术前 S-1 单药放化疗治疗局部进展期直肠癌的疗效和耐受性。
Efficacy and tolerability of preoperative chemoradiotherapy with S-1 alone for locally advanced rectal cancer.
机构信息
Department of Radiation Oncology, Graduate School of Biomedical Health Sciences, Hiroshima University. Hiroshima, Japan.
Department of Gastroenterological and Transplant Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University. Hiroshima, Japan.
出版信息
J Radiat Res. 2021 Mar 10;62(2):300-308. doi: 10.1093/jrr/rraa117.
Preoperative chemoradiotherapy with capecitabine or 5-fluorouracil is a standard treatment for locally advanced rectal cancer (LARC). S-1, a prodrug of 5-fluorouracil, is a candidate for this chemoradiotherapy regimen in Japan; however, treatment outcomes after S-1 treatment alone are not clear. This study aimed to assess the efficacy and tolerability of preoperative chemoradiotherapy with S-1 alone for LARC. We retrospectively evaluated 54 LARC patients who underwent preoperative chemoradiotherapy with S-1 alone in our institution between 2005 and 2017. The clinical tumor stage was cT2-3 in 31 patients and cT4 in 23 patients, and lymph node metastases were clinically evident in 31 patients. S-1, at a dose of 80 mg/m2/day, was orally administered during radiotherapy. A total dose of 45-50.4 Gy was delivered in 25-28 fractions (median: 50.4 Gy). Surgical resections were scheduled 6-10 weeks after chemoradiotherapy completion. The 3- and 5-year overall survival rates were 92.4 and 72.8%, respectively, with a median follow-up time of 51 months. The 3- and 5-year local control rates were 96.2 and 85.9%, respectively. A pathological complete response was observed in 7 patients (13.0%) at the time of surgery. Ten patients (18.5%) had grade 3 acute toxicities and 5 patients (9.3%) had grade 3 late toxicities. No grade 4 or 5 toxicities were observed. Preoperative chemoradiotherapy with S-1 alone followed by total mesorectal excision resulted in a low incidence of toxicities and comparable clinical results. Therefore, S-1 alone can be a treatment option for preoperative chemoradiotherapy in LARC patients.
术前卡培他滨或氟尿嘧啶化疗是局部进展期直肠癌(LARC)的标准治疗方法。替吉奥(S-1)是氟尿嘧啶的前体药物,是日本该放化疗方案的候选药物;然而,单独使用 S-1 治疗后的治疗效果尚不清楚。本研究旨在评估单独使用 S-1 进行术前放化疗治疗 LARC 的疗效和耐受性。我们回顾性评估了 2005 年至 2017 年期间在我院接受单独 S-1 术前放化疗的 54 例 LARC 患者。临床肿瘤分期为 cT2-3 期 31 例,cT4 期 23 例,临床淋巴结转移 31 例。S-1 剂量为 80mg/m2/天,在放疗期间口服给药。总剂量为 45-50.4Gy,分为 25-28 个分次(中位数:50.4Gy)。放化疗完成后 6-10 周安排手术切除。3 年和 5 年总生存率分别为 92.4%和 72.8%,中位随访时间为 51 个月。3 年和 5 年局部控制率分别为 96.2%和 85.9%。手术时观察到 7 例(13.0%)患者病理完全缓解。10 例(18.5%)患者出现 3 级急性毒性,5 例(9.3%)患者出现 3 级晚期毒性。未观察到 4 级或 5 级毒性。单独使用 S-1 进行术前放化疗,然后进行全直肠系膜切除术,毒性发生率低,临床效果相当。因此,S-1 可作为 LARC 患者术前放化疗的一种治疗选择。