AI Article Synopsis

  • Stereotactic radiotherapy (SRT) is being tested as a treatment for choroidal melanoma (CM) located near the optic nerve, with a focus on preserving vision while maintaining survival rates.
  • The study involved 20 patients and monitored outcomes like metastasis-free survival and visual acuity over a median follow-up of 5.1 years, with promising results showing high rates of both metrics.
  • Findings suggest that meaningful vision was preserved in a significant portion of patients, and the reduced-dose SRT approach is worth further exploration.

Article Abstract

Introduction: Stereotactic radiotherapy (SRT) is used for choroidal melanoma (CM) abutting the optic nerve. Visual acuity (VA) deterioration to ≤6/60 is common. We report a pilot study of reduced-dose SRT using 2 Gy/day, aiming to preserve vision without compromising survival.

Method: 60 Gy SRT was delivered in 30 fractions over 6 weeks. Liver metastasis surveillance was annual ultrasound. The primary endpoint was 5-year metastasis-free survival (5yMFS). Secondary endpoints were 2-year freedom from local progression (2yFFLP), VA, enucleation rate, and radiation toxicity.

Results: Twenty adults aged ≤70 years with T1-T2M0 CM without diabetes mellitus were enrolled. Median follow-up was 5.1 years. About 85% and 90% of tumours were ≤3 mm of the macula and optic disc, respectively. Median tumour height was 2.2 mm (range 1.0-4.4 mm), and median basal diameter was 8.2 mm (range: 4.3-15.0 mm). 5yMFS was 88% (95% CI: 61-97), and the 2yFFLP rate was 90% (95%: CI 66-97). There were three enucleations for disease progression. Final VA in retained eyes was ≥6/7.5 in 6 (30%), 6/9 to 6/12 in 5 (25%), 6/15 to 6/48 in 2 (10%), and ≤6/60 in 4 (20%) eyes. Retinopathy was the main cause of vision loss besides tumour progression.

Conclusion: Meaningful vision was preserved 5 years after SRT, despite high-risk tumour locations for vision loss. 2yFFLP and 5yMFS were acceptable. This dose fractionation warrants further investigation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11178344PMC
http://dx.doi.org/10.1159/000538022DOI Listing

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