Effectiveness and causes for failure of surveillance of CDKN2A-mutated melanoma families - 28/07/11
![](/templates/common/images/mail.png)
![](/templates/common/images/entites/lowast.gif)
Abstract |
Background |
For more than 25 years families with an increased susceptibility to melanoma have been under surveillance at our institution.
Objective |
We sought to investigate the effectiveness of surveillance for CDKN2A-mutated families and causes for failure of the program in patients with more advanced tumors.
Methods |
In a retrospective case-control study, Breslow thickness of melanomas diagnosed in relatives enrolled in the surveillance program were compared with melanomas of unscreened index patients. We investigated the influence of mode of detection and length of surveillance interval on outcome.
Results |
Surveillance melanomas (n = 226, median thickness: 0.50 mm) had a significantly lower Breslow thickness (multiplication factor: 0.61 [95% confidence interval 0.47-0.80], P < .001) than index melanomas (n = 40, median thickness: 0.98 mm). Index melanomas were more likely diagnosed with a Breslow thickness greater than 1.0 mm (odds ratio: 3.1 [95% confidence interval 1.2-8.1], P = .022). In all, 53% of surveillance melanomas were diagnosed during regular screens, 7% during patients’ first screen, 20% between regular screens, and 20% in patients who were noncompliant with the surveillance schedule. The majority of surveillance melanomas (58%) were detected within 6 months after the last screen. There was no correlation between tumor thickness and the length of the screening interval for tumors diagnosed within 24 months since the last screen.
Limitations |
The study is retrospective.
Conclusions |
Surveillance was associated with earlier detection of melanomas. Noncompliance was an important cause for failing surveillance. Shortening surveillance intervals may advance detection of tumors, but may paradoxically have little impact on prognosis.
Le texte complet de cet article est disponible en PDF.Key words : dysplastic nevus syndrome, genes, CDKN2A, melanoma, prevention and control
Abbreviations used : CI, LUMC, OR
Plan
Drs Kukutsch and Bergman contributed equally to this article. |
|
Recruitment and acquisition of data on part of the families described in this study was supported by the National Cancer Institute of the US National Institutes of Health, contract number CA83115 and the Dutch Cancer Society (RUL99-1932). |
|
Conflicts of interest: None declared. |
Vol 65 - N° 2
P. 289-296 - août 2011 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?