Hatashima Alycia, Shadman Mazyar, Raghunathan Vikram
Department of Pharmacy, University of Washington, Seattle, WA 98195, USA.
Division of Hematology and Medical Oncology, University of Washington, Seattle, WA 98195, USA.
Cancers (Basel). 2025 Jan 15;17(2):268. doi: 10.3390/cancers17020268.
Pathway inhibitors targeting Bruton tyrosine kinase (BTK) and B-cell lymphoma-2 (BCL-2) have dramatically changed the treatment landscape for both treatment-naïve and relapsed/refractory chronic lymphocytic leukemia (CLL). However, with increased utilization, a growing number of patients will experience progressive disease on both agents. This subgroup of "double refractory" patients has limited treatment options and poor prognosis. Chimeric antigen receptor (CAR)-T cells have transformed the treatment of relapsed/refractory B-cell malignancies. Although the earliest success of CAR-T cell therapy was in CLL, the clinical application of this modality has lagged until the recent approval of the first CAR-T cell product for CLL. In this review, we describe the current treatment options for upfront and subsequent therapies and the unmet need for novel agents highlighted by the burgeoning role and challenges of CAR-T cell therapy.
靶向布鲁顿酪氨酸激酶(BTK)和B细胞淋巴瘤-2(BCL-2)的通路抑制剂显著改变了初治和复发/难治性慢性淋巴细胞白血病(CLL)的治疗格局。然而,随着这些药物使用的增加,越来越多的患者在这两种药物治疗下都会出现疾病进展。这一“双重难治”亚组患者的治疗选择有限,预后较差。嵌合抗原受体(CAR)-T细胞已经改变了复发/难治性B细胞恶性肿瘤的治疗方式。尽管CAR-T细胞疗法最早在CLL中取得成功,但直到首个用于CLL的CAR-T细胞产品最近获批,这种治疗方式的临床应用一直滞后。在这篇综述中,我们描述了一线及后续治疗的当前治疗选择,以及CAR-T细胞疗法的新兴作用和挑战所凸显的对新型药物的未满足需求。