R. Mohty, Shaykha Alotaibi, M. Gadd, Yan Luo, Ricardo D. Parrondo, Hong Qin, M. Kharfan-Dabaja
{"title":"Chimeric Antigen Receptor T-cell Therapy for Chronic Lymphocytic Leukemia: What is the supporting evidence so far?","authors":"R. Mohty, Shaykha Alotaibi, M. Gadd, Yan Luo, Ricardo D. Parrondo, Hong Qin, M. Kharfan-Dabaja","doi":"10.46989/001c.88382","DOIUrl":null,"url":null,"abstract":"While acknowledging that newer therapies have improved survival rates in chronic lymphocytic leukemia (CLL), patients with high-risk disease features are at an increased risk of treatment failure. Allogeneic hematopoietic cell transplantation (allo-HCT) was traditionally offered as front-line consolidation in high-risk CLL; however, with the emergence of targeted therapies like Bruton tyrosine kinase (BTK) and B-cell lymphoma 2 (BCL-2) inhibitors, the role of allo-HCT has been relegated to later stages of the disease. Patients with relapsed/refractory (R/R) CLL who have failed both BTK and BCL-2 inhibitors represent a therapeutic challenge owing to a poor prognosis. Chimeric antigen receptor T-cell (CAR T) therapies targeting CD19 have improved response rates and overall survival in various types of R/R B-cell non-Hodgkin lymphomas. For CLL, no approved CAR T-cell therapies are yet available. Emerging data appear to show a therapeutic benefit of CAR T-cell therapy in patients with R/R CLL, even after failing an allo-HCT.","PeriodicalId":10368,"journal":{"name":"Clinical Hematology International","volume":"99 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Hematology International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46989/001c.88382","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
While acknowledging that newer therapies have improved survival rates in chronic lymphocytic leukemia (CLL), patients with high-risk disease features are at an increased risk of treatment failure. Allogeneic hematopoietic cell transplantation (allo-HCT) was traditionally offered as front-line consolidation in high-risk CLL; however, with the emergence of targeted therapies like Bruton tyrosine kinase (BTK) and B-cell lymphoma 2 (BCL-2) inhibitors, the role of allo-HCT has been relegated to later stages of the disease. Patients with relapsed/refractory (R/R) CLL who have failed both BTK and BCL-2 inhibitors represent a therapeutic challenge owing to a poor prognosis. Chimeric antigen receptor T-cell (CAR T) therapies targeting CD19 have improved response rates and overall survival in various types of R/R B-cell non-Hodgkin lymphomas. For CLL, no approved CAR T-cell therapies are yet available. Emerging data appear to show a therapeutic benefit of CAR T-cell therapy in patients with R/R CLL, even after failing an allo-HCT.
虽然新疗法提高了慢性淋巴细胞白血病(CLL)的存活率,但具有高危疾病特征的患者治疗失败的风险也在增加。异基因造血细胞移植(allo-HCT)传统上是作为高危CLL的一线巩固治疗手段;然而,随着布鲁顿酪氨酸激酶(BTK)和B细胞淋巴瘤2(BCL-2)抑制剂等靶向疗法的出现,allo-HCT的作用已被降至疾病的后期阶段。BTK和BCL-2抑制剂均无效的复发/难治(R/R)CLL患者预后较差,是治疗上的一大挑战。针对 CD19 的嵌合抗原受体 T 细胞(CAR T)疗法提高了各种复发性/难治性 B 细胞非霍奇金淋巴瘤的应答率和总生存率。对于 CLL,目前还没有获得批准的 CAR T 细胞疗法。新出现的数据似乎显示,CAR T 细胞疗法对 R/R CLL 患者有治疗效果,即使是异体肝细胞移植失败的患者。