Cancer Epidemiology and Services Research, Sydney School of Public Health, The University of Sydney, Sydney, New South Wales, Australia.
Sydney School of Public Health, The University of Sydney, Sydney, New South Wales, Australia.
JAMA Dermatol. 2014 Apr;150(4):434-44. doi: 10.1001/jamadermatol.2013.8890.
Currently, there is no comprehensive assessment of melanoma risk prediction models.
To systematically review published studies reporting multivariable risk prediction models for incident primary cutaneous melanoma for adults.
EMBASE, MEDLINE, PREMEDLINE, and Cochrane databases were searched to April 30, 2013. Eligible studies were hand searched and citation tracked. Two independent reviewers extracted information.
Nineteen studies reporting 28 melanoma prediction models were included. The number of predictors in the final models ranged from 2 to 13; the most common were nevi, skin type, freckle density, age, hair color, and sunburn history. There was limited reporting and substantial variation among the studies in model development and performance. Discrimination (the ability of the model to differentiate between patients with and without melanoma) was reported in 9 studies and ranged from fair to very good (area under the receiver operating characteristic curve, 0.62-0.86). Few studies assessed internal or external validity of the models or their use in clinical and public health practice. Of the published melanoma risk prediction models, the risk prediction tool developed by Fears and colleagues, which was designed for the US population, appears to be the most clinically useful and may also assist in identifying high-risk groups for melanoma prevention strategies.
Few melanoma risk prediction models have been comprehensively developed and assessed. More external validation and prospective evaluation will help translate melanoma risk prediction models into useful tools for clinical and public health practice.
目前,还没有全面评估黑色素瘤风险预测模型的方法。
系统评价发表的报告成年人原发性皮肤黑色素瘤多变量风险预测模型的研究。
截至 2013 年 4 月 30 日,检索了 EMBASE、MEDLINE、PREMEDLINE 和 Cochrane 数据库。手工检索了合格的研究,并进行了引文追踪。两名独立的审查员提取信息。
纳入了 19 项研究,报告了 28 个黑色素瘤预测模型。最终模型中的预测因子数量从 2 到 13 不等;最常见的是痣、皮肤类型、雀斑密度、年龄、头发颜色和晒伤史。研究在模型开发和性能方面的报告有限,且差异很大。有 9 项研究报告了区分有黑色素瘤和无黑色素瘤患者的能力(模型的区分能力),范围从一般到很好(接受者操作特征曲线下面积为 0.62-0.86)。很少有研究评估模型的内部或外部有效性,或其在临床和公共卫生实践中的应用。在已发表的黑色素瘤风险预测模型中,由 Fears 及其同事为美国人群开发的风险预测工具似乎最具临床实用性,也可能有助于确定黑色素瘤预防策略的高危人群。
少数黑色素瘤风险预测模型已经得到了全面的开发和评估。更多的外部验证和前瞻性评估将有助于将黑色素瘤风险预测模型转化为临床和公共卫生实践的有用工具。