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Volume 114, Issue 12, Pages 2309-2315.e2 (December 2007)


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Incidence of Uveal Melanoma in Europe

Gianni Virgili, MD1Corresponding Author Informationemail address, Gemma Gatta, MD2, Laura Ciccolallo, MSc2, Riccardo Capocaccia, MSc3, Annibale Biggeri, MD45, Emanuele Crocetti, MD6, Jean-Michel Lutz, MD7, Eugenio Paci, MD6, EUROCARE Working Group

Received 28 July 2006; received in revised form 29 January 2007; accepted 31 January 2007. published online 10 May 2007.

Purpose

To estimate incidence rates of uveal melanoma in Europe from 1983 to 1994.

Design

Incidence analysis of data from cancer registries adhering to the European Cancer Registry–based study on survival and care of cancer patients (EUROCARE) (cases diagnosed from 1983 to 1994).

Participants

Data of 6673 patients with ocular melanoma (as defined by International Classification of Diseases for Oncology morphology codes 8720 to 8780 [melanoma] and International Classification of Diseases 9 (ICD9) codes 190.0 [iris and ciliary body], 190.5 [retina], 190.6 [choroid], and 190.9 [unspecified ocular location]) from 33 cancer registries of 16 European countries.

Methods

Incidence rate ratios (IRRs) were obtained from a multilevel Poisson regression model.

Main Outcome Measures

Incidence rates and IRRs associated with demographic and geographic variables.

Results

Standardized incidence rates increased from south to north across registries, from a minimum of <2 per million in registries of Spain and southern Italy up to >8 per million in Norway and Denmark. The inclusion of tumors with unspecified ocular location (code 190.9) increased incidence rates in most United Kingdom registries, but not in the other geographic areas, where this code was seldom used for uveal melanomas. Incidence increased noticeably up to age 55 (IRR, 1.46 per 5 years; 95% confidence interval [CI], 1.36–1.57) but leveled off after age 75 (IRR, 0.99 per 5 years; 95% CI, 0.93–1.05), with intermediate levels midway (IRR, 1.18 per 5 years; 95% CI, 1.12–1.23). It was also higher in males (IRR, 1.22; 95% CI, 1.16–1.28). Rates were stable during the study period, but a cohort effect was evidenced, accounting for higher incidence rates in people born during the period 1910 to 1935 (P = 0.005). Incidence increased with latitude (P = 0.008), which explained most differences in rates among areas.

Conclusions

In this large series of uveal melanomas, we found stable incidence during the years 1983 to 1994. The north-to-south decreasing gradient supports the protective role of ocular pigmentation. European ophthalmologists should develop guidelines to standardize the coding of tumors treated conservatively using the ICD classification to improve the registration and surveillance of uveal melanoma by cancer registries.

Available online: May 10, 2007.

1 Department of Ophthalmology, University of Florence, Florence, Italy.

2 Epidemiology Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.

3 Laboratory of Epidemiology, Istituto Superiore di Sanità, Rome, Italy.

4 Department of Statistics “G. Parenti,” University of Florence, Florence, Italy.

5 Biostatistics Unit, Center for Study and Prevention of Cancer, Scientific Institute, Tuscany Region, Florence, Italy.

6 Clinical and Descriptive Epidemiology Unit, Center for Study and Prevention of Cancer, Scientific Institute, Tuscany Region, Florence, Italy.

7 Registre Genevois des Tumeurs, Geneva, Switzerland.

Corresponding Author InformationCorrespondence to Gianni Virgili, Department of Oto-Neuro-ophthalmological Surgical Sciences, University of Florence, Viale Morgagni 85, Florence 50134, Italy.

 Manuscript no. 2006-833.

Research supported by the EUROCARE-3 BIOMED-2 program, Brussels, Belgium (contract no. BMH4-CT98-3390); Compagnia di San Paolo, Torino, Italy; and European Community, Brussels, Belgium (grant no. SPC.2002303-DEP/01/19, “European Network of Cancer Registries: Survival of Adult Patients with Rare Tumors”). Dr Virgili’s work was partially supported by the Master of Epidemiology, University of Turin, Turin, Italy.

 For a list of the members of the Group, see “Appendix” (available at http://aaojournal.org).

PII: S0161-6420(07)00176-5

doi:10.1016/j.ophtha.2007.01.032


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