Faculty, Staff and Student Publications
Language
English
Publication Date
2-1-2023
Journal
Annals of Hematology
DOI
10.1007/s00277-022-05071-8
PMID
36635381
PMCID
PMC9889415
PubMedCentral® Posted Date
1-13-2023
PubMedCentral® Full Text Version
Post-print
Abstract
Red blood cell transfusion independence (RBC-TI) is an important goal in treating lower-risk myelodysplastic syndromes with ring sideroblasts. In the phase 3 MEDALIST study, RBC-TI of ≥ 8 weeks was achieved by significantly more luspatercept- versus placebo-treated patients in the first 24 weeks of treatment. In this post hoc analysis, we evaluated RBC transfusion units and visits based on patients' baseline transfusion burden level and the clinical benefit of luspatercept treatment beyond week 25 in initial luspatercept nonresponders (patients who did not achieve RBC-TI ≥ 8 weeks by week 25) but continued luspatercept up to 144 weeks. RBC transfusion burden, erythroid response, serum ferritin levels, and hemoglobin levels relative to baseline were evaluated. Through week 25, fewer RBC transfusion units and visits were observed in luspatercept-treated patients versus placebo, regardless of baseline transfusion burden. This continued through 144 weeks of luspatercept treatment, particularly in patients with low baseline transfusion burden. Sixty-eight patients were initial nonresponders at week 25 but continued treatment; most (81%) received the maximum dose of luspatercept (1.75 mg/kg). Sixteen percent achieved RBC-TI for ≥ 8 weeks during weeks 25-48, 26% had reduced RBC transfusion burden, 10% achieved an erythroid response, 44% had reduced serum ferritin, and hemoglobin levels increased an average of 1.3 g/dL from baseline. These data have implications for clinical practice, as transfusion units and visits are less in luspatercept-treated patients through week 25 regardless of baseline transfusion burden, and continuing luspatercept beyond week 25 can potentially provide additional clinical benefits for initial nonresponders.
Keywords
Humans, Ferritins, Hemoglobins, Immunoglobulin Fc Fragments, Myelodysplastic Syndromes, Recombinant Fusion Proteins, Activin Receptors, Type II, Myelodysplastic syndromes, Anemia, Luspatercept, Red blood cell transfusion independence, Health-related quality of life
Published Open-Access
yes
Recommended Citation
Germing, Ulrich; Fenaux, Pierre; Platzbecker, Uwe; et al., "Improved Benefit of Continuing Luspatercept Therapy: Sub-analysis of Patients With Lower-Risk MDS in the Medalist Study" (2023). Faculty, Staff and Student Publications. 5719.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/5719
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Bioinformatics Commons, Biomedical Informatics Commons, Genetic Phenomena Commons, Medical Genetics Commons, Oncology Commons
Comments
Trial registration: NCT02631070.