Prostate cancer detection following diagnosis of atypical small acinar proliferation.

Prostate cancer detection following diagnosis of atypical small acinar proliferation.
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诊断非典型小腺泡增殖后前列腺癌的检测。

DOI:
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发表时间:
2017
期刊:
The Canadian journal of urology
影响因子:
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通讯作者:
S. Eggener
S. Eggener
中科院分区:
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文献类型:
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作者:
Kyle J. Ericson;H. Wenger;A. Rosen;Kyle J. Kiriluk;G. Gerber;G. Paner;S. Eggener

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引言 报告诊断为不典型小腺泡细胞增生症(ASAP)后癌症的发生率和特征,并对当前的临床实践建议进行评论。 材料和方法 我们回顾了2008至2013年间在一家机构接受前列腺活检的患者。早期无癌症史的男性也包括在内。分析了接受重复前列腺活检的男性患者的临床病理特征,包括前列腺特异性抗原(PSA)、ASAP或癌症的存在、肿瘤体积、受累核心数量和Gleason评分。 结果 在1450名男性中,75名(5%)患者发现了ASAP。49例(65%)患者进行了重复活检。15例(31%)被诊断为癌症,10例(20%)为ASAP,24例(49%)为良性。PSA、年龄和ASAP核心数与癌症无关。12例(80%)诊断为Gleason 6病。在3名患者中发现了格里森≥7癌,占所有重复活检患者的6%。肿瘤平均线形体积3.2 mm,平均肿瘤体积14.2%。 结论 在当代的前列腺活检系列中,ASAP的发生率为5%。在患有ASAP的男性中,重复活检的癌症发生率为31%,绝大多数是低级别和低体积。在适当的临床情况下,ASAP患者可能在6个月内不需要重复活检。
INTRODUCTION To report the incidence and characteristics of cancer following a diagnosis of atypical small acinar proliferation (ASAP) and comment on current clinical practice recommendations. MATERIALS AND METHODS We reviewed patients that underwent prostate biopsy between 2008 and 2013 at a single institution. Men with ASAP without previous cancer were included. Clinicopathologic features including prostate-specific antigen (PSA), presence of ASAP or cancer, tumor volume, number of involved cores, and Gleason score were analyzed in men that received a repeat prostate biopsy. RESULTS Of 1450 men, ASAP was found in 75 (5%) patients. Repeat biopsy was performed in 49 (65%) patients. Fifteen (31%) were diagnosed with cancer, 10 (20%) with ASAP, and 24 (49%) were benign. PSA, age, and number of cores with ASAP were not associated with cancer. Gleason 6 disease was diagnosed in 12 (80%) patients. Gleason ≥ 7 cancer was found in 3 patients, or 6% of all patients with a repeat biopsy. The average linear amount of tumor was 3.2 mm, and the average tumor volume was 14.2%. CONCLUSION In a contemporary prostate biopsy series, the incidence of ASAP was 5%. Among men with ASAP, incidence of cancer at repeat biopsy was 31%, with the overwhelming majority being low grade and low volume. Patients with ASAP may not require repeat biopsy within 6 months in the appropriate clinical context.