Abd Ali Furat, Sievert Karl-Dietrich, Eisenblaetter Michel, Titze Barbara, Hansen Torsten, Barth Peter J, Titze Ulf
Bielefeld University, Medical School and University Medical Center OWL, Klinikum Lippe Detmold, Department of Urology, 32756 Detmold, Germany.
Bielefeld University, Medical School and University Medical Center OWL, Klinikum Lippe Detmold, Department of Diagnostic and Interventional Radiology, 32756 Detmold, Germany.
Cancers (Basel). 2023 Aug 1;15(15):3915. doi: 10.3390/cancers15153915.
The standard procedure for the diagnosis of prostate carcinoma involves the collection of 10-12 systematic biopsies (SBx) from both lobes. MRI-guided targeted biopsies (TBx) from suspicious foci increase the detection rates of clinically significant (cs) PCa. We investigated the extent to which the results of the TBx predicted the tumor board treatment decisions. SBx and TBx were acquired from 150 patients. Risk stratifications and recommendations for interventional therapy (prostatectomy and radiotherapy) or active surveillance were established by interdisciplinary tumor boards. We analyzed how often TBx alone were enough to correctly classify the tumors as well as to indicate interventional therapy and how often the findings of SBx were crucial for therapy decisions. A total of 28/39 (72%) favorable risk tumors were detected in TBx, of which 11/26 (42%) very-low-risk tumors were not detected and 8/13 (62%) low-risk tumors were undergraded. A total of 36/44 (82%) intermediate-risk PCa were present in TBx, of which 4 (9%) were underdiagnosed as a favorable risk tumor. A total of 12/13 (92%) high-risk carcinomas were detected and correctly grouped in TBx. The majority of csPCa were identified by the sampling of TBx alone. The tumor size was underestimated in a proportion of ISUP grade 1 tumors. Systematic biopsy sampling is therefore indicated for the next AS follow-up in these cases.
前列腺癌的标准诊断程序包括从双侧叶采集10 - 12次系统活检(SBx)。对可疑病灶进行MRI引导下的靶向活检(TBx)可提高临床显著性(cs)前列腺癌的检出率。我们研究了TBx结果对肿瘤委员会治疗决策的预测程度。从150例患者中获取了SBx和TBx。跨学科肿瘤委员会制定了风险分层以及介入治疗(前列腺切除术和放疗)或积极监测的建议。我们分析了仅TBx就足以正确分类肿瘤并指示介入治疗的频率,以及SBx的结果对治疗决策至关重要的频率。在TBx中总共检测出28/39(72%)的低风险肿瘤,其中11/26(42%)的极低风险肿瘤未被检测到,8/13(62%)的低风险肿瘤分级过低。在TBx中总共存在36/44(82%)的中风险前列腺癌,其中4例(9%)被漏诊为低风险肿瘤。在TBx中总共检测出12/13(92%)的高风险癌并正确分组。大多数csPCa仅通过TBx采样即可识别。部分ISUP 1级肿瘤的肿瘤大小被低估。因此,在这些病例的下一次积极监测随访中,建议进行系统活检采样。