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立体定向体部放疗治疗合并门静脉和/或下腔静脉癌栓的肝细胞癌的疗效。

Effectiveness of stereotactic body radiotherapy for hepatocellular carcinoma with portal vein and/or inferior vena cava tumor thrombosis.

机构信息

State Key Laboratory of Oncology in Southern China, Department of Radiation Oncology, Cancer Center, Sun Yat-sen University, Guangzhou, China.

出版信息

PLoS One. 2013 May 30;8(5):e63864. doi: 10.1371/journal.pone.0063864. Print 2013.

DOI:10.1371/journal.pone.0063864
PMID:23737955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3667854/
Abstract

BACKGROUND

To report the feasibility, efficacy, and toxicity of stereotactic body radiotherapy (SBRT) for the treatment of portal vein tumor thrombosis (PVTT) and/or inferior vena cava tumor thrombosis (IVCTT) in patients with advanced hepatocellular carcinoma (HCC).

MATERIALS AND METHODS

Forty-one patients treated with SBRT using volumetric modulated arc therapy (VMAT) for HCC with PVTT/IVCTT between July 2010 and May 2012 were analyzed. Of these, 33 had PVTT and 8 had IVCTT. SBRT was designed to target the tumor thrombosis and deliver a median total dose of 36 Gy (range, 30-48 Gy) in six fractions during two weeks.

RESULTS

The median follow-up was 10.0 months. At the time of analysis, 15 (36.6%) achieved complete response, 16 (39.0%) achieved partial response, 7 (17.1%) patients were stable, and three (7.3%) patients showed progressive disease. No treatment-related Grade 4/5 toxicity was seen within three months after SBRT. One patient had Grade 3 elevation of bilirubin. The one-year overall survival rate was 50.3%, with a median survival of 13.0 months. The only independent predictive factor associated with better survival was response to radiotherapy.

CONCLUSIONS

VMAT-based SBRT is a safe and effective treatment option for PVTT/IVCTT in HCC. Prospective randomized controlled trials are warranted to validate the role of SBRT in these patients.

摘要

背景

报道立体定向体部放疗(SBRT)治疗晚期肝细胞癌(HCC)合并门静脉癌栓(PVTT)和/或下腔静脉癌栓(IVCTT)的可行性、疗效和毒性。

材料和方法

分析了 2010 年 7 月至 2012 年 5 月期间采用容积旋转调强放疗(VMAT)治疗 HCC 合并 PVTT/IVCTT 的 41 例患者。其中 33 例有 PVTT,8 例有 IVCTT。SBRT 的设计目标是肿瘤血栓,并在两周内分 6 次给予中位总剂量 36Gy(范围 30-48Gy)。

结果

中位随访时间为 10.0 个月。在分析时,15 例(36.6%)完全缓解,16 例(39.0%)部分缓解,7 例(17.1%)患者病情稳定,3 例(7.3%)患者病情进展。SBRT 后 3 个月内未见治疗相关 4/5 级毒性。1 例患者出现胆红素 3 级升高。一年总生存率为 50.3%,中位生存时间为 13.0 个月。唯一与生存相关的独立预测因素是对放疗的反应。

结论

基于 VMAT 的 SBRT 是 HCC 合并 PVTT/IVCTT 的一种安全有效的治疗选择。需要前瞻性随机对照试验来验证 SBRT 在这些患者中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/79f8f54a4348/pone.0063864.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/360da65af662/pone.0063864.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/a5deb957a30c/pone.0063864.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/b04eff061ca2/pone.0063864.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/79f8f54a4348/pone.0063864.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/360da65af662/pone.0063864.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/a5deb957a30c/pone.0063864.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/b04eff061ca2/pone.0063864.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fc/3667854/79f8f54a4348/pone.0063864.g004.jpg

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