Abstract OT2-06-05: A randomized phase II study of peri-operative ipilimumab, nivolumab and cryoablation versus standard peri-operative care in women with residual triple negative early stage/resectable breast cancer after standard-of-care neoadjuvant chemotherapy

H. McArthur, E. Comen, S. Solomon, M. Rodine, C. Abaya, J. Leal, S. Patil, L. Norton
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引用次数: 2

Abstract

Background: Triple negative breast cancer (TNBC) is a biologically distinct subtype with high risk of early relapse, particularly for patients who do not achieve a pathological complete response (pCR) after neoadjuvant chemotherapy (NAC), with an event free survival of Methods: Eligible pts are aged ≥18 years, with ER, PR and HER2 negative operable tumors ≥ 1.0 cm after neoadjuvant taxane-based chemotherapy. Approximately 160 patients will be randomized to one of two arms: standard-of-care breast surgery (control arm) or ipi/nivo/cryo followed by standard-of-care breast surgery (intervention arm). Subjects randomized to the intervention arm will undergo percutaneous, ultrasound- (or MRI-) guided cryoablation with concurrent research core biopsy 7-10 days prior to surgery, and will receive a pre-operative infusion with ipilimumab at the dose of 1mg/kg IV, and nivolumab 240mg flat dose IV (1 to 5 days prior to cryoablation). After surgery, patients will receive three additional doses of nivolumab 240mg flat dose IV Q2 weeks. Adjuvant capecitabine is recommended for all participants and will be administered per standard-of-care at the treating physician9s discretion. Patients will be stratified by prior platinum administration, prior anthracycline administration, and clinical nodal status (positive versus negative) at enrollment. The primary endpoint is 3-year Event Free Survival (EFS). Secondary end points include Invasive Disease-Free Survival (IDFS), Distant Disease-Free Survival (DDFS), overall survival (OS) and safety. Exploratory correlative studies will be performed on tumor and serum to characterize the immunologic impact of the intervention and to explore predictors of efficacy and toxicity. Citation Format: McArthur HL, Comen EA, Solomon S, Rodine M, DiLauro Abaya C, Leal JHS, Patil S, Norton L. A randomized phase II study of peri-operative ipilimumab, nivolumab and cryoablation versus standard peri-operative care in women with residual triple negative early stage/resectable breast cancer after standard-of-care neoadjuvant chemotherapy [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr OT2-06-05.
OT2-06-05:一项随机II期研究,ipilimumab, nivolumab和冷冻消融与标准围手术期护理相比,在标准护理新辅助化疗后残余三阴性早期/可切除乳腺癌妇女
背景:三阴性乳腺癌(TNBC)是一种生物学上独特的亚型,具有早期复发的高风险,特别是对于新辅助化疗(NAC)后未达到病理完全缓解(pCR)的患者,其无事件生存期为:方法:符合条件的患者年龄≥18岁,ER, PR和HER2阴性可手术肿瘤≥1.0 cm新辅助紫杉烷化疗后。大约160名患者将随机分为两组:标准乳房手术组(对照组)或ipi/nivo/cryo后进行标准乳房手术组(干预组)。随机分配到干预组的受试者将在手术前7-10天接受经皮、超声(或MRI)引导下的冷冻消融,同时进行研究核心活检,并接受伊匹单抗1mg/kg IV的术前输注,纳武单抗240mg平剂量IV(冷冻消融前1 - 5天)。手术后,患者将接受三次额外剂量的nivolumab 240mg平剂量IV,每2周。辅助卡培他滨被推荐用于所有参与者,并将在治疗医师的判断下按照标准护理进行管理。在入组时,患者将根据既往铂类药物、既往蒽环类药物和临床淋巴结状态(阳性与阴性)进行分层。主要终点是3年无事件生存期(EFS)。次要终点包括侵袭性无病生存期(IDFS)、远处无病生存期(DDFS)、总生存期(OS)和安全性。将对肿瘤和血清进行探索性相关研究,以表征干预的免疫影响,并探索疗效和毒性的预测因素。引用本文:marthur HL, Comen EA, Solomon S, Rodine M, DiLauro Abaya C, Leal JHS, Patil S, Norton L. ipilimumab、nivolumab联合冷冻消融与标准新辅助化疗后残留三阴性早期/可切除乳腺癌围手术期护理的随机II期研究[摘要]。2018年圣安东尼奥乳腺癌研讨会论文集;2018年12月4-8日;费城(PA): AACR;中国癌症杂志2019;79(4增刊):OT2-06-05。
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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