Tumor shrinkage after simultaneous proton therapy for multiple hepatocellular carcinomas

There are no reports on shrinkage of multiple hepatocellular carcinomas (HCCs) after simultaneous treatment with radiotherapy. The purpose of the study was to examine the relationship between tumor shrinkage and treatment outcomes for several HCCs irradiated simultaneously using proton beam therapy (PBT). The subjects were 46 patients with multiple HCCs (95 lesions) who received PBT between January 2008 and December 2018. Overall survival (OS), local control (LC) and complete+partial response (CR + PR) rates were determined using the Kaplan-Meier method. The median follow-up period was 29.2 months and the 3-year OS was 50.3%. For the 95 lesions, the 3-year LC rate was 90.4% and the CR + PR rate was 85.2% at 3 years. Three combination protocols (referred to as A, B and C) were used for different lesions in the same patient: A (66 Gray (Gy) Relative biological effectiveness (RBE) in 10 fractions (fr))-B (72.6 Gy(RBE) in 22 fr) (22 lesions), A-C (74 Gy(RBE) in 37 fr) (15 lesions) and B-C (2 lesions). The 1-year CR + PR rates were 75.8% for A and 56.4% for B in A-B cases (P = 0.14), and 62.5% for A and 57.1% for C in A-C cases (P = 0.35). In the B-C group, there was only one patient with 2 lesions. The lesion treated with the B protocol reached CR + PR, while that treated with the C protocol did not reach CR + PR. These results show that some cases can have differences in tumor shrinkage after concurrent PBT for multiple HCCs, and that there is no significant relationship between dose and tumor shrinkage.

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Publication Details

Journal
Journal of Radiation Research
Published
2025-06-30
DOI
https://doi.org/10.1093/jrr/rraf044
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
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article

Tumor shrinkage after simultaneous proton therapy for multiple hepatocellular carcinomas

Keiichiro Baba, Masatoshi Nakamura, Taisuke Sumiya, Takashi Iizumi et al.
Journal of Radiation Research
Cancer, Hypoxia, and Metabolism
article

Tumor shrinkage after simultaneous proton therapy for multiple hepatocellular carcinomas

Keiichiro Baba, Masatoshi Nakamura, Taisuke Sumiya, Takashi Iizumi, Masashi Mizumoto, Yinuo Li, Hirokazu Makishima, Kei Nakai, Haruko Numajiri, Motohiro Murakami, Hideyuki Sakurai, Hikaru Niitsu, Takashi Saito, Yoshiko Oshiro, Toshiki Ishida
article en

Abstract

There are no reports on shrinkage of multiple hepatocellular carcinomas (HCCs) after simultaneous treatment with radiotherapy. The purpose of the study was to examine the relationship between tumor shrinkage and treatment outcomes for several HCCs irradiated simultaneously using proton beam therapy (PBT). The subjects were 46 patients with multiple HCCs (95 lesions) who received PBT between January 2008 and December 2018. Overall survival (OS), local control (LC) and complete+partial response (CR + PR) rates were determined using the Kaplan-Meier method. The median follow-up period was 29.2 months and the 3-year OS was 50.3%. For the 95 lesions, the 3-year LC rate was 90.4% and the CR + PR rate was 85.2% at 3 years. Three combination protocols (referred to as A, B and C) were used for different lesions in the same patient: A (66 Gray (Gy) Relative biological effectiveness (RBE) in 10 fractions (fr))-B (72.6 Gy(RBE) in 22 fr) (22 lesions), A-C (74 Gy(RBE) in 37 fr) (15 lesions) and B-C (2 lesions). The 1-year CR + PR rates were 75.8% for A and 56.4% for B in A-B cases (P = 0.14), and 62.5% for A and 57.1% for C in A-C cases (P = 0.35). In the B-C group, there was only one patient with 2 lesions. The lesion treated with the B protocol reached CR + PR, while that treated with the C protocol did not reach CR + PR. These results show that some cases can have differences in tumor shrinkage after concurrent PBT for multiple HCCs, and that there is no significant relationship between dose and tumor shrinkage.

Journal of Radiation ResearchVol. 66(5)
University of Tsukuba Hospital (JP), Tsukuba Medical Center Hospital (JP)
Openalex Percentile: Top 76%
Cancer, Hypoxia, and Metabolism
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