Clinical utility of skin cancer and melanoma risk scores for population screening: TRoPICS study

被引:6
作者
Shetty, A. [1 ]
Janda, M. [2 ]
Fry, K. [1 ]
Brown, S. [1 ]
Yau, B. [3 ]
Von Schuckmann, L. [1 ,3 ]
Thomas, S. [3 ]
Rayner, J. E. [1 ,3 ]
Spelman, L. [3 ]
Wagner, G. [3 ]
Jenkins, H. [3 ]
Lun, K. [3 ]
Parbery, J. [3 ]
Soyer, H. P. [1 ]
Neale, R. E. [4 ]
Green, A. C. [4 ]
Whiteman, D. C. [4 ]
Olsen, C. M. [1 ,4 ]
Khosrotehrani, K. [1 ]
机构
[1] Univ Queensland, UQ Diamantina Inst, Brisbane, Qld, Australia
[2] Univ Queensland, Ctr Hlth Serv Res, Brisbane, Qld, Australia
[3] Queensland Skin & Canc Fdn, Queensland Inst Dermatol, Brisbane, Qld, Australia
[4] QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
PREDICTION;
D O I
10.1111/jdv.17062
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Screening for skin cancer can be cost-effective if focused on high-risk groups. Risk prediction tools have been developed for keratinocyte cancers and melanoma to optimize advice and management. However, few have been validated in a clinical setting over the past few years. Objectives To assess the clinical utility of risk assessment tools to identify individuals with prevalent skin cancers in a volunteer-based screening clinic. Methods Participants were adults presenting for a skin check at a volunteer-based skin cancer screening facility. We used previously published tools, based on questionnaire responses, to predict melanoma and keratinocyte cancers [KCs; basal cell carcinoma (BCC) and squamous cell carcinoma (SCC)] and classified each participant into one of five risk categories. Participants subsequently underwent a full skin examination by a dermatologist. All suspicious lesions were biopsied, and all cancers were histopathologically confirmed. Results Of 789 people who presented to the clinic, 507 (64%) consented to the study. Twenty-two BCCs, 19 SCCs and eight melanomas were diagnosed. The proportion of keratinocyte cancers diagnosed increased according to risk category from <1% in the lowest to 24% in the highest risk category (P < 0.001). Subtype analysis revealed similar proportionate increases in BCC or SCC prevalence according to risk category. However, a similar proportion of melanoma cases were detected in the low-risk and high-risk groups. Conclusion The risk prediction model for keratinocyte cancers can reliably identify individuals with a significant skin cancer burden prior to a skin examination in the community setting. The prediction tool for melanoma needs to be tested in a larger sample exposed to a wider range of environmental risk factors.
引用
收藏
页码:1094 / 1098
页数:5
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