The purpose of this study is to understand the treatment patterns and clinical outcomes of myelodysplastic syndromes patients treated with luspatercept or erythropoiesis-stimulating agents
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Participant baseline demographics
Timeframe: Baseline
Luspatercept dose at treatment initiation
Timeframe: Baseline
Luspatercept dose at treatment discontinuation
Timeframe: Up to 50 months
Luspatercept dose change or escalation or reduction
Timeframe: Up to 50 months
Time from luspatercept initiation to the first occurrence of dose escalation
Timeframe: Up to 50 months
Proportion of participants that discontinued treatment
Timeframe: Up to 50 months
Time from treatment initiation to treatment discontinuation
Timeframe: Up to 50 months
Time from luspatercept/erythropoiesis stimulating agents treatment initiation to initiation of a new treatment for myelodysplastic syndromes
Timeframe: Up to 50 months