Premium
Dynamic contrast‐enhanced ultrasound parametric imaging for the detection of prostate cancer
Author(s) -
Postema Arnoud W.,
Frinking Peter J.A.,
Smeenge Martijn,
De Reijke Theo M.,
De la Rosette Jean J.M.C.H.,
Tranquart Francois,
Wijkstra Hessel
Publication year - 2016
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/bju.13116
Subject(s) - medicine , biopsy , prostate cancer , radiology , prostate , medical diagnosis , contrast enhanced ultrasound , ultrasound , prostate biopsy , cancer
Objective To investigate the value of dynamic contrast‐enhanced ( DCE )‐ultrasonography ( US ) and software‐generated parametric maps in predicting biopsy outcome and their potential to reduce the amount of negative biopsy cores. Materials and Methods For 651 prostate biopsy locations (82 consecutive patients) we correlated the interpretation of DCE ‐ US recordings with and without parametric maps with biopsy results. The parametric maps were generated by software which extracts perfusion parameters that differentiate benign from malignant tissue from DCE ‐ US recordings. We performed a stringent analysis (all tumours) and a clinical analysis (clinically significant tumours). We calculated the potential reduction in biopsies (benign on imaging) and the resultant missed positive biopsies (false‐negatives). Additionally, we evaluated the performance in terms of sensitivity, specificity negative predictive value ( NPV ) and positive predictive value ( PPV ) on a per‐prostate level. Results Based on DCE ‐ US , 470/651 (72.2%) of biopsy locations appeared benign, resulting in 40 false‐negatives (8.5%), considering clinically significant tumours only. Including parametric maps, 411/651 (63.1%) of the biopsy locations appeared benign, resulting in 23 false‐negatives (5.6%). In the per‐prostate clinical analysis, DCE ‐ US classified 38/82 prostates as benign, missing eight diagnoses. Including parametric maps, 31/82 prostates appeared benign, missing three diagnoses. Sensitivity, specificity, PPV and NPV were 73, 58, 50 and 79%, respectively, for DCE ‐ US alone and 91, 56, 57 and 90%, respectively, with parametric maps. Conclusion The interpretation of DCE ‐ US with parametric maps allows good prediction of biopsy outcome. A two‐thirds reduction in biopsy cores seems feasible with only a modest decrease in cancer diagnosis.