Development and external validation of a prognostic nomogram for metastatic uveal melanoma

Approximately 50% of patients with uveal melanoma (UM) will develop metastatic disease, usually involving the liver. The outcome of metastatic UM (mUM) is generally poor and no standard therapy has been established. Additionally, clinicians lack a validated prognostic tool to evaluate these patients...

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Veröffentlicht in:PloS one 2015-03, Vol.10 (3), p.e0120181-e0120181
Hauptverfasser: Valpione, Sara, Moser, Justin C, Parrozzani, Raffaele, Bazzi, Marco, Mansfield, Aaron S, Mocellin, Simone, Pigozzo, Jacopo, Midena, Edoardo, Markovic, Svetomir N, Aliberti, Camillo, Campana, Luca G, Chiarion-Sileni, Vanna
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Sprache:eng
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Zusammenfassung:Approximately 50% of patients with uveal melanoma (UM) will develop metastatic disease, usually involving the liver. The outcome of metastatic UM (mUM) is generally poor and no standard therapy has been established. Additionally, clinicians lack a validated prognostic tool to evaluate these patients. The aim of this work was to develop a reliable prognostic nomogram for clinicians. Two cohorts of mUM patients, from Veneto Oncology Institute (IOV) (N=152) and Mayo Clinic (MC) (N=102), were analyzed to develop and externally validate, a prognostic nomogram. The median survival of mUM was 17.2 months in the IOV cohort and 19.7 in the MC cohort. Percentage of liver involvement (HR 1.6), elevated levels of serum LDH (HR 1.6), and a WHO performance status=1 (HR 1.5) or 2-3 (HR 4.6) were associated with worse prognosis. Longer disease-free interval from diagnosis of UM to that of mUM conferred a survival advantage (HR 0.9). The nomogram had a concordance probability of 0.75 (SE .006) in the development dataset (IOV), and 0.80 (SE .009) in the external validation (MC). Nomogram predictions were well calibrated. The nomogram, which includes percentage of liver involvement, LDH levels, WHO performance status and disease free-interval accurately predicts the prognosis of mUM and could be useful for decision-making and risk stratification for clinical trials.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0120181