Detection of circulating tumor cells and micrometastases in Stage II, III, and IV breast cancer patients utilizing cytology and immunocytochemistry

Evaluation for circulating tumor cells and bone marrow micrometastases has generated considerable interest due to a potential association with disease recurrence and poor prognosis. In this study, we examined bone marrow and apheresis samples from Stage II, III, and IV patients (n 120) enrolled in v...

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Veröffentlicht in:Diagnostic cytopathology 2000-05, Vol.22 (5), p.323-328
Hauptverfasser: Fetsch, Patricia A., Cowan, Kenneth H., Weng, David E., Freifield, Allison, Filie, Armando C., Abati, Andrea
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container_end_page 328
container_issue 5
container_start_page 323
container_title Diagnostic cytopathology
container_volume 22
creator Fetsch, Patricia A.
Cowan, Kenneth H.
Weng, David E.
Freifield, Allison
Filie, Armando C.
Abati, Andrea
description Evaluation for circulating tumor cells and bone marrow micrometastases has generated considerable interest due to a potential association with disease recurrence and poor prognosis. In this study, we examined bone marrow and apheresis samples from Stage II, III, and IV patients (n 120) enrolled in various clinical breast cancer trials at the National Institutes of Health/National Cancer Institute. For each patient sample, two Diff‐Quik‐stained cytospins were reviewed for morphology, and approximately 1 × 106 cells were analyzed for the expression of cytokeratins using an avidin‐biotin immunoperoxidase method. Keratin‐positive malignant cells appearing as single cells or in small clusters were detected in bone marrow samples from Stage IV patients only (9/68, 13%) and detected in apheresis samples from both Stage III and IV patients (13/245, 5%). These findings indicate that the combination of cytomorphology with immunocytochemistry can be utilized for the investigation of circulating tumor cells and bone marrow micrometastases, and that positive results appear to correlate with high tumor stage/burden. Diagn. Cytopathol. 2000;22:323–328. Published 2000 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1097-0339(200005)22:5<323::AID-DC13>3.0.CO;2-L
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Cytopathol</addtitle><description>Evaluation for circulating tumor cells and bone marrow micrometastases has generated considerable interest due to a potential association with disease recurrence and poor prognosis. In this study, we examined bone marrow and apheresis samples from Stage II, III, and IV patients (n 120) enrolled in various clinical breast cancer trials at the National Institutes of Health/National Cancer Institute. For each patient sample, two Diff‐Quik‐stained cytospins were reviewed for morphology, and approximately 1 × 106 cells were analyzed for the expression of cytokeratins using an avidin‐biotin immunoperoxidase method. Keratin‐positive malignant cells appearing as single cells or in small clusters were detected in bone marrow samples from Stage IV patients only (9/68, 13%) and detected in apheresis samples from both Stage III and IV patients (13/245, 5%). 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Mammary gland</topic><topic>Humans</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Keratins</topic><topic>Medical sciences</topic><topic>micrometastases</topic><topic>Neoplasm Metastasis - diagnosis</topic><topic>Neoplasm Metastasis - pathology</topic><topic>Neoplasm Staging</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. 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subjects Biological and medical sciences
Biomarkers, Tumor
Breast Neoplasms - pathology
circulating tumor cells
cytokeratin
Female
Genital system. Mammary gland
Humans
immunocytochemistry
Immunohistochemistry
Investigative techniques, diagnostic techniques (general aspects)
Keratins
Medical sciences
micrometastases
Neoplasm Metastasis - diagnosis
Neoplasm Metastasis - pathology
Neoplasm Staging
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
title Detection of circulating tumor cells and micrometastases in Stage II, III, and IV breast cancer patients utilizing cytology and immunocytochemistry
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