Kim Daniel H, Wang-Chesebro Alice, Weinberg Vivian, Pouliot Jean, Chen Lee-May, Speight Joycelyn, Littell Ramey, Hsu I-Chow
Department of Radiation Oncology, University of California, San Francisco, CA, USA.
Int J Radiat Oncol Biol Phys. 2009 Dec 1;75(5):1329-34. doi: 10.1016/j.ijrobp.2009.01.002. Epub 2009 May 4.
We present clinical outcomes of image-guided brachytherapy using inverse planning simulated annealing (IPSA) planned high-dose rate (HDR) brachytherapy boost for locoregionally advanced cervical cancer.
From February 2004 through December 2006, 51 patients were treated at the University of California, San Francisco with HDR brachytherapy boost as part of definitive radiation for International Federation of Gynecology and Obstetrics Stage IB1 to Stage IVA cervical cancer. Of the patients, 46 received concurrent chemotherapy, 43 with cisplatin alone and 3 with cisplatin/5-fluorouracil. All patients had IPSA-planned HDR brachytherapy boost after whole-pelvis external radiation to a total tumor dose of 85 Gy or greater (for alpha/beta = 10). Toxicities are reported according to National Cancer Institute CTCAE v3.0 (Common Terminology Criteria for Adverse Events version 3.0) guidelines.
At a median follow-up of 24.3 months, there were no toxicities of Grade 4 or greater and the frequencies of Grade 3 acute and late toxicities were 4% and 2%, respectively. The proportion of patients having Grade 1 or 2 gastrointestinal and genitourinary acute toxicities was 48% and 52%, respectively. Low-grade late toxicities included Grade 1 or 2 vaginal, gastrointestinal, and hormonal toxicities in 31%, 18%, and 4% of patients, respectively. During the follow-up period, local recurrence developed in 2 patients, regional recurrence developed in 2, and new distant metastases developed in 15. The rates of locoregional control of disease and overall survival at 24 months were 91% and 86%, respectively.
Definitive radiation by use of inverse planned HDR brachytherapy boost for locoregionally advanced cervical cancer is well tolerated and achieves excellent local control of disease.
我们报告了使用逆向计划模拟退火(IPSA)计划的高剂量率(HDR)近距离放射治疗对局部晚期宫颈癌进行增敏治疗的临床结果。
从2004年2月至2006年12月,加利福尼亚大学旧金山分校对51例国际妇产科联盟(FIGO)IB1期至IVA期宫颈癌患者进行了HDR近距离放射治疗增敏,作为确定性放疗的一部分。其中46例患者接受了同步化疗,43例仅使用顺铂,3例使用顺铂/5-氟尿嘧啶。所有患者在全盆腔外照射至总肿瘤剂量85 Gy或更高(α/β=10)后,均接受了IPSA计划的HDR近距离放射治疗增敏。毒性反应按照美国国立癌症研究所CTCAE v3.0(不良事件通用术语标准第3.0版)指南进行报告。
中位随访24.3个月时,无4级或更高级别的毒性反应,3级急性和晚期毒性反应的发生率分别为4%和2%。1级或2级胃肠道和泌尿生殖系统急性毒性反应的患者比例分别为48%和52%。低级别晚期毒性反应包括1级或2级阴道、胃肠道和激素毒性反应,分别发生在31%、18%和4%的患者中。随访期间,2例患者出现局部复发,2例出现区域复发,15例出现新的远处转移。24个月时的局部区域疾病控制率和总生存率分别为91%和86%。
使用逆向计划的HDR近距离放射治疗增敏对局部晚期宫颈癌进行确定性放疗耐受性良好,且能实现出色的局部疾病控制。