摘要:比卡鲁胺联合核糖环尼治疗雄激素受体阳性三阴性乳腺癌的I期临床试验

M. Sharifi, K. Wisinski, M. Burkard, Amye J. Tevaarwerk, D. Tamkus, N. Chan, C. Truica, Oc Danciu, K. Hoskins, R. O'Regan
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引用次数: 6

摘要

背景:迄今为止,在表达雄激素受体(AR)的三阴性乳腺癌(TNBC)亚群中使用抗雄激素已显示出适度的反应率,表明大多数这些肿瘤具有抗雄激素耐药性。基于细胞周期蛋白D激酶(CDK)抑制剂逆转前列腺癌细胞对抗雄激素的耐药性的数据,我们假设使用CDK抑制剂可能增强ar阳性TNBC中抗雄激素的活性。方法:关键入选条件包括:中央确诊的AR阳性TNBC患者,定义为AR表达>0%;转移性疾病的既往治疗0 - 1线;以及可测量的疾病。患者接受比卡鲁胺150mg口服,每日一次,加核糖环尼3种剂量水平之一的治疗(见表)。结果:根据试验标准,74%的筛查患者AR表达阳性。每个剂量水平累积了3例患者。中位年龄为56岁,分别有6名和3名患者在一线和二线接受治疗。中位AR表达率为50%(范围5 - 75%)。有6名接受剂量水平1和2治疗的患者的毒性数据。未发现剂量限制性毒性。正如预期的那样,最常见的毒性是中性粒细胞减少(1例4级,2例3级)。2例患者出现3级高血压,1例出现3级淋巴细胞减少。2级或更低的毒性包括疲劳、恶心、高血糖和粘膜炎。1例患者出现1级QT间期延长。结论:比卡鲁胺与核波西尼合用可耐受,无不良反应。3名接受剂量水平3和剂量扩大治疗的患者的数据将包括在内。第二阶段的给药时间表将根据第一阶段的结果决定。引文格式:Sharifi M, Wisinski KB, Burkard ME, Tevaarwerk AJ, Tamkus D, Chan N, Truica C, Danciu O, Hoskins K, O9Regan RM。比卡鲁胺联合核糖环尼治疗雄激素受体阳性三阴性乳腺癌的I期临床试验[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):1-02-01。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract OT1-02-01: Phase I trial of bicalutamide and ribociclib in androgen receptor-positive triple negative breast cancer
Background: To date, the use of anti-androgens in the subset of triple negative breast cancers (TNBC) that express androgen receptor (AR) has shown modest response rates, indicating anti-androgen-resistance in the majority of these tumors. Based on data that Cyclin D kinase (CDK) inhibitors reverse resistance to anti-androgens in prostate cancer cell lines, we hypothesize that the use of CDK inhibition may enhance the activity of anti-androgens in AR-positive TNBC. Methods: Key eligibility include: patients with centrally confirmed AR-positive TNBC, defined as AR expression >0%; 0 to 1 line of prior therapy for metastatic disease; and measurable disease. Patients are treated with bicalutamide 150mg orally once daily plus ribociclib at one of 3 dose levels (see table). Results: AR expression was positive by trial criteria in 74% of screened patients. Three patients have been accrued at each dose level. Median age is 56 and 6 and 3 patients were treated in first and second-line settings, respectively. Median AR expression was 50% (range 5 to 75%). Toxicity data is available for 6-patients treated on dose levels 1 and 2. No dose-limiting toxicities were noted. As anticipated with ribociclib, the most common toxicity is neutropenia (1 patient grade 4 and 2 patients grade 3). Two patients experienced grade 3 hypertension and 1 experienced grade 3 lymphopenia. Grade 2 or lower toxicities included fatigue, nausea, hyperglycemia and mucositis. One patient experienced grade 1 QT interval prolongation. Conclusion: The combination of bicalutamide and ribociclib is tolerable without unexpected toxicities. Data on the 3-patients treated at dose level 3 and dose expansion will be included. Phase 2 dosing schedule will be decided based on phase 1 results. Citation Format: Sharifi M, Wisinski KB, Burkard ME, Tevaarwerk AJ, Tamkus D, Chan N, Truica C, Danciu O, Hoskins K, O9Regan RM. Phase I trial of bicalutamide and ribociclib in androgen receptor-positive triple negative 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 OT1-02-01.
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