López-Oreja Irene, Playa-Albinyana Heribert, Arenas Fabián, López-Guerra Mónica, Colomer Dolors
Experimental Therapies in Lymphoid Neoplasms, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain.
Centro de Investigación Biomédica en Red en Oncología (CIBERONC), 28029 Madrid, Spain.
Cancers (Basel). 2021 Jun 24;13(13):3150. doi: 10.3390/cancers13133150.
Chronic lymphocytic leukemia (CLL) is characterized by a high degree of genetic variability and interpatient heterogeneity. In the last decade, novel alterations have been described. Some of them impact on the prognosis and evolution of patients. The approval of BTK inhibitors, PI3K inhibitors and Bcl-2 inhibitors has drastically changed the treatment of patients with CLL. The effect of these new targeted therapies has been widely analyzed in -mutated cases, but few data exist about the response of patients carrying other recurrent mutations. In this review, we describe the biological pathways recurrently altered in CLL that might have an impact on the response to these new therapies together with the possibility to use new actionable targets to optimize treatment responses.
慢性淋巴细胞白血病(CLL)的特征是高度的基因变异性和患者间的异质性。在过去十年中,已发现了新的改变。其中一些改变会影响患者的预后和病情发展。BTK抑制剂、PI3K抑制剂和Bcl-2抑制剂的获批极大地改变了CLL患者的治疗方式。这些新型靶向疗法在有特定突变的病例中的疗效已得到广泛分析,但关于携带其他复发性突变患者的反应的数据却很少。在本综述中,我们描述了CLL中经常发生改变的生物学途径,这些途径可能会影响对这些新疗法的反应,同时探讨了使用新的可操作靶点来优化治疗反应的可能性。