Volume 118, Issue 1 pp. 185-188
Epidemiology

Elevation of thyroid cancer risk among cutaneous melanoma survivors

William Goggins

William Goggins

Centre for Epidemiology and Biostatistics, School of Public Health, Chinese University of Hong Kong, Hong Kong, China

Search for more papers by this author
Gilbert H. Daniels

Gilbert H. Daniels

Thyroid Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA

Search for more papers by this author
Hensin Tsao

Corresponding Author

Hensin Tsao

Department of Dermatology, Massachusetts General Hospital, Boston, MA, USA

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA, USA

Fax: +617-724-2745.

Department of Dermatology, Massachusetts General Hospital, Bartlett 622, 48 Blossom Street, Boston, MA 02114Search for more papers by this author
First published: 26 October 2005
Citations: 23

Abstract

Recent molecular studies have identified recurrent BRAF mutations in both cutaneous melanoma and thyroid malignancies. This relatively selective shared genetic vulnerability raises the possibility that these 2 tumors are connected through a common undisclosed pathogenic mechanism. To assess for possible associations between these 2 genetically related tumors at the population level, we calculated standardized incidence ratios (SIRs) for thyroid cancer (TC) among cutaneous melanoma (CM) survivors and CM among TC survivors using the National Cancer Institute's Surveillance, Epidemiology and End Result (SEER) database. Between 1973 and 2000, there were 73,274 and 27,138 cases of CM and TC cases, respectively. Overall, we found a 2.17-fold increase (p < 0.0000001) in the risk of TC after a diagnosis of CM. This augmented risk of TC is somewhat higher for males, for those diagnosed more recently and for the first 3 years after the CM diagnosis. We also detected a considerably smaller and borderline significant increased risk of CM (25%, p = 0.063) among the post-TC survivors. Of note, TC patients who received radiation therapy had a 57% increased risk of a subsequent CM (p = 0.034). Our study documents a strong unilateral risk of TC after CM. More studies are clearly needed to better delineate this mechanism. © 2005 Wiley-Liss, Inc.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.