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在经过学习曲线后,MRI 靶向活检诊断前列腺癌所需的核心数量会减少。

Number of cores needed to diagnose prostate cancer during MRI targeted biopsy decreases after the learning curve.

机构信息

Department of Urology, University of Iowa, Iowa City, IA.

Carver College of Medicine, University of Iowa, Iowa City, IA.

出版信息

Urol Oncol. 2022 Jan;40(1):7.e19-7.e24. doi: 10.1016/j.urolonc.2021.05.029. Epub 2021 Jun 27.

Abstract

INTRODUCTION

We hypothesized that the number of cores needed to detect prostate cancer would decrease with increasing MRI-targeted biopsy (TBx) experience.

METHODS

All patients undergoing TBx at our institution from May 2017 to August 2019 were enrolled in a prospectively maintained database. Five biopsy cores were obtained from each lesion ≥3 on PI-RADS v2.0 followed by a systematic 12-core biopsy. To assess learning curve, the study population was divided into quartiles by sequential biopsies. Clinically significant prostate cancer (csPC) was defined as Gleason Grade Group 2 or higher.

RESULTS

377 patients underwent prostate biopsy (533 lesions); 233 lesions (44%) were positive for prostate cancer and 173 lesions (32%) were csPC. There was a significant decline in the number of cores required for diagnosing any cancer (P < 0.001) and csPC (P < 0.05) after the first quartile. There was no difference when stratifying by PI-RADS score or lesion volume. Within the first quartile, limiting the biopsy to 3 cores would miss 16.2% of csPC, decreasing to 6.6% after approximately 100 patients.

CONCLUSION

MRI TBx is associated with a learning curve of approximately 100 cases. Four or 5 cores should be considered during the initial experience, but thereafter, 3 cores per lesion is sufficient to detect csPC.

摘要

介绍

我们假设,随着 MRI 靶向活检(TBx)经验的增加,检测前列腺癌所需的核心数量将会减少。

方法

我们机构于 2017 年 5 月至 2019 年 8 月期间进行 TBx 的所有患者均纳入前瞻性维护的数据库。每个 PI-RADS v2.0 评分≥3 的病变均获得 5 个活检核心,然后进行系统的 12 核活检。为了评估学习曲线,将研究人群按顺序活检分为四等份。临床显著前列腺癌(csPC)定义为 Gleason 分级组 2 或更高。

结果

377 名患者接受了前列腺活检(533 个病灶);233 个病灶(44%)为前列腺癌阳性,173 个病灶(32%)为 csPC。在第一个四分位数后,诊断任何癌症(P<0.001)和 csPC(P<0.05)所需的核心数量显著下降。按 PI-RADS 评分或病变体积分层时无差异。在第一个四分位数内,将活检限制在 3 个核心会错过 16.2%的 csPC,大约 100 例后降至 6.6%。

结论

MRI-TBx 与大约 100 例的学习曲线相关。在初始经验中应考虑使用 4 或 5 个核心,但此后,每个病变 3 个核心足以检测 csPC。

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