Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, 303 E Superior St, Lurie 3-103, Chicago, IL, 60611, USA.
Curr Hematol Malig Rep. 2021 Aug;16(4):325-335. doi: 10.1007/s11899-021-00637-1. Epub 2021 May 22.
The treatment options for chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) have expanded significantly in the last few years, including the use of new classes of oral small molecular inhibitors targeting the B cell receptor signaling pathway or the apoptosis machinery. Targeted therapy with or without immunotherapy has quickly emerged as a new standard for frontline treatment of CLL/SLL, though the previous standard chemoimmunotherapy (CIT) remains a treatment option. In this review, we present data from key clinical trials to evaluate the benefits and risks associated with different frontline treatment approaches.
We reviewed recently published and presented clinical trials on frontline CLL/SLL treatment, with particular focus on the comparison of CIT vs. targeted therapies, including inhibitors of Bruton's tyrosine kinase (BTK) or of the anti-apoptotic protein Bcl-2. Various BTK inhibitors as continuous treatment with or without anti-CD20 monoclonal antibodies have compared favorably to the conventional CITs in previously untreated CLL/SLL patients of various ages and comorbidities. Fixed duration treatment with the Bcl-2 inhibitor venetoclax combined with anti-CD20 monoclonal antibodies also showed superiority in clinical outcomes compared to CIT. Subgroup analysis interestingly showed that IgHV-mutated CLL/SLL might still derive similar benefits from CIT. Ongoing clinical trials are investigating combined targeted therapies of venetoclax plus a BTK inhibitor to try to further improve the efficacy while limiting the duration of treatment. Targeted therapies are becoming the new standard of care for frontline treatment of CLL/SLL although conventional CIT remains an option group of fit patients with low risk features. Novel strategies are being studied using targeted therapy combinations to optimize the depth of response in a time-limited fashion.
近年来,慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)的治疗选择有了显著的扩展,包括使用针对 B 细胞受体信号通路或凋亡机制的新型口服小分子抑制剂。靶向治疗联合或不联合免疫治疗已迅速成为 CLL/SLL 一线治疗的新标准,尽管之前的标准化疗免疫治疗(CIT)仍然是一种治疗选择。在这篇综述中,我们展示了来自关键临床试验的数据,以评估不同一线治疗方法的获益和风险。
我们回顾了最近发表的和报告的 CLL/SLL 一线治疗的临床试验,特别关注 CIT 与靶向治疗的比较,包括布鲁顿酪氨酸激酶(BTK)抑制剂或抗凋亡蛋白 Bcl-2 抑制剂。各种 BTK 抑制剂作为连续治疗,联合或不联合抗 CD20 单克隆抗体,与之前未治疗的不同年龄和合并症的 CLL/SLL 患者的传统 CIT 相比具有优势。固定疗程的 Bcl-2 抑制剂 venetoclax 联合抗 CD20 单克隆抗体治疗也显示出优于 CIT 的临床结局。有趣的亚组分析表明,IGHV 突变的 CLL/SLL 可能仍然从 CIT 中获得类似的获益。正在进行的临床试验正在研究 venetoclax 联合 BTK 抑制剂的联合靶向治疗,以尝试进一步提高疗效,同时限制治疗的持续时间。尽管传统 CIT 仍然是具有低风险特征的适合患者的选择,但靶向治疗正在成为 CLL/SLL 一线治疗的新标准。正在研究新的策略,使用靶向治疗联合以有限的时间限制方式优化反应的深度。