A clinical available decision support scheme for optimizing prostate biopsy based on mpMRI

被引:7
作者
Hou, Ying [1 ]
Jiang, Ke-Wen [1 ]
Zhang, Jing [1 ]
Bao, Mei-Ling [2 ]
Shi, Hai-Bin [1 ]
Qu, Jin-Rong [4 ,5 ]
Cheng, Gong [3 ]
Zhang, Yu-Dong [1 ]
机构
[1] Nanjing Med Univ, Dept Radiol, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Pathol, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Urol, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[4] Zhengzhou Univ, Dept Radiol, Affiliated Canc Hosp, Zhengzhou, Henan, Peoples R China
[5] Henan Canc Hosp, Zhengzhou, Henan, Peoples R China
关键词
ULTRASOUND-GUIDED BIOPSY; CANCER DETECTION; DIAGNOSTIC-ACCURACY; TARGETED BIOPSY; SYSTEM; NUMBER; MRI; AUA;
D O I
10.1038/s41391-021-00489-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Combined MRI/Ultrasound fusion targeted biopsy (TBx) and systematic biopsy (SBx) results in better prostate cancer (PCa) detection relative to either TBx or SBx alone, while at the cost of higher number of biopsy cores and greater detection of clinically insignificant PCa. We therefore developed and evaluated a simple decision support scheme for optimizing prostate biopsy based on multiparametric (mp) MRI assessment. Methods Total 229 patients with suspicion of PCa underwent mpMRI before combined TBx/SBx were retrospectively included. Impacts of MRI characteristics such as Prostate Imaging-Reporting and Data System (PI-RADS) score, lesion size, zonal origination, and location on biopsy performance were evaluated. A clinically available decision support scheme relying on mpMRI assessment was subsequently developed as a triage test to optimize prostate biopsy process. Cost (downgrade, upgrade, and biopsy core)-to-Effectiveness (detection rate) was systemically compared. Results TBx achieved comparable detection rate to combined TBx/SBx in diagnosis of PCa and clinically significant PCa (csPCa) (PCa, 59% [135/229] vs 60.7% [139/229]; csPCa, 45.9% [105/229] vs 47.2% [108/229]; p-values > 0.05) and outperformed SBx (PCa, 42.4% [97/229]; csPCa, 28.4% [65/229]; p-values < 0.001). Specially, in personalized decision support scheme, TBx accurately detected all PCa (72.5% [74/102]) in PI-RADS 5 and larger (>= 1 cm) PI-RADS 3-4 observations, adding SBx to TBx only resulted in 1.4% (1/74) upgrading csPCa. For smaller (<1 cm) PI-RADS 3-4 lesions, combined TBx/SBx resulted in relatively higher detection rate (51.2% [65/127] vs 48.0% [61/127]) and lower upgrading rate (30.6% [15/49] vs 36.7% [18/49]) than TBx. Conclusions The benefit of SBx added to TBx was largely restricted to smaller PI-RADS score 3-4 lesions. Using our personalized strategy of solo TBx for PI-RADS 5 and larger (>= 1 cm) PI-RADS score 3-4 lesions would avoid excess SBx in 44.5% (102/229) of all biopsy-naive patients without compromising detection rate.
引用
收藏
页码:727 / 734
页数:8
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