Division of Radiation Oncology, Department of Radiology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo 113-8677, Japan.
Department of Radiation Oncology, Kurashiki Central Hospital, Okayama 710-8602, Japan.
J Radiat Res. 2023 Jan 20;64(1):154-161. doi: 10.1093/jrr/rrac069.
This study assessed the efficacy of chemoradiotherapy for squamous cell carcinoma of the anal canal (SCCAC). Patients with T1-4N0-3M0 SCCAC received chemoradiotherapy with 5-fluorouracil (5-FU, 800 mg/m2/day, 96-h infusion) and mitomycin-C (MMC, 10 mg/m2 bolus). Patients treated with 3-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) were administered 36.0 Gy in 20 fractions or 49.5 Gy in 33 fractions for elective nodal irradiation and 59.4 Gy in 33 fractions for primary tumor and metastatic nodal irradiation. The sample size was considered sufficient to estimate 95% confidence intervals (CIs) for the true 2-year disease-free survival (DFS) within a width of +15% when the expected true 2-year DFS was 70%. The primary endpoint was 2-year DFS. The secondary endpoints were 2-year overall survival (OS), locoregional control (LC), colostomy-free survival (CFS) and adverse events. Thirty-one patients were enrolled between January 2014 and July 2019. The median follow-up was 33.3 months (range, 16.2-65.8 months). Among the 31 patients, 13%, 32%, 16% and 39% had stage I, II, IIIA and IIIB disease, respectively. Thirty patients were treated with IMRT. Complete response (CR) was achieved in 27 patients. The 2-year DFS, OS, LC and CFS rates were 77.4% (95% CI, 58.4-88.5%), 93.5% (95% CI, 76.6-98.3%), 83.9% (95% CI, 65.5-92.9%) and 80.6% (95% CI, 61.9-90.8%), respectively. One patient experienced grade 3 late adverse events; however, no grade ≥ 4 late adverse events occurred. Good DFS with a low rate of late adverse events was observed. Chemoradiotherapy with 5-FU and MMC was effective for SCCAC.
本研究评估了同步放化疗治疗肛管鳞癌(SCCAC)的疗效。T1-4N0-3M0 期 SCCAC 患者接受氟尿嘧啶(5-FU,800mg/m2/天,96 小时输注)和丝裂霉素 C(MMC,10mg/m2 推注)联合放化疗。接受三维适形放疗(3D-CRT)或调强放疗(IMRT)的患者,行选择性淋巴结照射 36.0Gy/20 次,原发肿瘤和转移淋巴结照射 59.4Gy/33 次,行同步放化疗。当预期 2 年无疾病生存率(DFS)为 70%时,样本量被认为足以估计真实 2 年 DFS 的 95%置信区间(CI),置信区间宽度为+15%。主要终点为 2 年 DFS。次要终点为 2 年总生存率(OS)、局部区域控制(LC)、无造口生存(CFS)和不良事件。2014 年 1 月至 2019 年 7 月期间,共纳入 31 例患者。中位随访时间为 33.3 个月(16.2-65.8 个月)。31 例患者中,Ⅰ期、Ⅱ期、ⅢA 期和ⅢB 期分别占 13%、32%、16%和 39%。30 例患者接受 IMRT 治疗。27 例患者达到完全缓解(CR)。2 年 DFS、OS、LC 和 CFS 率分别为 77.4%(95%CI,58.4-88.5%)、93.5%(95%CI,76.6-98.3%)、83.9%(95%CI,65.5-92.9%)和 80.6%(95%CI,61.9-90.8%)。1 例患者发生 3 级晚期不良事件,但无≥4 级晚期不良事件发生。观察到DFS 良好且晚期不良事件发生率低。5-FU 和 MMC 联合放化疗治疗 SCCAC 有效。