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Eur Urol Oncol. 2021 Aug;4(4):519-528. doi: 10.1016/j.euo.2020.11.008. Epub 2020 Dec 28.
2
Other and All-Cause Mortality among Men Diagnosed with Prostate Cancer in the PLCO Trial.在 PLCO 试验中被诊断患有前列腺癌的男性的其他和全因死亡率。
J Urol. 2021 May;205(5):1372-1378. doi: 10.1097/JU.0000000000001531. Epub 2020 Dec 22.
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Oncologic Outcomes after Localized Prostate Cancer Treatment: Associations with Pretreatment Prostate Magnetic Resonance Imaging Findings.局限性前列腺癌治疗后的肿瘤学结果:与治疗前前列腺磁共振成像结果的关系。
J Urol. 2021 Apr;205(4):1055-1062. doi: 10.1097/JU.0000000000001474. Epub 2020 Nov 18.
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Prostate cancer risk group is associated with other-cause mortality in men with localized prostate cancer.前列腺癌风险组与局限性前列腺癌男性的其他原因死亡率相关。
Can Urol Assoc J. 2020 Oct;14(10):E507-E513. doi: 10.5489/cuaj.6324.
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PI-RADS score is associated with biochemical control and distant metastasis in men with intermediate-risk and high-risk prostate cancer treated with radiation therapy.PI-RADS 评分与接受放疗的中危和高危前列腺癌男性的生化控制和远处转移相关。
Urol Oncol. 2020 Jun;38(6):600.e1-600.e8. doi: 10.1016/j.urolonc.2019.12.015. Epub 2020 Jan 15.
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Prediction of biochemical recurrence in prostate cancer patients who underwent prostatectomy using routine clinical prostate multiparametric MRI and decipher genomic score.使用常规临床前列腺多参数 MRI 和破译基因组评分预测前列腺切除术患者的生化复发。
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MRI 检测到的临床显著前列腺癌与前列腺切除术后的肿瘤学结果相关。

MRI-Detectability of Clinically Significant Prostate Cancer Relates to Oncologic Outcomes After Prostatectomy.

机构信息

Memorial Sloan Kettering Cancer Center, Department of Radiology, New York, NY.

Memorial Sloan Kettering Cancer Center, Department of Radiology, New York, NY.

出版信息

Clin Genitourin Cancer. 2022 Aug;20(4):319-325. doi: 10.1016/j.clgc.2022.04.001. Epub 2022 Apr 14.

DOI:10.1016/j.clgc.2022.04.001
PMID:35618599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10191247/
Abstract

INTRODUCTION/BACKGROUND: Magnetic resonance imaging (MRI) misses a proportion of "clinically significant" prostate cancers (csPC) as defined by histopathology criteria. The aim of this study was to analyze whether long-term oncologic outcomes differ between MRI-detectable and MRI-occult csPC.

PATIENTS AND METHODS

Retrospective analysis of 1449 patients with pre-prostatectomy MRI and csPC on prostatectomy specimens (ie, Grade group ≥2 or extraprostatic spread) between 2001-2006. T2-weighted MRIs were classified according to the Prostate Imaging Reporting and Data System into MRI-occult (categories 1, 2), MRI-equivocal (category 3), and MRI-detectable (categories 4, 5). Cumulative incidence of biochemical recurrence (BCR), metastatic disease, and cancer-specific mortality, estimated with competing risk models. The median follow-up in survivors was 11.0 years (IQR: 8.9-13.1).

RESULTS

In 188 (13%) cases, csPC was MRI-occult, 435 (30%) MRIs were equivocal, and 826 (57%) csPC were MRI-detectable. The 15-year cumulative incidence [95% CI] of BCR was 8.3% [2.2, 19.5] for MRI-occult cases, 17.4% [11.1, 24.8] for MRI-equivocal cases, and 43.3% [38.7, 47.8] for MRI-detectable cases (P < .001). The cumulative incidences of metastases were 0.61% [0.06, 3.1], 3.5% [1.5, 6.9], and 19.6% [15.4, 24.2] for MRI-occult, MRI-equivocal, and MRI-detectable cases, respectively (P < .001). There were no deaths from prostate cancer observed in patients with MRI-occult csPC, compared to an estimated 1.9% [0.54, 4.9], and 7.1 % [4.5, 10.6] for patients with MRI-equivocal and MRI-detectable cancer, respectively (P < .001).

CONCLUSION

Oncologic outcomes after prostatectomy for csPC differ between MRI-occult and MRI-detectable lesions. Judging the clinical significance of a negative prostate MRI based on histopathologic surrogates alone might be misleading.

MICROABSTRACT

Among 1449 patients with pre-prostatectomy MRI and clinically significant prostate cancer on prostatectomy histopathology, MRI-occult cancers (n = 188, 13%) were less likely to recur biochemically (8% vs. 43%, P < .001), metastasize (0.6% vs. 20%, P < .001), or lead to prostate cancer mortality (0% vs. 7%, P < .001) than MRI-detectable cancers (n = 826, 57%). MRI-occult cancers constitute a prognostically distinct subgroup among higher-grade prostate cancers.

摘要

介绍/背景:磁共振成像(MRI)漏诊了一部分组织病理学标准定义的“临床显著”前列腺癌(csPC)。本研究旨在分析 MRI 可检测和 MRI 隐匿性 csPC 的长期肿瘤学结局是否存在差异。

患者和方法

对 2001 年至 2006 年间行前列腺切除术的 1449 例术前 MRI 检查和 csPC 患者(即,Gleason 分级≥2 或外生扩散)进行回顾性分析。根据前列腺成像报告和数据系统(Prostate Imaging Reporting and Data System),T2 加权 MRI 分为 MRI 隐匿性(1、2 类)、MRI 可疑(3 类)和 MRI 可检测(4、5 类)。采用竞争风险模型估计生化复发(BCR)、转移性疾病和癌症特异性死亡率的累积发生率。幸存者的中位随访时间为 11.0 年(IQR:8.9-13.1)。

结果

在 188 例(13%)csPC 中 MRI 隐匿性,435 例(30%)MRI 可疑,826 例(57%)csPC 为 MRI 可检测。MRI 隐匿性病例的 15 年累积 BCR 发生率为 8.3%[2.2,19.5],MRI 可疑性病例为 17.4%[11.1,24.8],MRI 可检测性病例为 43.3%[38.7,47.8](P<0.001)。MRI 隐匿性、MRI 可疑性和 MRI 可检测性病例的转移累积发生率分别为 0.61%[0.06,3.1]、3.5%[1.5,6.9]和 19.6%[15.4,24.2](P<0.001)。在 MRI 隐匿性 csPC 患者中未观察到前列腺癌死亡,而 MRI 可疑性和 MRI 可检测性癌症患者的估计死亡率分别为 1.9%[0.54,4.9]和 7.1%[4.5,10.6](P<0.001)。

结论

前列腺切除术治疗 csPC 的肿瘤学结局在 MRI 隐匿性和 MRI 可检测性病变之间存在差异。仅根据组织病理学替代物判断阴性前列腺 MRI 的临床意义可能会产生误导。

微摘要

在 1449 例接受前列腺切除术的术前 MRI 检查和前列腺切除术后组织病理学证实为临床显著前列腺癌的患者中,MRI 隐匿性癌症(n=188,13%)发生生化复发(8% vs. 43%,P<0.001)、转移(0.6% vs. 20%,P<0.001)或导致前列腺癌死亡(0% vs. 7%,P<0.001)的可能性低于 MRI 可检测性癌症(n=826,57%)。MRI 隐匿性癌症构成了高级别前列腺癌中预后不同的亚组。