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引用次数: 0
摘要
靶向治疗是慢性淋巴细胞白血病(CLL)的一种有效治疗方法,在大多数临床情况下,其疗效优于传统的化学免疫疗法。除了某些年轻、体格健壮、免疫球蛋白重链可变区基因突变的患者外,大多数患者都能从持续使用BTK抑制剂或1年固定疗程的venetoclax-obinutuzumab作为CLL一线治疗的靶向疗法中获益。治疗选择取决于患者、治疗和疾病相关因素,包括患者偏好、伴随药物、合并症、治疗方案的安全性以及TP53畸变。临床试验正在积极研究使用或不使用 CD20 单克隆抗体同时抑制布鲁顿酪氨酸激酶(BTK)和 B 细胞淋巴瘤 2(BCL-2)蛋白的方法,该方法可使大多数患者获得深度应答(骨髓中检测不到最小残留病灶的比例为 52%-89%)。
Targeted therapy is a powerful treatment option in chronic lymphocytic leukemia (CLL) that has outperformed conventional chemoimmunotherapy in most clinical settings. Except for selected young, fit patients with a mutated immunoglobulin heavy chain variable region gene, most patients benefit from targeted therapy with either a continuous BTK inhibitor or 1-year fixed-duration venetoclax-obinutuzumab as first-line treatment of CLL. Treatment selection is driven by patient-, treatment-, and disease-related factors, encompassing patient preference, concomitant medications, comorbidities, safety profile of the regimen, and TP53 aberration. Clinical trials are actively investigating the simultaneous inhibition of Bruton's tyrosine kinase (BTK) and B-cell lymphoma 2 (BCL-2) proteins with or without a CD20 monoclonal antibody, which can achieve deep response in most patients (52%-89% undetectable minimal residual disease in bone marrow).