Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
J Clin Oncol. 2022 Nov 20;40(33):3848-3857. doi: 10.1200/JCO.21.02823. Epub 2022 Jun 15.
The combination of venetoclax and 5-azacitidine (5-AZA) for older or unfit patients with acute myeloid leukemia (AML) improves remission rates and survival compared with 5-AZA alone. We hypothesized that the addition of venetoclax to cladribine (CLAD)/low-dose araC (low-dose cytarabine [LDAC]) alternating with 5-AZA backbone may further improve outcomes for older patients with newly diagnosed AML.
This is a phase II study investigating the combination of venetoclax and CLAD/LDAC alternating with venetoclax and 5-AZA in older (≥ 60 years) or unfit patients with newly diagnosed AML. The primary objective was composite complete response (CR) rate (CR plus CR with incomplete blood count recovery); secondary end points were overall survival, disease-free survival (DFS), overall response rate, and toxicity.
A total of 60 patients were treated; median age was 68 years (range, 57-84 years). By European LeukemiaNet, 23%, 33%, and 43% were favorable, intermediate, and adverse risk, respectively. Fifty-six of 60 evaluable patients responded (composite CR: 93%) and 84% were negative for measurable residual disease. There was one death (2%) within 4 weeks. With a median follow-up of 22.1 months, the median overall survival and DFS have not yet been reached. The most frequent grade 3/4 nonhematologic adverse events were febrile neutropenia (n = 33) and pneumonia (n = 14). One patient developed grade 4 tumor lysis syndrome.
Venetoclax and CLAD/LDAC alternating with venetoclax and 5-AZA is an effective regimen among older or unfit patients with newly diagnosed AML. The rates of overall survival and DFS are encouraging. Further study of this non-anthracycline-containing backbone in younger patients, unfit for intensive chemotherapy, as well as comparisons to standard frontline therapies is warranted.
与单独使用 5-氮杂胞苷(5-AZA)相比,维奈克拉联合 5-氮杂胞苷(5-AZA)治疗年龄较大或不适合的急性髓系白血病(AML)患者可提高缓解率和生存率。我们假设,在 cladribine(CLAD)/低剂量阿糖胞苷(低剂量阿糖胞苷[LDAC])与 5-AZA 骨干交替的基础上加用 venetoclax 可能会进一步改善新诊断为 AML 的老年患者的预后。
这是一项评估 venetoclax 联合 CLAD/LDAC 与 venetoclax 联合 5-AZA 治疗新诊断为 AML 的年龄较大(≥60 岁)或不适合的患者的疗效和安全性的 II 期研究。主要终点为复合完全缓解率(CR)(CR 加不完全血细胞计数恢复的 CR);次要终点为总生存、无病生存(DFS)、总反应率和毒性。
共 60 例患者接受治疗;中位年龄为 68 岁(范围为 57-84 岁)。根据欧洲白血病网(European LeukemiaNet)标准,分别有 23%、33%和 43%的患者为低危、中危和高危。60 例可评估患者中有 56 例(复合 CR:93%)有反应,84%的患者为无残留疾病。4 周内有 1 例(2%)死亡。中位随访 22.1 个月时,中位总生存和 DFS尚未达到。最常见的 3/4 级非血液学不良事件为发热性中性粒细胞减少症(n=33)和肺炎(n=14)。1 例患者发生 4 级肿瘤溶解综合征。
venetoclax 联合 CLAD/LDAC 与 venetoclax 联合 5-AZA 是新诊断为 AML 的老年或不适合患者的有效治疗方案。总生存和 DFS 率令人鼓舞。在不适合强化化疗的年轻患者中进一步研究该非蒽环类骨干药物,以及与标准一线治疗的比较是必要的。