A Systematic Literature Review of Predictors of Erythropoiesis-Stimulating Agent Failure in Lower-Risk Myelodysplastic Syndromes
- PMID: 38731231
- PMCID: PMC11084325
- DOI: 10.3390/jcm13092702
A Systematic Literature Review of Predictors of Erythropoiesis-Stimulating Agent Failure in Lower-Risk Myelodysplastic Syndromes
Abstract
Erythropoiesis-stimulating agents (ESAs) are the first-line treatment option for anemia in patients with lower-risk myelodysplastic syndromes (LR-MDS). A systematic literature review was conducted to identify evidence of the association between prognostic factors and ESA response/failure in LR-MDS. MEDLINE, Embase, and relevant conferences were searched systematically for studies assessing the association between prognostic factors and ESA response/failure in adult patients. Of 1566 citations identified, 38 were included. Patient risk status in studies published from 2000 onwards was commonly assessed using the International Prognostic Scoring System (IPSS) or revised IPSS. ESA response was generally assessed using the International Working Group MDS criteria. Among the included studies, statistically significant relationships were found, in both univariate and multivariate analyses, between ESA response and the following prognostic factors: higher hemoglobin levels, lower serum erythropoietin levels, and transfusion independence. Furthermore, other prognostic factors such as age, bone marrow blasts, serum ferritin level, IPSS risk status, and karyotype status did not demonstrate statistically significant relationships with ESA response. This systematic literature review has confirmed prognostic factors of ESA response/failure. Guidance to correctly identify patients with these characteristics could be helpful for clinicians to provide optimal treatment.
Keywords: ESA failure; myelodysplastic syndromes; systematic literature review.
Conflict of interest statement
R. Boccia received grants or contracts from AbbVie, Amgen, AstraZeneca, Bristol Myers Squibb, Janssen, and Seagen; consultancy fees from AbbVie, Amgen, Bristol Myers Squibb, and Genmab; payment or honoraria from AbbVie, Amgen, Bristol Myers Squibb, Daiichi-Sankyo, Janssen, and Pharmacosmos; and participated on a data safety monitoring board or advisory board for Genmab. H. Xiao and A. Yucel are employees with and stock owners in Bristol Myers Squibb. S.L. Klijn is an employee with and stock owner in Bristol Myers Squibb, and has received consulting fees from Bayer, Bristol Myers Squibb, and Janssen. C. von Wilamowitz-Moellendorff, R. Raorane, and S. Deshpande are employees of Evidera, a research organization that was retained by Bristol Myers Squibb to conduct the research that is the subject of this manuscript.
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