Queensland Institute of Medical Research, PO Royal Brisbane Hospital, Australia.
Cancer Prev Res (Phila). 2010 Feb;3(2):233-45. doi: 10.1158/1940-6207.CAPR-09-0108. Epub 2010 Jan 19.
Epidemiologic research has shown convincingly that certain phenotypic attributes are associated with increased relative risks of melanoma. Although such findings have intrinsic utility, there have been few attempts to translate such knowledge into estimates of disease burden suitable for framing public health policy. We aimed to estimate the population attributable fraction (PAF) for melanoma associated with melanocytic nevi using relative risk estimates derived from a systematic review and meta-analysis. We identified eligible studies using citation databases, followed by manual review of retrieved references. Of 49 studies identified, 25 and 23, respectively, were included in meta-analyses of atypical and common nevi. For people with > or =1 atypical nevi, the summary relative risk was 3.63 (95% confidence interval, 2.85-4.62), with a PAF of 0.25. The relative risk increased by 1.017 (95% confidence interval, 1.014-1.020) for each common nevus; however, significant heterogeneity in risk estimates was observed. We estimated that 42% of melanomas were attributable to having > or =25 common nevi (PAF 25-49 nevi = 0.15; PAF > or =50 nevi = 0.27), whereas PAFs for low nevus counts were modest (PAF 0-10 nevi = 0.04; PAF 11-24 nevi = 0.07). We modeled PAF under scenarios of varying nevus prevalence; the highest melanoma burden was always among those with high nevus counts (PAF range of 0.31-0.62 for > or =25 common nevi). Patients with > or =25 common nevi and/or > or =1 atypical nevi are a high-risk group, which might be targeted for identification, screening, and education. This work is the necessary first step in designing targeted preventive strategies for melanoma, which must now be overlaid with information about cost and utility.
流行病学研究令人信服地表明,某些表型特征与黑色素瘤的相对风险增加有关。尽管这些发现具有内在的实用性,但很少有人试图将这些知识转化为适合制定公共卫生政策的疾病负担估计。我们旨在使用系统评价和荟萃分析得出的相对风险估计值,估算与黑色素细胞痣相关的黑色素瘤的人群归因分数(PAF)。我们使用引文数据库确定了合格的研究,然后手动审查了检索到的参考文献。在确定的 49 项研究中,分别有 25 项和 23 项研究纳入了非典型和常见痣的荟萃分析。对于有>或=1 个非典型痣的人,汇总相对风险为 3.63(95%置信区间,2.85-4.62),PAF 为 0.25。每增加一个常见痣,风险估计值增加 1.017(95%置信区间,1.014-1.020);然而,风险估计值存在显著的异质性。我们估计,42%的黑色素瘤归因于有>或=25 个常见痣(PAF 25-49 个痣=0.15;PAF>或=50 个痣=0.27),而低痣计数的 PAF 适中(PAF 0-10 个痣=0.04;PAF 11-24 个痣=0.07)。我们在不同痣患病率的情况下对 PAF 进行了建模;高痣计数的患者始终具有最高的黑色素瘤负担(PAF 范围为 0.31-0.62,>或=25 个常见痣)。有>或=25 个常见痣和/或>或=1 个非典型痣的患者是高危人群,可能需要进行识别、筛查和教育。这项工作是为黑色素瘤设计有针对性的预防策略的必要的第一步,现在必须将其与成本和效用信息叠加。