Division of Hematology-Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Division of Hematology, Mayo Clinic, Rochester, Minnesota.
Haematologica. 2024 Sep 1;109(9):2864-2872. doi: 10.3324/haematol.2024.285014.
Azacitidine/venetoclax is an active regimen in patients with newly diagnosed acute myeloid leukemia (AML). However, primary or secondary resistance to azacitidine/venetoclax is an area of unmet need and overexpression of MCL1 is suggested to be a potential resistance mechanism. Pevonedistat inhibits MCL1 through activation of NOXA, and pevonedistat/azacitidine has previously shown activity in AML. To assess the tolerability and efficacy of adding pevonedistat to azacitidine/ venetoclax in relapsed/refractory AML, we conducted a phase I, multicenter, open-label study in 16 adults with relapsed/ refractory AML. Patients were treated with azacitidine, venetoclax along with pevonedistat intravenously on days 1, 3 and 5 of each 28-day cycle at doses of 10, 15 or 20 mg/m2 in successive cohorts in the dose escalation phase. The impact of treatment on protein neddylation as well as expression of pro-apoptotic BCL2 family members was assessed. The recommended phase II dose of pevonedistat was 20 mg/m2. Grade 3 or higher adverse events included neutropenia (31%), thrombocytopenia (13%), febrile neutropenia (19%), anemia (19%), hypertension (19%) and sepsis (19%). The overall response rate was 46.7% for the whole cohort including complete remission in five of seven (71.4%) patients who had not previously been treated with the hypomethylating agent/venetoclax. No measurable residual disease was detected in 80.0% of the patients who achieved complete remission. The median time to best response was 50 (range, 23-77) days. Four patients were bridged to allogeneic stem cell transplantation. The combination of azacitidine, venetoclax and pevonedistat is safe and shows encouraging preliminary activity in patients with relapsed/refractory AML. (NCT04172844).
阿扎胞苷/维奈托克是新诊断为急性髓系白血病(AML)患者的有效治疗方案。然而,对阿扎胞苷/维奈托克的原发性或继发性耐药是一个未满足的需求领域,并且 MCL1 的过表达被认为是一种潜在的耐药机制。Pevonedistat 通过激活 NOXA 抑制 MCL1,并且 pevonedistat/阿扎胞苷在 AML 中已显示出活性。为了评估在复发性/难治性 AML 患者中添加 pevonedistat 到阿扎胞苷/维奈托克中的耐受性和疗效,我们在 16 名复发性/难治性 AML 成人中进行了一项 I 期、多中心、开放标签研究。患者在每个 28 天周期的第 1、3 和 5 天接受阿扎胞苷、维奈托克和静脉注射 pevonedistat,剂量为 10、15 或 20mg/m2,在剂量递增阶段的连续队列中。评估了治疗对蛋白泛素化以及促凋亡 BCL2 家族成员表达的影响。推荐的 pevonedistat Ⅱ期剂量为 20mg/m2。3 级或更高级别的不良事件包括中性粒细胞减少症(31%)、血小板减少症(13%)、发热性中性粒细胞减少症(19%)、贫血(19%)、高血压(19%)和败血症(19%)。整个队列的总缓解率为 46.7%,包括 7 名(71.4%)先前未接受低甲基化剂/维奈托克治疗的患者中有 5 名达到完全缓解。达到完全缓解的患者中有 80.0%未检测到可测量残留疾病。最佳反应的中位时间为 50 天(范围 23-77 天)。4 名患者桥接进行异基因干细胞移植。阿扎胞苷、维奈托克和 pevonedistat 的联合使用在复发性/难治性 AML 患者中安全且具有令人鼓舞的初步疗效。(NCT04172844)。