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抗体药物偶联物ENHERTU获批治疗HER2阳性不可切除的或转移性乳腺癌

2020-03-25 Allan MedSci原创

第一三共株式会社今日宣布,日本厚生劳动省(MHLW)批准了靶向HER2的抗体药物偶联物(ADC)ENHERTU(曲妥珠单抗deruxtecan),用于治疗HER2阳性不可切除的或复发性乳腺癌。

第一三共株式会社今日宣布,日本厚生劳动省(MHLW)批准了靶向HER2的抗体药物偶联物(ADC)ENHERTU®(曲妥珠单抗deruxtecan),用于治疗HER2阳性不可切除的或复发性乳腺癌患者。

此项批准是基于ENHERTU®(5.4 mg/kg)单药治疗的开放标签、单臂、关键性II期临床试验(DESTINY-Breast01研究)的最新结果。该研究招募了184例HER2阳性转移性乳腺癌患者(包括30例日本患者),结果显示,客观缓解率为64.1%,达到了该研究的主要终点。

日本第一三共公司肿瘤事业部负责人Wataru Takasaki博士说:“我们的日本研究人员致力于ADC技术,我们很高兴将ENHERTU®带入日本”。抗体药物偶联物(ADC)是通过一个化学链接将具有生物活性的小分子药物连接到单抗上,单抗作为载体将小分子药物靶向运输到目标细胞。

 

原始出处:

https://www.firstwordpharma.com/node/1710576?tsid=4

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    2020-05-25 lhlxtx
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Minerva Biotechnologies是一家生物制药公司,专注于开发癌症免疫疗法,近日宣布,美国FDA已批准huMNC2-CAR44 T细胞疗法的研究性新药申请(IND)。

MacroGenics宣布HER2单抗Margetuximab在转移性乳腺癌患者中的III期临床SOPHIA的第二次总体中期生存数据

MacroGenics宣布其靶向HER2单抗margetuximab在先前接受过抗HER2靶向疗法治疗的HER2阳性转移性乳腺癌患者中的3期SOPHIA研究的总体总体生存期(OS)结果。Margetuximab是一种研究性增强免疫力的单克隆抗体,源自该公司专有的Fc Optimization技术平台。

复发/转移性乳腺癌标志物临床应用专家共识(2019年版)

在个体化精准医学时代,包括组织活检和液体活检在内的肿瘤生物标志物检测在辅助制定复发/转移性乳腺癌的治疗方案和疗效监测中尤为重要,但目前其在临床诊疗应用中还缺乏统一的认识。为规范使用肿瘤生物标志物监测结果,中国抗癌协会肿瘤标志专业委员会乳腺癌标志物协作组和中国抗癌协会肿瘤标志专业委员会遗传性肿瘤标志物协作组组织相关专家,综合复发/转移性乳腺癌生物标志物检测领域的指南、共识、重要文献及我国临床实践,编

拓展阅读

Nature Medicine:科学运动助力抗癌:转移性乳腺癌患者的福音

该研究证明了结构化和个性化的运动干预可以显著改善MBC患者的身体疲劳和HRQOL,因此建议将监督的有氧和抗阻运动纳入MBC患者的支持性护理中。

Medicina:内分泌治疗联合曲妥珠单抗可改善HER-2阳性、激素受体阳性转移性乳腺癌

本研究旨在探讨在HER2阳性和HR阳性转移性乳腺癌(MBC)中使用T-DM1和内分泌治疗(ET)的益处。这项研究首次调查了ET与T-DM1联合治疗的益处。

JAMA NETW OPEN | ERBB2阳性转移性乳腺癌患者接受德喜曲妥珠单抗后接受图卡替尼联合治疗的效果观察

该研究旨在评估图卡替尼联合治疗对这类患者在接受德喜曲妥珠单抗后的效果,图卡替尼联合治疗在先前接受过德喜曲妥珠单抗治疗的ERBB2阳性转移性乳腺癌患者中显示出临床意义且安全可控。

JAMA ONCOL:口服化疗方案(长春瑞滨 + 环磷酰胺 + 卡培他滨)在ER+/ERBB2-转移性乳腺癌患者中的优势:METEORA-II随机临床试验结果

该试验比较了口服化疗方案(VEX)和静脉化疗方案(紫杉醇)在ER+/ERBB2-转移性乳腺癌患者中的疗效,口服VEX化疗方案可以显著延长ER+/ERBB2-转移性乳腺癌患者的TTF和PFS且安全可控。

CCR:血浆TP53突变当心!预测HR+/HER2-转移性乳腺癌预后差,与治疗无关

本研究对PEARL试验队列2中的患者进行了血浆ctDNA分析,收集基线和治疗期间血液样本,探索基线基因图谱和治疗期间血浆ctDNA动力学与疗效的相关性。

前沿进展 | HER2低表达浸润性乳腺癌特点及抗体偶联药物(ADC)在HER2低表达转移性乳腺癌的应用

广东省人民医院廖宁主任团队在BMC Medicine发表重磅研究,从临床病理、疾病预后,基因变异图谱层面阐明HER2低表达人群特征,为HER2低表达能否成为独立亚型提供参考。

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