Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong Province, China.
Department of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, Shandong Province, China.
Jpn J Clin Oncol. 2021 May 28;51(6):905-910. doi: 10.1093/jjco/hyab047.
The aim of the present study was to retrospectively evaluate the toxicity and efficacy of post-operative small pelvic intensity-modulated radiotherapy in early-stage cervical cancer patients with intermediate-risk factors.
Between 2012 and 2016, 151 patients who had cervical cancer (International Federation of Gynecology and Obstetrics stage I-IIA) with intermediate-risk factors were treated with post-operative small pelvic intensity-modulated radiotherapy. The median dose of 50.4 Gy in 28 fractions with small pelvic intensity-modulated radiotherapy was prescribed to the planning target volume. The intensity-modulated radiotherapy technique used was conventional fixed-field intensity-modulated radiotherapy or helical tomotherapy.
The median follow-up was 37 months. The 3-year disease-free survival and overall survival rates were 89 and 96%, respectively. A total of 144 patients (95.3%) were alive at the last follow-up. In total, 6 patients (3.9%) had recurrence: locoregional recurrence in 3 patients (2%), distant metastasis in 2 (1.3%), and both in 1 (0.6%). Diarrhoea was the most common acute toxicity. There were no patients suffering from acute or late grade ≥ 3 toxicity. Only 4 patients (2.6%) had late grade 2 toxicities.
For early-stage cervical cancer patients with intermediate-risk factors, post-operative small pelvic intensity-modulated radiotherapy was safe and well tolerated. The rates of acute and late toxicities were quite satisfactory.
本研究旨在回顾性评估中危因素的早期宫颈癌患者术后盆腔调强放疗的毒性和疗效。
2012 年至 2016 年间,151 例中危因素的宫颈癌(国际妇产科联合会分期 I-IIA)患者接受了术后盆腔调强放疗。计划靶区规定盆腔调强放疗 50.4Gy/28 次,中位剂量。调强放疗技术采用常规固定野调强放疗或螺旋断层放疗。
中位随访时间为 37 个月。3 年无病生存率和总生存率分别为 89%和 96%。末次随访时,144 例患者(95.3%)存活。共有 6 例(3.9%)患者复发:3 例(2%)局部区域复发,2 例(1.3%)远处转移,1 例(0.6%)两者均有。腹泻是最常见的急性毒性反应。无患者发生急性或晚期≥3 级毒性反应。仅有 4 例(2.6%)患者发生晚期 2 级毒性反应。
对于中危因素的早期宫颈癌患者,术后盆腔调强放疗安全且耐受性良好。急性和晚期毒性反应的发生率相当令人满意。