Abstract
IMiDs (immunomodulatory drugs from the thalidomide class) enhance hemoglobin F (HbF) production but are not yet approved for sickle cell disease (SCD). Here, we describe a case of severe SCD and multiple myeloma (MM) in which over 6 years of treatment with IMiDs and hydroxyurea led to sustained remission of SCD.
Keywords:
Fetal hemoglobin (HbF); Hydroxyurea; Multiple myeloma (MM); Pomalidomide; Sickle cell disease (SCD).
© 2025. The Author(s), under exclusive licence to Japanese Society of Hematology.
MeSH terms
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Anemia, Sickle Cell* / complications
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Anemia, Sickle Cell* / drug therapy
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Female
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Humans
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Hydroxyurea* / administration & dosage
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Hydroxyurea* / therapeutic use
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Immunologic Factors* / administration & dosage
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Immunologic Factors* / therapeutic use
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Male
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Middle Aged
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Multiple Myeloma* / complications
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Multiple Myeloma* / drug therapy
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Thalidomide* / administration & dosage
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Thalidomide* / analogs & derivatives
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Thalidomide* / therapeutic use
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Treatment Outcome
Substances
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Hydroxyurea
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Thalidomide
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Immunologic Factors