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A novel free-assembled template for interstitial brachytherapy of locally advanced cervical cancer: a dosimetric study

医学 近距离放射治疗 放射科 外科肿瘤学 核医学 放射治疗 医学物理学 宫颈癌 梅德林 肿瘤分期
作者
Ranxi Liang,Qian Peng,Gaoshu Yan,Jiabao Ma,Dandan Huang,bin bi,Ting Tang,Shun Lu,Xianliang Wang,Yan Tan,Jie Zhu
出处
期刊:BMC Cancer [BioMed Central]
标识
DOI:10.1186/s12885-026-17241-2
摘要

The application of guidance template in interstitial brachytherapy (ISBT) was expected to improve target coverage and sparing organs at risk for locally advanced cervical cancer (LACC). The purpose of this study was to compare dosimetric and procedural outcomes of template-guided ISBT against free-handed ISBT. Consecutive patients with the International Federation of Gynecology and Obstetrics (FIGO) 2018 stage of IB3, IIA2, and IIB to IVA were prospectively enrolled at Sichuan Cancer Hospital from February to September 2025. A novel 3D-printed free-assembled interstitial template (FAIT), featuring a tandem with optimized non-coplanar needle channels, was invented and utilized for ISBT. Each patient underwent both FAIT-guided and free-handed high-dose-rate ISBT within 3 days with a random sequence. Treatment plans were generated in the Oncentra planning system with a 600 cGy prescription, and dosimetric parameters including high-risk clinical target volume (HRCTV) D 90 , dose of organs at risk (OARs) (D 1cc and D 2cc for bladder, rectum, sigmoid and bowel) were extracted. The number of interstitial needles and implantation time were also recorded. Data were presented as mean ± standard deviation and compared using paired Student’s t -tests. Statistical significance was defined as P < 0.05. Fifty-five patients received both FAIT-guided and free-handed ISBT procedures after pelvic external beam radiotherapy (EBRT) of 45–50.4 Gy with 25–28 fractions. Most patients were stage ⅡB ( n = 34, 61.8%) and squamous cell carcinoma ( n = 49, 89.1%), and mean post-EBRT HRCTV volume was 61.8 ± 21.3 cm 3 . There was no significant difference on the number of needles used in FAIT-guided and free-handed ISBTs (4.88 ± 0.90 vs. 4.76 ± 1.24, P = 0.30). FAIT guidance shortened implantation time (5.83 ± 1.93 vs. 8.03 ± 2.71 min, P < 0.0001) and achieved higher HRCTV D 90 (611.38 ± 35.12 vs. 580.86 ± 64.65 cGy, P < 0.01), with similar OAR doses ( P > 0.05). Improved target volume dose coverage and shortened needle implantation time were achieved with the application of the novel 3D-printed FAIT in ISBT. This novel template had high clinical utility and was worthy of further promotion and application.
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