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. 2014 Jun;98(6):769-74.
doi: 10.1136/bjophthalmol-2013-303867. Epub 2013 Oct 29.

Genome-wide profiling is a clinically relevant and affordable prognostic test in posterior uveal melanoma

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Free PMC article

Genome-wide profiling is a clinically relevant and affordable prognostic test in posterior uveal melanoma

Nathalie Cassoux et al. Br J Ophthalmol. 2014 Jun.
Free PMC article

Abstract

Objective: This study investigated the capacity of genetic analysis of uveal melanoma samples to identify high-risk patients and discusses its clinical implications.

Methods: Patients with posterior uveal melanoma were prospectively enrolled. Tumour samples were derived from enucleated globe, fine-needle aspirates or endoresection. Chromosome 3 and 8 status was determined by array comparative genomic hybridisation (array-CGH). Patients were followed after treatment to detect metastasis.

Results: Four groups were classified by array-CGH. Patients were divided into disomy 3 and normal chromosome 8 (D3/8nl), disomy 3 and 8q gain (D3/8g), monosomy 3 and normal chromosome 8 (M3/8nl) and monosomy 3 and 8 or 8q gain (M3/8g). Median follow-up was 28 months (range: 1-147 months). At the end of the study, 128 patients (33.7%) had developed metastasis and 96 patients had died. Univariate Cox proportional hazard analysis showed that factors associated with metastasis included basal tumour diameter p=0.0007, tumour thickness p=0.01, mixed/epithelioid cell type p=0.0009 and genomic data p<0.0001. High-risk profile was more strongly associated with metastasis than the other prognostic factors p<0.001. Multivariate Cox modelling analysis showed that the status of chromosomes 3 and 8 were the only two variables that independently contributed to prognosis: monosomy 3 alone p=0.001 and monosomy 3 and 8q gain p<0.0001.

Conclusions: Array-CGH allowed identification of three prognostic groups with low, intermediate and high risk of developing metastasis. Array-CGH is a reliable and inexpensive method for uveal melanoma prognosis. This method is now currently used in France.

Keywords: Choroid; Diagnostic tests/Investigation; Genetics; Pathology.

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Figures

Figure 1
Figure 1
Four examples of Nimblegen 4×72 K comparative genomic hybridisation-array (array-CGH) profiles. From upper to lower: profiles from D3/8nl, M3/8nl, D3/8nl and M3/8 g groups. In these array-CGH profiles, every point represents the mean level of the probes over 400 kilobases. Chromosome imbalances are presented in log2 ratio.
Figure 2
Figure 2
Metastatic-free interval according to genomic results: M3/8nl (disomy 3, normal ch 8); D3/8g (disomy 3 ch 8 gain); M3/8nl (monosomy 3 normal ch.8) and M3/8g (monosomy 3 and ch 8 gain).

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