The University of Texas MD Anderson Cancer Center, 1400 Holcombe Blvd Unit 463, Houston, TX, 77030, USA.
University of Arizona Cancer Center, 1400 Holcombe Blvd Unit 463, Tucson, AZ, 77030, USA.
Curr Treat Options Oncol. 2020 Jun 29;21(8):63. doi: 10.1007/s11864-020-00767-3.
The standard of care first-line therapy for patients with advanced biliary tract cancers eligible for treatment continues to be the combination of gemcitabine and cisplatin. Based on the promising results of a phase II study, an ongoing multi-institutional phase III study is assessing the benefit of adding nab-paclitaxel to the chemotherapy doublet, and appropriate patients should be considered for enrollment at participating centers. We would recommend early comprehensive genomic profiling of patients' tumors to identify potentially targetable aberrations with available therapies. Results with therapeutic implications include tumors with microsatellite instability/deficient mismatch repair, alterations in FGFR, IDH1/2, and HER-2, and potentially other molecular vulnerabilities. Patients in whom a targetable genomic abnormality is found should be matched with appropriate agent. If a targetable fusion or mutation is not detected, patients eligible for second-line therapy should be considered for either clinical trial enrollment or a second-line cytotoxic chemotherapy regimen such as modified FOLFOX. Strategies incorporating immunotherapy into the treatment of patients with microsatellite stable advanced biliary tract cancers have yielded largely disappointing results thus far, and routine use of checkpoint inhibitors outside of a clinical trial is not recommended.
对于适合治疗的晚期胆道癌患者,标准的一线治疗方法仍然是吉西他滨和顺铂联合治疗。基于 II 期研究的有希望结果,一项正在进行的多机构 III 期研究正在评估在化疗双联方案中加入 nab-紫杉醇的获益,合适的患者应考虑在参与中心入组。我们建议对患者的肿瘤进行早期全面的基因组分析,以确定可用治疗方法中具有潜在靶向性的异常。具有治疗意义的结果包括微卫星不稳定/错配修复缺陷、FGFR、IDH1/2 和 HER-2 改变的肿瘤,以及潜在的其他分子弱点。发现具有可靶向基因组异常的患者应与适当的药物相匹配。如果未检测到可靶向融合或突变,应考虑有资格接受二线治疗的患者参加临床试验或二线细胞毒性化疗方案,如改良的 FOLFOX。迄今为止,将免疫疗法纳入微卫星稳定型晚期胆道癌患者治疗的策略产生的结果大多令人失望,因此不建议在临床试验之外常规使用检查点抑制剂。