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mpMRI preoperative staging in men treated with antiandrogen and androgen deprivation therapy before robotic prostatectomy.
Gold, Samuel A; VanderWeele, David J; Harmon, Stephanie; Bloom, Jonathan B; Karzai, Fatima; Hale, Graham R; Marhamati, Shawn; Rayn, Kareem N; Mehralivand, Sherif; Merino, Maria J; Gulley, James L; Bilusic, Marijo; Madan, Ravi A; Choyke, Peter L; Turkbey, Baris; Dahut, William; Pinto, Peter A.
Affiliation
  • Gold SA; Laboratory for Genitourinary Cancer Pathogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • VanderWeele DJ; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Harmon S; Clinical Research Directorate, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD.
  • Bloom JB; Laboratory for Genitourinary Cancer Pathogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Karzai F; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Hale GR; Laboratory for Genitourinary Cancer Pathogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Marhamati S; Laboratory for Genitourinary Cancer Pathogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD; Department of Urology, Georgetown University Hospital, Washington, DC.
  • Rayn KN; Laboratory for Genitourinary Cancer Pathogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Mehralivand S; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Merino MJ; Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Gulley JL; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Bilusic M; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Madan RA; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Choyke PL; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Turkbey B; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Dahut W; Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Pinto PA; Laboratory for Genitourinary Cancer Pathogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD. Electronic address: pintop@mail.nih.gov.
Urol Oncol ; 37(6): 352.e25-352.e30, 2019 06.
Article in En | MEDLINE | ID: mdl-31000430
INTRODUCTION: Using multiparametric magnetic resonance imaging (mpMRI), we sought to preoperatively characterize prostate cancer (PCa) in the setting of antiandrogen plus androgen deprivation therapy (AA-ADT) prior to robotic-assisted radical prostatectomy (RARP). We present our preliminary findings regarding mpMRI depiction of changes of disease staging features and lesion appearance in treated prostate. METHODS: Prior to RARP, men received 6 months of enzalutamide and goserelin. mpMRI consisting of T2 weighted, b = 2,000 diffusion weighted imaging, apparent diffusion coefficient mapping, and dynamic contrast enhancement sequences was acquired before and after neoadjuvant therapy. Custom MRI-based prostate molds were printed to directly compare mpMRI findings to H&E whole-mount pathology as part of a phase II clinical trial (NCT02430480). RESULTS: Twenty men underwent imaging and RARP after a regimen of AA-ADT. Positive predictive values for post-AA-ADT mpMRI diagnosis of extraprostatic extension, seminal vesicle invasion, organ-confined disease, and biopsy-confirmed PCa lesions were 71%, 80%, 80%, and 85%, respectively. Post-treatment mpMRI correctly staged disease in 15/20 (75%) cases with 17/20 (85%) correctly identified as organ-confined or not. Of those incorrectly staged, 2 were falsely positive for higher stage features and 1 was falsely negative. Post-AA-ADT T2 weighted sequences best depicted presence of PCa lesions as compared to diffusion weighted imaging and dynamic contrast enhancement sequences. CONCLUSION: mpMRI proved reliable in detecting lesion changes after antiandrogen therapy corresponding to PCa pathology. Therefore, mpMRI of treated prostates may be helpful for assessing men for surgical planning and staging.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatectomy / Prostatic Neoplasms / Robotic Surgical Procedures / Multiparametric Magnetic Resonance Imaging Type of study: Prognostic_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: Urol Oncol Journal subject: NEOPLASIAS / UROLOGIA Year: 2019 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatectomy / Prostatic Neoplasms / Robotic Surgical Procedures / Multiparametric Magnetic Resonance Imaging Type of study: Prognostic_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: Urol Oncol Journal subject: NEOPLASIAS / UROLOGIA Year: 2019 Document type: Article Country of publication: United States