4.3 Article

Proton beam therapy for hepatocellular carcinoma with bile duct invasion

Journal

BMC GASTROENTEROLOGY
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12876-023-02897-y

Keywords

Bile duct invasion; Bile duct tumor thrombosis; Hepatocellular carcinoma; Proton beam therapy; Radiation therapy

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The study aimed to clarify the efficacy and safety of proton beam therapy for hepatocellular carcinoma with bile duct invasion. The results showed that proton beam therapy is a feasible and tolerable treatment option for patients with bile duct invasion hepatocellular carcinoma.
AimHepatocellular carcinoma (HCC) with bile duct invasion (BDI) (BDIHCC) has a poor prognosis. Moreover, due to the paucity of reports, there is no consensus regarding optimal management of this clinical condition yet. The aim of this study was to clarify the efficacy and safety of proton beam therapy (PBT) for BDIHCC.MethodsBetween 2009 and 2018, 15 patients with BDIHCC underwent PBT at our institution. The overall survival (OS), local control (LC), and progression-free survival (PFS) curves were constructed using the Kaplan-Meier method. Toxicities were assessed using the Common Terminology Criteria of Adverse Events version 4.0.ResultsThe median follow-up time was 23.4 months (range, 7.9-54.3). The median age was 71 years (range, 58-90 years). Many patients were Child A (n = 8, 53.3%) and most had solitary tumors (n = 11, 73.3%). Additionally, most patients had central type BDI (n = 11, 73%). The median tumor size was 4.0 cm (range, 1.5-8.0 cm). The 1-, 2-, and 3-year OS rates were 80.0%, 58.7% and 40.2%, respectively, and the corresponding LC and PFS rates were 93.3%, 93.3%, and 74.7% and 72.7%, 9.7%, and 0.0%, respectively. Acute grade 1/2 dermatitis (n = 7, 46.7%), and grades 2 (n = 1, 6.7%) and 3 (n = 1, 6.7%) cholangitis were observed. Late toxicities such as grade 3 gastric hemorrhage and pleural effusion were observed. No toxicities of grade 4 or higher were observed.ConclusionsPBT was feasible with tolerable toxicities for the treatment of BDIHCC.

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