Jiao Dechao, Wu Gang, Ren Jianzhuang, Han Xinwei
Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Oncotarget. 2016 Dec 27;7(52):87523-87531. doi: 10.18632/oncotarget.11983.
This retrospective study aimed to demonstrate and compare the safety and effectiveness of computed tomography-guided radiofrequency ablation (RFA) and 125I-seed brachytherapy for painful bone metastases after failure of external beam radiotherapy (EBRT). From June 2013 to October 2015, 79 patients with moderate-to-severe pain caused by metastatic bone lesions who underwent either RFA (n = 41) or 125I-seed brachytherapy (n = 38) were enrolled. Pain in patients was measured using the brief pain inventory (BPI) before treatment, 1 week after treatment, and 3 months after treatment. Response rates were assessed by measuring the changes in pain and incorporation of changes in the analgesic requirements. At baseline, 1 week, and 3 months, the mean worst pain scores of BPI were 7.8, 5.4, and 2.7, respectively, for the RFA group and 7.7, 6.1, and 2.8, respectively, for the brachytherapy group. At 1 week, the complete and partial response rates were 12% and 59%, respectively, in the RFA group compared with 3% and 45%, respectively, in the brachytherapy group. At 3 months, the complete and partial response rates were 23% and 58%, respectively, in the RFA group compared with 24% and 52% in the brachytherapy group (p = 0.95). The response rates in the RFA group were significantly higher than those in the brachytherapy group at 1 week (p = 0.32), but comparable at 3 weeks (p = 0.95). Both groups had low rates of complications and no treatment-related mortality. In conclusion, the short-term curative efficiency of RFA was better than that of brachytherapy, but the log-term efficiency of both treatments was equal.
这项回顾性研究旨在论证并比较计算机断层扫描引导下的射频消融(RFA)和¹²⁵I粒子近距离放射治疗对外照射放疗(EBRT)失败后的疼痛性骨转移瘤的安全性和有效性。2013年6月至2015年10月,纳入了79例因转移性骨病变导致中重度疼痛且接受了RFA(n = 41)或¹²⁵I粒子近距离放射治疗(n = 38)的患者。在治疗前、治疗后1周和治疗后3个月,使用简明疼痛量表(BPI)对患者的疼痛进行测量。通过测量疼痛变化和镇痛药需求变化来评估缓解率。在基线、1周和3个月时,RFA组BPI的平均最严重疼痛评分分别为7.8、5.4和2.7,近距离放射治疗组分别为7.7、6.1和2.8。在1周时,RFA组的完全缓解率和部分缓解率分别为12%和59%,而近距离放射治疗组分别为3%和45%。在3个月时,RFA组的完全缓解率和部分缓解率分别为23%和58%,近距离放射治疗组为24%和52%(p = 0.95)。RFA组在1周时的缓解率显著高于近距离放射治疗组(p = 0.32),但在3周时相当(p = 0.95)。两组的并发症发生率均较低,且无治疗相关死亡。总之,RFA的短期疗效优于近距离放射治疗,但两种治疗的长期疗效相当。