活检季节对活检Gleason评分的重要性:日照是否有影响?

Guila Delouya, Daniel Taussky
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引用次数: 0

摘要

摘要:昼夜节律时钟受阳光照射的强烈影响,前列腺癌已被证明与其成反比。我们调查了加拿大魁北克省蒙特利尔市的PCa侵袭性是否会随着暴露在阳光下的时间长短而有所不同。我们分析了1995年1月至2023年12月期间3447例接受局部PCa初级放疗的患者。我们调查了进行诊断性活检的月份是否与原发性Gleason评分(pGS)为4或5的更频繁诊断相关。我们将活检月份分为四个季度(Q1-4)。采用多变量逻辑回归预测pGS为4或5,并根据年龄和活检年份进行调整。在一年中最后3个月,pGS为4或5的活检次数明显减少(P = 0.027) (Q4;19.0%),高于第一季度(22.9%)。年龄、前列腺特异性抗原(PSA)水平、活检阳性次数在Q4和Q1-3之间无显著差异。在多因素logistic回归分析中,第4季度活检可显著预测pGS 4或5的风险较低(优势比[or]: 0.77, 95%可信区间[CI]: 0.63-0.93, P = 0.007),年龄较大(P < 0.001),但与活检年份无关(P = 0.76)。总之,第四季度活检的患者在诊断活检中出现pGS 4或5的风险比前9个月活检的患者低23%。我们的结果并不是因果关系的证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The importance of the season of biopsy on the Gleason score on biopsy: does exposure to sunshine have an influence?

Abstract: The circadian clock is strongly influenced by the sun exposure and prostate cancer has been shown to be inversely proportional to it. We investigated whether PCa aggressiveness in Montreal, Quebec, Canada, differs over the months during or following potentially longer exposure to sunlight. We analyzed 3447 patients treated between January 1995 and December 2023 with primary radiotherapy for localized PCa. We investigated whether the month when diagnostic biopsy was performed was associated with a more frequent diagnosis of a primary Gleason score (pGS) of 4 or 5. We grouped the months of biopsy into the four quarters (Q1-4) of the year. Multivariable logistic regression was used to predict a pGS of 4 or 5, adjusted for age and year of biopsy. There were significantly fewer biopsies (P = 0.027) with pGS 4 or 5 in the last 3 months of the year (Q4; 19.0%) than those in Q1-3 (22.9%). Age, prostate-specific antigen (PSA) level, and the number of positive biopsies were not significantly different between Q4 versus Q1-3. In multivariate logistic regression analysis, a biopsy in Q4 was significantly predictive of a lower risk of pGS 4 or 5 (odds ratio [OR]: 0.77, 95% confidence interval [CI]: 0.63-0.93, P = 0.007), as was older age (P < 0.001), but not the year of biopsy (P = 0.76). In conclusion, patients biopsied during Q4 had a 23% lower risk of a pGS 4 or 5 on diagnostic biopsy than those biopsied during the previous 9 months. Our results are not a proof of causality.

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