Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
Pract Radiat Oncol. 2013 Jan-Mar;3(1):26-31. doi: 10.1016/j.prro.2012.02.005. Epub 2012 Apr 3.
To assess the toxicity and efficacy of intensity modulated radiation therapy (IMRT) combined with chemotherapy in treatment of anal cancer.
We examined the records of 34 consecutive patients who received chemoradiation therapy with IMRT as initial treatment for squamous cell carcinoma of the anus between June 2005 and January 2009. The median radiation dose was 50.4 Gy (range, 48.6-57.6 Gy). Chemotherapy was given concurrently: 5-fluorouracil alone in 1 patient and combination 5-fluorouracil and mitomycin C in all others. Endpoints included local control and survival, as well as toxicity. Acute and late toxicity was scored with the Common Terminology Criteria for Adverse Events version 3.0.
Twenty-eight patients presented with T1 and T2 disease and 6 with T3 and T4 disease. Fourteen patients had regional nodal metastases. The median age was 59 years (range, 46-85 years). Median follow-up in surviving patients was 22 months. The estimated 2-year survival was 93% (95% confidence interval, 76%-98%). Three patients (9%) had local relapse (estimated 2-year local control, 90%; 95% confidence interval, 74%-97%). One patient had relapse in a regional node. Acute grade 3-4 hematologic toxicity was observed in 20 patients (59%). Other acute grade 3 or grade 4 toxicity included the gastrointestinal tract in 3 patients (9%) and skin in 5 patients (15%). Two patients (6%) had late grade 3 or grade 4 gastrointestinal tract toxicity.
Treatment of anal squamous cell carcinoma with IMRT and chemotherapy is effective and has an acceptable toxicity profile.
评估调强放疗(IMRT)联合化疗治疗肛门癌的毒性和疗效。
我们回顾了 2005 年 6 月至 2009 年 1 月期间,34 例连续接受 IMRT 同期放化疗作为肛门鳞癌初始治疗的患者的记录。中位放疗剂量为 50.4Gy(范围 48.6-57.6Gy)。同期化疗:1 例采用氟尿嘧啶单药,其余均采用氟尿嘧啶联合丝裂霉素 C。终点包括局部控制和生存以及毒性。采用不良事件通用术语标准 3.0 版对急性和迟发性毒性进行评分。
28 例患者为 T1 和 T2 期,6 例为 T3 和 T4 期。14 例患者有区域淋巴结转移。中位年龄为 59 岁(范围 46-85 岁)。生存患者的中位随访时间为 22 个月。估计 2 年生存率为 93%(95%置信区间 76%-98%)。3 例(9%)患者发生局部复发(估计 2 年局部控制率为 90%,95%置信区间 74%-97%)。1 例患者发生区域淋巴结复发。20 例(59%)患者出现急性 3-4 级血液学毒性。其他急性 3 级或 4 级毒性包括 3 例(9%)胃肠道毒性和 5 例(15%)皮肤毒性。2 例(6%)患者发生迟发性 3 级或 4 级胃肠道毒性。
IMRT 和化疗治疗肛门鳞癌有效,且毒性谱可接受。