Campos Elisabete do Vale, Pinto Ricardo
Universidade do Porto, Faculdade de Medicina, Porto, Portugal.
Centro Hospitalar São João, Porto, Portugal.
Hematol Transfus Cell Ther. 2019 Apr-Jun;41(2):169-177. doi: 10.1016/j.htct.2018.09.001. Epub 2018 Dec 29.
Older patients with acute myeloid leukemia are particularly difficult to treat, as they have a high risk of comorbidities, poor performance status and less tolerability to chemotherapy, as well as a more aggressive disease biology, responsible for the resistance to treatment. There is a need to explore novel therapeutic agents that are more effective and tolerable. Venetoclax, a BCL-2 inhibitor is a promising agent, as BCL-2 overexpression is present in 84% of acute myeloid leukemia patients at diagnosis and 95% of patients at relapse and has been associated with leukemia cell survival, chemotherapy resistance and poor prognosis.
To review the available data about venetoclax in acute myeloid leukemia and how it can influence the treatment in older patients.
Using the Pubmed database, we selected 29 articles published within the last 15 years, considering preclinical and clinical trials and review studies that combined venetoclax with acute myeloid leukemia.
Venetoclax has demonstrated promising results in preclinical and clinical trials, especially in patients with poor prognosis and the IDH mutation, with an excellent side-effect profile. However, resistance seems to develop rapidly with venetoclax monotherapy, because of antiapoptotic escape mechanisms.
While the results with the use of venetoclax seem encouraging, it is not likely that targeting a single pathway will result in long-term disease control. The solution includes the use of combined therapy to block resistance mechanisms and enhance apoptosis, by reducing MCL-1, increasing BIM or inhibiting the complex IV in the mitochondria.
老年急性髓系白血病患者特别难以治疗,因为他们存在高合并症风险、体能状态差、对化疗耐受性低,以及疾病生物学行为更具侵袭性,导致对治疗产生耐药性。有必要探索更有效且耐受性更好的新型治疗药物。维奈克拉,一种BCL-2抑制剂,是一种有前景的药物,因为在84%的急性髓系白血病患者诊断时及95%的复发患者中存在BCL-2过表达,且其与白血病细胞存活、化疗耐药及预后不良相关。
综述关于维奈克拉治疗急性髓系白血病的现有数据,以及它如何影响老年患者的治疗。
使用PubMed数据库,我们选择了过去15年内发表的29篇文章,纳入临床前和临床试验以及将维奈克拉与急性髓系白血病相结合的综述研究。
维奈克拉在临床前和临床试验中已显示出有前景的结果,特别是在预后不良和异柠檬酸脱氢酶(IDH)突变的患者中,且副作用较小。然而,由于抗凋亡逃逸机制,维奈克拉单药治疗似乎会迅速产生耐药性。
虽然使用维奈克拉的结果似乎令人鼓舞,但仅靶向单一途径不太可能实现长期疾病控制。解决方案包括使用联合疗法来阻断耐药机制并通过降低MCL-1、增加BIM或抑制线粒体复合物IV来增强细胞凋亡。