Nonmyeloablative Allogeneic Stem Cell Transplantation for Chronic Myelogenous Leukemia in the Imatinib Era

被引:11
|
作者
Champlin, Richard [1 ]
de Lima, Marcos
Kebriaei, Partow
Rondon, Gabriela
Fisher, Tobi
Jabbour, Elias
Cortes, Jorge E.
Kantarjian, Hagop
Anderlini, Paolo
Alousi, Amin
Hosing, Chitra
Shpall, Elizabeth
Popat, Uday
Qazilbash, Muzaffar
Andersson, Borje
Giralt, Sergio
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
来源
关键词
Busulfan; Chronic myeloid leukemia; Fludarabine; G raft-versus-host disease; Preparative regimen; CHRONIC MYELOID-LEUKEMIA; BONE-MARROW-TRANSPLANTATION; GRAFT-VERSUS-LEUKEMIA; DONOR LEUKOCYTE INFUSIONS; ADOPTIVE IMMUNOTHERAPY; INTERFERON-ALPHA; CHRONIC-PHASE; PREPARATIVE REGIMENS; HEMATOPOIETIC TRANSPLANTATION; HEMATOLOGIC MALIGNANCIES;
D O I
10.3816/CLM.2009.s.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Allogeneic stem cell transplantation (ASCT) is a potentially curative treatment for patients with chronic myelogenous leukemia (CML) and was previously considered the preferred treatment for newly diagnosed CML. The success of imatinib has changed treatment recommendations, and allogeneic transplants are now reserved for imatinib treatment failures. Previous imatinib treatment does not compromise the results of ASCT, but patients with overt transformed disease have poor results. It is unclear whether patients whose disease is considered to have failed imatinib should be referred immediately for ASCT or receive treatment with a second-generation tyrosine kinase inhibitors (TKI). Patients whose disease fails 2 TKIs should receive ASCT if possible. Nonmyeloablative preparative regimens reduce the toxicity and treatment-related mortality associated with the transplantation procedure and allow transplantations to be performed in older and medically infirm patients. This approach, including posttransplantation treatment with TKIs and donor lymphocyte infusion, produces a high fraction of durable molecular complete remissions.
引用
收藏
页码:S261 / S265
页数:5
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