Abstract OT2-07-01: DETECT V/CHEVENDO – Comparison of dual HER2-targeted therapy with trastuzumab plus pertuzumab in combination with chemo- or endocrine therapy in addition with CDK4/6 inhibition in patients with HER2-positive and hormone-receptor positive metastatic breast cancer

Sabrina Krause, T. Friedl, T. Fehm, T. Romashova, P. Fasching, A. Schneeweiss, V. Müller, F. Taran, A. Polasik, M. Tzschaschel, A. D. Gregorio, F. Meier-Stiegen, W. Janni, J. Huober
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Abstract

Background: Metastatic breast cancer (MBC) is usually an incurable disease and maintenance of quality of life (QoL) is one of the main aims of therapy. In patients with HER2-positive MBC taxane-based chemotherapy in combination with dual HER2 targeted therapy with trastuzumab and pertuzumab,is the standard of care. Adverse events are well-known side effects of any cytostatic treatment and can seriously impact the patients9 QoL. The synergistic combination of dual HER2-targeted therapy with trastuzumab and pertuzumab plus endocrine therapy might offer a better treatment option for these patients. First clinical trials suggest an additional benefit when a CDK4/6 inhibitor is added to the combination of endocrine therapy and anti HER2 treatment. DETECT V is a randomized phase III study comparing the safety and efficacy of trastuzumab plus pertuzumab and the CDK 4/6 inhibitor ribociclib in combination with either endocrine therapy or chemotherapy. Trial design: Patients with HER2 positive and hormone-receptor positive MBC are 1:1 randomized to receive trastuzumab and pertuzumab combined with endocrine therapy and ribociclib or to chemotherapy with trastuzumab and pertuzumab followed by maintenance therapy with trastuzumab, pertuzumab, endocrine therapy and ribociclib. Chemotherapy and the endocrine agents can be chosen from a variety of available regimens according to the physicians discretion. Specific aims: The primary objective of this study is to compare safety and tolerability in both arms, as assessed by the occurrence of AEs during the treatment period. Secondary endpoints are progression free survival, overall survival, quality-adjusted survival using the quality-adjusted time without symptoms and toxicity (Q-TWiST) method. A translational program is included investigating detection and phenotyping of circulating tumor cells (CTC)-and the assessment of marker expression on CTCs in order to validate an endocrine responsiveness score. Present accrual and target accrual: The DETECT V trial started 2015 in the Dept. of Gynecology, University of Ulm and at the up to 120 sites in Germany. Until June 2018 97 patients with HER2-positive, hormone-receptor positive metastatic breast cancer have been enrolled. A sample size of 270 patients is planned. Contact information: Jens Huober, University of Ulm, Dept of Gynecology, Breast Center, jens.huober@uniklinik-ulm.de Sabrina Krause, University of Ulm, Dept of Gynecology, sabrina.krause@uniklinik-ulm.de Citation Format: Krause S, Friedl T, Fehm T, Romashova T, Fasching PA, Schneeweiss A, Muller V, Taran F-A, Polasik A, Tzschaschel M, De Gregorio A, Meier-Stiegen F, Janni W, Huober J. DETECT V/CHEVENDO – Comparison of dual HER2-targeted therapy with trastuzumab plus pertuzumab in combination with chemo- or endocrine therapy in addition with CDK4/6 inhibition in patients with HER2-positive and hormone-receptor positive metastatic 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 OT2-07-01.
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OT2-07-01: DETECT V/CHEVENDO -在her2阳性和激素受体阳性转移性乳腺癌患者中,曲妥珠单抗+帕妥珠单抗联合化疗或内分泌治疗以及CDK4/6抑制的双重her2靶向治疗的比较
背景:转移性乳腺癌(MBC)通常是一种无法治愈的疾病,维持生活质量(QoL)是治疗的主要目的之一。在HER2阳性MBC患者中,紫杉烷为基础的化疗联合曲妥珠单抗和帕妥珠单抗的双重HER2靶向治疗是标准的护理。不良事件是任何细胞抑制剂治疗的众所周知的副作用,可严重影响患者的生活质量。双her2靶向治疗与曲妥珠单抗和帕妥珠单抗加内分泌治疗的协同联合可能为这些患者提供更好的治疗选择。首次临床试验表明,在内分泌治疗和抗HER2治疗的联合治疗中加入CDK4/6抑制剂会有额外的益处。DETECT V是一项随机III期研究,比较曲妥珠单抗+帕妥珠单抗和cdk4 /6抑制剂核糖环尼联合内分泌治疗或化疗的安全性和有效性。试验设计:HER2阳性和激素受体阳性MBC患者1:1随机接受曲妥珠单抗和帕妥珠单抗联合内分泌治疗和核波西尼,或曲妥珠单抗和帕妥珠单抗化疗,然后曲妥珠单抗、帕妥珠单抗、内分泌治疗和核波西尼维持治疗。化疗和内分泌药物可以根据医生的判断从各种可用的方案中选择。具体目的:本研究的主要目的是比较两组的安全性和耐受性,通过治疗期间不良事件的发生来评估。次要终点是无进展生存期、总生存期、质量调整生存期(使用无症状和毒性的质量调整时间)(Q-TWiST)方法。翻译程序包括研究循环肿瘤细胞(CTC)的检测和表型,以及CTC上标记物表达的评估,以验证内分泌反应性评分。当前累积和目标累积:2015年在乌尔姆大学妇科和德国多达120个地点开始了DETECT V试验。截至2018年6月,已有97例her2阳性、激素受体阳性转移性乳腺癌患者入组。计划样本量为270例。联系方式:Jens Huober,乌尔姆大学,妇科,乳房中心,jens.huober@uniklinik-ulm.de Sabrina Krause,乌尔姆大学,妇科,sabrina.krause@uniklinik-ulm.deKrause S, Friedl T, Fehm T, Romashova T, Fasching PA, Schneeweiss A, Muller V, Taran F-A, Polasik A, Tzschaschel M, De Gregorio A, Meier-Stiegen F, Janni W, Huober J. DETECT V/CHEVENDO - her2阳性和激素受体阳性转移性乳腺癌患者化疗或内分泌联合抑制CDK4/6的her2靶向治疗比较[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):OT2-07-01。
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