4.6 Review

Recent advances in systemic therapy for advanced intrahepatic cholangiocarcinoma

Journal

LIVER CANCER
Volume -, Issue -, Pages -

Publisher

KARGER
DOI: 10.1159/000531458

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Background: The incidence of intrahepatic cholangiocarcinoma (IHCCA) is increasing globally, making it a major global health issue. Conventionally, systemic therapy has been the mainstay of treatment for advanced cholangiocarcinoma. This review discusses recent advances in systemic treatments for patients with IHCCA. Summary: The addition of durvalumab to a gemcitabine plus cisplatin (GemCis) regimen has significantly improved overall survival (OS) in the phase 3 TOPAZ-1 trial and is recommended as the standard first-line treatment. Second-line fluoropyrimidine plus oxaliplatin and fluoropyrimidine plus nanoliposomal irinotecan have shown benefits in treating patients without actionable alterations. Targeted agents have shown efficacy in treating patients with actionable genomic alterations. Immune checkpoint inhibitors are being investigated for previously treated patients. Key Messages: Recent advances in systemic treatments have improved clinical outcomes for advanced IHCCA patients. However, resistance and tumor progression remain challenges, and further efforts are needed to improve outcomes.
Background The incidence of intrahepatic cholangiocarcinoma (IHCCA) is rising around the world. The disease is becoming a major global health issue. Conventionally, most patients with cholangiocarcinoma present with advanced disease and systemic therapy is the mainstay of treatment. This review discusses recent advances in systemic treatments for patients with IHCCA.Summary The addition of durvalumab to a gemcitabine plus cisplatin (GemCis) regimen has significantly improved overall survival (OS) in the phase 3 TOPAZ-1 trial and is currently recommended as a standard first-line treatment. The phase 3 ABC-06 and phase 2b NIFTY trials have shown the benefit of second-line fluoropyrimidine plus oxaliplatin, and fluoropyrimidine plus nanoliposomal irinotecan, respectively. They have provided a treatment option for patients without actionable alterations who progressed to first-line therapy. For patients with actionable genomic alterations, including FGFR2 rearrangement, IDH1 mutation, BRAF mutation, and ERBB2 amplification, targeted agents have shown encouraging efficacy in several phase 2-3 trials, and are recommended as subsequent treatments. Immune checkpoint inhibitors are being investigated for the treatment of previously treated patients, although only a small proportion of patients showed durable responses.Key Messages Recent advances in systemic treatments have improved clinical outcomes in patients with advanced IHCCA. However, most patients eventually show resistance to the treatment and tumor progression occurs within a year. Indeed, there should be further efforts to improve the outcomes of patients with advanced IHCCA.

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