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培尼达司他联合阿扎胞苷对比阿扎胞苷单药治疗高危骨髓增生异常综合征/慢性粒单核细胞白血病或低比例骨髓原始细胞急性髓系白血病。

Pevonedistat plus azacitidine vs azacitidine alone in higher-risk MDS/chronic myelomonocytic leukemia or low-blast-percentage AML.

机构信息

INSERM U944, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Saint Louis and University of Paris, Paris, France.

Federal Almazov North-West Medical Research Centre, Saint-Petersburg, Russia.

出版信息

Blood Adv. 2022 Sep 13;6(17):5132-5145. doi: 10.1182/bloodadvances.2022007334.

Abstract

PANTHER is a global, randomized phase 3 trial of pevonedistat+azacitidine (n = 227) vs azacitidine monotherapy (n = 227) in patients with newly diagnosed higher-risk myelodysplastic syndromes (MDS; n = 324), higher-risk chronic myelomonocytic leukemia (n = 27), or acute myeloid leukemia (AML) with 20% to 30% blasts (n = 103). The primary end point was event-free survival (EFS). In the intent-to-treat population, the median EFS was 17.7 months with pevonedistat+azacitidine vs 15.7 months with azacitidine (hazard ratio [HR], 0.968; 95% confidence interval [CI], 0.757-1.238; P = .557) and in the higher-risk MDS cohort, median EFS was 19.2 vs 15.6 months (HR, 0.887; 95% CI, 0.659-1.193; P = .431). Median overall survival (OS) in the higher-risk MDS cohort was 21.6 vs 17.5 months (HR, 0.785; P = .092), and in patients with AML with 20% to 30% blasts was 14.5 vs 14.7 months (HR, 1.107; P = .664). In a post hoc analysis, median OS in the higher-risk MDS cohort for patients receiving >3 cycles was 23.8 vs 20.6 months (P = .021) and for >6 cycles was 27.1 vs 22.5 months (P = .008). No new safety signals were identified, and the azacitidine dose intensity was maintained. Common hematologic grade ≥3 treatment emergent adverse events were anemia (33% vs 34%), neutropenia (31% vs 33%), and thrombocytopenia (30% vs 30%). These results underscore the importance of large, randomized controlled trials in these heterogeneous myeloid diseases and the value of continuing therapy for >3 cycles. The trial was registered on clinicaltrials.gov as #NCT03268954.

摘要

PANTHER 是一项全球性、随机的 3 期临床试验,评估了 pevonedistat+阿扎胞苷(n = 227)与阿扎胞苷单药治疗(n = 227)在新诊断的高危骨髓增生异常综合征(MDS;n = 324)、高危慢性髓单核细胞白血病(n = 27)或 20%至 30%原始细胞的急性髓系白血病(AML;n = 103)患者中的疗效。主要终点是无事件生存(EFS)。在意向治疗人群中,pevonedistat+阿扎胞苷组的中位 EFS 为 17.7 个月,阿扎胞苷组为 15.7 个月(风险比 [HR],0.968;95%置信区间 [CI],0.757-1.238;P =.557),高危 MDS 队列的中位 EFS 为 19.2 个月 vs 15.6 个月(HR,0.887;95%CI,0.659-1.193;P =.431)。高危 MDS 队列的中位总生存(OS)为 21.6 个月 vs 17.5 个月(HR,0.785;P =.092),20%至 30%原始细胞的 AML 患者为 14.5 个月 vs 14.7 个月(HR,1.107;P =.664)。在事后分析中,高危 MDS 队列中接受 >3 个周期治疗的患者中位 OS 为 23.8 个月 vs 20.6 个月(P =.021),接受 >6 个周期治疗的患者中位 OS 为 27.1 个月 vs 22.5 个月(P =.008)。未发现新的安全性信号,阿扎胞苷剂量强度保持不变。常见的血液学≥3 级治疗相关不良事件为贫血(33% vs 34%)、中性粒细胞减少(31% vs 33%)和血小板减少(30% vs 30%)。这些结果突出表明,在这些异质性髓系疾病中,大型随机对照试验具有重要意义,并且继续治疗 >3 个周期具有重要意义。该试验在 clinicaltrials.gov 上注册,编号为 #NCT03268954。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22a4/9631625/e2a7e94503ae/advancesADV2022007334absf1.jpg

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