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异体移植在新型治疗时代的慢性淋巴细胞白血病患者中的作用:综述。

Role of allogeneic transplantation in patients with chronic lymphocytic leukemia in the era of novel therapies: a review.

机构信息

Department of Hematology/Oncology and Cell Therapy, Western Pennsylvania Cancer Institute, 4800 Friendship Ave, Pittsburgh, PA 15224, USA.

Section of Bone Marrow Transplant and Cell Therapy, Division of Hematology/Oncology and Cell Therapy, Rush University Medical Center, 1725 West Harrison Street, Suite 809, Chicago, IL, USA.

出版信息

Ther Adv Hematol. 2014 Oct;5(5):139-52. doi: 10.1177/2040620714550773.

Abstract

Chronic lymphocytic leukemia (CLL) is the most common form of adult leukemia and is characterized by a highly variable clinical course. In the past decade, several prognostic risk factors have been identified facilitating the classification of CLL into various risk groups. Patients with poor risk disease, such as poor cytogenetics or relapsing after purine-based analogues, had limited therapeutic options, with allogeneic hematopoietic cell transplantation (allo-SCT) the only known therapy with curative potential. More recently, the introduction of novel agents inhibiting the B-cell receptor pathway, and the early success with chimeric antigen receptor T cells offers an effective and relatively safe option for this poor prognostic group which holds promise in the future. Alternatively, the use of reduced intensity conditioning regimens in the allo-SCT setting has led to a significant decrease in nonrelapse mortality to 16-23%, making it an attractive therapeutic option. No recent guidelines have been developed since these novel therapies became available regarding the optimal time to allo-SCT in this patient population. The advent of these novel and highly active therapeutic agents, therefore, warrants a reappraisal of the role and timing of allo-SCT in patients with CLL. In this article, we summarize the literature regarding the novel therapeutic agents available today as well as focus on the efficacy and safety of allo-SCT.

摘要

慢性淋巴细胞白血病(CLL)是成人白血病中最常见的类型,其临床过程高度可变。在过去的十年中,已经确定了几种预后危险因素,有助于将 CLL 分为不同的风险组。患有不良风险疾病的患者,如不良细胞遗传学或嘌呤类似物治疗后复发,治疗选择有限,异基因造血细胞移植(allo-SCT)是唯一具有治愈潜力的治疗方法。最近,新型抑制 B 细胞受体途径的药物的引入,以及嵌合抗原受体 T 细胞的早期成功,为这一预后不良的患者群体提供了一种有效且相对安全的选择,未来前景广阔。或者,在 allo-SCT 环境中使用强度降低的调理方案,可将非复发死亡率显著降低至 16-23%,使其成为一种有吸引力的治疗选择。由于这些新型治疗方法的出现,自这些新型疗法问世以来,尚未制定关于该患者群体中 allo-SCT 的最佳时机的最新指南。因此,这些新型、高度有效的治疗药物的出现,需要重新评估 allo-SCT 在 CLL 患者中的作用和时机。在本文中,我们总结了有关当今可用的新型治疗药物的文献,并重点介绍了 allo-SCT 的疗效和安全性。

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