Abstract

Introductionconjunctival melanomas have high local relapse rates. Oncologic and visual outcomes can be improved with proton therapy and no-touch surgery.Material and methodsa monocentric retrospective study of consecutive patients treated with surgery and proton therapy for conjunctival melanoma was conducted. Proton therapy was performed to a total dose of 45 Grays physical dose delivered in eight fractions over two weeks.ResultsNinety-two patients were included. The mean age was 63-year-old. 65.2% of patients had primary acquired melanosis. The mean tumor thickness and diameter was 2.5 mm and 7.0 mm respectively. The clinical stage was T1 in 71.6% of cases, with a quadrangular involvement of more than 90° in 69% of cases. Conjunctival melanomas were of epithelioid cell-type in 40% of cases. Mean follow-up was 4.7 years. Five-year local failure rate was 33.2%. Of 25 local recurrences, 14 were marginal/out-of-field, 4 in-field, others were undetermined. First surgery at expert center resulted in 24.3% of local failure at 5 years versus 38.7% if performed elsewhere (p = 0.41). Salvage exenteration was performed in 13 patients. Tumor stage and quadrangular involvement were significant factors for local failure. Five-year progression-free survival and cause-specific death rates were 61.5 and 3.6%. Stage and epithelioid type were associated with poorer progression-free survival. Trophic toxicity occurred in 22.9% of patients and was treated locally, with grafts in 7 patients. Glaucoma and cataract occurred in 13 and 22 patients respectively. Prognostic factors for visual deterioration were age, tumor extent (multifocality, quadrangular involvement > 180°) and cryotherapy.Conclusions5-year local failure rate after postoperative proton therapy for conjunctival melanoma was of 33.2%. Radiation-induced complications were overall manageable.

Highlights

  • Conjunctival melanomas are rare but deadly tumors of the ocular surface

  • Conjunctival melanomas were of epithelioid cell-type in 40% of cases

  • We evaluated the patterns of failure, progression-free survival and prognostic factors, toxicity and visual outcomes in patients with conjunctival melanomas referred to our tertiary-care institution and all treated with surgery and proton therapy

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Summary

Introduction

Conjunctival melanomas are rare but deadly tumors of the ocular surface. Substantial increase in incidence of conjunctival melanoma has been reported in the last decades with up to 0.8 cases per million inhabitants [1, 2] in Caucasians. There is some racial and Thariat et al Radiation Oncology (2019) 14:239 margins without touching the tumor [7, 8]. It may be associated with absolute alcohol corneal epitheliectomy in case of corneal involvement and cryotherapy of the cut conjunctival edge [9, 10]. Adjuvant conjunctival radiotherapy can be performed using proton therapy, brachytherapy or electron beam radiation therapy [12,13,14,15]

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