The purpose of this study is to evaluate the treatment patterns and clinical outcomes in adults with lower-risk MDS (LR-MDS) who were erythropoiesis-stimulating agents (ESA)-naïve and received luspatercept treatment in China
Study Type
OBSERVATIONAL
Enrollment
80
According to the product label
Zhijian Xiao
Tianjin, China
Participant red blood cell transfusion independence
Time frame: Up to 12-weeks
Participants mean hemoglobin (Hb) increase ≥1.5 g/dL
Time frame: Up to 12-weeks
Participant transfusion independence and increase in hemoglobin (Hb)
Time frame: Up to 48 weeks
Duration of luspatercept monotherapy treatment
Time frame: Up to 48 weeks
Health Care Resource Utilization (HCRU)
Time frame: Up to 48 weeks
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