医学
阿替唑单抗
肝细胞癌
不利影响
贝伐单抗
内科学
放射治疗
危险系数
肿瘤科
胃肠病学
泌尿科
癌症
化疗
置信区间
无容量
免疫疗法
作者
Chung‐Wei Su,Wei Teng,Eric Yi-Liang Shen,Bing‐Shen Huang,Po‐Ting Lin,Ming‐Mo Hou,Tsung‐Han Wu,Din‐Li Tsan,Chia‐Hsun Hsieh,Ching‐Ting Wang,Pei‐Mei Chai,Chun‐Yen Lin,Shi‐Ming Lin,Chen‐Chun Lin
出处
期刊:Oncologist
[AlphaMed Press]
日期:2024-03-26
卷期号:29 (7): e922-e931
被引量:26
标识
DOI:10.1093/oncolo/oyae048
摘要
BACKGROUND: Atezolizumab plus bevacizumab (atezo-bev) has been recommended for advanced hepatocellular carcinoma (HCC). High-dose external beam radiotherapy (RT) is recognized for its excellent local tumor control. The efficacy and safety of concurrent atezo-bev with RT for highly advanced HCC has been minimally explored. METHODS: In this preliminary retrospective study, we assessed patients with highly advanced HCC, characterized by Vp4 portal vein thrombosis or tumors exceeding 50% of liver volume, who received concurrent atezo-bev and RT (group A). Group A included 13 patients who received proton radiation at a dose of 72.6 GyE in 22 fractions, and one patient who received photon radiation at a dose of 54 Gy in 18 fractions. This group was compared with 34 similar patients treated atezo-bev alone as a control (group B). The primary objectives were to evaluate the objective response rate (ORR), overall survival (OS), and safety. RESULTS: Baseline characteristics were similar between groups, except for a higher incidence of Vp4 portal vein thrombosis in group A (78.6% vs. 21.4%, P = .05). Group A achieved a higher ORR (50.0% vs. 11.8%, P < .01) and a longer OS (not reached vs. 5.5 months, P = .01) after a median follow-up of 5.2 months. Multivariate analysis indicated that concurrent RT independently favored longer OS (hazard ratio: 0.18; 95% CI, 0.05-0.63, P < .01). Group A did not increase any grade adverse events (78.6% vs. 58.8%, P = .19) or severe adverse events of grade ≥ 3 (14.3% vs. 14.7%, P = .97) compared to group B. CONCLUSIONS: The concurrent high-dose external beam radiotherapy appears to safely enhance the effectiveness of atezolizumab plus bevacizumab for highly advanced patients with HCC. Further studies are warranted to confirm these findings.
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