Feasibility of additional radiotherapy in patients with advanced hepatocellular carcinoma treated with atezolizumab plus bevacizumab.

Journal of Liver Cancer Pub Date : 2023-09-01 Epub Date: 2023-05-16 DOI:10.17998/jlc.2023.04.14
Tae Hyun Kim, Bo Hyun Kim, Yu Ri Cho, Young-Hwan Koh, Joong-Won Park
{"title":"Feasibility of additional radiotherapy in patients with advanced hepatocellular carcinoma treated with atezolizumab plus bevacizumab.","authors":"Tae Hyun Kim,&nbsp;Bo Hyun Kim,&nbsp;Yu Ri Cho,&nbsp;Young-Hwan Koh,&nbsp;Joong-Won Park","doi":"10.17998/jlc.2023.04.14","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aim: </strong>Radiotherapy (RT) is an effective local treatment for hepatocellular carcinoma (HCC). However, whether additional RT is safe and effective in patients with advanced HCC receiving atezolizumab plus bevacizumab remains unclear. This retrospective cohort study aimed to evaluate the feasibility of additional RT in these patients.</p><p><strong>Methods: </strong>Between March and October 2021, we retrospectively analyzed seven patients with advanced HCC who received RT during treatment with atezolizumab plus bevacizumab. The median prescribed RT dose was 35 Gy (range, 33-66). Freedom from local progression (FFLP), progression-free survival (PFS), and overall survival (OS) after RT were analyzed.</p><p><strong>Results: </strong>The median follow-up duration after RT was 14.2 months (range, 10.0-18.6). Of the seven patients, disease progression was noted in six (85.7%), the sites of disease progression were local in two (28.6%), intrahepatic in four (57.1%), and extrahepatic in four (57.1%). The median time of FFLP was not reached, and PFS and OS times were 4.0 (95% confidence interval [CI], 3.6-4.5) and 14.8% (95% CI, 12.5-17.2) months, respectively. The 1-year FFLP, PFS, and OS rates were 60% (95% CI, 43.8-76.2), 0%, and 85.7% (95% CI, 75.9-95.5), respectively. Grade 3 or higher hematologic adverse events (AEs) were not observed, but grade 3 nonhematologic AEs unrelated to RT were observed in one patient.</p><p><strong>Conclusions: </strong>The addition of RT may be feasible in patients with advanced HCC treated with atezolizumab plus bevacizumab. However, further studies are required to validate these findings.</p>","PeriodicalId":16226,"journal":{"name":"Journal of Liver Cancer","volume":" ","pages":"330-340"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/97/3d/jlc-2023-04-14.PMC10565546.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Liver Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17998/jlc.2023.04.14","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/5/16 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Background/aim: Radiotherapy (RT) is an effective local treatment for hepatocellular carcinoma (HCC). However, whether additional RT is safe and effective in patients with advanced HCC receiving atezolizumab plus bevacizumab remains unclear. This retrospective cohort study aimed to evaluate the feasibility of additional RT in these patients.

Methods: Between March and October 2021, we retrospectively analyzed seven patients with advanced HCC who received RT during treatment with atezolizumab plus bevacizumab. The median prescribed RT dose was 35 Gy (range, 33-66). Freedom from local progression (FFLP), progression-free survival (PFS), and overall survival (OS) after RT were analyzed.

Results: The median follow-up duration after RT was 14.2 months (range, 10.0-18.6). Of the seven patients, disease progression was noted in six (85.7%), the sites of disease progression were local in two (28.6%), intrahepatic in four (57.1%), and extrahepatic in four (57.1%). The median time of FFLP was not reached, and PFS and OS times were 4.0 (95% confidence interval [CI], 3.6-4.5) and 14.8% (95% CI, 12.5-17.2) months, respectively. The 1-year FFLP, PFS, and OS rates were 60% (95% CI, 43.8-76.2), 0%, and 85.7% (95% CI, 75.9-95.5), respectively. Grade 3 or higher hematologic adverse events (AEs) were not observed, but grade 3 nonhematologic AEs unrelated to RT were observed in one patient.

Conclusions: The addition of RT may be feasible in patients with advanced HCC treated with atezolizumab plus bevacizumab. However, further studies are required to validate these findings.

Abstract Image

Abstract Image

Abstract Image

atezolizumab联合贝伐单抗治疗晚期肝细胞癌患者额外放疗的可行性。
背景/目的:放射治疗(RT)是治疗肝细胞癌(HCC)的一种有效的局部治疗方法。然而,在接受atezolizumab联合贝伐单抗治疗的晚期HCC患者中,额外的RT是否安全有效仍不清楚。这项回顾性队列研究旨在评估在这些患者中进行额外RT的可行性。方法:在2021年3月至10月期间,我们回顾性分析了7名在atezolizumab联合贝伐单抗治疗期间接受RT的晚期HCC患者。规定的中位RT剂量为35 Gy(范围33-66)。分析RT后无局部进展(FFLP)、无进展生存期(PFS)和总生存期(OS)。结果:RT后的中位随访时间为14.2个月(范围为10.0-18.6)。在7名患者中,有6名患者(85.7%)出现疾病进展,2名患者出现局部疾病进展(28.6%),4名患者出现肝内疾病进展(57.1%),4例患者出现肝外疾病进展(5.71%),PFS和OS时间分别为4.0个月(95%可信区间[CI],3.6-4.5)和14.8%(95%置信区间,12.5-17.2)。1年的FFLP、PFS和OS发生率分别为60%(95%CI,43.8-76.2)、0%和85.7%(95%CI:75.9-95.5)。未观察到3级或更高级别的血液学不良事件(AE),但在一名患者中观察到与RT无关的3级非血液学AE。结论:在接受atezolizumab联合贝伐单抗治疗的晚期HCC患者中,加入RT可能是可行的。然而,还需要进一步的研究来验证这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信