Allogeneic Hematopoietic Stem-Cell Transplantation for Myelofibrosis: A Practical Review
Author(s) -
Nosha Farhadfar,
Sonia Cerquozzi,
Mrinal M. Patnaik,
Ayalew Tefferi
Publication year - 2016
Publication title -
journal of oncology practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.555
H-Index - 60
eISSN - 1935-469X
pISSN - 1554-7477
DOI - 10.1200/jop.2016.013268
Subject(s) - myelofibrosis , medicine , myeloproliferative neoplasm , hepatosplenomegaly , hematopoietic stem cell transplantation , constitutional symptoms , disease , transplantation , stem cell , haematopoiesis , oncology , intensive care medicine , immunology , bone marrow , biology , genetics
Myelofibrosis is a myeloproliferative neoplasm with cardinal features of extramedullary hematopoiesis, hepatosplenomegaly, cytopenias, and constitutional symptoms that result in shortened survival and leukemic transformation. It is a disease predominantly of the elderly, and currently available therapies only offer symptom control without curative benefit or ability to alter disease progression. Allogeneic hematopoietic stem-cell transplant (HSCT) is the only potentially curative intervention; however, this is only feasible in younger and medically fit patients and selectively offered to those with high-risk disease. Despite ongoing advancements, HSCT is associated with substantial morbidity and mortality, and the determination of which patients with myelofibrosis are ideal candidates and the selection of the opportune moment to proceed with transplantation remains challenging. This review summarizes our current recommendations for the role of and indications for HSCT in myelofibrosis.
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