Prospective Study of Quantitation of Plasma DNA Levels in the Diagnosis of Malignant versus Benign Prostate Disease
Purpose: The aim of this study was to determine the potential of cell-free DNA levels as a diagnostic marker for prostate cancer, having first established the effect that blood sample processing has on this measurement. Experimental Design: A total of 152 blood samples were collected prospectively f...
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Published in: | Clinical cancer research Vol. 11; no. 4; pp. 1394 - 1399 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Philadelphia, PA
American Association for Cancer Research
15-02-2005
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Subjects: | |
Online Access: | Get full text |
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Summary: | Purpose: The aim of this study was to determine the potential of cell-free DNA levels as a diagnostic marker for prostate cancer,
having first established the effect that blood sample processing has on this measurement.
Experimental Design: A total of 152 blood samples were collected prospectively from patients before their prostate biopsy and 25 from men in two
distinct control groups. Blood was processed to yield three components: one-spin plasma ( n = 68), two-spin plasma ( n = 152), and serum ( n = 56 ) samples.
Results: Having established the effect of sample preparation on the measured DNA level, the more reliable two-spin plasma sample was
used to determine the relationship between DNA and the presence of prostate cancer. Those patients with cancer ( n = 78) had a significantly higher level of DNA compared with the control groups ( P < 0.0001 and P < 0.0001). However, DNA levels in patients with a benign biopsy ( n = 74) were significantly higher than the 78 patients confirmed to have cancer ( P = 0.02).
Conclusions: We conclude that the sample type used in the quantitation of cell-free DNA has an effect on the level reported. Elevated
levels are present in the two-spin plasma samples of patients with prostate cancer compared with healthy controls but are
not of diagnostic value during the management of prostate cancer. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-04-1237 |