Central Nervous System Relapse in Adults with Acute Lymphoblastic Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation

被引:42
|
作者
Hamdi, Amir [1 ]
Mawad, Raya [2 ,3 ]
Bassett, Roland [1 ]
di Stasi, Antonio [1 ]
Ferro, Roberto [1 ]
Afrough, Aimaz [1 ]
Ram, Ron [4 ,5 ]
Dabaja, Bouthaina [1 ]
Rondon, Gabriela [1 ]
Champlin, Richard [1 ]
Sandmaier, Brenda M. [2 ,3 ]
Doney, Kristine [2 ,3 ]
Bar, Merav [2 ,3 ]
Kebriaei, Partow [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[3] Univ Washington, Seattle, WA 98195 USA
[4] Rabin Med Ctr, Inst Hematol, Bone Marrow Transplantat Unit, Petah Tiqwa, Israel
[5] Tel Aviv Univ, IL-69978 Tel Aviv, Israel
基金
美国国家卫生研究院;
关键词
Acute lymphoblastic leukemia; Central nervous system relapse; Allogeneic hematopoietic stem cell transplantation; BONE-MARROW-TRANSPLANTATION; ACUTE LYMPHOCYTIC-LEUKEMIA; RISK GROUPS; PROPHYLAXIS; REMISSION; CHEMOTHERAPY; THERAPIES; SEQUELAE; OUTCOMES; EBMT;
D O I
10.1016/j.bbmt.2014.07.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central nervous system (CNS) relapse after allogeneic hematopoietic stem cell transplantation (HSCT) confers a poor prognosis in adult patients with acute lymphoblastic leukemia (ALL). Preventing CNS relapse after HSCT remains a therapeutic challenge, and criteria for post-HSCT CNS prophylaxis have not been addressed. In a 3-center retrospective analysis, we reviewed the data for 457 adult patients with ALL who received a first allogeneic HSCT in first or second complete remission (CR). All patients received CNS prophylaxis as part of their upfront therapy for ALL, but post-transplantation CNS prophylaxis practice varied by institution and was administered to 48% of the patients. Eighteen patients (4%) developed CNS relapse after HSCT (isolated CNS relapse, n = 8; combined bone marrow and CNS relapse, n = 10). Patients with a previous history of CNS involvement with leukemia had a significantly higher rate for CNS relapse (P = .002), and pretransplantation CNS involvement was the only risk factor for post-transplantation CNS relapse found in this study. We failed to find a significant effect of post-transplantation CNS prophylaxis to prevent relapse after transplantation. Furthermore, no benefit for post-transplantation CNS prophylaxis could be detected when a subgroup analysis of patients with (P = .10) and without previous CNS involvement (P = .52) was performed. Finally, we could not find any significant effect for intensity of the transplantation conditioning regimen on CNS relapse after HSCT. In conclusion, CNS relapse is an uncommon event after HSCT for patients with ALL in CR1 or CR2, but with higher risk among patients with CNS involvement before transplantation. Furthermore, neither the use of post-HSCT CNS prophylaxis nor the intensity of the HSCT conditioning regimen made a significant difference in the rate of post-HSCT CNS relapse. (C) 2014 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1767 / 1771
页数:5
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