eJHaem | |
Improved donor chimerism in relapse myelofibrosis post allogenic stem cell transplant with azacitidine and oral decitabine—First case report | |
article | |
Verna Cheung1  Fotios V. Michelis3  Hassan Sibai1  | |
[1] Princess Margaret Cancer Centre;University of Toronto;Hans Messner Allogeneic Transplant Program, Princess Margaret Cancer Centre, University Health Network | |
关键词: allogenic stem cell transplant; hypomethylating agent; myeloid lineage chimerism; primary myelofibrosis; | |
DOI : 10.1002/jha2.611 | |
来源: Wiley | |
【 摘 要 】
To date, allogenic stem cell transplant (ASCT) remains the only potential curative option for patients with primary myelofibrosis (PMF). However, relapse rates and associated mortality remain a concern. A second ASCT may not be feasible due to advancing age, declined functional status, donor unavailability, toxicities associated with a second ASCT. Herein, we report the first case of utilizing initially azacitidine and subsequently oral decitabine + cedazuridine (decitabine), in the context of relapsed PMF post-ASCT. Utilizing both hypomethylating agents provided disease control and improved donor/myeloid lineage chimerism levels, and the patient also remained transfusion independent, with preserved functional status and quality of life.
【 授权许可】
Unknown
【 预 览 】
Files | Size | Format | View |
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RO202307080004837ZK.pdf | 333KB | download |