Abstract GS2-07: PHARE randomized trial final results comparing 6 to 12 months of trastuzumab in adjuvant early breast cancer

X. Pivot, G. Romieu, M. Debled, J. Pierga, P. Kerbrat, T. Bachelot, M. Espié, A. Lortholary, P. Fumoleau, D. Serin, J. Jacquin, C. Jouannaud, M. Rios, S. Abadie-Lacourtoisie, L. Venat-Bouvet, L. Cany, S. Catala, D. Khayat, L. Gambotti, I. Pauporté, C. Mercier, S. Paget‐Bailly, J. Henriques, J. Grouin
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引用次数: 4

Abstract

Since 2005, 12 months of trastuzumab added to chemotherapy alone is the standard of care in patients with HER2-positive breast cancer. PHARE (9Protocol for Herceptin® as Adjuvant therapy with Reduced Exposure9) is the first trial comparing a reduction of adjuvant trastuzumab versus the standard 12 months. In 2012, the first analysis failed to prove that 6-months was non-inferior to 12-months of adjuvant trastuzumab (NCT00381901). The current presentation reports the final analysis. Methods: The trial was sponsored by the French National Cancer Institute (INCa) (www.e-cancer.fr), and approved by central Ethical Committee on May 15 th 2006. Patients with HER2-positive early breast cancer were randomly assigned between 12 and 6 months of adjuvant trastuzumab duration. The randomization was stratified by concomitant or sequential trastuzumab administration with chemotherapy, estrogen receptor (ER) status and center. The primary objective was non-inferiority of 6- versus 12-months arms in the intent to treat population, in terms of disease-free survival (DFS) with a pre-specified hazard margin of 1.15. Overall Survival (OS) and metastasis free survival (MFS) were secondary endpoints. Results: A total of 3380 patients were randomized, their median age was 54 years (21-86). Patients and disease characteristics were well balanced between the two arms. No involved axillary node was observed in 54.5% of cases, 41.7% of tumors were ER negative. At a median follow-up of 7.5 years, 704 events counting for DFS were observed. Between the 12- and 6-months arms, the adjusted Hazard Ratio (HR) for DFS rates was 1.08 (95%CI: 0.93-1.25; p=0.39) favoring the longer exposure. The 1.15 margin of non-inferiority was included in the 95%CI. No heterogeneity in terms of treatment effect was observed, no significant difference for trastuzumab duration effects was found in any subgroups.For OS and MFS, the adjusted HR were 1.13 (95%CI 0.92-1.39) and 1.15 (95%CI 0.96-1.37), respectively. Conclusion: The choice of the non-inferiority margin will remain inherently a subject of controversy especially in the context of oncology trials where the primary outcome is survival and the least additional death could be considered unacceptable questioning the very feasibility of such trials. Nevertheless, PHARE failed to show that 6 months of adjuvant trastuzumab was non-inferior to 12 months. The standard of care should remain 12 months of adjuvant trastuzumab. Citation Format: Pivot X, Romieu G, Debled M, Pierga J-Y, Kerbrat P, Bachelot T, Espie M, Lortholary A, Fumoleau P, Serin D, Jacquin J-P, Jouannaud C, Rios M, Abadie-Lacourtoisie S, Venat-Bouvet L, Cany L, Catala S, Khayat D, Gambotti L, Pauporte I, Faure Mercier C, Paget-Bailly S, Henriques J, Grouin J-M. PHARE randomized trial final results comparing 6 to 12 months of trastuzumab in adjuvant early breast cancer [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 GS2-07.
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GS2-07: PHARE随机试验的最终结果比较了6个月和12个月曲妥珠单抗在辅助早期乳腺癌中的作用
自2005年以来,12个月的曲妥珠单抗单独化疗是her2阳性乳腺癌患者的标准治疗。PHARE(赫赛汀作为减少暴露的辅助治疗方案)是第一个比较曲妥珠单抗与标准12个月辅助治疗减少的试验。2012年,首个分析未能证明6个月的辅助曲妥珠单抗(NCT00381901)不劣于12个月。当前的报告报告了最后的分析。方法:该试验由法国国家癌症研究所(INCa) (www.e-cancer.fr)主办,并于2006年5月15日获得中央伦理委员会批准。her2阳性早期乳腺癌患者被随机分配12至6个月的辅助曲妥珠单抗疗程。随机分组根据曲妥珠单抗与化疗同时或顺序给药、雌激素受体(ER)状态和中心进行分层。主要目标是6个月组与12个月组在治疗人群中的非劣效性,就无病生存(DFS)而言,预先指定的危险裕度为1.15。总生存期(OS)和无转移生存期(MFS)是次要终点。结果:共纳入3380例患者,中位年龄54岁(21-86岁)。患者和疾病特征在两组之间得到了很好的平衡。54.5%的病例未见腋窝淋巴结受累,41.7%的肿瘤为ER阴性。在中位7.5年的随访中,观察到704例DFS事件。在12个月和6个月组中,DFS率的调整风险比(HR)为1.08 (95%CI: 0.93-1.25;P =0.39),有利于较长时间的曝光。95%CI包括1.15的非劣效性裕度。在治疗效果方面没有观察到异质性,在任何亚组中曲妥珠单抗持续时间效应没有发现显著差异。OS组和MFS组调整后的HR分别为1.13 (95%CI 0.92-1.39)和1.15 (95%CI 0.96-1.37)。结论:非劣效边际的选择仍然是一个固有的争议话题,特别是在肿瘤试验的背景下,主要结果是生存,最小的额外死亡可能被认为是不可接受的,质疑这种试验的可行性。然而,PHARE未能证明6个月的辅助曲妥珠单抗治疗不逊于12个月。标准护理应保持12个月的辅助曲妥珠单抗治疗。引用格式:Pivot X, Romieu G, Debled M, Pierga J- y, Kerbrat P, Bachelot T, Espie M, Lortholary A, Fumoleau P, Serin D, Jacquin J-P, Jouannaud C, Rios M, abdie - lacourtoisie S, Venat-Bouvet L, Cany L, Catala S, Khayat D, Gambotti L, Pauporte I, Faure Mercier C, Paget-Bailly S, Henriques J, Grouin J-M。PHARE随机试验的最终结果比较了6个月和12个月曲妥珠单抗在辅助早期乳腺癌中的作用[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;癌症杂志,2019;79(4增刊):摘要nr GS2-07。
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Abstract GS4-02: E2112: Randomized phase 3 trial of endocrine therapy plus entinostat/placebo in patients with hormone receptor-positive advanced breast cancer. A trial of the ECOG-ACRIN cancer research group Abstract GS3-07: Identifying patients whose symptoms are under-recognized during breast radiotherapy: Comparison of patient and physician reports of toxicity in a multicenter cohort Abstract GS2-03: Pathological complete response after neoadjuvant chemotherapy and impact on breast cancer recurrence and mortality, stratified by breast cancer subtypes and adjuvant chemotherapy usage: Individual patient-level meta-analyses of over 27,000 patients Abstract GS5-01: A randomized community-based trial of an angiotensin converting enzyme inhibitor, lisinopril or a beta blocker, carvedilol for the prevention of cardiotoxicity in patients with early stage HER2-positive breast cancer receiving adjuvant trastuzumab Abstract GS4-02: Regional lymph node irradiation in early stage breast cancer: An EBCTCG meta-analysis of 13,000 women in 14 trials
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