Devimistat (CPI-613) With Modified Fluorouarcil, Oxaliplatin, Irinotecan, and Leucovorin (FFX) Versus FFX for Patients With Metastatic Adenocarcinoma of the Pancreas: The Phase III AVENGER 500 Study.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-11-01 Epub Date: 2024-08-01 DOI:10.1200/JCO.23.02659
Philip A Philip, Vaibhav Sahai, Nathan Bahary, Amit Mahipal, Anup Kasi, Caio Max S Rocha Lima, Angela T Alistar, Paul E Oberstein, Talia Golan, Jean-Philippe Metges, Jill Lacy, Christos Fountzilas, Charles D Lopez, Michel Ducreux, Pascal Hammel, Mohamed Salem, David Bajor, Al B Benson, Sanjeev Luther, Timothy Pardee, Eric Van Cutsem
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引用次数: 0

Abstract

Purpose: Metastatic pancreatic adenocarcinoma (mPC) remains a difficult-to-treat disease. Fluorouarcil, oxaliplatin, irinotecan, and leucovorin (FFX) is a standard first-line therapy for mPC for patients with a favorable performance status and good organ function. In a phase I study, devimistat (CPI-613) in combination with modified FFX (mFFX) was deemed safe and exhibited promising efficacy in mPC.

Methods: The AVENGER 500 trial (ClinicalTrials.gov identifier: NCT03504423) is a global, randomized phase III trial conducted at 74 sites across six countries to investigate the efficacy and safety of devimistat in combination with mFFX (experimental arm) compared with standard-dose FFX (control arm) in treatment-naïve patients with mPC. Treatment, administered in once-every-2-weeks cycles until disease progression or intolerable toxicity, included intravenous devimistat at 500 mg/m2 total per day on days 1 and 3 in the experimental arm. The primary end point of the study was overall survival (OS).

Results: Five hundred and twenty-eight patients were randomly assigned (266 in the experimental arm and 262 in the control arm). The median OS was 11.10 months for devimistat plus mFFX versus 11.73 months for FFX (hazard ratio [HR], 0.95 [95% CI, 0.77 to 1.18]; P = .655) and median progression-free survival was 7.8 months versus 8.0 months, respectively (HR, 0.99 [95% CI, 0.76 to 1.29]; P = .94). Grade ≥3 treatment-emergent adverse events with >10% frequency in the devimistat plus mFFX arm versus the FFX arm were neutropenia (29.0% v 34.5%), diarrhea (11.2% v 19.6%), hypokalemia (13.1% v 14.9%), anemia (13.9% v 13.6%), thrombocytopenia (11.6% v 13.6%), and fatigue (10.8% v 11.5%), respectively.

Conclusion: Devimistat in combination with mFFX did not improve long- and short-term mPC patient outcomes compared with standard FFX. There were no new toxicity signals with the addition of devimistat.

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Devimistat(CPI-613)与改良氟脲嘧啶、奥沙利铂、伊立替康和亮菌素(FFX)治疗胰腺转移性腺癌患者的对比研究:AVENGER 500 III 期研究。
目的:转移性胰腺腺癌(mPC)仍然是一种难以治疗的疾病。氟脲嘧啶、奥沙利铂、伊立替康和亮菌素(FFX)是治疗胰腺癌的标准一线疗法,适用于表现良好、器官功能良好的患者。在一项I期研究中,devimistat(CPI-613)与改良FFX(mFFX)联用被认为是安全的,并且对mPC具有良好的疗效:AVENGER 500试验(ClinicalTrials.gov标识符:NCT03504423)是一项全球性的随机III期试验,在6个国家的74个地点进行,目的是研究devimistat联合mFFX(试验组)与标准剂量FFX(对照组)相比,对治疗无效的mPC患者的疗效和安全性。治疗以每两周一次的周期进行,直至疾病进展或出现不可耐受的毒性,其中实验组每天静脉注射500 mg/m2的devimistat,剂量为第1天和第3天。研究的主要终点是总生存期(OS):研究随机分配了528名患者(实验组266人,对照组262人)。devimistat 加 mFFX 的中位 OS 为 11.10 个月,而 FFX 为 11.73 个月(危险比 [HR],0.95 [95% CI,0.77 至 1.18];P = .655);中位无进展生存期分别为 7.8 个月和 8.0 个月(HR,0.99 [95% CI,0.76 至 1.29];P = .94)。在devimistat联合mFFX治疗组与FFX治疗组中,频率大于10%的≥3级治疗突发不良事件分别为中性粒细胞减少(29.0%对34.5%)、腹泻(11.2%对19.6%)、低钾血症(13.1%对14.9%)、贫血(13.9%对13.6%)、血小板减少(11.6%对13.6%)和疲劳(10.8%对11.5%):与标准FFX相比,Devimistat与mFFX联用并不能改善mPC患者的长期和短期预后。加入地维司他后没有出现新的毒性信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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