Table 2.

Retrospective studies supporting the use of erythropoiesis stimulating agents (ESAs) in MDS patients.

Study groupStudy designNResultsComments
MDS indicates myelodysplastic syndromes; ESA, erythropoiesis stimulating agent; HR, hazard ratio; CSF, colony stimulating factor; GFM, Groupe Francophone Myelodysplasies; GF, growth factor; IWG, International Working Group. 
Nordic17  Matched cohort of ESA-treated Nordic patients to untreated Pavia patients 121 Nordic 237 Pavia, Italy Survival advantage for ESA-treated group (HR = .61, P = .002) Nordic patients were treated with combination ESAs and CSFs. Survival improvement mainly in patients with low transfusion needs. 
GFM18  Matched cohort of ESA-treated GFM patients with untreated IMRAW patients 403 GFM Survival advantage for ESA-treated group (HR = .43, 95% CI: .25–.72) GFM patients were treated with epogen or darbepoietin 
Cleveland12  Systematic review of 162 trials published from 1985–2005 comparing ESA-treated patients with non-GF-treated patients 1587 ESA 1005 Non-GF Survival advantage for ESA-treated group at 2 years follow-up (79% vs. 68%, P = .005) Included only lower-risk MDS patients and used IWG response criteria. Differences remained significant in multivariate analyses controlling for baseline characteristic differences. 
Study groupStudy designNResultsComments
MDS indicates myelodysplastic syndromes; ESA, erythropoiesis stimulating agent; HR, hazard ratio; CSF, colony stimulating factor; GFM, Groupe Francophone Myelodysplasies; GF, growth factor; IWG, International Working Group. 
Nordic17  Matched cohort of ESA-treated Nordic patients to untreated Pavia patients 121 Nordic 237 Pavia, Italy Survival advantage for ESA-treated group (HR = .61, P = .002) Nordic patients were treated with combination ESAs and CSFs. Survival improvement mainly in patients with low transfusion needs. 
GFM18  Matched cohort of ESA-treated GFM patients with untreated IMRAW patients 403 GFM Survival advantage for ESA-treated group (HR = .43, 95% CI: .25–.72) GFM patients were treated with epogen or darbepoietin 
Cleveland12  Systematic review of 162 trials published from 1985–2005 comparing ESA-treated patients with non-GF-treated patients 1587 ESA 1005 Non-GF Survival advantage for ESA-treated group at 2 years follow-up (79% vs. 68%, P = .005) Included only lower-risk MDS patients and used IWG response criteria. Differences remained significant in multivariate analyses controlling for baseline characteristic differences. 
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