Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome

The Prostate Pub Date : 2024-04-17 DOI:10.1002/pros.24711
Eli Marie Grindedal, Manuela Zucknick, Astrid Stormorken, Elin Rønne, Nora M. Tandstad, William B. Isaacs, Karol Axcrona, Lovise Mæhle
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Abstract

BackgroundPathogenic germline variants in the mismatch repair (MMR) genes are associated with an increased risk of prostate cancer (PCa). Since 2010 we have recommended MMR carriers annual PSA testing from the age of 40. Prospective studies of the outcome of long‐term PSA screening are lacking. This study aimed to investigate the incidence and characteristics of PCa in Norwegian MMR carriers attending annual PSA screening (PSA threshold >3.0 ng/mL) to evaluate whether our recommendations should be continued.MethodsThis is a prospective observational study of 225 male MMR carriers who were recommended annual PSA screening by the Section of Inherited Cancer, Oslo University Hospital from 2010 and onwards. Incidence and tumor characteristics (age, PSA at diagnosis, Gleason score, TNM score) were described. IHC and MSI‐analyses were done on available tumors. Standardized incidence ratio (SIR) was calculated based on data from the Cancer Registry of Norway.ResultsTwenty‐two of 225 (9.8%) had been diagnosed with PCa, including 10/69 (14.5%) MSH2 carriers and 8/61 (13.1%) MSH6 carriers. Ten of 20 (50%) tumors had Gleason score ≥4 + 3 on biopsy and 6/11 (54.5%) had a pathological T3a/b stage. Eight of 17 (47.1%) tumors showed abnormal staining on IHC and 3/13 (23.1%) were MSI‐high. SIR was 9.54 (95% CI 5.98–14.45) for all MMR genes, 13.0 (95% CI 6.23–23.9) for MSH2 and 13.74 for MSH6 (95% CI 5.93–27.08).ConclusionsOur results indicate that the MMR genes, and especially MSH2 and MSH6, are associated with a significant risk of PCa, and a high number of tumors show aggressive characteristics. While the impact of screening on patient outcomes remains to be more firmly established, the high SIR values we observe provide support for continued PSA screening of MSH2 and MSH6 carriers. Studies are needed to provide optimal recommendations for PSA‐threshold and to evaluate whether MLH1 and PMS2 carriers should not be recommended screening.
挪威林奇综合征男性前列腺癌 PSA 筛查 10 年的结果
背景错配修复(MMR)基因中的致病性种系变异与前列腺癌(PCa)风险的增加有关。自 2010 年起,我们建议 MMR 基因携带者从 40 岁起每年进行一次 PSA 检测。目前还缺乏对长期 PSA 筛查结果的前瞻性研究。本研究旨在调查参加年度PSA筛查(PSA阈值为3.0纳克/毫升)的挪威MMR携带者中PCa的发病率和特征,以评估是否应继续执行我们的建议。方法这是一项前瞻性观察研究,研究对象是奥斯陆大学医院遗传性癌症科建议从2010年起每年进行PSA筛查的225名男性MMR携带者。研究描述了发病率和肿瘤特征(年龄、诊断时的PSA、Gleason评分、TNM评分)。对现有肿瘤进行了 IHC 和 MSI 分析。结果225人中有22人(9.8%)被诊断为PCa,其中包括10/69(14.5%)名MSH2携带者和8/61(13.1%)名MSH6携带者。20例肿瘤中有10例(50%)活检时Gleason评分≥4 + 3,6/11例(54.5%)病理分期为T3a/b。17个肿瘤中有8个(47.1%)在IHC上出现异常染色,3/13(23.1%)为MSI-高。所有 MMR 基因的 SIR 为 9.54 (95% CI 5.98-14.45),MSH2 为 13.0 (95% CI 6.23-23.9),MSH6 为 13.74 (95% CI 5.93-27.08)。虽然筛查对患者预后的影响还有待进一步确定,但我们观察到的高SIR值支持继续对MSH2和MSH6基因携带者进行PSA筛查。还需要进行研究,以提供 PSA 临界值的最佳建议,并评估是否不应建议 MLH1 和 PMS2 携带者进行筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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