Allogeneic haematopoietic cell transplantation for myelofibrosis in 30 patients 60-78 years of age

作者：Samuelson Scott; Sandmaier Brenda M; Heslop Helen E; Popat Uday; Carrum George; Champlin Richard E; Storb Rainer; Prchal Josef T; Gooley Theodore A; Deeg H Joachim^*

来源：British Journal of Haematology, 2011, 153(1): 76-82.

DOI：10.1111/j.1365-2141.2011.08582.x

• myelofibrosis
• older patients
• haematopoietic cell transplantation

P>We analysed the results of haematopoietic cell transplantation (HCT) in 30 patients aged 60-78 (median 65) years, with primary myelofibrosis or myelofibrosis evolving from antecedent polycythaemia vera or essential thrombocythaemia. Donors were human leucocyte antigen (HLA)-identical siblings (N = 15) or unrelated individuals (N = 15). Various conditioning regimens were used, ranging from very low intensity (fludarabine plus 2 Gy total body irradiation) to high dose (busulfan plus cyclophosphamide). Stem cell sources were granulocyte colony-stimulating factor mobilized peripheral blood progenitor cells in 29 patients and marrow in one patient. Sustained engraftment was documented in 27 of 30 patients. Day -100 mortality was 13%. With a median follow-up of 22 (range 0 center dot 5-69) months, 3-year overall survival and progression-free survival were 45% and 40%, respectively. Currently, 13 patients are surviving. Seven patients died with disease progression at 0 center dot 5-22 months, and 10 patients died from other causes at 1 center dot 5-37.5 months after HCT. While the selection of older patients for transplantation was probably biased, the present results are encouraging. Motivated older patients with myelofibrosis without substantial comorbid conditions should be offered the option of allogeneic HCT.

• 出版日期2011-4