Stereotactic body radiation therapy in primary liver tumor: Local control, outcomes and toxicities

IF 2.7 3区 医学 Q3 ONCOLOGY
Ludovic Hernandez , Laure Parent , Victoire Molinier , Bertrand Suc , Françoise Izar , Elisabeth Moyal , Jean-Marie Peron , Philippe Otal , Amélie Lusque , Anouchka Modesto
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Abstract

Objective

Stereotactic body radiation therapy (SBRT) is a therapeutic option in the guidelines for liver primaries after standard strategies like surgery or thermoablation have failed. To assess its efficacy and safety, we reviewed all patients treated by SBRT for a hepatocellular carcinoma (HCC) over a six-year period.

Methods and materials

The study included all patients treated by SBRT for HCC between April 2015 and November 2021 in the University Cancer Institute at Toulouse-Oncopole. All patients were inoperable and not eligible for thermoablation, or after a failure. All tumor sizes were included and cirrhosis up to Child-Pugh B was accepted. Local control (LC), overall survival (OS) and progression-free survival (PFS) were estimated by the Kaplan-Meier method. Treatment response was assessed using mRECIST criteria. Toxicity was graded using CTCAE (v4.0).

Results

One hundred and nine patients with 118 lesions were treated. Half underwent prior standard treatment. Median dose was 50 Grays in five fractions for most patients. Chronic liver disease represented 90.8 % of cases with a median age of 69 years. Median tumor size was 4.0 cm. Median follow-up was 22.2 months [95 %CI: 15.1–30.4]. LC, OS and PFS at two years were 82.4 % [95 %CI: 71.3; 89.5], 73.2 % [95 %CI: 61.5; 81.8] and 35.8 % [95 %CI: 25.1; 46.7], respectively. Acute toxicities occurred in 20.2 % of patients, including 10.1 % grade 3–4 and 1.8 % grade 5. Late toxicities occurred in 5.5 % of patients including 4.6 % grade 3–4. Grade ≥ 3 toxicity was related to digestive perforation or liver failure.

Conclusion

SBRT provides good LC with an acceptable safety profile. It can be used in several settings such as salvage therapy or in combination with validated treatment. Prospective randomized trials are needed to validate SBRT as a standard alternative.
原发性肝肿瘤的立体定向体放射治疗:局部控制、疗效和毒性
目的立体定向体放射治疗(SBRT)是手术或热消融等标准策略失败后,肝脏原发癌治疗指南中的一种治疗方案。为评估其疗效和安全性,我们回顾了六年来所有接受 SBRT 治疗的肝细胞癌(HCC)患者。所有患者均无法手术,不符合热消融条件,或治疗失败。所有肿瘤大小均包括在内,肝硬化程度达到Child-Pugh B均可接受。局部控制率(LC)、总生存率(OS)和无进展生存率(PFS)采用卡普兰-梅耶法估算。治疗反应采用 mRECIST 标准进行评估。采用 CTCAE(v4.0)对毒性进行分级。半数患者之前接受过标准治疗。大多数患者的中位剂量为50格雷,分5次进行。慢性肝病患者占 90.8%,中位年龄为 69 岁。肿瘤中位大小为 4.0 厘米。中位随访时间为 22.2 个月[95 %CI:15.1-30.4]。两年的LC、OS和PFS分别为82.4% [95 %CI: 71.3; 89.5]、73.2% [95 %CI: 61.5; 81.8]和35.8% [95 %CI: 25.1; 46.7]。20.2%的患者出现急性毒性反应,其中10.1%为3-4级,1.8%为5级。5.5%的患者出现晚期毒性反应,其中4.6%为3-4级。≥3级毒性与消化道穿孔或肝功能衰竭有关。它可用于多种情况,如挽救治疗或与有效治疗联合使用。需要进行前瞻性随机试验来验证 SBRT 作为标准替代疗法的有效性。
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来源期刊
Clinical and Translational Radiation Oncology
Clinical and Translational Radiation Oncology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.30
自引率
3.20%
发文量
114
审稿时长
40 days
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