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影像引导下大分割放疗治疗门静脉癌栓型肝细胞癌的疗效与安全性:一项回顾性多中心研究

Efficacy and safety of image-guided hypofractionated radiotherapy for hepatocellular carcinoma with portal vein tumor thrombosis: a retrospective, multicenter study.

作者信息

Lee Sang Min, Choi Jin Hwa, Yoon Jung-Hwan, Kim Yoon Jun, Yu Su Jong, Lee Jeong-Hoon, Kang Hyun-Cheol, Chie Eui Kyu, Kim Kyung Su

机构信息

Department of Radiation Oncology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.

Department of Radiation Oncology, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Republic of Korea.

出版信息

BMC Cancer. 2025 Apr 21;25(1):736. doi: 10.1186/s12885-025-13739-3.

Abstract

BACKGROUND

External beam radiation therapy (RT) has shown promising effects for hepatocellular carcinoma (HCC) patients with portal vein tumor thrombosis (PVTT) in recent studies. However, there is still a lack of consensus on the optimal RT scheme for PVTT treatment. We evaluated the efficacy and safety of image-guided 10-fraction hypofractionated RT in these patients.

METHODS

Between January 2016 and March 2022, a total of 95 HCC patients with PVTT received 10-fraction hypofractionated image-guided radiation therapy (IGRT) at two institutes, and 69 patients were analyzed. Follow-up imaging was performed at three-month intervals after the completion of RT. The extent of PVTT was described according to the Liver Cancer Study Group of Japan classification: Vp1 = segmental portal vein branch, Vp2 = right/left anterior/posterior portal vein, Vp3 = right/left portal vein, and Vp4 = main portal vein. Response evaluation was performed using Response Evaluation Criteria in Solid Tumors, version 1.1. Freedom from local progression (FFLP), progression-free survival (PFS), and overall survival (OS) were calculated from the start date of RT.

RESULTS

The median prescribed dose of 50 Gy (range: 40-50 Gy; biologically effective dose [BED]: 56-75Gy) was delivered in 10 fractions. In this cohort, 4.3% of patients had Vp1, 20.3% had Vp2, 37.7% had Vp3, and 37.7% had Vp4. Median Planning target volume was 105.3 cc (interquartile range [IQR], 74.1-179.4 cc). Fifty-two (75.4%) patients received 50 Gy. With a median follow-up of 10.2 months (IQR, 6-21 months), the median OS was 20.3 months, and 1-year FFLP, PFS, and OS rates were 88.7%, 26.9%, and 62.2%, respectively. At 3 months follow-up, 13.0% had a complete response, 36.2% had a partial response, 46.4% had a stable disease and 4.4% had a progressive disease. In the multivariate analysis, alpha-fetoprotein level ≥ 600 IU/ml (hazard ratio [HR] 2.06, p = 0.03), Child-Pugh Class B or C (HR 2.30, p = 0.02), and stage IVA or IVB (4.05, p = 0.02) were significantly related to OS. During the follow-up period, there were 2 (2.9%) cases of grade ≥ 3 toxicity: grade 3 liver enzyme elevation (n = 1), and acute cholangitis (n = 1).

CONCLUSIONS

Hypofractionated RT demonstrated promising local PVTT control and OS rates with acceptable toxicity. These data suggest that 10-fraction image-guided hypofractionated RT (BED: 56-75 Gy) is a feasible treatment option for PVTT in HCC patients.

摘要

背景

近期研究表明,外照射放疗(RT)对伴有门静脉癌栓(PVTT)的肝细胞癌(HCC)患者显示出有前景的疗效。然而,对于PVTT治疗的最佳放疗方案仍缺乏共识。我们评估了图像引导下10次分割的低分割放疗在这些患者中的疗效和安全性。

方法

2016年1月至2022年3月期间,共有95例伴有PVTT的HCC患者在两家机构接受了10次分割的图像引导下低分割放疗(IGRT),对69例患者进行了分析。放疗结束后每隔三个月进行一次随访成像。根据日本肝癌研究组的分类描述PVTT的范围:Vp1 = 门静脉分支段,Vp2 = 右/左前/后门静脉,Vp3 = 右/左门静脉,Vp4 = 门静脉主干。使用实体瘤疗效评价标准1.1版进行疗效评估。从放疗开始日期计算无局部进展生存期(FFLP)、无进展生存期(PFS)和总生存期(OS)。

结果

10次分割给予的中位处方剂量为50 Gy(范围:40 - 50 Gy;生物等效剂量[BED]:56 - 75 Gy)。在该队列中,4.3%的患者为Vp1,20.3%为Vp2,37.7%为Vp3,37.7%为Vp4。中位计划靶体积为105.3 cc(四分位间距[IQR],74.1 - 179.4 cc)。52例(75.4%)患者接受了50 Gy的剂量。中位随访时间为10.2个月(IQR,6 - 21个月),中位OS为20.3个月,1年FFLP、PFS和OS率分别为88.7%、26.9%和62.2%。在3个月随访时,13.0%的患者完全缓解,36.2%部分缓解,46.4%疾病稳定,4.4%疾病进展。在多变量分析中,甲胎蛋白水平≥600 IU/ml(风险比[HR] 2.06,p = 0.03)、Child-Pugh B级或C级(HR 2.30,p = 0.02)以及IV A期或IV B期(4.05,p = 0.02)与OS显著相关。在随访期间,有2例(2.9%)≥3级毒性反应:3级肝酶升高(n = 1)和急性胆管炎(n = 1)。

结论

低分割放疗显示出有前景的局部PVTT控制率和OS率,且毒性可接受。这些数据表明,10次分割的图像引导下低分割放疗(BED:56 - 75 Gy)是HCC患者PVTT的一种可行治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acc6/12010600/9aed31da2a6f/12885_2025_13739_Fig1_HTML.jpg

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