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Progressive hypofractionated carbon-ion radiotherapy for hepatocellular carcinoma: Combined analyses of 2 prospective trials
https://repo.qst.go.jp/records/48574
https://repo.qst.go.jp/records/4857451b1cc69-f3a7-4359-ba42-c23773a288d1
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2018-03-14 | |||||
タイトル | ||||||
タイトル | Progressive hypofractionated carbon-ion radiotherapy for hepatocellular carcinoma: Combined analyses of 2 prospective trials | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Kasuya, Goro
× Kasuya, Goro× Katou, Hirotoshi× Yasuda, Shigeo× Tsuji, Hiroshi× Yamada, Shigeru× Haruyama, Yasuo× Kobashi, Gen× Ebner, Daniel× Okada, Naomi× Makishima, Hirokazu× Miyazaki, Masaru× Kamada, Tadashi× Tsujii, Hirohiko× 粕谷 吾朗× 加藤 博敏× 安田 茂雄× 辻 比呂志× 山田 滋× 春山 康夫× 小橋 元× エブナー ダニエル× 岡田 直美× 牧島 弘和× 宮崎 勝× 鎌田 正× 辻井 博彦 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | BACKGROUND: \nThe objective of this study was to evaluate the safety and efficacy of carbon-ion radiotherapy (CIRT) in patients with hepatocellular carcinoma (HCC) with stepwise dose escalation and hypofractionation in 2 combined prospective trials. \nMETHODS: \nSequential phase 1/2 (protocol 9603) and phase 2 (protocol 0004) trials were conducted for patients with histologically proven HCC. The phase 1 component of protocol 9603 was a dose-escalation study; CIRT was delivered in 12, 8, or 4 fractions. After determination of the recommended dose, 2 phase 2 trials were performed in an expanded cohort, and the data were pooled to analyze toxicity, local control, and overall survival. \nRESULTS: \nIn the phase 1 component of protocol 9603, 69.6, 58.0, and 52.8 Gy (relative biological effectiveness [RBE]) in 12, 8, and 4 fractions, respectively, constituted the maximum tolerated doses, and 52.8 Gy (RBE) in 4 fractions was established as the recommended dose regimen for the 2 phase 2 studies. In 124 patients with a total of 133 lesions, few severe adverse effects occurred, and local-control and overall survival rates at 1, 3, and 5 years were 94.7% and 90.3%, 91.4% and 50.0%, and 90.0% and 25.0%, respectively; this included 1-, 3-, and 5-year local-control rates of 97.8%, 95.5%, and 91.6%, respectively, in the phase 2 study. In a multivariate analysis, Child-Pugh class B and the presence of a tumor thrombus were significant factors for mortality. \nCONCLUSIONS: \nThe safety and efficacy of CIRT in 12, 8, and 4 fractions were confirmed, with 52.8 Gy (RBE) in 4 fractions established as the recommended treatment course for eligible HCC patients. Cancer 2017. © 2017 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. |
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書誌情報 |
Cancer 巻 123, 号 20, p. 3955-3965, 発行日 2017-06 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0008-543X | |||||
PubMed番号 | ||||||
識別子タイプ | PMID | |||||
関連識別子 | 28662297 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1002/cncr.30816 |