Storandt Michael H, Kurniali Peter C, Mahipal Amit, Jin Zhaohui
Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Department of Hematology/Medical Oncology, Sanford Cancer Center, Bismarck, ND 58501, USA.
Life (Basel). 2023 Oct 16;13(10):2066. doi: 10.3390/life13102066.
Primary tumor resection and liver transplantation are the only curative treatment options for the management of cholangiocarcinoma (CCA). However, for patients with advanced or metastatic disease, palliative systemic therapy remains the only treatment option. The development of targeted therapeutics has begun to shift the treatment paradigm in CCA. Targets of interest in CCA include mutated isocitrate dehydrogenase-1 (mIDH-1), human epidermal growth factor receptor 2 (HER2) overexpression/amplification, and fibroblast growth factor receptor 2 () fusion, in addition to less frequently observed targets such as , deficient mismatch repair/high microsatellite instability (dMMR/MSI-H), and high tumor mutation burden (TMB-H). These targets are observed in varying frequency among patients with intrahepatic CCA and extrahepatic CCA. Multiple novel therapies have been developed to exploit each of these targets, with some having received United States Food and Drug Administration approval for use in the second-line setting. In the current review, we discuss targets of interest in CCA and summarize current evidence evaluating available therapies directed at these targets.
原发性肿瘤切除和肝移植是胆管癌(CCA)治疗仅有的治愈性选择。然而,对于晚期或转移性疾病患者,姑息性全身治疗仍然是唯一的治疗选择。靶向治疗药物的发展已开始改变CCA的治疗模式。CCA中令人感兴趣的靶点包括异柠檬酸脱氢酶-1突变(mIDH-1)、人表皮生长因子受体2(HER2)过表达/扩增和成纤维细胞生长因子受体2()融合,此外还有一些较少见的靶点,如、错配修复缺陷/微卫星高度不稳定(dMMR/MSI-H)和高肿瘤突变负荷(TMB-H)。这些靶点在肝内CCA和肝外CCA患者中的出现频率各不相同。已经开发了多种新型疗法来针对这些靶点,其中一些已获得美国食品药品监督管理局批准用于二线治疗。在本综述中,我们讨论了CCA中令人感兴趣的靶点,并总结了评估针对这些靶点的现有疗法的当前证据。