Endoportal Radiofrequency Ablation and Stent Placement in Patients with Portal Vein Tumor Thrombosis from Hepatocellular Carcinoma: A Study on Feasibility and Safety

Author:

Mizandari Malkhaz1,Gotsiridze Elene1,Keshavarz Pedram23ORCID,Nezami Nariman4567ORCID,Azrumelashvili Tamta1,Nejati Seyed Faraz8ORCID,Habib Nagy9ORCID,Chiang Jason2ORCID,Raman Steven S.2

Affiliation:

1. Department of Diagnostic & Interventional Radiology, New Hospitals, Tbilisi 0114, Georgia

2. Department of Radiological Sciences, David Geffen School of Medicine, University of California, Los Angeles (UCLA), Los Angeles, CA 10833, USA

3. School of Science and Technology, The University of Georgia, Tbilisi 0114, Georgia

4. Department of Radiology, MedStar Georgetown University Hospital, Washington, DC 20007, USA

5. Georgetown University School of Medicine, Washington, DC 20007, USA

6. Lombardi Comprehensive Cancer Center, Washington, DC 20007, USA

7. The Fischell Department of Bioengineering, University of Maryland College Park, College Park, MD 20742, USA

8. Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06510, USA

9. Department of Surgery and Cancer, Imperial College London, London SW7 2BX, UK

Abstract

Background: Hepatocellular carcinoma (HCC) is the most common type of liver cancer, with 10–40% of cases involving portal vein tumor thrombosis (PVTT), leading to poor outcomes and a short survival. The effectiveness of PVTT treatment in patients with HCC is still controversial. Methods: This prospective dual-center study cohort comprised 60 patients with HCC and PVTT who underwent PVR-EPRFA-ST using a novel intravascular radiofrequency system followed by vascular stent placement across the PVTT stenosed segment under fluoroscopy guidance. Results: PVR-EPRFA-ST was technically and clinically successful in 54/60 (90%) and 37/54 (68.5%) patients, respectively. The mean tumor size, PVTT length, post-ablation luminal diameter, and median duration of the recanalized PV patency were 8.6 ± 3.4 cm, 4.1 ± 2.1 cm, 10.3 ± 1.8 mm, and 13.4 months. Higher technical and clinical success rates were associated with a longer survival (177 ± 17.3 days, HR: 0.3, 95%CI 0.12–0.71, p = 0.04; and 233 ± 18.3 days, HR: 0.14, 0.07–0.27, p < 0.001). A shorter survival was associated with Child–Pugh C (HR: 2.7, p = 0.04), multiple tumors (HR: 1.81, p = 0.03), and PVTT length (HR: 1.16, p = 0.04). Conclusions: PVR-EPRFA-ST was feasible and effective for the treatment of selected patients with PVTT, especially in patients with Child–Pugh A/B, single tumors, or a shorter PVTT length.

Publisher

MDPI AG

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