Comparison of risk stratification tools in predicting outcomes of patients with higher-risk myelodysplastic syndromes treated with azanucleosides

被引:65
作者
Zeidan, A. M. [1 ]
Sekeres, M. A. [2 ]
Garcia-Manero, G. [3 ]
Steensma, D. P. [4 ]
Zell, K. [2 ]
Barnard, J. [2 ]
Ali, N. A.
Zimmerman, C. [2 ]
Roboz, G. [6 ]
DeZern, A. [7 ]
Nazha, A. [2 ]
Jabbour, E. [3 ]
Kantarjian, H. [3 ]
Gore, S. D. [1 ]
Maciejewski, J. P. [2 ]
List, A. [5 ]
Komrokji, R.
机构
[1] Yale Univ, Sect Hematol, Dept Internal Med, Yale Comprehens Canc Ctr, 333 Cedar St,POB 208028, New Haven, CT 06520 USA
[2] Cleveland Clin, Dept Translat Hematol & Oncol Res, Leukemia Program, Cleveland, OH 44106 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[5] H Lee Moffitt Canc Ctr & Res Inst, Dept Malignant Hematol, Tampa, FL USA
[6] Cornell Univ, Weill Med Coll, Dept Med, New York, NY 10021 USA
[7] Johns Hopkins Univ, Dept Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
关键词
PROGNOSTIC SCORING SYSTEM; LEUKEMIA GROUP-B; CONVENTIONAL CARE REGIMENS; ACUTE MYELOID-LEUKEMIA; RANDOMIZED PHASE-III; HYPOMETHYLATING AGENTS; MOLECULAR MUTATIONS; ELDERLY-PATIENTS; GENETIC-BASIS; AZACITIDINE;
D O I
10.1038/leu.2015.283
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Established prognostic tools in patients with myelodysplastic syndromes (MDS) were largely derived from untreated patient cohorts. Although azanucleosides are standard therapies for higher-risk (HR)-MDS, the relative prognostic performance of existing prognostic tools among patients with HR-MDS receiving azanucleoside therapy is unknown. In the MDS Clinical Research Consortium database, we compared the prognostic utility of the International Prognostic Scoring System (IPSS), revised IPSS (IPSS-R), MD Anderson Prognostic Scoring System (MDAPSS), World Health Organization-based Prognostic Scoring System (WPSS) and the French Prognostic Scoring System (FPSS) among 632 patients who presented with HR-MDS and were treated with azanucleosides as the first-line therapy. Median follow-up from diagnosis was 15.7 months. No prognostic tool predicted the probability of achieving an objective response. Nonetheless, all five tools were associated with overall survival (OS, P = 0.025 for the IPSS, P = 0.011 for WPSS and P<0.001 for the other three tools). The corrected Akaike Information Criteria, which were used to compare OS with the different prognostic scoring systems as covariates (lower is better) were 4138 (MDAPSS), 4156 (FPSS), 4196 (IPSS-R), 4186 (WPSS) and 4196 (IPSS). Patients in the highest-risk groups of the prognostic tools had a median OS from diagnosis of 11 - 16 months and should be considered for up-front transplantation or experimental approaches.
引用
收藏
页码:649 / 657
页数:9
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