Risk of cancer in patients with biopsy-proven giant cell arteritis

Objective. Results of previous studies investigating the association between GCA and malignancy are conflicting. We performed a study of the risk of cancer in patients with biopsy-proven GCA. Methods. Patients with biopsy-proven GCA were identified from pathology reports of temporal artery biopsies...

Full description

Saved in:
Bibliographic Details
Published inRheumatology (Oxford, England) Vol. 49; no. 4; pp. 756 - 759
Main Authors Hill, Catherine L., Cole, Antonia, Rischmueller, Maureen, Dodd, Thomas, Coleman, Mark, Tucker, Graeme, Roberts-Thomson, Peter
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.04.2010
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Objective. Results of previous studies investigating the association between GCA and malignancy are conflicting. We performed a study of the risk of cancer in patients with biopsy-proven GCA. Methods. Patients with biopsy-proven GCA were identified from pathology reports of temporal artery biopsies from the major pathology laboratories in South Australia (SA). All subjects with biopsy-proven GCA were linked to the SA Cancer Registry to identify cases of cancer until 31 December 2006. Standardized incidence ratios (SIRs) for cancer were determined using the age- and gender-specific rates for SA. Results. There were 226 cases of biopsy-proven GCA (163 females and 63 males). Thirty-one cases were diagnosed with cancer, following the diagnosis of biopsy-proven GCA. There was no increased risk of cancer among those with biopsy-proven GCA, following the diagnosis of GCA compared with the general population (SIR 1.2; 95% CI 0.8, 1.6). Conclusion. This cohort study did not demonstrate any increased risk for malignancy in subjects with biopsy-proven GCA.
Bibliography:istex:C4AF0A7A10DC4F7386A351C1CDF5C3392D802DEC
ark:/67375/HXZ-F9SHVQDH-7
ArticleID:kep409
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1462-0324
1462-0332
1462-0332
DOI:10.1093/rheumatology/kep409