Li Juan, Fu Shuying, Ye Chunmei, Li Jun
Department of Hematology, Taixing People's Hospital Affiliated to Yangzhou University, Taixing, China; Institute of Hematology, affiliated hospital of Yangzhou University, Taixing, China.
Department of Hematology, Taixing People's Hospital Affiliated to Yangzhou University, Taixing, China; Institute of Hematology, affiliated hospital of Yangzhou University, Taixing, China.
Leuk Res. 2025 Jan;148:107638. doi: 10.1016/j.leukres.2024.107638. Epub 2024 Dec 18.
Acute myeloid leukemia (AML) is a complex hematological malignancy predominantly affecting the elderly, with a median diagnosis age of 68 years. Despite advances in treatment, elderly AML patients face suboptimal survival outcomes, with an estimated 5-year survival rate below 20 %. Epigenetic dysregulation, notably DNA methylation, is a key factor in the progression of myelodysplastic syndromes (MDS) to AML. This review examines various combination regimens involving azacitidine (AZA), including those with lenalidomide, histone deacetylase inhibitors (HDACi), kinase inhibitors, metabolic enzyme inhibitors, monoclonal antibodies, immune checkpoint inhibitors, and anti-apoptotic protein inhibitors. Notable among these are the combinations with venetoclax, which has demonstrated remarkable efficacy in phase III trials, and the emerging IDH inhibitors ivosidenib and enasidenib, which have shown significant clinical benefits in patients with IDH mutations. While combination therapies with AZA hold great promise, challenges persist, including translating in vitro synergies to in vivo efficacy and identifying optimal regimens for specific patient populations. Cumulative toxicities may also offset clinical benefits, necessitating rigorous clinical trial design. Future research must focus on refining combination strategies, optimizing dosages and sequences, and thoroughly evaluating therapeutic efficacy and safety to advance the treatment of AML and improve patient outcomes.
急性髓系白血病(AML)是一种复杂的血液系统恶性肿瘤,主要影响老年人,中位诊断年龄为68岁。尽管治疗取得了进展,但老年AML患者的生存结果仍不理想,估计5年生存率低于20%。表观遗传失调,尤其是DNA甲基化,是骨髓增生异常综合征(MDS)进展为AML的关键因素。本综述探讨了涉及阿扎胞苷(AZA)的各种联合治疗方案,包括与来那度胺、组蛋白去乙酰化酶抑制剂(HDACi)、激酶抑制剂、代谢酶抑制剂、单克隆抗体、免疫检查点抑制剂和抗凋亡蛋白抑制剂的联合方案。其中值得注意的是与维奈克拉的联合方案,该方案在III期试验中已显示出显著疗效,以及新兴的异柠檬酸脱氢酶(IDH)抑制剂艾伏尼布和恩杂鲁胺,它们在IDH突变患者中已显示出显著的临床益处。虽然与AZA的联合治疗前景广阔,但挑战依然存在,包括将体外协同作用转化为体内疗效,以及为特定患者群体确定最佳治疗方案。累积毒性也可能抵消临床益处,因此需要严谨的临床试验设计。未来的研究必须集中在优化联合策略、优化剂量和用药顺序,以及全面评估治疗效果和安全性,以推进AML的治疗并改善患者预后。