Lenvatinib radiofrequency ablation sequential therapy offers survival benefits for patients with unresectable hepatocellular carcinoma at intermediate stage and the liver reserve of Child–Pugh A category: A multicenter study

Author:

Zhang Ying123ORCID,Numata Kazushi1,Imajo Kento45,Uojima Haruki6,Funaoka Akihiro1,Komiyama Satoshi1,Ogushi Katsuaki1,Chuma Makoto1,Irie Kuniyasu2,Kokubu Shigehiro4,Yoneda Masato7,Kobayashi Takashi7,Hidaka Hisashi6ORCID,Fukushima Taito8,Kobayashi Satoshi8,Morimoto Manabu8,Kagawa Tatehiro9ORCID,Hattori Nobuhiro10,Watanabe Tsunamasa10,Iwase Shigeru11,Maeda Shin2

Affiliation:

1. Gastroenterological Center Yokohama City University Medical Center Yokohama Japan

2. Department of Gastroenterology Yokohama City University Graduate School of Medicine Yokohama Japan

3. Department of Medical Ultrasound Ningbo Medical Center Lihuili Hospital Ningbo China

4. Department of Gastroenterology Shin‐Yurigaoka General Hospital Kawasaki Japan

5. Minimally Invasive Surgical and Medical Oncology Fukushima Medical University Fukushima Japan

6. Department of Gastroenterology, Internal Medicine Kitasato University School of Medicine Sagamihara Japan

7. Department of Gastroenterology and Hepatology Yokohama City University Graduate School of Medicine Yokohama Japan

8. Hepatobiliary and Pancreatic Medical Oncology Kanagawa Cancer Center Hospital Yokohama Japan

9. Division of Gastroenterology and Hepatology Department of Internal Medicine Tokai University School of Medicine Isehara Japan

10. Division of Gastroenterology and Hepatology Department of Internal Medicine St. Marianna University School of Medicine Kawasaki Japan

11. Department of Gastroenterology Fujisawa City Hospital Fujisawa Japan

Abstract

AbstractAimThis study aims to evaluate the efficacy and safety of lenvatinib radiofrequency ablation (RFA) sequential therapy for certain hepatocellular carcinoma (HCC) patients.MethodsOne hundred and nineteen patients with unresectable HCC in the intermediate stage with Child–Pugh A were retrospectively recruited in a multicenter setting. Those in the lenvatinib RFA sequential therapy group received lenvatinib initially, followed by RFA and the retreatment with lenvatinib. The study compared overall survival (OS), progression‐free survival (PFS), tumor response, and adverse events (AEs) between patients undergoing sequential therapy and lenvatinib monotherapy.ResultsAfter propensity score matching, 25 patients on sequential therapy and 50 on monotherapy were evaluated. Independent factors influencing OS were identified as sequential therapy, modified albumin–bilirubin (mALBI) grade, and relative dose intensity (%) with hazard ratios (HRs) of 0.381 (95% confidence interval [CI], 0.186–0.782), 2.220 (95% CI, 1.410–3.493), and 0.982 (95% CI, 0.966–0.999), respectively. Stratified analysis based on mALBI grades confirmed the independent influence of treatment strategy across all mALBI grades for OS (HR, 0.376; 95% CI, 0.176–0.804). Furthermore, sequential therapy was identified as an independent factor of PFS (HR, 0.382; 95% CI, 0.215–0.678). Sequential therapy significantly outperformed monotherapy on survival benefits (OS: 38.27 vs. 18.96 months for sequential therapy and monotherapy, respectively, p = 0.004; PFS: 13.80 vs. 5.32 months for sequential therapy and monotherapy, respectively, p < 0.001). Sequential therapy was significantly associated with complete response by modified Response Evaluation Criteria in Solid Tumors (odds ratio, 63.089). Ten of 119 patients experienced grade 3 AEs, with no AE beyond grade 3 observed.ConclusionLenvatinib RFA sequential therapy might offer favorable tolerability and potential prognostic improvement compared to lenvatinib monotherapy.

Publisher

Wiley

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