Department of Radiation Oncology, University Hospital, LMU Munich, Germany.
Department of Radiation Oncology, University Hospital, LMU Munich, Germany.
Gynecol Oncol. 2022 Sep;166(3):576-581. doi: 10.1016/j.ygyno.2022.06.019. Epub 2022 Jun 25.
The aim of this study was to evaluate the clinical outcome in locally advanced cervical cancer (LACC) after image-guided adaptive brachytherapy (IGABT) with combined intracavitary and interstitial (IC/IS) techniques using the hybrid Venezia applicator (Elekta AB, Sweden).
LACC patients (UICC Stage IIB - IVB) treated with radiochemotherapy followed by IGABT with the hybrid IC/IS Venezia applicator at a single institution were retrospectively analyzed. Treatment comprised EBRT of the pelvis with 45 Gy and concomitant weekly cisplatin chemotherapy (40 mg/m) followed by MRI-based IGABT. Dosimetry, oncological outcome and toxicity were investigated.
Forty-six patients underwent a total of 184 fractions of IGABT between 2017 and 2020. Median follow-up was 24 months. Combined IC/IS techniques were used in 40 patients (87%). The median HRCTV volume was 31.2 cm and the median HRCTV D was 92.3 Gy (EQD2). The median D was 74.8 Gy for bladder, 57.9 Gy for rectum, 60.0 Gy for sigmoid and 52.2 Gy for bowel (EQD2). The 3-yr actuarial rates were 97.6% for local control, 97.6% for pelvic control, 59.9% for distant metastasis-free survival and 81.6% for overall survival. The crude rate for G2 and G3 late toxicity was 21.7% and 4.3%.
IGABT with the hybrid Venezia applicator and a pronounced use of a combined IC/IS technique achieved high target doses, while maintaining low doses to organs at risk, leading to excellent local control and overall survival rates with acceptable toxicity.
本研究旨在评估采用混合 Venezia 施源器(Elekta AB,瑞典)联合腔内和间质(IC/IS)技术的图像引导自适应近距离放疗(IGABT)在局部晚期宫颈癌(LACC)患者中的临床疗效。
回顾性分析在一家机构接受放化疗后行 IGABT 治疗的 LACC 患者(UICC 分期 IIB-IVB)。治疗包括盆腔外照射 45 Gy 并同期每周给予顺铂化疗(40mg/m),随后行基于 MRI 的 IGABT。评估剂量学、肿瘤学结局和毒性。
2017 年至 2020 年期间,46 例患者共行 184 次 IGABT。中位随访时间为 24 个月。40 例患者(87%)采用了联合 IC/IS 技术。中位 HRCTV 体积为 31.2cm,HRCTV D 为 92.3Gy(EQD2)。膀胱 D 中位值为 74.8Gy,直肠为 57.9Gy,乙状结肠为 60.0Gy,肠道为 52.2Gy(EQD2)。3 年局部控制、盆腔控制、无远处转移生存和总生存的累积率分别为 97.6%、97.6%、59.9%和 81.6%。G2 和 G3 级晚期毒性的发生率分别为 21.7%和 4.3%。
采用混合 Venezia 施源器和联合腔内和间质技术的 IGABT 可实现高靶区剂量,同时保持对危及器官的低剂量,从而获得优异的局部控制率和总生存率,毒性可接受。