Clinical outcomes using a 3D printed tandem-needle-template and the EMBRACE-II planning aims for image guided adaptive brachytherapy in locally advanced cervical cancer

被引:8
|
作者
Cobussen, Anne [1 ,2 ,4 ]
Petric, Primoz [1 ,3 ]
Wulff, Christian Nielsen [1 ]
Buus, Simon [1 ]
Spejlborg, Harald [1 ]
Nielsen, Soren Kynde [1 ]
Traberg, Anders [1 ]
Meisner, Bjarne [1 ]
Hokland, Steffen [1 ]
Lindegaard, Jacob Christian [1 ]
机构
[1] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
[2] MAASTRO Clin, Dept Radiat Oncol, Maastricht, Netherlands
[3] Zurich Univ Hosp, Dept Radiat Oncol, Zurich, Switzerland
[4] MAASTRO, Dept Radiat Oncol, Doctor Tanslaan 12, NL-6229 ET Maastricht, Netherlands
关键词
Cervical cancer; image guided adaptive brachytherapy; 3d-printing; interstitial; treatment individualization; DOSE-RATE BRACHYTHERAPY; WORKING GROUP; COMBINED INTRACAVITARY; MRI; APPLICATORS; PARAMETERS; IMPROVES; VOLUME; RECOMMENDATIONS; RADIOTHERAPY;
D O I
10.1080/0284186X.2023.2246642
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Extensive local disease or narrow vagina may compromise brachytherapy (BT) in patients with cervical cancer. This is the first study to analyze long-term outcomes of using 3D printed vaginal tandem-needle templates (3DP TNT) for transvaginal insertion of needles in parallel (P) or parallel and oblique (P & O) direction to the tandem.Material and methods: All patients treated with BT using 3DP TNT from 2015-2020 were included. Decision to use a 3DP TNT and preplanning were made after 4-5 weeks of external beam radiotherapy, based on gynecological examination and MRI with a tandem-ring applicator in situ. The TNT was 3D-printed in house consisting of a circular template with P & O holes for guidance of plastic needles and a shaft fitting the uterine tandem. Thus, the radioactive source was never in direct contact with the 3DP TNT. The TNT was 3D printed in a standard or personalized configuration. Planning aims were based on the Embrace II protocol.Results: 101 patients (median age of 63 years) were included: 49 with P needles only and 52 with P & O needles. Personalized TNT was used in 19 patients in the P & O group. Performance status (WHO) was > 0 in 48%. FIGO(2018) stage III-IV was present in 77%. T-score at diagnosis and BT was 9.1 and 6.3 respectively, with a significantly higher T-score in the P & O compared to P group. The mean high-risk CTV D90 was 93 Gy with no significant difference between the two groups. Three-year local control rates were 85%, 95%, 75% for the overall, P- and P & O group respectively and 68%, 80% and 56% for cancer specific survival. Grade & GE;3 treatment related complications were observed in 10 (10%) patients.Conclusions: 3DP TNT for BT in cervical cancer provides successful management of very extensive local disease and/or unfavorable anatomy with the possibility for treatment individualization.
引用
收藏
页码:1470 / 1478
页数:9
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