Response to erythropoietic‐stimulating agents in patients with chronic myelomonocytic leukemia
- 5 September 2015
- journal article
- research article
- Published by Wiley in European Journal of Haematology
- Vol. 97 (1) , 33-38
Abstract
Background: The efficacy of erythropoietic‐stimulating agents (ESA) in chronic myelomonocytic leukemia (CMML) is unknown. Our objective was to analyze erythroid response (ER) and overall survival (OS) in a series of 94 patients with CMML treated with ESA.Methods: We analyzed a series of 94 patients with CMML treated with ESA included in the Spanish and Düsseldorf‐MDS registries.Findings: ER was observed in 64% of patients and red blood cell (RBC) transfusion independence in 31%. The median duration of ER was 7 months (range, 0–88). CPSS and EPO level were significantly associated with ER in multivariate analysis (P = 0.003). Considering only patients with CPSS low‐ or intermediate‐1‐risk group, the absence of RBC transfusion dependence and erythropoietin (EPO) level predicted ER (P = 0.003 and P = 0.008, respectively). In multivariate analysis, only the EPO level retained its prognostic value (P = 0.029). Achievement of ER correlated with a better survival since ER evaluation (P = 0.016).Interpretation: The CPSS and EPO levels are adequate tools to select CMML patients with symptomatic anemia who may benefit from treatment with ESA. A significant ER to ESA is expected in anemic patients with low/intermediate‐1 CMML risk by the CPSS and a low endogenous serum EPO level.Keywords
Funding Information
- Josep Carreras Leukemia Research Institute (RD12/0036/0029)
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