Bose Prithviraj, Gandhi Varsha
Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Department of Experimental Therapeutics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Fac Rev. 2021 Feb 26;10:22. doi: 10.12703/r/10-22. eCollection 2021.
The therapeutic landscape of chronic lymphocytic leukemia (CLL) underwent a paradigm shift in 2014 with the approval of ibrutinib, which binds covalently to the C481 residue of Bruton's tyrosine kinase (BTK) and irreversibly inhibits it. A number of large, phase 3 trials conducted in both the frontline and the relapsed/refractory settings resulted in the approval of ibrutinib for all CLL. Indeed, the role of chemoimmunotherapy in CLL is fast dwindling. The limitations of ibrutinib, e.g. the development of resistance-conferring C481 BTK mutations and the toxicity issues of atrial fibrillation and bleeding, in particular, have also become apparent with longer-term follow-up. This has spurred the development of second-generation, irreversible inhibitors with greater selectivity for BTK and third-generation, reversible BTK inhibitors to address C481 site mutations. The last 3 years have also witnessed enormous growth in the therapeutic role of the B-cell lymphoma 2 (BCL-2) antagonist venetoclax, initially approved (in 2016) only for patients with relapsed, 17p-deleted CLL. Venetoclax, in combination with CD20 antibodies, is currently approved for both treatment-naïve and relapsed/refractory patients, regardless of genomic subtype. Robust results have also been reported for ibrutinib plus venetoclax, and "triple" combinations of a BTK inhibitor, venetoclax, and obinutuzumab are now being pursued. The major questions facing the field at present are how best to select patients for BTK inhibitor monotherapy versus venetoclax/obinutuzumab upfront, what to do after failure of both BTK inhibitor(s) and venetoclax, and the ideal way to integrate measurable residual disease data into decisions regarding treatment choice, duration, and discontinuation.
2014年,随着依鲁替尼获批,慢性淋巴细胞白血病(CLL)的治疗格局发生了范式转变。依鲁替尼可与布鲁顿酪氨酸激酶(BTK)的C481残基共价结合并不可逆地抑制它。在一线和复发/难治性治疗环境中进行的多项大型3期试验导致依鲁替尼获批用于所有CLL患者。事实上,化疗免疫疗法在CLL中的作用正在迅速减弱。随着长期随访,依鲁替尼的局限性,例如导致耐药的C481 BTK突变的出现以及房颤和出血等毒性问题也变得明显。这促使了对BTK具有更高选择性的第二代不可逆抑制剂以及针对C481位点突变的第三代可逆BTK抑制剂的开发。过去3年中,B细胞淋巴瘤2(BCL-2)拮抗剂维奈克拉的治疗作用也有了巨大增长,它最初(2016年)仅被批准用于复发的、17p缺失的CLL患者。维奈克拉与CD20抗体联合使用,目前已获批用于初治和复发/难治性患者,无论其基因组亚型如何。依鲁替尼加维奈克拉也报告了强有力的结果,目前正在探索BTK抑制剂、维奈克拉和奥妥珠单抗的“三联”组合。该领域目前面临的主要问题是如何最好地选择患者进行BTK抑制剂单药治疗与维奈克拉/奥妥珠单抗一线治疗,在BTK抑制剂和维奈克拉均失败后该怎么做,以及将可测量的残留疾病数据纳入治疗选择、持续时间和停药决策的理想方法。