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How I reduce and treat posttransplant relapse of MDS.
Mina, Alain; Greenberg, Peter L; Deeg, H Joachim.
Afiliação
  • Mina A; Myeloid Malignancies Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD.
  • Greenberg PL; Department of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA.
  • Deeg HJ; Fred Hutchinson Cancer Center, Seattle, WA.
Blood ; 143(14): 1344-1354, 2024 Apr 04.
Article em En | MEDLINE | ID: mdl-38306658
ABSTRACT
ABSTRACT Allogeneic hematopoietic stem cell transplantation (HSCT) is the only potentially curative option for patients with high-risk myelodysplastic syndromes (MDS). Advances in conditioning regimens and supportive measures have reduced treatment-related mortality and increased the role of transplantation, leading to more patients undergoing HSCT. However, posttransplant relapse of MDS remains a leading cause of morbidity and mortality for this procedure, necessitating expert management and ongoing results analysis. In this article, we review treatment options and our institutional approaches to managing MDS relapse after HSCT, using illustrative clinical cases that exemplify different clinical manifestations and management of relapse. We address areas of controversy relating to conditioning regimen intensity, chemotherapeutic bridging, and donor selection. In addition, we discuss future directions for advancing the field, including (1) the need for prospective clinical trials separating MDS from acute myeloid leukemia and focusing on posttransplant relapse, as well as (2) the validation of measurable residual disease methodologies to guide timely interventions.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article