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慢性淋巴细胞白血病治疗的当前方法和新型药物

英文原题:Current Approaches and Novel Agents in the Treatment of Chronic Lymphocytic Leukemia.

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Current Approaches and Novel Agents in the Treatment of Chronic Lymphocytic Leukemia.

PubMed 2024/06/07(内容时间) JCO Oncol Pract Q1 · IF 5.5(JCR 2025)

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中文摘要

慢性淋巴细胞白血病(CLL)治疗已从传统化学免疫疗法(CIT)发展至越来越多的靶向和生物疗法。随机试验证实,共价布鲁顿酪氨酸激酶抑制剂(cBTKi)优于 CIT;阿可替尼和泽布替尼等第二代药物的疗效/安全性特征似乎优于伊布替尼。非共价 BTK 抑制剂吡托布替尼在 cBTKi 治疗失败后显示出显著活性,且耐受性良好。BCL-2 抑制剂维奈克拉联合抗 CD20 药物(通常为奥妥珠单抗),作为初始治疗或 cBTKi 治疗失败后的方案,疗效很高;许多患者可达到微小残留病灶不可检测状态。具有前景的新策略包括 BTK 降解剂、双特异性抗体和CAR-T 细胞疗法。显而易见,CIT 已过时,目前及未来的靶向治疗将持续改善 CLL 患者结局。

展开英文摘要原文

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.

论文信息

作者
Cheson BD、Sharman JP
第一作者单位
Center for Cancer and Blood Disorders, Bethesda, MD.United States
通讯作者单位
Willamette Valley Cancer Institute, Medical Director of Hematology Research: Sara Cannon, Eugene, OR.
文献类型
综述
期刊
JCO oncology practice2024 Oct
原文标识
PubMed 38848511 · DOI 10.1200/OP.23.00770