Adamson Adewole S, Naik Geetanjali, Jones Mark A, Bell Katy Jl
Department of Internal Medicine (Division of Dermatology), Dell Medical School at The University of Texas at Austin, Austin, Texas, USA
The University of Texas Health Science Center at Houston, Houston, Texas, USA.
BMJ Evid Based Med. 2024 May 22;29(3):156-161. doi: 10.1136/bmjebm-2023-112460.
To quantify the proportion of melanoma diagnoses (invasive and in situ) in the USA that might be overdiagnosed.
In this ecological study, incidence and mortality data were collected from the Surveillance, Epidemiology and End Results 9 registries database. DevCan software was used to calculate the cumulative lifetime risk of being diagnosed with melanoma between 1975 and 2018, with adjustments made for changes in longevity and risk factors over the study period.
USA.
White American men and women (1975-2018).
The primary outcome was excess lifetime risk of melanoma diagnosis between 1976 and 2018 (adjusted for year 2018 competing mortality and changes in risk factors), which was inferred as likely overdiagnosis. The secondary outcome was an excess lifetime risk of melanoma diagnosis in each year between 1976 and 2018 (adjusted and unadjusted).
Between 1975 and 2018 the adjusted lifetime risk of being diagnosed with melanoma (invasive and in situ) increased from 3.2% (1 in 31) to 6.4% (1 in 16) among white men, and from 1.6% (1 in 63) to 4.5% (1 in 22) among white women. Over the same period, the adjusted lifetime risk of being diagnosed with melanoma in situ increased from 0.17% (1 in 588) to 2.7% (1 in 37) in white men and 0.08% (1 in 1250) to 2.0% (1 in 50) in white women. An estimated 49.7% of melanomas diagnosed in white men and 64.6% in white women were overdiagnosed in 2018. Among people diagnosed with melanomas in situ, 89.4% of white men and 85.4% of white women were likely overdiagnosed in 2018.
Melanoma overdiagnosis among white Americans is significant and increasing over time with an estimated 44 000 overdiagnosed in men and 39 000 in women in 2018. A large proportion of overdiagnosed melanomas are in situ cancers, pointing to a potential focus for intervention.
量化美国可能被过度诊断的黑色素瘤(侵袭性和原位性)诊断比例。
在这项生态学研究中,从监测、流行病学和最终结果9登记数据库收集发病率和死亡率数据。使用DevCan软件计算1975年至2018年间被诊断为黑色素瘤的累积终生风险,并对研究期间寿命和风险因素的变化进行调整。
美国。
美国白人男性和女性(1975 - 2018年)。
主要结局是1976年至2018年间黑色素瘤诊断的终生风险过高(根据2018年的竞争死亡率和风险因素变化进行调整),推断为可能的过度诊断。次要结局是1976年至2018年间每年黑色素瘤诊断的终生风险过高(调整和未调整)。
1975年至2018年间,美国白人男性中被诊断为黑色素瘤(侵袭性和原位性)的调整后终生风险从3.2%(1/31)增至6.4%(1/16),白人女性从1.6%(1/63)增至4.5%(1/22)。同期,美国白人男性中被诊断为原位黑色素瘤的调整后终生风险从0.17%(1/588)增至2.7%(1/37),白人女性从0.08%(1/1250)增至2.0%(1/50)。估计2018年美国白人男性中49.7%的黑色素瘤诊断以及白人女性中64.6%的黑色素瘤诊断属于过度诊断。在被诊断为原位黑色素瘤的人群中,2018年估计89.4%的白人男性和85.4%的白人女性可能被过度诊断。
美国白人中黑色素瘤过度诊断情况严重且随时间增加,2018年估计男性有44000例、女性有39000例被过度诊断。很大一部分被过度诊断的黑色素瘤是原位癌,这指出了一个潜在的干预重点。