The Daffodil Centre, The University of Sydney, a Joint Venture with Cancer Council New South Wales, Sydney, NSW, Australia.
School of Public Health and Preventative Medicine, Monash University, Melbourne, VIC, Australia.
Br J Cancer. 2023 Jan;128(1):71-79. doi: 10.1038/s41416-022-02027-7. Epub 2022 Nov 1.
The association between cutaneous melanoma and subsequent risk of prostate cancer (PC) was examined in a large population-based cohort study.
Male participants in the Sax Institute's 45 and Up Study (Australia) were recruited between 2006 and 2009. Questionnaire data and linked administrative health data from the Centre for Health Record Linkage and Services Australia identified melanomas diagnosed between 1/1/1994 and 12 months before Study recruitment (i.e., between 2005 and 2008), incident PCs, primary healthcare utilisation and prostate-specific antigen (PSA) tests. Men were excluded from the current analyses if they had a recorded PC or other cancer diagnosis other than melanoma and non-melanoma skin cancer prior to recruitment. Multivariable Cox regression was used to estimate hazard ratios (HRs) adjusting for PSA-testing frequency before PC diagnosis.
Of 96,548 eligible men, 1899 were diagnosed with melanoma during the melanoma diagnosis period and 3677 incident PC diagnosed during follow-up (latest date 31/12/2013). Men with melanoma diagnosis had increased risk of a subsequent PC diagnoses (vs. no melanoma; fully adjusted HR = 1.32; 95% CI: 1.09-1.60). There was weak evidence of higher risks of a subsequent PC diagnosis for men diagnosed with more than one melanoma compared to men diagnosed with only one melanoma (p = 0.077), and if first melanoma diagnosis was 10 to 15 years before Study recruitment (fully adjusted HR = 2.05; 95% CI [1.35, 3.12]).
Melanoma diagnosis was associated with increased risk of subsequent PC diagnosis, after adjusting for PSA testing and primary healthcare utilisation. While our ability to adjust for PC screening reduced risk of detection bias, we acknowledge that residual confounding from increased medical surveillance after melanoma diagnoses cannot be entirely ruled out.
在一项大型基于人群的队列研究中,研究了皮肤黑色素瘤与随后发生前列腺癌(PC)的风险之间的关联。
澳大利亚萨克研究所的 45 岁及以上研究中的男性参与者于 2006 年至 2009 年期间招募。问卷数据和来自澳大利亚健康记录链接中心和服务的链接行政健康数据确定了 1994 年 1 月 1 日至研究招募前 12 个月(即 2005 年至 2008 年)期间诊断的黑色素瘤、新发 PC、初级保健利用和前列腺特异性抗原(PSA)检测。如果男性在招募前已经有记录的 PC 或除黑色素瘤和非黑色素瘤皮肤癌以外的其他癌症诊断,则排除在当前分析之外。多变量 Cox 回归用于估计风险比(HRs),并在 PC 诊断前 PSA 检测频率的基础上进行调整。
在 96548 名合格男性中,1899 名男性在黑色素瘤诊断期间被诊断患有黑色素瘤,3677 名男性在随访期间被诊断患有新发 PC(最新日期为 2013 年 12 月 31 日)。诊断出黑色素瘤的男性患随后 PC 诊断的风险增加(与无黑色素瘤相比;完全调整后的 HR=1.32;95%CI:1.09-1.60)。与诊断出一种黑色素瘤的男性相比,诊断出多种黑色素瘤的男性随后诊断出 PC 的风险更高,而诊断出第一种黑色素瘤的时间距离研究招募前 10 至 15 年的男性(完全调整后的 HR=2.05;95%CI[1.35,3.12])。
在调整 PSA 检测和初级保健利用后,黑色素瘤诊断与随后 PC 诊断的风险增加相关。虽然我们能够调整 PC 筛查以降低检测偏差的风险,但我们承认,无法完全排除黑色素瘤诊断后增加的医疗监测所带来的残余混杂因素。