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前列腺癌升级和升期对生化复发和癌症特异性生存的影响。

The Impact of Prostate Cancer Upgrading and Upstaging on Biochemical Recurrence and Cancer-Specific Survival.

机构信息

Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, 03101 Vilnius, Lithuania.

Vilnius University Hospital Santaros Kinikos, 08661 Vilnius, Lithuania.

出版信息

Medicina (Kaunas). 2020 Feb 4;56(2):61. doi: 10.3390/medicina56020061.

Abstract

Significant numbers of prostate cancer (PCa) patients experience tumour upgrading and upstaging between prostate biopsy and radical prostatectomy (RP) specimens. The aim of our study was to investigate the role of grade and stage increase on surgical and oncological outcomes. Upgrading and upstaging rates were analysed in 676 treatment-naïve PCa patients who underwent RP with subsequent follow-up. Positive surgical margin (PSM), biochemical recurrence (BCR), metastasis-free survival (MFS), overall (OS) and cancer specific survival (CSS) were analysed according to upgrading and upstaging. Upgrading was observed in 29% and upstaging in 22% of PCa patients. Patients undergoing upgrading or upstaging were 1.5 times more likely to have a PSM on RP pathology. Both upgrading and upstaging were associated with increased risk for BCR: 1.8 and 2.1 times, respectively. Mean time to BCR after RP was 2.1 years in upgraded cases and 2.7 years in patients with no upgrading ( <0.001), while mean time to BCR was 1.9 years in upstaged and 2.8 years in non-upstaged cases ( <0.001). Grade and stage increase after RP were associated with inferior MFS rates and ten-year CSS: 89% vs. 98% for upgrading ( = 0.039) and 87% vs. 98% for upstaging ( = 0.008). Currently used risk stratification models are associated with substantial misdiagnosis. Pathological upgrading and upstaging have been associated with inferior surgical results, substantial higher risk of BCR and inferior rates of important oncological outcomes, which should be considered when counselling PCa patients at the time of diagnosis or after definitive therapy.

摘要

大量前列腺癌 (PCa) 患者在前列腺活检和根治性前列腺切除术 (RP) 标本之间经历肿瘤升级和分期升级。我们研究的目的是探讨分级和分期增加对手术和肿瘤学结果的影响。

对 676 例接受 RP 治疗的初治 PCa 患者进行了研究,这些患者随后进行了随访。根据升级和分期情况,分析了阳性手术切缘 (PSM)、生化复发 (BCR)、无转移生存 (MFS)、总生存 (OS) 和癌症特异性生存 (CSS)。在 29%的 PCa 患者中观察到升级,在 22%的患者中观察到分期升级。接受升级或分期升级的患者在 RP 病理上发生 PSM 的可能性是前者的 1.5 倍。升级和分期升级均与 BCR 风险增加相关:分别为 1.8 倍和 2.1 倍。RP 后发生 BCR 的平均时间在升级病例中为 2.1 年,在未升级病例中为 2.7 年 ( <0.001),而在升级病例中为 1.9 年,在未升级病例中为 2.8 年 ( <0.001)。RP 后分级和分期的增加与较差的 MFS 率和 10 年 CSS 相关:升级为 89%比 98% ( = 0.039),分期升级为 87%比 98% ( = 0.008)。目前使用的风险分层模型与大量误诊相关。病理升级和分期升级与手术结果较差、BCR 风险显著增加以及重要肿瘤学结果的发生率降低相关,在诊断时或在根治性治疗后为 PCa 患者提供咨询时应考虑这些因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c2/7074013/053353fad7d8/medicina-56-00061-g001.jpg

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