
[10]  
BRUNNING RD, 2008, WHO CLASSIFICATION T, V1, P88