Allogeneic hematopoietic cell transplantation for mycosis fungoides and Sezary syndrome

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作者
M J Lechowicz
H M Lazarus
J Carreras
G G Laport
C S Cutler
P H Wiernik
G A Hale
D Maharaj
R P Gale
P A Rowlings
C O Freytes
A M Miller
J M Vose
R T Maziarz
S Montoto
D G Maloney
P N Hari
机构
[1] Emory University Hospital,Division of Blood and Marrow Transplantation
[2] Seidman Cancer Center,Division of Experimental Medicine, Department of Medicine
[3] University Hospitals Case Medical Center,Division of Hematology/Oncology
[4] Center for International Blood and Marrow Transplant Research,undefined
[5] Medical College of Wisconsin,undefined
[6] Stanford University Medical Center,undefined
[7] Dana Farber Cancer Institute,undefined
[8] Our Lady of Mercy Medical Center,undefined
[9] Pediatric Hematology/Oncology/BMT,undefined
[10] All Children’s Hospital,undefined
[11] South Florida Bone Marrow Stem Cell Transplant Institute,undefined
[12] Section of Hematology,undefined
[13] Imperial College,undefined
[14] Calvary Mater Newcastle,undefined
[15] HAPS-Pathology North,undefined
[16] University of Newcastle,undefined
[17] New South Wales,undefined
[18] Australia,undefined
[19] South Texas Veterans Health Care System and University of Texas Health Science Center San Antonio,undefined
[20] Baylor University Medical Center,undefined
[21] The Nebraska Medical Center,undefined
[22] Center for Hematologic Malignancies,undefined
[23] Oregon Health and Science University,undefined
[24] Barts Cancer Institute,undefined
[25] Queen Mary University of London,undefined
[26] Fred Hutchinson Cancer Research Center,undefined
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摘要
We describe outcomes after allogeneic hematopoietic cell transplantation (HCT) for mycosis fungoides and Sezary syndrome (MF/SS). Outcomes of 129 subjects with MF/SS reported to the Center for the International Blood and Marrow Transplant from 2000–2009. Median time from diagnosis to transplant was 30 (4–206) months and most subjects were with multiply relapsed/ refractory disease. The majority (64%) received non-myeloablative conditioning (NST) or reduced intensity conditioning (RIC). NST/RIC recipients were older in age compared with myeloablative recipients (median age 51 vs 44 years, P=0.005) and transplanted in recent years. Non-relapse mortality (NRM) at 1 and 5 years was 19% (95% confidence interval (CI) 12–27%) and 22% (95% CI 15–31%), respectively. Risk of disease progression was 50% (95% CI 41–60%) at 1 year and 61% (95% CI 50–71%) at 5 years. PFS at 1 and 5 years was 31% (95% CI 22–40%) and 17% (95% CI 9–26%), respectively. OS at 1 and 5 years was 54% (95% CI 45–63%) and 32% (95% CI 22–44%), respectively. Allogeneic HCT in MF/SS results in 5-year survival in approximately one-third of patients and of those, half remain disease-free.
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页码:1360 / 1365
页数:5
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