Prostate-specific antigen testing patterns and prostate cancer stage at diagnosis in older Ohio cancer patients.

IF 2.2 4区 医学 Q3 ONCOLOGY Cancer Causes & Control Pub Date : 2024-12-01 Epub Date: 2024-09-03 DOI:10.1007/s10552-024-01908-x
Sajan N Patel, Long Vu, Holly E Hartman, Weichuan Dong, Siran M Koroukian, Johnie Rose
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Abstract

Background: Prostate cancer (PCa) screening recommendations do not support prostate-specific antigen (PSA) screening for older men. Such screening often occurs, however. It is, therefore, important to understand how frequently and among which subgroups screening occurs, and the extent of distant stage PCa diagnoses among screened older men.

Methods: Using the 2014-2016 linked Ohio Cancer Incidence Surveillance System (OCISS) and Medicare administrative database, we identified men 68 and older diagnosed with PCa and categorized their PSA testing in the three years preceding diagnosis as screening or diagnostic. We conducted multivariable logistic regression analysis to identify correlates of screening PSA and to determine whether screening PSA is independently associated with distant stage disease.

Results: Our study population included 3034 patients (median age: 73 years). 62.1% of PCa patients underwent at least one screening-based PSA in the three years preceding diagnosis. Older age (75-84 years: aOR [95% CI]: 0.84 [0.71, 0.99], ≥ 85: aOR: 0.27 [0.19, 0.38]), and frailty (aOR: 0.51 [0.37, 0.71]) were associated with lower screening. Screening was associated with decreased odds of distant stage disease (aOR: 0.55 [0.42, 0.71]). However, older age (75-84 years: aOR: 2.43 [1.82, 3.25], ≥ 85: aOR: 10.57 [7.05, 15.85]), frailty (aOR: 5.00 [2.78, 9.31]), and being separated or divorced (aOR: 1.64 [1.01, 2.60]) were associated with increased distant stage PCa.

Conclusion: PSA screening in older men is common, though providers appear to curtail PSA screening as age and frailty increase. Screened older men are diagnosed at earlier stages, but the harms of screening cannot be assessed.

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俄亥俄州老年癌症患者诊断时的前列腺特异性抗原检测模式和前列腺癌分期。
背景:前列腺癌(PCa)筛查建议不支持对老年男性进行前列腺特异性抗原(PSA)筛查。然而,这种筛查经常进行。因此,了解筛查的频率、筛查的亚群体以及接受筛查的老年男性中远期 PCa 诊断的程度非常重要:利用 2014-2016 年俄亥俄州癌症发病监测系统 (OCISS) 和医疗保险管理数据库,我们确定了确诊为 PCa 的 68 岁及以上男性,并将他们在确诊前三年的 PSA 检测分为筛查型和诊断型。我们进行了多变量逻辑回归分析,以确定筛查 PSA 的相关性,并确定筛查 PSA 是否与远期疾病独立相关:我们的研究对象包括 3034 名患者(中位年龄:73 岁)。62.1%的 PCa 患者在确诊前三年内至少接受了一次 PSA 筛查。高龄(75-84 岁:aOR [95% CI]:0.84 [0.71, 0.99];≥ 85 岁:aOR:0.27 [0.19, 0.38])和体弱(aOR:0.51 [0.37, 0.71])与筛查率较低有关。筛查与远期疾病几率的降低有关(aOR:0.55 [0.42, 0.71])。然而,年龄较大(75-84 岁:aOR:2.43 [1.82, 3.25];≥ 85 岁:aOR:10.57 [7.05, 15.85])、体弱(aOR:5.00 [2.78, 9.31])、分居或离婚(aOR:1.64 [1.01, 2.60])与远期 PCa 增高有关:结论:PSA筛查在老年男性中很常见,但随着年龄和体弱程度的增加,医疗服务提供者似乎会减少PSA筛查。接受筛查的老年男性可在较早阶段得到诊断,但筛查的危害尚无法评估。
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来源期刊
Cancer Causes & Control
Cancer Causes & Control 医学-公共卫生、环境卫生与职业卫生
CiteScore
3.90
自引率
4.30%
发文量
130
审稿时长
6.6 months
期刊介绍: Cancer Causes & Control is an international refereed journal that both reports and stimulates new avenues of investigation into the causes, control, and subsequent prevention of cancer. By drawing together related information published currently in a diverse range of biological and medical journals, it has a multidisciplinary and multinational approach. The scope of the journal includes: variation in cancer distribution within and between populations; factors associated with cancer risk; preventive and therapeutic interventions on a population scale; economic, demographic, and health-policy implications of cancer; and related methodological issues. The emphasis is on speed of publication. The journal will normally publish within 30 to 60 days of acceptance of manuscripts. Cancer Causes & Control publishes Original Articles, Reviews, Commentaries, Opinions, Short Communications and Letters to the Editor which will have direct relevance to researchers and practitioners working in epidemiology, medical statistics, cancer biology, health education, medical economics and related fields. The journal also contains significant information for government agencies concerned with cancer research, control and policy.
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