Published online Jul 15, 2025. doi: 10.4251/wjgo.v17.i7.108650
Revised: May 19, 2025
Accepted: June 4, 2025
Published online: July 15, 2025
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Intrahepatic cholangiocarcinoma (ICC) is an aggressive malignancy with limited treatment options and a poor prognosis, particularly in unresectable or metastatic cases. Tri-modal strategies combining systemic chemotherapy, targeted therapies, and immune checkpoint inhibitors have demonstrated synergistic effects in converting unresectable ICC to resectable status and improving patient survival.
A 39-year-old male presented with unresectable stage IIIB ICC (cT3N1M0), abdominal pain, and elevated carbohydrate antigen (CA) 19-9 levels. He received tri-modal therapy consisting of gemcitabine-oxaliplatin hepatic arterial infusion chemotherapy (GEMOX-HAIC), lenvatinib (8 mg daily), and toripalimab (160 mg every three weeks). After five cycles, significant tumor shrinkage and normalization of CA19-9 levels enabled a left hepatectomy. Complications, including biliary stenosis and liver abscesses, were managed with biliary stenting and percutaneous drainage, which allowed for the continuation of chemotherapy. Postoperative pathological examination confirmed a pathological complete response. At the last follow-up, the patient had maintained 29 months of disease-free survival post-resection and was continuing postoperative therapy.
This case highlights the potential of a tri-modal therapy combining GEMOX-HAIC, lenvatinib, and toripalimab to convert unresectable ICC to a resectable status, thereby potentially improving patient survival by surgical resection. Further clinical trials investigating this regimen are warranted.
Core Tip: This report details an unresectable advanced intrahepatic cholangiocarcinoma (ICC) patient treated with first-line GEMOX-HAIC, lenvatinib, and toripalimab. This tri-modal therapy led to successful R0 resection and complete pathological remission. The patient achieved 29 months of disease-free survival. This rare case highlights a regimen enabling surgical resection and long-term survival in advanced ICC and discusses multidisciplinary management of severe biliary complications. However, as a single case, generalizability is limited. The regimen's efficacy and safety warrant validation in prospective, multi-center clinical trials.