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CLL 的 CAR-T 细胞治疗:我们治疗工具箱中的新成员?

英文原题:CAR T-cell therapy for CLL: a new addition to our treatment toolbox?

查看英文原题

CAR T-cell therapy for CLL: a new addition to our treatment toolbox?

PubMed 2023/03/01(内容时间) Clin Adv Hematol Oncol Q4 · IF 2(JCR 2025)

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中文摘要

近年来,随着新型药物问世,高危慢性淋巴细胞白血病(CLL)的治疗发生了重大变革。布鲁顿酪氨酸激酶(BTK)抑制剂,如ibrutinib、acalabrutinib和zanubrutinib,可有效控制各治疗线的CLL,包括具有高危特征的患者。BTK抑制剂可序贯使用或与BCL2抑制剂venetoclax联合应用。因此,在当前治疗时代,曾是高危患者主要治疗方法的标准化疗和异基因干细胞移植(allo-SCT)已很少采用。尽管这些新型药物疗效卓越,仍有部分患者发生疾病进展。嵌合抗原受体(CAR)T细胞疗法已获批用于若干B细胞恶性肿瘤并显示疗效,但用于CLL仍处于研究阶段。多项研究显示,CAR-T 细胞疗法有望使CLL患者获得长期缓解,且与传统治疗方法相比安全性较好。本综述重点回顾CLL CAR-T 疗法的部分文献,包括关键在研研究的中期结果,并着重讨论近期研究进展。

展开英文摘要原文

Treatment of high-risk chronic lymphocytic leukemia (CLL) has undergone a revolution in recent years with the introduction of novel agents. Bruton kinase inhibitors (BTK) inhibitors, such as ibrutinib, acalabrutinib, and zanubrutinib, are effective at controlling CLL in all lines of therapy, including in patients with high-risk features. BTK inhibitors can be used in sequence or in combination with the BCL2 inhibitor venetoclax. As a result, standard chemotherapy and allogeneic stem cell transplant (allo-SCT)-once major treatment approaches in high-risk patients-are used much less commonly in the current era.

Despite the outstanding efficacy of these novel agents, a proportion of patients still experience disease progression. Chimeric antigen receptor (CAR) T-cell therapy has received regulatory approval for several B-cell malignancies in which it has shown efficacy, but it remains investigational for CLL.

Several studies have shown the potential for long-term remission in CLL with CAR T-cell therapy, with a favorable safety profile compared with conventional approaches. This review focuses on selected literature on CAR T-cell therapy for CLL, including the interim results of key ongoing studies, with an emphasis on recent research.

论文信息

作者
Iovino L、Shadman M
单位
Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.United States
文献类型
综述
期刊
Clinical advances in hematology & oncology : H&O2023 Mar
原文标识
PubMed 36867557