2024
DOI: 10.3389/fimmu.2024.1378432
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The state of the art in the treatment of severe aplastic anemia: immunotherapy and hematopoietic cell transplantation in children and adults

Agnieszka Piekarska,
Katarzyna Pawelec,
Anna Szmigielska-Kapłon
et al.

Abstract: Acquired aplastic anemia (AA) is an immune-mediated bone marrow (BM) failure where marrow disruption is driven by a cytotoxic T-cell–mediated autoimmune attack against hematopoietic stem cells. The key diagnostic challenge in children, but also in adults, is to exclude the possible underlying congenital condition and myelodysplasia. The choice of treatment options, either allogeneic hematopoietic cell transplantation (alloHCT) or immunosuppressive therapy (IST), depends on the patient’s age, comorbidities, and… Show more

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Cited by 5 publications
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“…Patients with benign disease have a 70 to 90 percent success rate when they receive a transplant from a sibling with compatible tissue. However, when a referral is received from an unrelated person, the success rate drops to 36% to 65% [9]. Data show that the three-year survival rate for multiple myeloma and Hodgkin lymphoma patients after stem cell transplantation is 79% [10].…”
Section: Introductionmentioning
confidence: 99%
“…Patients with benign disease have a 70 to 90 percent success rate when they receive a transplant from a sibling with compatible tissue. However, when a referral is received from an unrelated person, the success rate drops to 36% to 65% [9]. Data show that the three-year survival rate for multiple myeloma and Hodgkin lymphoma patients after stem cell transplantation is 79% [10].…”
Section: Introductionmentioning
confidence: 99%