Can Conventional Magnetic Resonance Imaging, Prostate Needle Biopsy, or Their Combination Predict the Laterality of Clinically Localized Prostate Cancer?
详细信息查看全文 | 推荐本文 |
摘要
| Figures/TablesFigures/Tables | ReferencesReferences

Objective

To evaluate conventional magnetic resonance imaging (MRI), prostate needle biopsy (PBx), and the combination of both tests in predicting the laterality of final specimen pathology after radical prostatectomy.

Methods

A total of 574 radical prostatectomy cases that had PBx with at least 12 cores and preoperative prostate MRI with pelvic coil were included. We analyzed the clinicopathologic data with laterality based on PBx and MRI. Unilateral disease in combination was defined as unilateral cancer in PBx and at the same time MRI findings of undetectable or ipsilateral disease. Cohen's kappa (魏) was used to measure agreement between the laterality data.

Results

There were a total of 316 (55.1%) unilateral cancers detected by PBx, whereas there were 139 (24.2%) cases in the final specimen pathology. MRI resulted in 119 (20.7%) undetectable and 205 (35.7%) unilateral cancers. Cancer laterality based on final specimen pathology had only fair agreements with PBx (魏 = 0.286), MRI (魏 = 0.200), and their combination (k = .291). The positive predictive values to predict pathologic concurrent unilaterality were only 30.4%(96/316), 25.9%(53/205), and 34.8%(72/207), respectively. These trends were similar in low-risk cases.

Conclusion

Preoperative PBx, MRI, and the combination of both methods had only a fair correlation with the laterality of prostate cancer (PC), even in low-risk cases. Approximately two thirds of cases diagnosed as unilateral disease by contemporary PBx, MRI, or their combination were not concurrent unilateral disease in final pathology. This should be recognized when planning nerve-sparing surgery and potentially for candidate selection for focal therapy to treat PC.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700