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Risk Stratification by Urinary PCA3 Testing Prior to MRI-US Fusion-Targeted Prostate Biopsy among Men with No Previous History of Biopsy

Fenstermaker, Michael; Mendhiratta, Neil; Bjurlin, Marc A; Meng, Xiaosong; Rosenkrantz, Andrew B; Huang, Richard; Deng, Fang Ming; Zhou, Ming; Huang, William C; Lepor, Herbert; Taneja, Samir S
OBJECTIVES: To determine whether a combination of PCA3 and MRI suspicion score (mSS) could further optimize detection of prostate cancer on MRF-TB among men with no previous history of biopsy. MATERIALS AND METHODS: 187 men presenting to our institution between 6/12 and 8/14 who underwent multiparametric MRI and PCA3 prior to MRF-TB. Biopsy results, stratified by biopsy indication and PCA3 score, were recorded. Receiver operating characteristics (ROC) curves and multivariable logistic regressions were utilized to model the association of PCA3 and mSS with cancer detection on MRF-TB. RESULTS: PCA3 is associated with cancer detection on MRF-TB for men with no prior biopsies (AUC = 0.67, 95% CI 0.59-0.76). Using a cutoff of >/=35, PCA3 was associated with cancer risk among men with mSS 2-3 (p=0.004), but not among those with mSS 4-5 (p=0.340). The interaction of PCA3 and mSS demonstrated significantly higher discrimination for cancer than mSS alone (AUC: 0.83 vs. 0.79, p=0.0434). CONCLUSIONS: Urinary PCA3 is associated with mSS and the detection of cancer on MRF-TB for men with no prior biopsies. PCA3 notably demonstrates a high negative predictive value among mSS 2-3. However, in the case of high suspicion mpMRI, PCA3 is not associated with cancer detection on MRF-TB adding little to cancer diagnosis. Further studies are needed to evaluate the utility of PCA3 in predicting cancer among men with normal mpMRI.
PMID: 27562202
ISSN: 1527-9995
CID: 2221652

Complications After Systematic, Random, and Image-guided Prostate Biopsy

Borghesi, Marco; Ahmed, Hashim; Nam, Robert; Schaeffer, Edward; Schiavina, Riccardo; Taneja, Samir; Weidner, Wolfgang; Loeb, Stacy
CONTEXT: Prostate biopsy (PB) represents the gold standard method to confirm the presence of cancer. In addition to traditional random or systematic approaches, a magnetic resonance imaging (MRI)-guided technique has been introduced recently. OBJECTIVE: To perform a systematic review of complications after transrectal ultrasound (TRUS)-guided, transperineal, and MRI-guided PB. EVIDENCE ACQUISITION: We performed a systematic literature search of Web of Science, Embase, and Scopus databases up to October 2015, according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. Complications and mortality following random, systematic, and image-guided PBs were reviewed. Eighty-five references were included. EVIDENCE SYNTHESIS: The most frequent complication after PB was minor and self-limiting bleeding (hematuria and hematospermia), regardless of the biopsy approach. Occurrence of rectal bleeding was comparable for traditional TRUS-guided and image-guided PBs. Almost 25% of patients experienced lower urinary tract symptoms, but only a few had urinary retention, with higher rates after a transperineal approach. Temporary erectile dysfunction was not negligible, with a return to baseline after 1-6 mo. The incidence of infective complications is increasing, with higher rates among men with medical comorbidities and older age. Transperineal and in-bore MRI-targeted biopsy may reduce the risk of severe infectious complications. Mortality after PB is uncommon, regardless of biopsy technique. CONCLUSIONS: Complications after PB are frequent but often self-limiting. The incidence of hospitalization due to severe infections is continuously increasing. The patient's general health status, risk factors, and likelihood of antimicrobial resistance should be carefully appraised before scheduling a PB. PATIENT SUMMARY: We reviewed the variety and incidence of complications after prostate biopsy. Even if frequent, complications seldom represent a problem for the patient. The most troublesome complications are infections. To minimize this risk, the patient's medical condition should be carefully evaluated before biopsy.
PMID: 27543165
ISSN: 1873-7560
CID: 2219482

Re: Tissue-Based Genomics Augments Post-Prostatectomy Risk Stratification in a Natural History Cohort of Intermediate- and High-Risk Men [Comment]

Taneja, Samir S
PMID: 26699962
ISSN: 1527-3792
CID: 2548552

Re: Use, Complications, and Costs of Stereotactic Body Radiotherapy for Localized Prostate Cancer

Taneja, Samir S
PMID: 27845107
ISSN: 1527-3792
CID: 2548502

Re: Duration of Androgen Suppression before Radiotherapy for Localized Prostate Cancer: Radiation Therapy Oncology Group Randomized Clinical Trial 9910 [Comment]

Taneja, Samir S
PMID: 26699964
ISSN: 1527-3792
CID: 2548542

Re: Redirecting Abiraterone Metabolism to Fine-Tune Prostate Cancer Anti-Androgen Therapy

Taneja, Samir S
PMID: 27751453
ISSN: 1527-3792
CID: 2548512

Re: The Effect of a Pure Anti-Inflammatory Therapy on Reducing Prostate-Specific Antigen Levels in Patients Diagnosed with a Histologic Prostatitis

Taneja, Samir S
PMID: 27751452
ISSN: 1527-3792
CID: 2548522

Re: Lethal Prostate Cancer in the PLCO Cancer Screening Trial

Taneja, Samir S
PMID: 27845108
ISSN: 1527-3792
CID: 2548492

Re: Nanoparticle-Enabled Selective Destruction of Prostate Tumor Using MRI-Guided Focal Photothermal Therapy

Taneja, Samir S
PMID: 27845145
ISSN: 1527-3792
CID: 2548482

Re: Chemohormonal Therapy in Metastatic Hormone-Sensitive Prostate Cancer [Comment]

Taneja, Samir S
PMID: 26699961
ISSN: 1527-3792
CID: 2548562