Rao Yuan James, Chundury Anupama, Schwarz Julie K, Hassanzadeh Comron, DeWees Todd, Mullen Daniel, Powell Matthew A, Mutch David G, Grigsby Perry W
Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
University of Missouri - Kansas City School of Medicine, Kansas City, Missouri.
Adv Radiat Oncol. 2017 Feb 28;2(2):148-158. doi: 10.1016/j.adro.2017.02.006. eCollection 2017 Apr-Jun.
The objective of this study was to present the treatment technique and evaluate clinical outcomes after intensity modulated radiation therapy (IMRT) for vulvar cancer.
This retrospective study included 39 patients with squamous cell carcinoma of the vulva treated with IMRT from 2005 to 2015. There were 21 patients treated with postoperative IMRT, 13 with definitive IMRT, and 5 with preoperative IMRT. Tumor staging was Federation of Gynecology and Obstetrics stage I in 6, stage II in 7, stage III in 19, and stage IV in 7 patients. Concurrent chemotherapy was administered to 14 patients. Brachytherapy was delivered in 8 patients.
The median follow-up was 34 months (range, 3.3-71). Median IMRT dose to patients receiving pre- or postoperative IMRT was 5040 cGy (range, 5040-6080). Median combined IMRT and brachytherapy dose to gross tumor was 7000 cGy (range, 5040-7520) in those treated with definitive RT. The 3-year locoregional control (LRC) and overall survival for those receiving postoperative RT were 89% and 67%, respectively. The 3-year LRC and overall survival for those receiving definitive IMRT were 42% and 49%, respectively. In patients receiving definitive or neoadjuvant IMRT, 69% had complete clinical response and 44% had complete pathologic response. The actuarial 3-year inguinal recurrence rate was 7%. There were no acute grade 3-4 hematological, gastrointestinal, or genitourinary toxicities. There were no late grade 3-4 gastrointestinal or genitourinary toxicities.
IMRT for vulvar cancer is associated with high rates of LRC in the postoperative setting and limited radiation-related toxicity. Durable LRC of disease after definitive IMRT remains challenging, and several refinements to our treatment technique are suggested.
本研究的目的是介绍外阴癌调强放射治疗(IMRT)的治疗技术并评估临床疗效。
这项回顾性研究纳入了2005年至2015年期间接受IMRT治疗的39例外阴鳞状细胞癌患者。其中21例接受术后IMRT治疗,13例接受根治性IMRT治疗,5例接受术前IMRT治疗。肿瘤分期为国际妇产科联盟(FIGO)I期6例,II期7例,III期19例,IV期7例。14例患者接受了同步化疗。8例患者接受了近距离放疗。
中位随访时间为34个月(范围3.3 - 71个月)。接受术前或术后IMRT患者的IMRT中位剂量为5040 cGy(范围5040 - 6080)。接受根治性放疗患者的IMRT与近距离放疗联合的肿瘤总中位剂量为7000 cGy(范围5040 - 7520)。接受术后放疗患者的3年局部区域控制率(LRC)和总生存率分别为89%和67%。接受根治性IMRT患者的3年LRC和总生存率分别为42%和49%。接受根治性或新辅助IMRT的患者中,69%有完全临床缓解,4%有完全病理缓解。3年腹股沟复发率的精算值为7%。无3 - 4级急性血液学、胃肠道或泌尿生殖系统毒性反应。无3 - 4级晚期胃肠道或泌尿生殖系统毒性反应。
外阴癌的IMRT在术后环境中具有较高的LRC率且放疗相关毒性有限。根治性IMRT后疾病的持久LRC仍然具有挑战性,建议对我们的治疗技术进行一些改进。