Piffoux Max, Leary Alexandra, Follana Philippe, Abdeddaim Cyril, Joly Florence, Bin Sylvie, Bonjour Maxime, Boulai Anais, Callens Celine, Villeneuve Laurent, Alexandre Marine, Schwiertz Verane, Freyer Gilles, Rodrigues Manuel, You Benoit
Medical Oncology, Hospices Civils de Lyon, EPSILYON, Lyon, France; GINECO, Paris, France.
Medical Oncology, Institut Gustave Roussy, Villejuif, France; GINECO, Paris, France.
Nat Commun. 2025 Feb 20;16(1):1821. doi: 10.1038/s41467-025-56914-7.
Endometrial cancers are characterized by frequent alterations in the PI3K-AKT-mTor, IGF1 and DNA repair signaling pathways. Concomitant inhibition of these pathways was warranted. ENDOLA phase I/II trial (NCT02755844) was designed to assess the safety/efficacy of the triplet combination of the PARP inhibitor olaparib, metronomic cyclophosphamide (50 mg daily), and PI3K-AKT-mTor inhibitor metformin (1500 mg daily) in women with recurrent endometrial carcinomas. Olaparib dose-escalation (100-300 mg twice-a-day (bid)) was used to determine the recommended-phase II-trial-dose (RP2D, primary endpoint), followed by an expansion cohort to determine the non-progression rate at 10 weeks (NPR-10w, secondary endpoint). 31 patients were treated. Olaparib RP2D was defined as 300 mg bid. The tolerability was acceptable, and grade 3-4 adverse events (51% patients) were mainly hematological. The NPR-10w was 61.5%, and the median progression-free survival (mPFS) was 5.2 months. In a post-hoc analysis, when explored by molecular subtypes/alterations, longer PFS were observed in patients with tumors characterized by a non-specific-molecular-profile (NSMP, n = 4; mPFS, 9.1 months), and by both TP53 altered & high number of large genomic alterations (LGA ≥ 8)(n = 10, mPFS, 8.6 months)). The analyses about kinetics of circulating biomarkers and pharmacodynamic effects are not reported here. In total, the benefit/toxicity ratio of the all-oral olaparib/cyclophosphamide/metformin regimen was favorable in heavily pretreated patients with recurrent endometrial cancer.
子宫内膜癌的特征是PI3K-AKT-mTor、IGF1和DNA修复信号通路频繁改变。有必要同时抑制这些通路。ENDOLA I/II期试验(NCT02755844)旨在评估PARP抑制剂奥拉帕利、节拍性环磷酰胺(每日50毫克)和PI3K-AKT-mTor抑制剂二甲双胍(每日1500毫克)三联组合对复发性子宫内膜癌女性的安全性/疗效。采用奥拉帕利剂量递增(每日两次,每次100 - 300毫克)来确定推荐的II期试验剂量(RP2D,主要终点),随后进行扩大队列研究以确定10周时的无进展率(NPR - 10w,次要终点)。31名患者接受了治疗。奥拉帕利的RP2D定义为每日两次,每次300毫克。耐受性可接受,3 - 4级不良事件(51%的患者)主要为血液学方面的。NPR - 10w为61.5%,中位无进展生存期(mPFS)为5.2个月。在事后分析中,按分子亚型/改变进行探索时,在具有非特异性分子谱(NSMP,n = 4;mPFS,9.1个月)以及TP53改变且大量基因组改变数量较多(LGA≥8)(n = 10,mPFS,8.6个月)的肿瘤患者中观察到更长的PFS。此处未报告关于循环生物标志物动力学和药效学效应的分析。总体而言,对于接受过大量治疗的复发性子宫内膜癌患者,全口服奥拉帕利/环磷酰胺/二甲双胍方案的获益/毒性比是有利的。