Department of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Leukemia Research Institute, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Blood Cancer J. 2022 Dec 19;12(12):169. doi: 10.1038/s41408-022-00770-x.
Venetoclax (VEN) combined with azacitidine (AZA) or decitabine (DEC) has been approved for older adults with acute myeloid leukemia (AML) unfit for intensive chemotherapy based on the pivotal VIALE-A trial. However, this trial only compared AZA + VEN with AZA monotherapy. Therefore, we compared the outcomes of consecutive older adults (65 years or older) with newly diagnosed AML who received DEC (n = 230) or DEC + VEN (n = 74) after propensity score matching to construct a one-to-one matched cohort by the nearest neighbor algorithm. The median overall survival was longer in the DEC + VEN group than in the DEC group (13.4 months vs. 8.3 months, p = 0.01). The median event-free survivals were 8.6 and 5.8 months in the DEC + VEN and DEC groups, respectively (p = 0.02). The response rate (complete response, complete response with incomplete hematologic recovery, and morphologic leukemia-free state) was significantly higher in the DEC + VEN group than in the DEC group (70.3% vs. 24.3%, p < 0.01). The 30-day (2.7% vs. 9.5%, p = 0.17) and 60-day (9.5% vs. 18.9%, p = 0.16) mortality rates did not differ between the two groups, nor did the median hospitalization and transfusion rates (hospitalization: 23 days vs. 21 days, p = 0.20; red blood cells: 3.2 units/month vs. 3.5 units/month, p = 0.73; platelets: 2.7 units/month vs. 2.3 units/months, p = 0.48). Of those who received DEC + VEN and became leukemia-free, 29% underwent allogeneic stem cell transplantation and had excellent survival outcomes (one-year survival: 79.4%; one-year non-relapse mortality: 13.3%). This study is the first to provide real-world evidence that DEC + VEN has superior outcomes to DEC monotherapy.
维奈克拉(VEN)联合阿扎胞苷(AZA)或地西他滨(DEC)已基于关键性 VIALE-A 试验被批准用于不适合强化化疗的老年急性髓系白血病(AML)患者。然而,该试验仅比较了 AZA+VEN 与 AZA 单药治疗。因此,我们比较了连续的老年(65 岁或以上)新诊断为 AML 的患者接受 DEC(n=230)或 DEC+VEN(n=74)的结局,这些患者是在倾向评分匹配后通过最近邻算法构建一对一匹配队列的。与 DEC 组相比,DEC+VEN 组的中位总生存期更长(13.4 个月比 8.3 个月,p=0.01)。DEC+VEN 组和 DEC 组的中位无事件生存期分别为 8.6 个月和 5.8 个月(p=0.02)。DEC+VEN 组的反应率(完全缓解、不完全血液学恢复的完全缓解和形态学白血病无状态)明显高于 DEC 组(70.3%比 24.3%,p<0.01)。两组的 30 天(2.7%比 9.5%,p=0.17)和 60 天(9.5%比 18.9%,p=0.16)死亡率无差异,中位住院和输血率也无差异(住院:23 天比 21 天,p=0.20;红细胞:3.2 单位/月比 3.5 单位/月,p=0.73;血小板:2.7 单位/月比 2.3 单位/月,p=0.48)。在接受 DEC+VEN 治疗并实现白血病无残留的患者中,29%接受了异基因造血干细胞移植,且具有优异的生存结局(1 年生存率:79.4%;1 年非复发死亡率:13.3%)。这项研究首次提供了真实世界的数据,表明 DEC+VEN 比 DEC 单药治疗具有更好的结局。