Recently, it was shown that the combination of 4K and mpMRI (4K-mpMRI) outperforms both tests individually in both area under the curve (AUC) and decision curve analyses6. However, attempts at devising a practical algorithm for 4K-mpMRI have yielded relatively weak sensitivities and low negative predictive values (NPV). In this presented study, the authors attempted to validate the combination of 4K-mpMRI and devise an improved algorithm for the identification of csPCa while limiting unnecessary prostate biopsies.
This was a retrospective study analyzing patients considered at risk for PCa and tested with 4K and mpMRI between the years 2016 and 2018. The primary outcome of csPCa was defined as Gleason grade group (GGG) >= 2 on prostate biopsy. 4K and mpMRI were compared via receiver operating characteristic (ROC) curves and logistic regression, and a model combining the two was tested for accuracy and efficiency. The 4K test was stratified to low (<7.5%) vs. high (>7.5%) risk disease, and mpMRI was stratified to PIRADS 3-5 vs. 0-2. The entire cohort consisted of 233 patients, and their basic clinical details are demonstrated in Table 1.
Table 1 – Basic clinical data of patients analyzed in the study:
mpMRI results of csPCa and non-csPCa stratified by the PIRADS score are shown in table 2, and the biopsy results are shown in table 3. The biopsy results demonstrate that 177/233 (76%) had either a negative or GGG =1 biopsy result, meaning that 76% of the biopsies should potentially have been avoided.
Table 2 – mpMRI results:
Table 3 -Biopsy results
The univariable and multivariable models identified an association between csPCa and both 4K and mpMRI, as shown in table 4. The combination of 4K+mpMRI had resulted in an AUC of 0.796, and a sensitivity of 93%, specificity of 71%, positive predictive value of 50%, and a NPV of 97%, which is quite impressive.
Table 4 – Univariable and multivariable models:
Dr. Lubin concluded his excellent presentation and stated that the combination of 4K+mpMRI might be a potentially useful screening test, maintaining high sensitivity and dramatically improving specificity. Larger prospective multicenter studies are obviously needed to validate these results before widespread clinical implementation.
Presented by: Marc Lubin, MD, Mount Sinai Hospital, New-York, USA
Written by: Hanan Goldberg, MD, Urologic Oncology Fellow (SUO), University of Toronto, Princess Margaret Cancer Centre @GoldbergHanan at American Urological Association's 2019 Annual Meeting (AUA 2019), May 3 – 6, 2019 in Chicago, Illinois
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