Multicenter prospective study of stereotactic body radiotherapy for previously untreated solitary primary hepatocellular carcinoma: The STRSPH study

Aim To prospectively evaluate the efficacy and safety of stereotactic body radiotherapy (SBRT) for patients with previously untreated solitary primary hepatocellular carcinoma (HCC). Methods The main eligibility criteria included the following: (1) primary solitary HCC; (2) no prior treatment for HC...

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Veröffentlicht in:Hepatology research 2021-04, Vol.51 (4), p.461-471
Hauptverfasser: Kimura, Tomoki, Takeda, Atsuya, Sanuki, Naoko, Ariyoshi, Keisuke, Yamaguchi, Takuhiro, Imagumbai, Toshiyuki, Katoh, Norio, Eriguchi, Takahisa, Oku, Yohei, Ozawa, Shuichi, Tsurugai, Yuichiro, Kokubo, Masaki, Shimizu, Shinichi, Ishikura, Satoshi
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container_end_page 471
container_issue 4
container_start_page 461
container_title Hepatology research
container_volume 51
creator Kimura, Tomoki
Takeda, Atsuya
Sanuki, Naoko
Ariyoshi, Keisuke
Yamaguchi, Takuhiro
Imagumbai, Toshiyuki
Katoh, Norio
Eriguchi, Takahisa
Oku, Yohei
Ozawa, Shuichi
Tsurugai, Yuichiro
Kokubo, Masaki
Shimizu, Shinichi
Ishikura, Satoshi
description Aim To prospectively evaluate the efficacy and safety of stereotactic body radiotherapy (SBRT) for patients with previously untreated solitary primary hepatocellular carcinoma (HCC). Methods The main eligibility criteria included the following: (1) primary solitary HCC; (2) no prior treatment for HCC; (3) Child–Turcotte–Pugh score of seven or less; and (4) unsuitability for or refusal of surgery and radiofrequency ablation (RFA). The prescribed dose of SBRT was 40 Gy in five fractions. The primary endpoint was 3‐year overall survival (OS); the secondary endpoints included local progression‐free survival (LPFS), local control (LC), and adverse events. The accrual target was 60 patients, expecting a 3‐year OS of 70% with a 50% threshold. Results Between 2014 and 2018, 36 patients were enrolled; enrollment was closed early because of slow accrual. The median tumor size was 2.3 cm. The median follow‐up at the time of evaluation was 20.8 months. The 3‐year OS was 78% (95% confidence interval [CI]: 53%–90%). The 3‐year LPFS and LC proportion were 73% (95% CI: 48%–87%) and 90% (95% CI: 65%–97%), respectively. Grade 3 or higher SBRT‐related toxicities were observed in four patients (11%), and grade five toxicities were not observed. Conclusions This study showed acceptably low incidence of SBRT‐related toxicities. LC and OS after SBRT were comparable for previously untreated solitary HCC for patients unfit for resection and RFA. Although a definitive conclusion cannot be drawn by this study, the promising results indicate that SBRT may be an alternative option in the management of early HCC.
doi_str_mv 10.1111/hepr.13595
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Methods The main eligibility criteria included the following: (1) primary solitary HCC; (2) no prior treatment for HCC; (3) Child–Turcotte–Pugh score of seven or less; and (4) unsuitability for or refusal of surgery and radiofrequency ablation (RFA). The prescribed dose of SBRT was 40 Gy in five fractions. The primary endpoint was 3‐year overall survival (OS); the secondary endpoints included local progression‐free survival (LPFS), local control (LC), and adverse events. The accrual target was 60 patients, expecting a 3‐year OS of 70% with a 50% threshold. Results Between 2014 and 2018, 36 patients were enrolled; enrollment was closed early because of slow accrual. The median tumor size was 2.3 cm. The median follow‐up at the time of evaluation was 20.8 months. The 3‐year OS was 78% (95% confidence interval [CI]: 53%–90%). The 3‐year LPFS and LC proportion were 73% (95% CI: 48%–87%) and 90% (95% CI: 65%–97%), respectively. Grade 3 or higher SBRT‐related toxicities were observed in four patients (11%), and grade five toxicities were not observed. Conclusions This study showed acceptably low incidence of SBRT‐related toxicities. LC and OS after SBRT were comparable for previously untreated solitary HCC for patients unfit for resection and RFA. Although a definitive conclusion cannot be drawn by this study, the promising results indicate that SBRT may be an alternative option in the management of early HCC.</description><identifier>ISSN: 1386-6346</identifier><identifier>EISSN: 1872-034X</identifier><identifier>DOI: 10.1111/hepr.13595</identifier><identifier>PMID: 33217113</identifier><language>eng</language><publisher>Netherlands: Wiley Subscription Services, Inc</publisher><subject>Adverse events ; clinical trial phase II ; Hepatocellular carcinoma ; Liver cancer ; multicenter study ; Patients ; Radiation therapy ; stereotactic body radiotherapy ; Surgery ; Survival</subject><ispartof>Hepatology research, 2021-04, Vol.51 (4), p.461-471</ispartof><rights>2020 The Japan Society of Hepatology</rights><rights>2020 The Japan Society of Hepatology.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). 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Grade 3 or higher SBRT‐related toxicities were observed in four patients (11%), and grade five toxicities were not observed. Conclusions This study showed acceptably low incidence of SBRT‐related toxicities. LC and OS after SBRT were comparable for previously untreated solitary HCC for patients unfit for resection and RFA. Although a definitive conclusion cannot be drawn by this study, the promising results indicate that SBRT may be an alternative option in the management of early HCC.</abstract><cop>Netherlands</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33217113</pmid><doi>10.1111/hepr.13595</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6480-8418</orcidid><orcidid>https://orcid.org/0000-0003-3959-2114</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Adverse events
clinical trial phase II
Hepatocellular carcinoma
Liver cancer
multicenter study
Patients
Radiation therapy
stereotactic body radiotherapy
Surgery
Survival
title Multicenter prospective study of stereotactic body radiotherapy for previously untreated solitary primary hepatocellular carcinoma: The STRSPH study
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