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和记黄埔启动HMPL-453治疗晚期肝内胆管癌的II期试验

2020-09-03 Allan MedSci原创

HMPL‑453是针对FGFR 1、2和3的新型、高度选择性小分子抑制剂。

肝内胆管癌(IHCC)是一种在胆管内细胞中发展的癌症。中国每年有390,000例新病例,占2018年全球肝癌年发病率的近50%。IHCC是第二大最常见的原发性恶性肝肿瘤,仅次于肝细胞癌(HCC)。大约10-15%的IHCC患者患有FGFR2融合的肿瘤。IHCC患者的长期生存要比HCC差,这可能与区域性和远端转移的倾向高以及缺乏有效的全身治疗选择有关。

HMPL‑453是针对FGFR 1、2和3的新型、高度选择性小分子抑制剂。在临床前研究中,HMPL‑453与其他同类药物相比,具有更强的效力和更好的激酶选择性。目前,和记黄埔已开始进行HMPL-453治疗IHCC的II期临床研究。

该临床研究是一项单臂、多中心、开放标签的II期研究,旨在评估HMPL-453在至少一项系统治疗失败的晚期FGFR2融合IHCC患者中的疗效、安全性和药代动力学。主要终点是客观反应率(ORR);次要终点包括疾病控制率(DCR)、响应时间(DoR)、无进展生存期(PFS)和总体生存期(OS)。有关其他详细信息,请访问Clinicaltrials.gov(NCT04353375)。

 

原始出处:

https://www.firstwordpharma.com/node/1754550?tsid=4

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    2021-08-14 xuyong536
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    2020-09-03 124b1980m56暂无昵称

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复旦大学附属中山医院副院长周俭教授:“肝内胆管癌发病率约占原发性肝脏恶性肿瘤的15~20%,且呈上升趋势。大部分肝内胆管癌病人初次就诊时常伴有局部侵犯或远处转移而失去手术根治机会。以吉西他滨联合铂类的化疗方案被推荐为治疗晚期胆管癌的一线方案,客观反应率(ORR)为15~26%,且常发生耐药。目前,临床上缺乏其他有效的治疗药物和方案。” FGFR靶向药物的横空出世解决了胆管癌患者的燃眉之急,今

AACR 2020:肝内胆管癌的FGFR2一个新型突变被发现

胆道癌包括肝内胆管癌(IHCC),肝外胆管癌(EHCC)和胆囊癌(GBC)。这些癌症在临床,病理和生物学上都具有异质性,而且都具有侵袭性,预后差,可用的治疗方法也很少。迄今为止发现的潜在可操作的基因组

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中山经验:肝内胆管癌外科综合治疗的创新实践

近期,复旦大学附属中山医院史颖弘教授分享了肝内胆管癌的外科综合治疗中山经验。肝癌在线特将精华整理成文,以飨读者。

揭秘!LI-RADS分类成肝硬化与CHB患者胆管癌术后预后新风向标

近期,发表于Liver Cancer的一项多中心研究,明确了LI-RADS分类与AJCC指南一起使用时,是否可以为ICCA提供额外的术后预后价值,肝癌在线特此报道。

探索与实践 | 肝内胆管癌的外科综合治疗进展

近期,海军军医大学第三附属医院东方肝胆外科医院王葵教授分享了“肝内胆管癌的外科综合治疗”。肝胆相照平台特将精华整理成文,以飨读者。

European Radiology:使用钇-90微球治疗局部晚期肝内胆管癌的价值

现阶段,使用钇-90 (Y90)微球的选择性内放射治疗(SIRT)作为iCCA的化疗联合治疗最近显示出有临床前景的效果,因为其能够通过肿瘤供血动脉选择性地提供高剂量辐射。

论文解读|Ying Tong教授团队揭示肝内胆管癌中癌症扩散的新机制

这项研究探讨了PDPN+癌相关成纤维细胞(CAFs)通过内皮-间质转化(MEndT)在促进肿瘤相关淋巴管生成中的关键作用。

特别关注|乙型肝炎相关肝内胆管癌的发病机制

本文就HBV-ICC发生的主要机制,以及该领域的最新研究进展进行综述。

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