Department of Radiation Oncology, Nagoya City University Hospital, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan.
Department of Radiation Oncology, Ichinomiya Municipal Hospital, 2-2-22 Bunkyo, Ichinomiya, Aichi 491-8558, Japan.
J Radiat Res. 2023 Jul 18;64(4):720-727. doi: 10.1093/jrr/rrad039.
We aimed to examine outcomes and toxicities of intensity-modulated radiation therapy (IMRT) with the central shielding (CS) technique for patients with uterine cervical cancer. This retrospective study included 54 patients with International Federation of Gynecology and Obstetrics IB-IVA cancer. Whole pelvic radiotherapy or extended-field radiotherapy were performed at the dose of 50.4 Gy in 28 fractions with helical tomotherapy (HT). Six patients had para-aortic lymph node metastases. The CS technique with HT was utilized after a total dose of 28.8-41.4 Gy to reduce doses to the rectum and bladder. The prescribed dose of intracavitary brachytherapy was mainly 18-24 Gy in three or four fractions at point A. Concurrent chemotherapy was used for 47 patients (87%). Median follow-up time was 56 months. Seventeen patients (31%) developed recurrence. The recurrence of the cervix was observed in two patients (4%). The 5-year rates of the locoregional control, progression-free survival (PFS) and overall survival were 79, 66 and 82%, respectively. Among several factors evaluated, histological type of adenocarcinoma was only a significantly worse prognostic factor for PFS by multivariate analysis (hazard ratio, 4.9 [95% confidence interval, 1.3-18], P = 0.018). Grade 2 or higher late toxicities were observed in nine patients (17%). Two patients (4%) each had grade 3 proctitis and grade 3 ileus, respectively. No grade 4 toxicity or treatment-related death was observed. The results suggest that IMRT with the CS technique allows a high local control without increasing the risk of complications for cervical cancer patients.
我们旨在研究子宫颈癌患者采用中央屏蔽(CS)技术的调强放疗(IMRT)的结果和毒性。这项回顾性研究纳入了 54 例国际妇产科联合会(FIGO)IB-IVA 期癌症患者。采用螺旋断层放疗(HT)进行全盆腔放疗或扩展野放疗,剂量为 50.4Gy,共 28 次。6 例患者有腹主动脉旁淋巴结转移。在总剂量达到 28.8-41.4Gy 后,采用 HT 实施 CS 技术以降低直肠和膀胱的剂量。腔内近距离放疗的处方剂量主要为 18-24Gy,在 A 点处分为 3 或 4 次。47 例患者(87%)采用了同期化疗。中位随访时间为 56 个月。17 例患者(31%)出现复发。宫颈复发见于 2 例患者(4%)。局部区域控制、无进展生存期(PFS)和总生存期的 5 年率分别为 79%、66%和 82%。在评估的多个因素中,多因素分析显示腺癌的组织学类型仅为 PFS 的一个显著不良预后因素(风险比,4.9[95%置信区间,1.3-18],P=0.018)。9 例患者(17%)出现 2 级或以上晚期毒性。分别有 2 例患者(4%)各出现 3 级直肠炎和 3 级肠梗阻。未观察到 4 级毒性或与治疗相关的死亡。结果表明,对于宫颈癌患者,采用 CS 技术的 IMRT 可实现高局部控制率,而不会增加并发症的风险。