急性白血病异基因造血干细胞移植后的维持治疗研究进展

Research progress on maintenance therapy following allogeneic hematopoietic stem cell transplantation for acute leukemia

  • 摘要: 急性白血病(acute leukemia,AL)是来源于造血干细胞的恶性克隆性疾病,分为急性淋巴细胞白血病(acute lymphoblastic leukemia,ALL)和急性髓细胞白血病(acute myeloid leukemia,AML)两大类。异基因造血干细胞移植(allogeneic hematopoietic stem cell transplantation,allo-HSCT)是AL患者获得长期生存有力的手段,但移植后复发仍然是导致其死亡的主要原因。移植前状态、移植预处理、移植后复发防治均影响移植后的复发。目前,有部分患者移植后维持治疗的研究开展,包括表观遗传学药物、靶向药物、免疫药物等移植后维持治疗。本文主要讨论移植后维持治疗与预后的关系,综述近年来急性白血病allo-HSCT后维持治疗的方法、治疗结局和潜在的不良反应。

     

    Abstract: Acute leukemia (AL) is a malignant clonal disease caused by hematopoietic stem cells. Depending on the cell type involved, AL is classified as acute lymphoblastic leukemia (ALL) or acute myeloid leukemia (AML). Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is an important and effective treatment for patients with AL to achieve long-term survival. However, recurrence after transplantation remains the primary cause of death. Pretransplantation status, transplantation conditioning, and prevention of post-transplantation relapse affects post-transplantation outcomes. This review focuses on post-transplantation maintenance therapy. Several studies on post-transplantation maintenance therapy are discussed, including research on post-transplantation maintenance therapy with epigenetic drugs, targeted drugs, and immunologic drugs.

     

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