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Prostate Cancer Disseminated Tumor Cells are Rarely Detected in the Bone Marrow of Patients with Localized Disease Undergoing Radical Prostatectomy across Multiple Rare Cell Detection Platforms.
Chalfin, Heather J; Glavaris, Stephanie A; Malihi, Paymaneh D; Sperger, Jamie M; Gorin, Michael A; Lu, Changxue; Goodwin, C Rory; Chen, Yan; Caruso, Emily A; Dumpit, Ruth; Kuhn, Peter; Lang, Joshua M; Nelson, Peter S; Luo, Jun; Pienta, Kenneth J.
Afiliación
  • Chalfin HJ; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address: heather.chalfin@jhmi.edu.
  • Glavaris SA; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Malihi PD; Bridge Institute, University of Southern California, Los Angeles, California.
  • Sperger JM; Department of Medicine, University of Wisconsin Carbone Cancer Center, Madison, Wisconsin.
  • Gorin MA; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Lu C; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Goodwin CR; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Chen Y; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Caruso EA; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Dumpit R; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Kuhn P; Bridge Institute, University of Southern California, Los Angeles, California.
  • Lang JM; Department of Medicine, University of Wisconsin Carbone Cancer Center, Madison, Wisconsin.
  • Nelson PS; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Luo J; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Pienta KJ; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
J Urol ; 199(6): 1494-1501, 2018 06.
Article en En | MEDLINE | ID: mdl-29339080
ABSTRACT

PURPOSE:

Prostate circulating tumor cells escape into peripheral blood and enter bone marrow as disseminated tumor cells, representing an early step before conventionally detectable metastasis. It is unclear how frequently this occurs in localized disease and existing detection methods rely on epithelial markers with low specificity and sensitivity. We used multiple methodologies of disseminated tumor cell detection in bone marrow harvested at radical prostatectomy. MATERIALS AND

METHODS:

Bone marrow was harvested from 208 clinically localized cases, 16 controls and 5 metastatic cases with peripheral blood obtained from 37 metastatic cases. Samples were evaluated at 4 centers with 4 distinct platforms using antibody enrichment with the AdnaTest (Qiagen®) or VERSA (versatile exclusion based rare sample analysis), or whole sample interrogation with the RareCyte platform (Seattle, Washington) or HD-SCA (high definition single cell assay) using traditional epithelial markers and prostate specific markers. We investigated the sensitivity and specificity of these markers by evaluating expression levels in control and metastatic cases.

RESULTS:

EpCAM, NKX3.1 and AR were nonspecifically expressed in controls and in most samples using AdnaTest with no relation to perioperative variables. Only 1 patient with localized disease showed positive results for the prostate specific marker PSA. With the VERSA platform no localized case demonstrated disseminated tumor cells. With the RareCyte and HD-SCA platforms only a single patient had 1 disseminated tumor cell.

CONCLUSIONS:

Evaluation across multiple platforms revealed that epithelial markers are nonspecific in bone marrow and, thus, not suitable for disseminated tumor cell detection. Using prostate specific markers disseminated tumor cells were typically not detected in patients with localized prostate cancer.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Prostatectomía / Neoplasias de la Próstata / Médula Ósea / Células Neoplásicas Circulantes Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Prostatectomía / Neoplasias de la Próstata / Médula Ósea / Células Neoplásicas Circulantes Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article