Reduced-intensity conditioning with fludarabine and busulfan for allogeneic hematopoietic cell transplantation in elderly or infirm patients with advanced myeloid malignancies

被引:0
作者
Dominik Schneidawind
Birgit Federmann
Corina Buechele
Andrea Helwig
Jörg Schmohl
Wichard Vogel
Christoph Faul
Lothar Kanz
Wolfgang A. Bethge
机构
[1] Stanford University,Division of Blood and Marrow Transplantation, Department of Medicine
[2] Eberhard Karls Universität Tübingen,Institute of Pathology and Neuropathology
[3] Stanford University,Department of Pathology
[4] University Hospital Tübingen,Department of Hematology and Oncology
来源
Annals of Hematology | 2016年 / 95卷
关键词
Allogeneic HCT; RIC; Myeloid malignancies; Aged patients; Fludarabine; Busulfan;
D O I
暂无
中图分类号
学科分类号
摘要
We report a retrospective single-center analysis of 112 consecutive patients that underwent allogeneic hematopoietic cell transplantation (HCT) after reduced-intensity conditioning (RIC) with fludarabine (FLU) and busulfan (BU) for the treatment of acute myeloid leukemia (AML), myelodysplastic syndrome (MDS) and myeloproliferative syndrome (MPS) from 2005 to 2014. Three-year event-free survival (EFS) and overall survival (OS) were 46 and 58 %, respectively. Patients ≥60 years of age showed a similar outcome compared to younger patients (3-year OS 55 vs. 61 %, p = 0.96; 3-year EFS 46 vs. 46 %, p = 0.82). Cumulative incidence of non-relapse mortality (NRM) at 3 years adjusted for relapse as competing risk was 25 % for patients aged <60 years and 15 % for older patients (p = 0.15). Infusions of higher CD34+ blood stem cell doses were associated with a significantly better outcome in the elderly subgroup (3-year OS 82 vs. 39 %, p = 0.007). Moreover, complete donor chimerism at day +100 was associated with a significantly improved survival (3-year OS 69 vs. 23 %, p = 0.003). In conclusion, our data suggest that RIC with FLU/BU enables long-term disease-free survival even in an elderly patient population. Age has no negative impact on the outcome of allogeneic HCT, and decision for transplant should be based on disease risk and performance status rather than age alone.
引用
收藏
页码:115 / 124
页数:9
相关论文
共 470 条
[1]  
Xie Y(2003)Trends in leukemia incidence and survival in the United States (1973-1998) Cancer 97 2229-2235
[2]  
Davies SM(2012)Cancer statistics, 2012 CA Cancer J Clin 62 10-29
[3]  
Xiang Y(2009)Age-related risk profile and chemotherapy dose response in acute myeloid leukemia: a study by the German Acute Myeloid Leukemia Cooperative Group J Clin Oncol 27 61-69
[4]  
Robison LL(2006)Age and acute myeloid leukemia Blood 107 3481-3485
[5]  
Ross JA(2015)Influence of age on outcome after allogeneic hematopoietic cell transplantation: a single center study in patients aged 60 Bone Marrow Transplant 50 427-31
[6]  
Siegel R(2010)Effect of age on outcome of reduced-intensity hematopoietic cell transplantation for older patients with acute myeloid leukemia in first complete remission or with myelodysplastic syndrome J Clin Oncol 28 1878-1887
[7]  
Naishadham D(1998)Nonmyeloablative stem cell transplantation and cell therapy as an alternative to conventional bone marrow transplantation with lethal cytoreduction for the treatment of malignant and nonmalignant hematologic diseases Blood 91 756-763
[8]  
Jemal A(2003)Graft-versus-host disease following allogeneic transplantation from HLA-identical sibling with antithymocyte globulin-based reduced-intensity preparative regimen Blood 102 470-476
[9]  
Buchner T(2012)Graft-versus-host disease induced graft-versus-leukemia effect: greater impact on relapse and disease-free survival after reduced intensity conditioning Biol Blood Marrow Transplant 18 1727-1733
[10]  
Berdel WE(2012)Potent graft-versus-leukemia effect after reduced-intensity allogeneic SCT for intermediate-risk AML with FLT3-ITD or wild-type NPM1 and CEBPA without FLT3-ITD Biol Blood Marrow Transplant 18 1845-1850