The rate of increase in the numbers of primary sporadic basal cell carcinomas during follow up is associated with age at first presentation.

Basal cell carcinoma (BCC) patients demonstrate marked variation in tumour numbers and site. Previous studies also show an association between age at first BCC presentation and development of BCC on the trunk. In this study we have investigated the association between age at first presentation and the rate of development of truncal and non-truncal tumours in 747 patients with BCC. We used negative binomial regression analysis to show that increasing age at first presentation was associated with an increased rate of BCC development (rate ratio 1.01/year, 95% CI 1.01-1.02, P < 0.001). In particular, development of tumours was greater in cases aged 60.0-69.9, 70.0-79.9 and 80.0-89.9 years than in those 40.0-49.9 years (P = 0.05, 0.01 and 0.039, respectively). While few cases aged over 70 years of age first present with a truncal BCC, the numbers of BCC/year were greater than in those with a head/neck BCC. The data suggest different genetic factors mediate the appearance of BCC in patients of different ages particularly those aged above and below 60 years.

[1]  R. Westendorp,et al.  Differences in age, site distribution, and sex between nodular and superficial basal cell carcinoma indicate different types of tumors. , 1998, The Journal of investigative dermatology.

[2]  R. Strange,et al.  Models for determining genetic susceptibility and predicting outcome. , 2002, Methods in molecular biology.

[3]  G. Wilson,et al.  Aggressive basal cell carcinoma in young patients: fact or fiction? , 2000, British Journal of Plastic Surgery.

[4]  H. Mukhtar Skin Cancer: Mechanisms and Human Relevance , 1994 .

[5]  N. Cox,et al.  Basal cell carcinoma in young adults , 1992, The British journal of dermatology.

[6]  Andrew G Smith,et al.  Presentation with multiple cutaneous basal cell carcinomas: association of glutathione S-transferase and cytochrome P450 genotypes with clinical phenotype. , 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[7]  J. Lear,et al.  Truncal site and detoxifying enzyme polymorphisms significantly reduce time to presentation of further primary cutaneous basal cell carcinoma. , 1997, Carcinogenesis.

[8]  A. Aupérin,et al.  Basal Cell Carcinoma in Young Adults: Not More Aggressive than in Older Patients , 1999, Dermatology.

[9]  R. Strange,et al.  Risk Factors for Basal Cell Carcinoma in the UK: Case-Control Study in 806 Patients , 1997, Journal of the Royal Society of Medicine.

[10]  H. Tsou,et al.  Role of PTCH and p53 genes in early-onset basal cell carcinoma. , 2001, The American journal of pathology.

[11]  Andrew G Smith,et al.  Basal cell carcinoma , 2000, Cancer.

[12]  J. Klotz,et al.  Statistical methods for the analysis of tumor multiplicity data. , 1981, Cancer research.

[13]  R. Corona,et al.  p53 mutations and chromosome instability in basal cell carcinomas developed at an early or late age. , 1997, Cancer research.

[14]  J. Lear,et al.  Cutaneous basal cell carcinomas , 2001, Cancer.

[15]  L Grossman,et al.  DNA repair and aging in basal cell carcinoma: a molecular epidemiology study. , 1993, Proceedings of the National Academy of Sciences of the United States of America.