a Department of Oncology , University of Turin Medical School , Turin , Italy.
b Medical Oncology , Candiolo Cancer Institute - FPO- IRCCS , Candiolo , Italy.
Expert Opin Emerg Drugs. 2018 Mar;23(1):63-75. doi: 10.1080/14728214.2018.1444749. Epub 2018 Feb 28.
Biliary tract cancers (BTCs) are a heterogeneous group of cancers, characterized by low incidence but poor prognosis. Even after complete surgical resection for early stage, relapse is frequent and the lack of effective treatments contributes to the dismal prognosis. To date, the only standard treatment in first-line is cisplatin/gemcitabine combination, whereas no standard in 2nd-line has been defined. Hence, the current goal is to better understand the biology of BTCs, discovering new treatment methods and improving clinical outcomes. Areas covered: The development of next-generation-sequencing has unveiled the picture of the molecular signatures characterizing BTCs, leading to the identification of actionable mutations in biomarker-driven clinical trials. In this review we will cover the genetic landscape of BTC, focusing on the efficacy of existing treatments. Furthermore, we will discuss emerging molecular targets and evaluate the findings of pre-clinical studies. Finally, the encouraging results of clinical trials involving targeted therapies or immunotherapy will be reviewed. Expert opinion: FGFR fusion rearrangements and IDH1 or IDH2 mutations are the most promising targeted treatments under evaluation. In addition, innovative trial design will allow to offer a chance for tailored medicine to infrequent subgroups of BTCs patients based on their molecular features rather than their histology.
胆道癌(BTC)是一组异质性癌症,其发病率低,但预后差。即使在早期完全手术切除后,复发也很常见,缺乏有效的治疗方法导致预后不佳。迄今为止,一线治疗的唯一标准是顺铂/吉西他滨联合治疗,而二线治疗尚无标准。因此,目前的目标是更好地了解 BTC 的生物学特性,发现新的治疗方法并改善临床结果。
下一代测序的发展揭示了 BTC 的分子特征图谱,导致在生物标志物驱动的临床试验中确定了可操作的突变。在这篇综述中,我们将介绍 BTC 的遗传特征,重点介绍现有治疗方法的疗效。此外,我们将讨论新出现的分子靶点,并评估临床前研究的结果。最后,将回顾涉及靶向治疗或免疫疗法的临床试验的令人鼓舞的结果。
FGFR 融合重排和 IDH1 或 IDH2 突变是最有前途的正在评估的靶向治疗方法。此外,创新的试验设计将使基于 BTC 患者的分子特征而不是其组织学为罕见亚组患者提供定制药物的机会。