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首页> 外文期刊>European radiology >Histopathological to multiparametric MRI spatial mapping of extended systematic sextant and MR/TRUS-fusion-targeted biopsy of the prostate
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Histopathological to multiparametric MRI spatial mapping of extended systematic sextant and MR/TRUS-fusion-targeted biopsy of the prostate

机译:延长系统六分子和先生/ Trus-Fusion-靶向活检的延长系统六分子的多次MRI空间映射的组织病理学

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PurposeMRI has limited ability to detect multifocal disease or the full extent of prostate involvement with clinically significant prostate cancer (sPC). We compare the spatial co-localization at sextant resolution of MRI lesions and histopathological mapping by combined targeted and extended systematic biopsies.Materials and methodsSextants were mapped for sPC (ISUP group 2) by 24-core transperineal systematic biopsies in 316 patients with suspicion for sPC and by MR lesions of PI-RADS score of 3. The gold standard is combined systematic (median 23 cores) and targeted biopsies.ResultsOf 316 men, 121 (38%) harbored sPC. Of these 121 patients, 4 (3%) had a negative MRI. MRI correctly identified 117/121 (97%) patients with sPC. In these patients, mpMRI missed no additional sPC in 96 (82%), while MRI-negative sPC lesions were present in 21 patients (18%). Of 1896 sextants, 379 (20%) harbored sPC. MR-positive sextants contained sPC in 26% (337/1275), compared to 7% (42/621) in MR-negative sextants. On a patient basis, sensitivity was 0.97, specificity 0.22, positive predictive value 0.43, and negative predictive value 0.91. On a sextant basis, sensitivity was 0.73, specificity 0.38, positive predictive value 0.26, and negative predictive value 0.93.ConclusionMpMRI mapping agreed well with histopathology with, at the observed sPC prevalence and on a patient basis, excellent sensitivity and negative predictive value, and acceptable specificity and positive predictive value for sPC. However, 18% of sPC was outside the mpMRI mapped region, quantifying limitations of MRI for complete localization of disease extent.Key Points center dot Currently, exclusive MRI mapping of the prostate for focal treatment planning cannot be recommended, as significant prostate cancer may remain untreated in a substantial number of cases.center dot At the observed sPC prevalence and on a patient basis, mpMRI has excellent sensitivity and NPV, and acceptable specificity and PPV for detection of prostate cancer, supporting its use to detect suspicious lesions before biopsy.center dot Despite the excellent global performance, 18% of sPC was outside the mpMRI mapped region even when a security margin of 10mm was considered, indicating that prostate MRI has limited ability to completely map all cancer foci within the prostate.
机译:Purposemri在临床上有明显的前列腺癌(SPC)中有有限的检测多焦疾病或前列腺疾病的全部程度。我们将Spxtant分辨率的空间共定位与MRI病变和组织病理学映射的组合分辨率进行比较,并通过组合靶向和扩展系统活检。在316例SPC怀疑的316名患者中,将SPC(ISUP组2)进行SPC(ISUP组2)的材料和方法映射并通过PI-RADS的病变的损伤3.金标准组合系统(中位数23个核心)和靶向活组织检查。316名男性,121(38%)Harbored SPC。在这121名患者中,4个(3%)有一个负MRI。 MRI正确鉴定了117/121(97%)SPC患者。在这些患者中,MPMRI在96名(82%)中没有额外的SPC,而MRI阴性SPC病变存在于21例(18%)中。 1896年塞列特,379(20%)有束缚的SPC。 MR阳性六分含量为26%(337/1275)的SPC,而MR阴性六分为7%(42/621)。在患者的基础上,敏感性为0.97,特异性0.22,阳性预测值0.43和负预测值0.91。在六分之基础上,敏感性为0.73,特异性0.38,阳性预测值0.26和负预测值0.93。在观察到的SPC患病率和患者的基础上,良好的敏感性和负面预测值以及良好的敏感性和负面预测值均匀,敏感性和负面预测值均匀,敏感性效率为0.73,阳性预测值0.26和负预测值0.93。 SPC可接受的特异性和阳性预测值。然而,18%的SPC在MPMRI映射区域之外,量化MRI的限制以完成疾病程度的完全定位.Key点中心点目前,不能推荐局灶性治疗规划前列腺的独家MRI映射,因为重要的前列腺癌可能留下在观察到的SPC患病率和患者的基础上未经治疗,MPMRI具有优异的敏感性和NPV,以及用于检测前列腺癌的可接受的特异性和PPV,支持其用于检测活检前的可疑病变.Center DOT尽管全球性能优异,但即使考虑了10毫米的安全率,18%的SPC也在MPMRI映射区域之外,表明前列腺MRI能够在前列腺内完全映射所有癌症患者的能力有限。

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