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局部晚期宫颈癌应用混合施源器行腔内/间质近距离放疗的临床疗效。

Clinical outcome of combined intracavitary / interstitial brachytherapy using a hybrid applicator in locally advanced cervical cancer.

机构信息

Department of Radiation Oncology, University Hospital, LMU Munich, Germany.

Department of Radiation Oncology, University Hospital, LMU Munich, Germany.

出版信息

Gynecol Oncol. 2022 Sep;166(3):576-581. doi: 10.1016/j.ygyno.2022.06.019. Epub 2022 Jun 25.

Abstract

OBJECTIVE

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).

METHODS

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.

RESULTS

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%.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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%。

结论

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。

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