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
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Participant red blood cell transfusion independence
Timeframe: Up to 12-weeks
Participants mean hemoglobin (Hb) increase ≥1.5 g/dL
Timeframe: Up to 12-weeks