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Survival of patients with recurrent uveal melanoma after treatment with radiation therapy
  1. Anne M Lane,
  2. Caleb Hartley,
  3. Ashley K Go,
  4. Frances Wu,
  5. Evangelos S Gragoudas,
  6. Ivana K Kim
  1. Ocular Melanoma Center, Retina Service, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, USA
  1. Correspondence to Ms Anne M Lane, Ocular Melanoma Center, Retina Service, Massachusetts Eye and Ear, Boston, Massachusetts, USA; alane{at}meei.harvard.edu

Abstract

Background/aims We evaluated a large cohort of patients treated for local recurrence of choroidal or ciliary body melanomas at the Massachusetts Eye and Ear (MEE) to quantify the risk of melanoma-related mortality associated with recurrence, independent of other risk factors.

Methods Patients treated with radiation therapy from 1982 to 2017 were identified through the Uveal Melanoma Registry at MEE. Competing risks regression was performed to investigate the risk of melanoma-related mortality associated with recurrence, treating recurrence as a time-varying covariate.

Results Of 4196 patients treated, 4043 patients remained recurrence-free and 153 patients experienced a recurrence (median follow-up: 9.9 years). Median time from initial treatment to recurrence was 30.5 months (range: 2.0–238.7). Seventy-nine (69.9%) patients with recurrences and 826 (37.9%) patients in the recurrence-free group died of metastatic uveal melanoma (p<0.001). Median time from initial treatment to melanoma-related death was 4.9 years (1.0–31.8) for patients who developed recurrences and 4.3 years (0.59–33.8) for patients who did not (p=0.17). Five-year and 10-year probabilities of melanoma-related mortality were 9.5% and 15.0%, respectively, in patients without local recurrences compared with 32.0% and 46.6% in patients with recurrences (p<0.001).

Conclusion These data confirm previous reports that local recurrence is associated with an increased risk of dying of melanoma and quantify the risk that can be attributed to local recurrence independent of other risk factors. This group of patients should be strongly considered for adjuvant therapies when available.

  • Choroid
  • Neoplasia

Data availability statement

Data are available upon reasonable request. Data are available upon reasonable request. Deidentified data are stored in the Uveal Melanoma Repository at MassEye and Ear. Any requests to access these data would require Institutional Review Board approval.

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Data availability statement

Data are available upon reasonable request. Data are available upon reasonable request. Deidentified data are stored in the Uveal Melanoma Repository at MassEye and Ear. Any requests to access these data would require Institutional Review Board approval.

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Footnotes

  • Contributors Study conception and design: AML, ESG, IKK; data acquisition: CH and AKG; analysis and/or interpretation of results: AML, ESG, FW, IKK; manuscript preparation and feedback: AML, CH, AKG, ESG, FW, IKK; guarantor: IKK.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests Dr. Kim receives research support from Aura Biosciences and Allergan and is a consultant for Castle Biosciences. Dr. Gragoudas is a consultant for Aura Biosciences.Ms. Lane, Mr. Hartley, Ms. Go, and Dr. Wu have no competing interests to disclose.

  • Provenance and peer review Not commissioned; externally peer reviewed.