April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
PET/CT for Initial Screening of Metastatic Uveal Melanoma: Analysis of 333 Patients
Author Affiliations & Notes
  • Aurelien Freton
    The New York Eye Cancer Center, New York, New York
  • Kimberley Chin
    The New York Eye Cancer Center, New York, New York
  • Robert Rout
    The New York Eye Cancer Center, New York, New York
  • Lawrence B. Tena
    The Beth Israel Comprehensive Cancer Center, New York, New York
  • Paul T. Finger
    The New York Eye Cancer Center, New York, New York
  • Footnotes
    Commercial Relationships  Aurelien Freton, None; Kimberley Chin, None; Robert Rout, None; Lawrence B. Tena, None; Paul T. Finger, None
  • Footnotes
    Support  Eye Cancer Foundation
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 3285. doi:
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      Aurelien Freton, Kimberley Chin, Robert Rout, Lawrence B. Tena, Paul T. Finger; PET/CT for Initial Screening of Metastatic Uveal Melanoma: Analysis of 333 Patients. Invest. Ophthalmol. Vis. Sci. 2011;52(14):3285.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To report our experience with whole body Positron Emission Tomography/Computed Tomography (PET/CT) screening for metastatic uveal melanoma.

Methods: : 333 consecutive patients were diagnosed with uveal melanoma and underwent screening for metastatic disease with PET/CT and liver function tests. PET/CT results suspicious for metastatic melanoma prompted further biopsies, blood tests, imaging and/or clinical evaluations for confirmation.

Results: : Seven of 333 (2.1%) patients were found to have metastatic choroidal melanoma. Ten (3.3%) were diagnosed with synchronous second cancers and 28 (8.4%) had benign lesions. The most common metastatic sites were liver (n=7), osseous (n=2), lungs, brain, spleen, lymph nodes and subcutaneous tissue (each n=1). Liver function tests were within normal limits in all metastatic patients. Using AJCC-UICC tumor staging criteria, one of the primary tumors was classified as T3, and 6 were T4. By COMS criteria, there was 1 medium and 6 large melanomas. PET/CT significantly improved the yield of metastases detection in T4 tumors in comparison to previous reports.

Conclusions: : Our findings support the use of PET/CT as a screening procedure for metastatic disease in uveal melanoma patients, especially in patients with large tumors that present an increased risk for patent metastatic disease at time of diagnosis.

Keywords: tumors • melanoma • imaging/image analysis: clinical 
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