Center for Blood Disorders and Stem Cell Transplantation, Swedish Cancer Institute, 1221 Madison St, Seattle, WA, 98104, USA.
J Hematol Oncol. 2021 Apr 26;14(1):69. doi: 10.1186/s13045-021-01054-w.
Treatment decisions for patients with chronic lymphocytic leukemia (CLL) are dependent on symptoms and classification into high-, medium-, or low-risk categories. The prognosis for CLL hinges, in part, on the presence or absence of less-favorable genetic aberrations, including del(17p), del(11q), TP53 dysfunction, and IGHV mutations, as these markers are associated with worse treatment response. Promising results from multiple clinical trials show emerging therapies targeting Burton tyrosine kinase, B-cell leukemia/lymphoma 2, and phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta result in better outcomes and prolonged progression-free survival for patients both with and without certain high-risk aberrations. Favorable outcomes using these novel oral targeted therapies, either alone or in combination with other treatments such as anti-CD20 antibodies, has led to their use almost entirely supplanting chemoimmunotherapy in the treatment of CLL. In this narrative review, we summarize the current clinical evidence for the use of targeted mono- and combination therapies for CLL, discuss new and next-generation treatment approaches currently in development, and provide insight into areas of unmet need for the treatment of patients with CLL.
慢性淋巴细胞白血病(CLL)患者的治疗决策取决于症状和风险分类(高、中、低)。CLL 的预后部分取决于是否存在不太有利的遗传异常,包括 del(17p)、del(11q)、TP53 功能障碍和 IGHV 突变,因为这些标志物与较差的治疗反应相关。多项临床试验的可喜结果表明,针对 Burton 酪氨酸激酶、B 细胞白血病/淋巴瘤 2 和磷脂酰肌醇 4,5-二磷酸 3-激酶催化亚单位 delta 的新兴疗法可改善患者的预后,并延长无论是否存在某些高危异常患者的无进展生存期。这些新型口服靶向治疗单独使用或与抗 CD20 抗体等其他治疗联合使用的良好结果,几乎完全取代了 CLL 的化疗免疫治疗。在这篇叙述性综述中,我们总结了目前针对 CLL 使用靶向单药和联合治疗的临床证据,讨论了目前正在开发的新型和下一代治疗方法,并深入探讨了 CLL 患者治疗中未满足的需求领域。