Obesity paradox in uveal melanoma: high body mass index is associated with low metastatic risk

Br J Ophthalmol. 2024 Mar 20;108(4):578-587. doi: 10.1136/bjo-2022-322877.

Abstract

Background: Metabolic factors and obesity may influence the development and progression of cancer. In this study, we examine their association with the risk of developing metastases of uveal melanoma.

Methods: Data on metabolic factors, medications, serum leptin levels, tumour leptin receptor RNA expression and clinical outcomes were examined in three cohorts. HRs for metastasis and cumulative incidences of melanoma-related mortality were calculated, and the levels of tumour leptin receptor expression were compared with prognostic factors including BAP1 mutation, and tumour cell morphology.

Results: Of 581 patients in the main cohort, 116 (20%) were obese and 7 (1 %) had metastatic disease at presentation. In univariate Cox regressions, tumour diameter, diabetes type II and use of insulin were associated with metastases, but patients with obesity had a lower risk. The beneficial prognostic implication of obesity was retained in multivariate regressions. In competing risk analyses, the incidence of melanoma-related mortality was significantly lower for patients with obesity. Serum leptin levels≥median were associated with a reduced risk for metastasis, independent of patient sex and cancer stage in a separate cohort (n=80). Similarly, in a third cohort (n=80), tumours with BAP1 mutation and epithelioid cells had higher leptin receptor RNA expression levels, which have a negative correlation with serum leptin levels.

Conclusion: Obesity and elevated serum leptin levels are associated with a lower risk for developing metastases and dying from uveal melanoma.

Keywords: Choroid; Epidemiology; Neoplasia; Pathology.

MeSH terms

  • Body Mass Index
  • Humans
  • Leptin
  • Melanoma* / pathology
  • Obesity / complications
  • Obesity Paradox
  • Prognosis
  • RNA
  • Receptors, Leptin / genetics
  • Tumor Suppressor Proteins
  • Uveal Neoplasms* / pathology

Substances

  • Leptin
  • Receptors, Leptin
  • Tumor Suppressor Proteins
  • RNA

Supplementary concepts

  • Uveal melanoma