How Many Targeted Biopsy Cores are Needed for Clinically Significant Prostate Cancer Detection during Transperineal Magnetic Resonance Imaging Ultrasound Fusion Biopsy?


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 28 7 2020
medline: 25 11 2020
entrez: 28 7 2020
Statut: ppublish

Résumé

In this study we determined the optimal number of transperineal magnetic resonance imaging ultrasound fusion targeted biopsy cores per lesion needed for the detection of clinically significant prostate cancer. A total of 101 patients with at least 1 lesion with a PI-RADS® (Prostate Imaging Reporting and Data System) score of 3 or greater were recruited prospectively. At least 4 transperineal magnetic resonance imaging ultrasound fusion targeted biopsy cores per lesion were performed, followed by systematic biopsy. The Kappa test was used to evaluate the consistency of the clinically significant prostate cancer detection rate between different targeted biopsy cores and 4 or more cores, which was regarded as reference standard. In the total cohort of 101 patients 49 (48.5%), 55 (54.5%) and 57 (56.4%) were diagnosed with clinically significant prostate cancer by systematic biopsy, targeted biopsy or targeted biopsy plus systematic biopsy, respectively. As for the total of 161 lesions, the clinically significant prostate cancer detection rate based on 1, 2, 3, or 4 or more targeted biopsy cores was made in 27.3%, 32.9%, 37.3% and 39.1%, respectively. Three cores showed great consistency with 4 or more cores in clinically significant prostate cancer detection rate (Kappa coefficient of 0.961, p <0.001) with a sensitivity of 95.2% (95% CI 85.8-98.8), and only missed 3 lesions harboring clinically significant prostate cancer. Similar results were obtained in cases with PI-RADS 3 or 4 or maximal diameter of less than 1.5 cm. Three targeted biopsies per lesion were suitable during transperineal magnetic resonance imaging ultrasound fusion biopsy, especially for lesions of PI-RADS 3 or 4, or small lesions (maximal diameter less than 1.5 cm), which may help to tailor targeted prostate biopsy procedures.

Identifiants

pubmed: 32716686
doi: 10.1097/JU.0000000000001302
doi:

Substances chimiques

KLK3 protein, human EC 3.4.21.-
Kallikreins EC 3.4.21.-
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1202-1208

Commentaires et corrections

Type : CommentIn

Auteurs

Gang Song (G)

Department of Urology, Peking University First Hospital, Beijing, China.
Institute of Urology, Peking University, Beijing, China.
National Urological Cancer Center of China, Beijing, China.

Mingjian Ruan (M)

Department of Urology, Peking University First Hospital, Beijing, China.
Institute of Urology, Peking University, Beijing, China.
National Urological Cancer Center of China, Beijing, China.

He Wang (H)

Department of Radiology, Peking University First Hospital, Beijing, China.

Yu Fan (Y)

Department of Urology, Peking University First Hospital, Beijing, China.
Institute of Urology, Peking University, Beijing, China.
National Urological Cancer Center of China, Beijing, China.

Qun He (Q)

Department of Urology, Peking University First Hospital, Beijing, China.
Institute of Urology, Peking University, Beijing, China.
National Urological Cancer Center of China, Beijing, China.

Zhiyong Lin (Z)

Department of Radiology, Peking University First Hospital, Beijing, China.

Xueying Li (X)

Department of Statistics, Peking University First Hospital, Beijing, China.

Peng Li (P)

Department of Ultrasound, Peking University First Hospital, Beijing, China.

Xiaoying Wang (X)

Department of Radiology, Peking University First Hospital, Beijing, China.

Zhisong He (Z)

Department of Urology, Peking University First Hospital, Beijing, China.
Institute of Urology, Peking University, Beijing, China.
National Urological Cancer Center of China, Beijing, China.

Liqun Zhou (L)

Department of Urology, Peking University First Hospital, Beijing, China.
Institute of Urology, Peking University, Beijing, China.
National Urological Cancer Center of China, Beijing, China.

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Classifications MeSH