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Methods. A total of 4070 patients with primary uveal melanoma [ICD-<br />

O-2] codes C69.3 [choroid], C69.4 [ciliary body and iris], and C69.2<br />

[retina] derived from the Surveillance, Epidemiology, and End Results<br />

(SEER) database. The significance of trends were determined using chisquare<br />

test.<br />

Results. There were 4070 cases of uveal melanoma representing 3.1%<br />

of all recorded cases of melanoma.<br />

The majority of cases (98.3%) were reported by hospitals. Histopathologic<br />

confirmation was available in 72.1% of cases. The mean age-adjusted<br />

incidence was 5.1 per million, with 97.8% of cases occurring in the white<br />

population. No change in the 5-year relative survival rate (81.6%) was<br />

observed.<br />

Conclusions. The age-adjusted incidence (5.1 per million) has remained<br />

unchanged from 1973 to 2008. Despite a shift toward more conservative<br />

treatments, survival has not improved during this time period.<br />

Financial disclosure. None<br />

453 Ump126<br />

FISH: MAKING HEADS OR TAILS OF TECHNIQUES<br />

M. Turell1, R. Tubbs2 , C. Biscotti3 , Y. Sun2, Y. Saunthararajah4, P.<br />

Triozzi 5, A. Singh1 (turellm2@ccf.org)<br />

1. Cole Eye Institute; 2. Department of Molecular Pathology; 3.<br />

Department of Anatomic Pathology; 4. Hematologic Oncology & Blood<br />

Disorders; 5. Solid Tumor Oncology, Cleveland Clinic Foundation,<br />

Cleveland, OH<br />

Purpose. Tumor monosomy 3 confers a poor prognosis in patients<br />

with uveal melanoma. A critical review of the literature pertaining to<br />

techniques and procedures used for fluorescence in situ hybridization<br />

(FISH) detection of monosomy 3 was performed in order to compare<br />

practice patterns across oncology centers worldwide.<br />

Methods. A PubMed literature search was conducted for studies related<br />

to FISH-based uveal melanoma prognostication published between<br />

January 1, 1997 and January 1, 2011.<br />

Results. A total of 29 publications were relevant to this review.<br />

Significant variability was found in both clinical features (tumor size<br />

and location) and the specific FISH techniques that have been used to<br />

assess monosomy 3 status in uveal melanoma. In particular, parameters<br />

including tissue sampling Methods (fresh tissue [n=14], fine-needle<br />

aspiration biopsy [n=6], and paraffin-embedded tissue [n=9]), selection<br />

of FISH probes (centromeric [n=25], locus-specific probes [n=6], whole<br />

chromosome paints [n=2], and unspecified [n=2]), number of cells<br />

counted (range: 40-500), and cut-point (range 5-60%) used to determine<br />

monosomy 3 status varied widely.<br />

Conclusions. FISH to detect monosomy 3 in uveal melanoma has not<br />

been performed in a standardized manner. This likely affects reported<br />

Results and limits Conclusions regarding clinical utility.<br />

Financial disclosure. This work was supported by a Falk Trust grant and a Research to Prevent<br />

Blindness Challenge Grant, Department of Ophthalmology, Cleveland Clinic Lerner College of<br />

Medicine.<br />

116

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