Departments of aRadiation Oncology bRadiology cInternal Medicine, Division of Hematology and Oncology, Tri-Service General Hospital, National Defense Medical Center dSchool of Public Health, National Defence Medical Center, Taipei, Taiwan, ROC.
Eur J Gastroenterol Hepatol. 2014 Mar;26(3):345-52. doi: 10.1097/MEG.0000000000000032.
The role of stereotactic ablative radiotherapy (SABR) in patients with hepatocellular carcinoma (HCC) who are refractory to or unsuitable for transarterial chemoembolization remains unclear. We examined the efficacy and safety of Cyberknife SABR and its effect on survival in this group of HCC patients.
From June 2008 to June 2011, 53 patients with 68 tumors of unresectable HCC were treated using Cyberknife SABR. The tumors measured 1.1-13 cm (median, 4.3 cm). The median prescribed dose was 40 Gy in four to five fractions over 4-5 consecutive working days.
The median follow-up period was 13.1 months for all patients and 18.1 months for the living patients. Objective responses were observed in 48 of 67 tumors (71.6%), including 22 tumors (32.8%) with complete responses. The 1- and 2-year in-field failure-free rate was 73.3 and 66.8%, respectively. Out-field intrahepatic recurrence was the main cause of treatment failure (28/52 patients). The median survival time was 20.0 months, and the 1- and 2-year overall survival rate was 70.1 and 45.4%, respectively. Multivariable analysis showed that Eastern Cooperative Oncology Group performance status (≤1 vs. >1) and tumor response (responder vs. nonresponder) were independent prognostic factors for overall survival. Radiation-induced liver disease, including classic and nonclassic types, developed in five patients (9.4%). Other acute toxicities were generally mild and tolerable.
Our findings supported the feasibility of SABR as a salvage treatment for HCC when transarterial chemoembolization was ineffective or technically unsuitable. Additional efforts to improve the response rate and reduce out-field recurrence are required.
立体定向消融放疗(SABR)在经动脉化疗栓塞(TACE)治疗无效或不适用的肝细胞癌(HCC)患者中的作用尚不清楚。我们研究了 Cyberknife SABR 在这组 HCC 患者中的疗效和安全性及其对生存的影响。
从 2008 年 6 月至 2011 年 6 月,53 例 68 个不可切除 HCC 患者接受 Cyberknife SABR 治疗。肿瘤大小为 1.1-13cm(中位数,4.3cm)。中位处方剂量为 40Gy,分 4-5 次,连续 4-5 个工作日完成。
所有患者的中位随访时间为 13.1 个月,存活患者的中位随访时间为 18.1 个月。67 个肿瘤中观察到 48 个(71.6%)有客观反应,其中 22 个(32.8%)完全缓解。1 年和 2 年的靶区无失败率分别为 73.3%和 66.8%。靶区外肝内复发是治疗失败的主要原因(52 例中有 28 例)。中位生存时间为 20.0 个月,1 年和 2 年的总生存率分别为 70.1%和 45.4%。多变量分析显示,东部肿瘤协作组表现状态(≤1 与>1)和肿瘤反应(应答者与无应答者)是总生存的独立预后因素。5 例(9.4%)发生放射性肝损伤,包括经典型和非经典型。其他急性毒性通常较轻且可耐受。
我们的研究结果支持在 TACE 无效或技术上不适用时,SABR 作为 HCC 的挽救性治疗是可行的。需要进一步努力提高反应率并降低靶区外复发率。