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. 2020 May;6(3):210-218.
doi: 10.1159/000504312. Epub 2019 Dec 11.

Practice Patterns for the Treatment of Uveal Melanoma with Iodine-125 Plaque Brachytherapy: Ocular Oncology Study Consortium Report 5

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Practice Patterns for the Treatment of Uveal Melanoma with Iodine-125 Plaque Brachytherapy: Ocular Oncology Study Consortium Report 5

Christina Binder et al. Ocul Oncol Pathol. 2020 May.

Abstract

Background: Treatment planning for I-125 plaque therapy for uveal melanoma has advanced significantly since the Collaborative Ocular Melanoma Study trial, with more widely available image-guided planning and improved dosimetry.

Objective: We evaluated real-world practice patterns for I-125 plaque brachytherapy in the United States by studying practice patterns at centers that comprise the Ocular Oncology Study Consortium (OOSC).

Methods: The OOSC database and responses to a treatment practice survey were evaluated. The database contains treatment information from 9 institutions. Patients included in the database were treated between 2010 and 2014. The survey was conducted in 2018 and current treatment planning methods and prescriptions were queried.

Results: Examination of the OOSC database revealed that average doses to critical structures were highly consistent, with the exception of one institution. Survey responses indicated that most centers followed published guidelines regarding dose and prescription point. Dose rate ranged from 51 to 118 cGy/h. As of 2018, most institutions use pre-loaded plaques and fundus photographs and/or computed tomography or magnetic resonance imaging in planning.

Conclusions: While there were differences in dosimetric practices, overall agreement in plaque brachytherapy practices was high among OOSC institutions. Clinical margins and planning systems were similar among institutions, while prescription dose, dose rates, and dosimetry varied.

Keywords: Brachytherapy; Treatment practices; Uveal melanoma.

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Conflict of interest statement

P.M.: consultant − Castle Biosciences, Optos Inc.; personal fees − Santen, Spark Therapeutics. J. William Harbour: consultant and royalties − Castle Biosciences. Miguel Materin and A.C.S.: consultant − Castle Biosciences. Thomas Aaberg Jr.: consultant − Castle Biosciences, Alcon, Baush, and Lomb, True Vision, Regeneron. Peter Hovland: advisory panel − Castle Biosciences. D.G.K.: scientific advisory board, own equity, and royalties − Lumicell Inc., co-founder and own equity − XRAD therapeutics. Research support: Merck, Eli Lilly, and Bristol-Myers Squibb. Jesse Berry: consultant − Immunocore. A.H.S.: consultant − Castle Biosciences, Immunocore. The other authors have no conflicts of interest to disclose.

Figures

Fig. 1
Fig. 1
Choice of plaque size and clinical margin. a Plaque size increases with largest basal diameter. Mean and SD are shown. b There is no difference in clinical margin per plaque size. Mean and SD are shown. c 2–3 mm is the most common clinical margin, and ≤2 and 3–4 mm are also prevalent. d Peripapillary lesions were treated with the largest clinical margins.

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