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Sequential Prostate Magnetic Resonance Imaging in Newly Diagnosed High-risk Prostate Cancer Treated with Neoadjuvant Enzalutamide is Predictive of Therapeutic Response.
Karzai, Fatima; Walker, Stephanie M; Wilkinson, Scott; Madan, Ravi A; Shih, Joanna H; Merino, Maria J; Harmon, Stephanie A; VanderWeele, David J; Cordes, Lisa M; Carrabba, Nicole V; Bright, John R; Terrigino, Nicolas T; Chun, Guinevere; Bilusic, Marijo; Couvillon, Anna; Hankin, Amy; Williams, Monique N; Lis, Rosina T; Ye, Huihui; Choyke, Peter L; Gulley, James L; Sowalsky, Adam G; Turkbey, Baris; Pinto, Peter A; Dahut, William L.
Afiliação
  • Karzai F; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Walker SM; Molecular Imaging Program, NCI, NIH, Bethesda, Maryland.
  • Wilkinson S; Laboratory for Genitourinary Cancer Pathogenesis, NCI, NIH, Bethesda, Maryland.
  • Madan RA; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Shih JH; Division of Cancer Treatment and Diagnosis, Biometric Research Program, NCI, NIH, Rockville, Maryland.
  • Merino MJ; Laboratory of Pathology, NCI, NIH, Bethesda, Maryland.
  • Harmon SA; Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc., NCI Campus at Frederick, Frederick, Maryland.
  • VanderWeele DJ; Laboratory for Genitourinary Cancer Pathogenesis, NCI, NIH, Bethesda, Maryland.
  • Cordes LM; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Carrabba NV; Laboratory for Genitourinary Cancer Pathogenesis, NCI, NIH, Bethesda, Maryland.
  • Bright JR; Laboratory for Genitourinary Cancer Pathogenesis, NCI, NIH, Bethesda, Maryland.
  • Terrigino NT; Laboratory for Genitourinary Cancer Pathogenesis, NCI, NIH, Bethesda, Maryland.
  • Chun G; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Bilusic M; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Couvillon A; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Hankin A; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Williams MN; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Lis RT; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Ye H; Department of Pathology, Ronald Reagan UCLA Medical Center, Los Angeles, California.
  • Choyke PL; Molecular Imaging Program, NCI, NIH, Bethesda, Maryland.
  • Gulley JL; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
  • Sowalsky AG; Laboratory for Genitourinary Cancer Pathogenesis, NCI, NIH, Bethesda, Maryland.
  • Turkbey B; Molecular Imaging Program, NCI, NIH, Bethesda, Maryland.
  • Pinto PA; Urologic Oncology Branch, NCI, NIH, Bethesda, Maryland.
  • Dahut WL; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland. dahutw@mail.nih.gov.
Clin Cancer Res ; 27(2): 429-437, 2021 01 15.
Article em En | MEDLINE | ID: mdl-33023952
ABSTRACT

PURPOSE:

For high-risk prostate cancer, standard treatment options include radical prostatectomy (RP) or radiotherapy plus androgen deprivation therapy (ADT). Despite definitive therapy, many patients will have disease recurrence. Imaging has the potential to better define characteristics of response and resistance. In this study, we evaluated prostate multiparametric MRI (mpMRI) before and after neoadjuvant enzalutamide plus ADT. PATIENTS AND

METHODS:

Men with localized intermediate- or high-risk prostate cancer underwent a baseline mpMRI and mpMRI-targeted biopsy followed by a second mpMRI after 6 months of enzalutamide and ADT prior to RP. Specimens were sectioned in the same plane as mpMRI using patient-specific 3D-printed molds to permit mpMRI-targeted biopsies to be compared with the same lesion from the RP. Specimens were analyzed for imaging and histologic correlates of response.

RESULTS:

Of 39 patients enrolled, 36 completed imaging and RP. Most patients (92%) had high-risk disease. Fifty-eight lesions were detected on baseline mpMRI, of which 40 (69%) remained measurable at 6-month follow-up imaging. Fifty-five of 59 lesions (93%) demonstrated >50% volume reduction on posttreatment mpMRI. Three of 59 lesions (5%) demonstrated growth in size at follow-up imaging, with two lesions increasing more than 3-fold in volume. On whole-mount pathology, 15 patients demonstrated minimal residual disease (MRD) of <0.05 cc or pathologic complete response. Low initial mpMRI relative tumor burden was most predictive of MRD on final pathology.

CONCLUSIONS:

Low relative lesion volume at baseline mpMRI was predictive of pathologic response. A subset of patients had limited response. Selection of patients based on these metrics may improve outcomes in high-risk disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Protocolos de Quimioterapia Combinada Antineoplásica / Imageamento por Ressonância Magnética Multiparamétrica Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Protocolos de Quimioterapia Combinada Antineoplásica / Imageamento por Ressonância Magnética Multiparamétrica Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article