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Very distal apical prostate tumours: identification on multiparametric MRI at 3 Tesla

Nix, Jeffrey W. ; Turkbey, Baris ; Hoang, Anthony ; Volkin, Dmitry ; Yerram, Nitin ; Chua, Celene ; Linehan, W. Marston ; Wood, Bradford ; Choyke, Peter ; Pinto, Peter A.

BJU International, December 2012, Vol.110(11b), pp.E694-E700 [Periódico revisado por pares]

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  • Título:
    Very distal apical prostate tumours: identification on multiparametric MRI at 3 Tesla
  • Autor: Nix, Jeffrey W. ; Turkbey, Baris ; Hoang, Anthony ; Volkin, Dmitry ; Yerram, Nitin ; Chua, Celene ; Linehan, W. Marston ; Wood, Bradford ; Choyke, Peter ; Pinto, Peter A.
  • Assuntos: Prostate Cancer ; Mri ; Distal Apical Region ; Biopsy
  • É parte de: BJU International, December 2012, Vol.110(11b), pp.E694-E700
  • Descrição: To purchase or authenticate to the full-text of this article, please visit this link: http://onlinelibrary.wiley.com/doi/10.1111/j.1464-410X.2012.11503.x/abstract Byline: Jeffrey W. Nix(3), Baris Turkbey(1), Anthony Hoang(3), Dmitry Volkin(3), Nitin Yerram(3), Celene Chua(3), W. Marston Linehan(3), Bradford Wood(2), Peter Choyke(1), Peter A. Pinto(3) Keywords: prostate cancer; MRI; distal apical region; biopsy Study Type - Diagnosis (case series) Level of Evidence 4 What's known on the subject? and What does the study add? MRI has been shown to improve prostate cancer detection rates. Pinto et al. (J Urol 2011; 86: 1281-5) reported their outcomes on 101 patients with low, moderate or high suspicion lesions on multiparametric MRI that were subsequently targeted via an MRI/ultrasound fusion biopsy platform. The prostate cancer detection rates were 27%, 66% and 89% respectively. Sciarra et al. (Clin Cancer Res 2010; 16: 1875-83) performed a prospective trial in 180 patients with prior negative biopsy and persistent PSA elevation. Patients were randomized to either MRI targeted biopsy followed by random 12-core TRUS biopsy vs random TRUS guided biopsy alone. Prostate cancer detection in the MRI targeted group was 45.5% vs 24.4% in the random group. Although MRI has been shown to improve prostate cancer detection rates, there has not previously been any work looking at the ability of MRI to detect prostate cancer localized to the very distal apex of the prostate. This is an important topic in that it might lead clinicians to counsel their patients in treatment decisions if it is felt that a treatment might not treat this section of the prostate well, e.g. high intensity focused ultrasound therapy that might spare the distal apex. OBJECTIVE To describe an undescribed 'very distal' apical prostate cancer on multiparametric MRI (mpMRI) since apical prostate cancer can be difficult to detect in transrectal ultrasound guided biopsy and might therefore be missed in treatment decisions such as high intensity focused ultrasound or surgical therapy. PATIENTS AND METHODS From January 2011 to December 2012 a total of 210 consecutive patients underwent 3 T mpMRI with endorectal coil followed by our previously described MRI/ultrasound image fused and directed TRUS biopsies. Patients also underwent 12-core TRUS sextant biopsies. The inclusion criteria required at least one distal apical prostate lesion visualized on mpMRI and targeted for biopsy. RESULTS A total of 38 men (median age 62 years, median PSA 7.68 ng/dL) were identified as having distal apical prostate cancer on mpMRI. Thirteen patients (34%) had a prior diagnosis of cancer and were on active surveillance protocols while 25 (66%) did not. Of those patients, 21 (55%) had undergone a median of two prior negative biopsies. Twenty-two patients (58%) were positive on biopsy for prostate cancer. On breakdown of patients who were positive, 17 (77%) were positive on TRUS random biopsies and 21 (95%) were positive on MRI targeted biopsies with the majority of patients having multifocal disease. At the distal apical lesions of interest, 80% were positive on MRI targeted biopsy. In addition 33% of these patients were upgraded based on MRI targeted biopsy at the distal lesion. CONCLUSIONS Very distal apical prostate cancer can be accurately detected and sampled with mpMRI and subsequent MRI/ultrasound fusion biopsy. This may aid clinicians and patients in decision making for therapeutic modalities. Author Affiliation: (3)National Institute of Health, National Cancer Institute, Urologic Oncology Branch (1)National Institute of Health, National Cancer Institute, Molecular Imaging Program (2)National Institute of Health, Diagnostic Radiology Division, Clinical Center, Bethesda, MD, USA Correspondence: (*) Jeffrey W. Nix, National Cancer Institute, Urologic Oncology Branch, 10 Center Drive, MSC 1107, CRC Room 1-5940W, Bethesda, MD 20892, USA. e-mail: jeffrey.nix@nih.gov Accepted for publication 11 July 2012 CAPTION(S): Supporting info item Testosterone levels and percentage of biopsy affected by tumour. Linear regression between the variables testosterone and percentage of tumour representation in the biopsy sample is displayed (P 0.01). In our centre, the tumour burden in the biopsy is expressed as the percentage of tumour in each prostatic lobe, ranging from >0% to 100%. Thus, the percentage of tumour represented in the biopsy adding the two prostatic lobes ranges from >0% to 200%. Testosterone levels and progression risk. Tumours were subclassified depending on their D'Amico risk of progression: low risk, PSA 10, DRE [less than or equal to] T2a and Gleason score [less than or equal to]6; intermediate risk, PSA 10-20, DRE = T2b and Gleason score 7; high risk, PSA > 20 or DRE a[yen] T2c or Gleason score a[yen]8. Low risk, testosterone 470 [+ or -] 171 ng/dL; intermediate risk, testosterone 445 [+ or -] 151 ng/dL; high risk, testosterone 365 [+ or -] 162 ng/dL; P= 0.03.

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