Kim Sang Won, Oh Dongryul, Park Hee Chul, Lim Do Hoon, Shin Sung Wook, Cho Sung Ki, Gwak Geum-Youn, Choi Moon Seok, Paik Yong Han, Paik Seung Woon
Department of Radiation Oncology, Yeungnam University Medical Center, Daegu, Korea.
Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Radiat Oncol J. 2014 Mar;32(1):14-22. doi: 10.3857/roj.2014.32.1.14. Epub 2014 Mar 27.
To evaluate the safety and efficacy of transcatheter arterial chemoembolization (TACE) followed by radiotherapy (RT) in treatment-naïve patients with locally advanced hepatocellular carcinoma (HCC).
ELIGIBILITY CRITERIA WERE AS FOLLOWS: newly diagnosed with HCC, the Barcelona Clinic Liver Cancer stage C, Child-Pugh class A or B, and no prior treatment for HCC. Patients with extrahepatic spread were excluded. A total of 59 patients were retrospectively enrolled. All patients were treated with TACE followed by RT. The time interval between TACE and RT was 2 weeks as per protocol. A median RT dose was 47.25 Gy10 as the biologically effective dose using the α/β = 10 (range, 39 to 65.25 Gy10).
At 1 month, complete response was obtained in 3 patients (5%), partial response in 27 patients (46%), stable disease in 13 patients (22%), and progressive disease in 16 patients (27%). The actuarial one- and two-year OS rates were 60.1% and 47.2%, respectively. The median OS was 17 months (95% confidence interval, 5.6 to 28.4 months). The median time to progression was 4 months (range, 1 to 35 months). Grade 3 or greater liver enzyme elevation occurred in only two patients (3%) after RT. Grade 3 gastroduodenal toxicity developed in two patients (3%).
The combination treatment of TACE followed by RT with two-week interval was safe and it showed favorable outcomes in treatment-naïve patients with locally advanced HCC. A prospective randomized trial is needed to validate these results.
评估经动脉化疗栓塞术(TACE)联合放疗(RT)用于初治局部晚期肝细胞癌(HCC)患者的安全性和疗效。
纳入标准如下:新诊断为HCC,巴塞罗那临床肝癌分期为C期,Child-Pugh肝功能分级为A或B级,且既往未接受过HCC治疗。排除肝外转移患者。共回顾性纳入59例患者。所有患者均先接受TACE治疗,随后接受RT治疗。按照方案,TACE与RT之间的时间间隔为2周。使用α/β = 10计算生物学等效剂量,中位RT剂量为47.25 Gy10(范围为39至65.25 Gy10)。
1个月时,3例患者(5%)获得完全缓解,27例患者(46%)获得部分缓解,13例患者(22%)病情稳定,16例患者(27%)病情进展。1年和2年总生存率分别为60.1%和47.2%。中位总生存期为17个月(95%置信区间为5.6至28.4个月)。中位疾病进展时间为4个月(范围为1至35个月)。RT后仅2例患者(3%)出现3级或更高级别的肝酶升高。2例患者(3%)发生3级胃十二指肠毒性反应。
TACE联合RT且间隔2周的联合治疗是安全的,在初治局部晚期HCC患者中显示出良好的疗效。需要进行前瞻性随机试验来验证这些结果。