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Article: Efficacy and feasibility of 3D printed redesigned Venezia™ applicator for treating advanced cervix and recurrent endometrial cancer

TitleEfficacy and feasibility of 3D printed redesigned Venezia™ applicator for treating advanced cervix and recurrent endometrial cancer
Authors
Keywords3D printed applicator
Advanced cervix
Image guided brachytherapy
Interstitial and intracavitary brachytherapy
Recurrent endometrial cancer
Issue Date1-Oct-2023
PublisherScientific Research Publishing
Citation
International Journal of Medical Physics,Clinical Engineering and Radiation Oncology, 2023, v. 114 How to Cite?
Abstract

Purpose: Venezia™ is an interstitial brachytherapy applicator for treating advanced cervical and vaginal vault recurrent cancer. However, there are limitations that lead to suboptimal target coverage. 3D printing introduction allows the redesign of Venezia™ for bulky and irregular-shaped tumors. Methods: This study first describes three new designs included: 1) add-on needles template allowed for an extra layer of straight and oblique needles, 2) redesigned vaginal cap so straight and oblique needles can be used together and 3) redesigned central tube allowed vaginal vault interstitial needle insertion. Drawbacks to original Venezia™ and rationale for using these new designs were discussed. Dosimetric analysis by comparing the original Venezia™ with new design for 10 cases in Oncentra treatment planning system v4.5 (Elekta, Stockholm, Sweden) to observe the dose differences in gross tumor volume (GTV), high risk clinical target volume (HRCTV), intermediate clinical target volume (IRCTV) and organs at risk. Results: For the dosimetric comparison, there were statistically significantly increased median minimal dose to 98% (D98%) of GTV, 90% (D90%) of HRCTV, and IRCTV for the new design with p-value of 0.008, 0.005 and 0.0018, respectively. Comparing the physical dose of D98% of GTV, D90% of HRCTV, and IRCTV when using the new design, it averagely increased by 11.7%, 8.0%, 19.4%, respectively per fraction. Conclusions: Dosimetric comparison revealed the new designs increased the dose to GTV, HRCTV and IRCTV and fulfilled the dose constraints of bladder, rectum and sigmoid. The 3D printed new design is biocompatible, inexpensive and can be patient specific.


Persistent Identifierhttp://hdl.handle.net/10722/347639
ISSN

 

DC FieldValueLanguage
dc.contributor.author Lee, Venus W.Y.-
dc.contributor.authorYip, Winnie W.L.-
dc.contributor.authorTang, Steven Y.K.-
dc.contributor.authorLeung, Mike P.H.-
dc.contributor.authorKwan, Keith K.K.-
dc.contributor.authorLiu, Alex C.H.-
dc.contributor.authorChan, Vincent Ngai Yui-
dc.contributor.authorWu, Jenna W.S.-
dc.contributor.authorCheng, Jean N.S.-
dc.contributor.authorChiang, Chi Leung-
dc.contributor.authorHo-Fun Lee, Victor-
dc.date.accessioned2024-09-26T00:30:18Z-
dc.date.available2024-09-26T00:30:18Z-
dc.date.issued2023-10-01-
dc.identifier.citationInternational Journal of Medical Physics,Clinical Engineering and Radiation Oncology, 2023, v. 114-
dc.identifier.issn2168-5436-
dc.identifier.urihttp://hdl.handle.net/10722/347639-
dc.description.abstract<p>Purpose: Venezia™ is an interstitial brachytherapy applicator for treating advanced cervical and vaginal vault recurrent cancer. However, there are limitations that lead to suboptimal target coverage. 3D printing introduction allows the redesign of Venezia™ for bulky and irregular-shaped tumors. Methods: This study first describes three new designs included: 1) add-on needles template allowed for an extra layer of straight and oblique needles, 2) redesigned vaginal cap so straight and oblique needles can be used together and 3) redesigned central tube allowed vaginal vault interstitial needle insertion. Drawbacks to original Venezia™ and rationale for using these new designs were discussed. Dosimetric analysis by comparing the original Venezia™ with new design for 10 cases in Oncentra treatment planning system v4.5 (Elekta, Stockholm, Sweden) to observe the dose differences in gross tumor volume (GTV), high risk clinical target volume (HRCTV), intermediate clinical target volume (IRCTV) and organs at risk. Results: For the dosimetric comparison, there were statistically significantly increased median minimal dose to 98% (D98%) of GTV, 90% (D90%) of HRCTV, and IRCTV for the new design with p-value of 0.008, 0.005 and 0.0018, respectively. Comparing the physical dose of D98% of GTV, D90% of HRCTV, and IRCTV when using the new design, it averagely increased by 11.7%, 8.0%, 19.4%, respectively per fraction. Conclusions: Dosimetric comparison revealed the new designs increased the dose to GTV, HRCTV and IRCTV and fulfilled the dose constraints of bladder, rectum and sigmoid. The 3D printed new design is biocompatible, inexpensive and can be patient specific.</p>-
dc.languageeng-
dc.publisherScientific Research Publishing-
dc.relation.ispartofInternational Journal of Medical Physics,Clinical Engineering and Radiation Oncology-
dc.subject3D printed applicator-
dc.subjectAdvanced cervix-
dc.subjectImage guided brachytherapy-
dc.subjectInterstitial and intracavitary brachytherapy-
dc.subjectRecurrent endometrial cancer-
dc.titleEfficacy and feasibility of 3D printed redesigned Venezia™ applicator for treating advanced cervix and recurrent endometrial cancer-
dc.typeArticle-
dc.identifier.doi10.1016/j.ejmp.2023.103150-
dc.identifier.pmid37757501-
dc.identifier.scopuseid_2-s2.0-85172313964-
dc.identifier.volume114-
dc.identifier.eissn2168-5444-
dc.identifier.issnl2168-5436-

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