治疗慢性淋巴细胞白血病的现有方法和新型新药。

IF 4.7 3区 医学 Q1 ONCOLOGY JCO oncology practice Pub Date : 2024-10-01 Epub Date: 2024-06-07 DOI:10.1200/OP.23.00770
Bruce D Cheson, Jeff P Sharman
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引用次数: 0

摘要

CLL的治疗方法已从传统的化学免疫疗法(CIT)发展到越来越多的靶向和生物疗法。随机试验表明,共价酪氨酸激酶抑制剂(cBTKis)的疗效优于CIT,而阿卡布替尼和扎努布替尼等第二代化合物似乎比伊布替尼具有更有利的疗效/安全性。非共价 BTKi pirtobrutinib 在 cBTKis 治疗失败后显示出令人印象深刻的活性,而且相当耐受。Bcl-2 抑制剂 venetoclax 加上 CD20(一般为 obinutuzumab),作为初始治疗或 cBTKi 治疗失败后的治疗,可提供高水平的疗效,许多患者可达到检测不到的最小残留疾病状态。前景看好的新方法包括 BTK 降解剂、双特异性抗体和嵌合抗原受体 T 细胞(CAR-T)疗法。显而易见的是,CIT疗法已经过时,目前和未来的靶向疗法将继续改善慢性淋巴细胞白血病患者的治疗效果。
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Current Approaches and Novel Agents in the Treatment of Chronic Lymphocytic Leukemia.

The treatment of CLL has evolved from traditional chemoimmunotherapy (CIT) to an increasing number of targeted and biologic approaches. Randomized trials have demonstrated superiority of covalent bruton tyrosine kinase inhibitors (cBTKis) over CIT, and second-generation compounds such as acalabrutinib and zanubrutinib appear to have a more favorable efficacy/safety profile than ibrutinib. The noncovalent BTKi, pirtobrutinib, has shown impressive activity after failure of the cBTKis and is quite tolerable. The Bcl-2 inhibitor venetoclax plus a CD20, generally obinutuzumab, provides a high level of efficacy as initial treatment or after failure on a cBTKi, with many patients achieving a state of undetectable minimal residual disease. Promising novel approaches include BTK degraders, bispecific antibodies, and chimeric antigen receptor T-cell (CAR-T)-cell therapy. What is clear is that CIT is archaic, and current and future targeted approaches will continue to improve the outcome for patients with chronic lymphocytic leukemia.

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CiteScore
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自引率
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518
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