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Proton Beam Therapy for Hepatocellular Carcinoma: Multicenter Prospective Registry Study in Japan.
Mizumoto, Masashi; Ogino, Hiroyuki; Okumura, Toshiyuki; Terashima, Kazuki; Murakami, Masao; Ogino, Takashi; Tamamura, Hiroyasu; Akimoto, Tetsuo; Waki, Takahiro; Katoh, Norio; Araya, Masayuki; Onoe, Tsuyoshi; Takagi, Masaru; Iwata, Hiromitsu; Numajiri, Haruko; Okimoto, Tomoaki; Uchinami, Yusuke; Maruo, Kazushi; Shibuya, Kei; Sakurai, Hideyuki.
  • Mizumoto M; Department of Radiation Oncology, University of Tsukuba, Tsukuba, Ibaraki, 305-8576, Japan. Electronic address: mizumoto@pmrc.tsukuba.ac.jp.
  • Ogino H; Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City University West Medical Center, Nagoya, 462-8508, Japan.
  • Okumura T; Department of Radiation Oncology, University of Tsukuba, Tsukuba, Ibaraki, 305-8576, Japan.
  • Terashima K; Department of Radiology, Hyogo Ion Beam Medical Center, Tatsuno, Hyogo, 679-5165, Japan.
  • Murakami M; Department of Radiation Oncology, Southern Tohoku Proton Therapy Center, Koriyama, Fukushima, 963-8052, Japan.
  • Ogino T; Medipolis Proton Therapy and Research Center, 4423 Higashikata, Ibusuki, Kagoshima, 891-0304, Japan.
  • Tamamura H; Proton Therapy Center, Fukui Prefectural Hospital, Fukui, Fukui, 910-8526, Japan.
  • Akimoto T; Department of Radiation Oncology, National Cancer Center Hospital East, Chiba, 277-8577, Japan.
  • Waki T; Department of Radiology, Tsuyama Chuo Hospital, Tsuyama, Okayama, 708-0841, Japan.
  • Katoh N; Department of Radiation Oncology, Hokkaido University Institute of Medicine, Hokkaido, 060-8648, Japan.
  • Araya M; Proton Therapy Center, Aizawa Hospital, Matsumoto, Nagano, 390-8510, Japan.
  • Onoe T; Radiation and Proton Therapy Center, Shizuoka Cancer Center, Nagaizumi, Suntou-gun, Shizuoka, 411-8777, Japan.
  • Takagi M; Department of Radiation Oncology, Sapporo Teishinkai Hospital, Sapporo, Hokkaido, 065-0033, Japan.
  • Iwata H; Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City University West Medical Center, Nagoya, 462-8508, Japan.
  • Numajiri H; Department of Radiation Oncology, University of Tsukuba, Tsukuba, Ibaraki, 305-8576, Japan.
  • Okimoto T; Department of Radiology, Hyogo Ion Beam Medical Center, Tatsuno, Hyogo, 679-5165, Japan.
  • Uchinami Y; Department of Radiation Oncology, Hokkaido University Institute of Medicine, Hokkaido, 060-8648, Japan.
  • Maruo K; Department of Biostatistics, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, 305-8575, Japan.
  • Shibuya K; Department of Radiation Oncology, Gunma University Graduate School of Medicine, Maebashi, 371-8511, Japan.
  • Sakurai H; Department of Radiation Oncology, University of Tsukuba, Tsukuba, Ibaraki, 305-8576, Japan.
Int J Radiat Oncol Biol Phys ; 118(3): 725-733, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-37778422
PURPOSE: A prospective multicenter registry study was started May 2016 in Japan to evaluate the efficacy and safety of proton beam therapy (PBT) for hepatocellular carcinoma (HCC). METHODS AND MATERIALS: Patients who received PBT for HCC from May 2016 to June 2018 were registered in the database of the Particle Beam Therapy Committee and Subcommittee of the Japanese Society for Radiation Oncology. Overall survival (OS), progression-free survival (PFS), and local recurrence were evaluated. RESULTS: Of the 755 registered patients, 576 with initial PBT and no duplicate cancer were evaluated. At final follow-up, 322 patients were alive and 254 had died. The median follow-up period for survivors was 39 months (0-58 months). The median OS time of the 576 patients was 48.8 months (95% CI, 42.0-55.6 months) and the 1-, 2-, 3-, and 4-year OS rates were 83.8% (95% CI, 80.5%-86.6%), 68.5% (64.5%-72.2%), 58.2% (53.9%-62.2%), and 50.1% (44.9%-55.0%), respectively. Recurrence was observed in 332 patients, including local recurrence in 45 patients. The median PFS time was 14.7 months (95% CI, 12.4-17.0 months) and the 1-, 2-, 3-, and 4-year PFS rates were 55.2% (95% CI, 51.0%-59.2%), 37.5% (33.5%-41.5%), 30.2% (26.3%-34.2%), and 22.8% (18.5%-27.4%), respectively. The 1-, 2-, 3-, and 4-year OS rates were significantly higher for tumor size <5 versus 5 to 10 cm (P < .001) and <5 versus ≥10 cm (P < .001); Child-Pugh score A/B versus C (P < .001); and distance of the tumor from the gastrointestinal tract <1 versus 1 to 2 cm (P < .008) and <1 versus >2 cm (P < .001). At final follow-up, 27 patients (4.7%) had late adverse events of grade 3 or higher, with liver failure (n = 7), and dermatitis (n = 7) being most common. CONCLUSIONS: This multicenter prospective data registry indicated that PBT for HCC gives good therapeutic effects (3-year local control rate of 90%) with a low risk of severe late adverse events.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Terapia de Protones / Neoplasias Hepáticas Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Terapia de Protones / Neoplasias Hepáticas Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2024 Tipo del documento: Article