PO.CTP01.03 · 进行中的临床试验
一项III期研究,评估GLSI-100(GP2 + GM-CSF)在新辅助和术后辅助抗HER2治疗后存在残留疾病或高危PCR的乳腺癌患者中的疗效和安全性,Flamingo-01
Phase III study to evaluate the efficacy and safety of GLSI-100 (GP2 + GM-CSF) in breast cancer patients with residual disease or high-risk PCR after both neo-adjuvant and postoperative adjuvant anti-HER2 therapy, Flamingo-01
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作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
背景:GP2是HER2/neu蛋白的一种九个氨基酸的生物肽,与粒细胞-巨噬细胞集落刺激因子(GM-CSF)联合给药,可刺激靶向HER2/neu表达癌症的免疫应答,该联合方案称为GLSI-100。
方法:这项III期试验是一项前瞻性、随机、双盲、多中心研究(NCT05232916)。在1年基于曲妥珠单抗的治疗后,将在前6个月内皮内注射6剂GLSI-100或安慰剂,并在随后的2.5年内给予5剂后续加强针。试验的参与者持续时间为3年治疗加额外1年随访。
研究规模——中期分析:将入组约498例患者。为检测浸润性乳腺癌无病生存(IBCFS)中0.3的风险比,需要28个事件。当至少发生14个事件时,将进行优效性和无效性的中期分析。如果安慰剂患者的年事件发生率为2.4%或更高,则该样本量提供80%的检验效能。最多将有250例非HLA-A*02受试者入组开放标签组。
入选标准:患者群体由以下关键入选标准定义:1)HER2/neu阳性且HLA-A*02,2)新辅助治疗后存在残留疾病或高危pCR(就诊时III期),3)排除IV期,以及4)已完成至少90%计划的基于曲妥珠单抗的治疗。
试验目的:试验目的为:1)确定GP2治疗是否增加IBCFS,2)评估GP2的安全性特征,以及3)监测对治疗的免疫应答并评估其与疗效和安全性的关系。
研究状态:该研究正在美国和欧洲最多150个中心积极招募和入组患者。
联系信息:Greenwich LifeSciences, Inc. Stafford, TX 邮箱:Flamingo-01@greenwichlifesciences.com 网站:greenwichlifesciences.com
资助:本试验由Greenwich LifeSciences支持。
查看英文原文 English abstract
Background : GP2 is a biologic nine amino acid peptide of the HER2/ neu protein delivered in combination with Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) that stimulates an immune response targeting HER2/neu expressing cancers, the combination known as GLSI-100.
Methods : This Phase III trial is a prospective, randomized, double-blinded, multi-center study ( NCT05232916 ). After 1 year of trastuzumab-based therapy, 6 intradermal injections of GLSI-100 or placebo will be administered over the first 6 months and 5 subsequent boosters will be administered over the next 2.5 years. The participant duration of the trial will be 3 years treatment plus 1 additional year follow-up.
Study Size - Interim Analysis : Approximately 498 patients will be enrolled. To detect a hazard ratio of 0.3 in invasive breast cancer free survival (IBCFS), 28 events will be required. An interim analysis for superiority and futility will be conducted when at least 14 events have occurred. This sample size provides 80% power if the annual rate of events in placebo patients is 2.4% or greater. Up to 250 non-HLA-A*02 subjects will be enrolled in an open-label arm.
Eligibility Criteria : The patient population is defined by these key eligibility criteria: 1) HER2/neu positive and HLA-A*02, 2) Residual disease or High risk pCR (Stage III at presentation) post neo-adjuvant therapy, 3) Exclude Stage IV, and 4) Completed at least 90% of planned trastuzumab-based therapy.
Trial Objectives : The trial objectives are to: 1) Determine if GP2 therapy increases IBCFS, 2) Assess the safety profile of GP2, and 3) Monitor immunologic responses to treatment and assess relationship to efficacy and safety.
Study Status : The study is actively recruiting and enrolling patients in the US and Europe at up to 150 sites.
Contact Information : Greenwich LifeSciences, Inc. Stafford, TX Email: Flamingo-01@greenwichlifesciences.com Website: greenwichlifesciences.com
Funding : This trial is supported by Greenwich LifeSciences.
利益披露 Disclosure
J. Thompson,
Greenwich LifeSciences Employment, Stock, Stock Option.
S. Patel,
Greenwich LifeSciences Employment, Stock, Stock Option.
M. Patel,
Greenwich LifeSciences Employment, Stock, Stock Option.
A. Tammareddi,
Greenwich LifeSciences Employment, Stock, Stock Option.
F. Daugherty,
Greenwich LifeSciences Independent Contractor, Stock, Stock Option.
M. Rimawi,
Daiichi Sankyo Other, Consulting/Honorarium.
AstraZeneca Other, Consulting/Honorarium.
Genentech Other, Consulting/Honorarium.
Novartis Other, Consulting/Honorarium.
Pfizer Other, Consulting/Honorarium.
Greenwich LifeSciences ).
Tempus Other, Consulting/Honorarium.
Stemline Other, Consulting/Honorarium.
Gilead Other, Consulting/Honorarium.