Abstract | PURPOSE OF REVIEW: RECENT FINDINGS: The introduction of Janus kinase inhibitors for myelofibrosis have ushered in a new era for treatment of constitutional symptoms and splenomegaly in myelofibrosis, but the effect of these agents on the natural history of the disease has yet to be clearly defined. Reduced intensity transplants have emerged as the preferred option with recent evidence suggesting fludarabine and melphalan as the optimal conditioning regimen. SUMMARY:
Myelofibrosis is a rare hematologic malignancy with limited curative therapeutic options. Significant advances in our understanding of disease pathogenesis have led to new targets and new therapeutic options are forthcoming. Hematopoietic stem cell transplantation is at present the only treatment with curative intent; however, the selection of patients who are likely to be best served by this procedure is difficult. As myelofibrosis is an extremely rare disease, randomized clinical trials specifically investigating the role of transplantation in myelofibrosis are unlikely to occur, thus current decision making processes are best guided by retrospective analyses from registry databases and single institution experiences.
|
Authors | Angela G Fleischman, Richard T Maziarz |
Journal | Current opinion in hematology
(Curr Opin Hematol)
Vol. 20
Issue 2
Pg. 130-6
(Mar 2013)
ISSN: 1531-7048 [Electronic] United States |
PMID | 23314844
(Publication Type: Journal Article, Review)
|
Chemical References |
- Protein Kinase Inhibitors
|
Topics |
- Decision Making
- Hematopoietic Stem Cell Transplantation
(methods)
- Humans
- Patient Selection
- Primary Myelofibrosis
(therapy)
- Protein Kinase Inhibitors
(therapeutic use)
- Transplantation Conditioning
(methods)
|