{"title":"Exploratory case series of conversion to carbon ion radiotherapy after systemic therapy in advanced hepatocellular carcinoma.","authors":"Haruka Anzai, Chihiro Miwa, Sadahisa Ogasawara, Makoto Fujiya, Hiroki Kurosaki, Takahiro Tsuchiya, Ryohei Yoshino, Keiichi Katayama, Midori Sawada, Teppei Akatsuka, Ryo Izai, Takuya Yonemoto, Sae Yumita, Keisuke Koroki, Masanori Inoue, Masato Nakamura, Naoya Kanogawa, Shingo Nakamoto, Hirokazu Makishima, Makoto Shinoto, Masaru Wakatsuki, Shigeru Yamada, Hitoshi Ishikawa, Jun Kato","doi":"10.1007/s13691-025-00839-x","DOIUrl":null,"url":null,"abstract":"<p><p>Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality, with advanced cases often presenting macrovascular invasion (MVI) or extrahepatic spread (EHS), limiting curative options. Latest systemic therapies, such as atezolizumab plus bevacizumab, have demonstrated potential in converting advanced HCC into treatable states. Carbon ion radiotherapy (C-ion RT), with its superior dose localization and biological effectiveness, has emerged as a promising treatment for advanced HCC. This retrospective exploratory case series reviewed eight patients with advanced HCC who received C-ion RT following systemic therapy at a single Japanese institution between 2021 and 2023. Data collection and follow-up were completed in October 2024. During the study period, 188 patients with advanced HCC received systemic therapy at our institution. Among these, 176 patients (93.6%) continued systemic therapy alone or received additional transarterial chemoembolization (TACE) for local disease control, while 12 patients (6.4%) were evaluated for curative-intent local therapy through multidisciplinary discussion. Patients were considered for conversion therapy after showing tumor shrinkage or loss of contrast enhancement during systemic therapy, but surgical resection was judged infeasible due to poor liver function or surgical tolerance. Therefore, C-ion RT was selected to treat all residual intrahepatic lesions. Clinical characteristics, treatment details, radiological responses, and safety outcomes were evaluated. The median age was 71 years, with 62.5% presenting MVI and 62.5% having tumors ≥ 90 mm in diameter. Systemic therapy included atezolizumab plus bevacizumab in seven cases and lenvatinib in one case. Following systemic therapy, C-ion RT achieved radiological cancer-free (rCF) status in five patients, including four with MVI and three with major portal vein invasion (Vp4). No clinically meaningful deterioration in liver function was observed during treatment, and adverse events were minimal. Patients achieving rCF maintained short-term disease control. Median follow-up was 11 months (range, 5-16). This exploratory case series suggests that C-ion RT following systemic therapy may be a feasible and safe local consolidation approach for highly selected patients with advanced HCC. C-ion RT achieved short-term local control without deterioration of liver function in this small cohort. Given the limited sample size and follow-up duration, these findings are preliminary and warrant validation in prospective studies with larger cohorts to establish its role in multidisciplinary management.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13691-025-00839-x.</p>","PeriodicalId":13703,"journal":{"name":"International Cancer Conference Journal","volume":"15 2","pages":"195-202"},"PeriodicalIF":0.5000,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13038779/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Cancer Conference Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s13691-025-00839-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality, with advanced cases often presenting macrovascular invasion (MVI) or extrahepatic spread (EHS), limiting curative options. Latest systemic therapies, such as atezolizumab plus bevacizumab, have demonstrated potential in converting advanced HCC into treatable states. Carbon ion radiotherapy (C-ion RT), with its superior dose localization and biological effectiveness, has emerged as a promising treatment for advanced HCC. This retrospective exploratory case series reviewed eight patients with advanced HCC who received C-ion RT following systemic therapy at a single Japanese institution between 2021 and 2023. Data collection and follow-up were completed in October 2024. During the study period, 188 patients with advanced HCC received systemic therapy at our institution. Among these, 176 patients (93.6%) continued systemic therapy alone or received additional transarterial chemoembolization (TACE) for local disease control, while 12 patients (6.4%) were evaluated for curative-intent local therapy through multidisciplinary discussion. Patients were considered for conversion therapy after showing tumor shrinkage or loss of contrast enhancement during systemic therapy, but surgical resection was judged infeasible due to poor liver function or surgical tolerance. Therefore, C-ion RT was selected to treat all residual intrahepatic lesions. Clinical characteristics, treatment details, radiological responses, and safety outcomes were evaluated. The median age was 71 years, with 62.5% presenting MVI and 62.5% having tumors ≥ 90 mm in diameter. Systemic therapy included atezolizumab plus bevacizumab in seven cases and lenvatinib in one case. Following systemic therapy, C-ion RT achieved radiological cancer-free (rCF) status in five patients, including four with MVI and three with major portal vein invasion (Vp4). No clinically meaningful deterioration in liver function was observed during treatment, and adverse events were minimal. Patients achieving rCF maintained short-term disease control. Median follow-up was 11 months (range, 5-16). This exploratory case series suggests that C-ion RT following systemic therapy may be a feasible and safe local consolidation approach for highly selected patients with advanced HCC. C-ion RT achieved short-term local control without deterioration of liver function in this small cohort. Given the limited sample size and follow-up duration, these findings are preliminary and warrant validation in prospective studies with larger cohorts to establish its role in multidisciplinary management.
Supplementary information: The online version contains supplementary material available at 10.1007/s13691-025-00839-x.
期刊介绍:
This online-only journal publishes original case reports on all types of cancer. In particular, we welcome not only case reports of educational value in the diagnosis and treatment of cancers, but also reports on molecularly analyzed cancer cases, including gene mutations, gene fusions, gene expression, and changes in copy number, regardless of their known clinical significance. Assessing the molecular analysis of a tumor usually requires a “cancer conference” in which experts from various fields discuss it. Even if the authors and their respective “cancer conference” were unable to determine the clinical significance of molecular changes at the time of submission and publication, their data may provide evidence that will help the scientific community develop precision medicine solutions in the future. We welcome case reports with reviews of the literature on similar cases, as they are more useful and valuable to readers than are reports of rare cases. International Cancer Conference Journal is the official publication of the Japan Society of Clinical Oncology (JSCO).
- Presents an online-only collection of original case reports on all types of cancer
- In particular, welcomes molecularly analyzed cancer cases
- The Official Publication of the Japan Society of Clinical Oncology (JSCO)