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Editorials |
Pain Research & Nuffield Department of Anaesthetics, University of Oxford, Oxford Radcliffe Hospital, The Churchill, Oxford OX3 7LJ, UK, Fax +44 1865 226978, e-mail andrew.moore@pru.ox.ac.uk
In this issue of Clinical Chemistry (pp 158894),
Junker et al. elegantly try to tease out the usefulness of the
percentage of free prostate-specific antigen (PSA) (that fraction not
bound to proteins like
-antichymotrypsin) in making the differential
diagnosis of prostate cancer and benign prostatic hyperplasia (BPH).
Their approach was to select samples from well-defined patients, 30
with BPH and 50 with cancer, and subject them to analysis by four
commercial systems for analyzing the free and total PSA in serum. At a
sensitivity of 95%, negative predictive values and the proportion of
men with BPH who may be spared prostate biopsy were calculated.
There were differences between the assays. Absolute values reported for
control materials with different amounts of complexed PSA varied by
factors of 2 or more between the assays, and the proportion of free PSA
calculated from control materials was consistently lower in the CIS and
DPC methods than in the Boehringer and Hybritech methods. Negative
predictive values at 95% sensitivity had confidence intervals that
were wide (reflecting the limited number of samples), and those of all
four methods overlapped. But the bottom line was that, on this set of
samples, three of the four assay systems might prevent 40% or more of
men with BPH from having unnecessary (and painful) prostate biopsies;
the Hybritch method produced much
References
The following articles in journals at HighWire Press have cited this article:
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J. Peter, C. Unverzagt, T. N. Krogh, O. Vorm, and W. Hoesel Identification of Precursor Forms of Free Prostate-specific Antigen in Serum of Prostate Cancer Patients by Immunosorption and Mass Spectrometry Cancer Res., February 1, 2001; 61(3): 957 - 962. [Abstract] [Full Text] |
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J. Peter, C. Unverzagt, and W. Hoesel Analysis of Free Prostate-specific Antigen (PSA) after Chemical Release from the Complex with {alpha}1-Antichymotrypsin (PSA-ACT) Clin. Chem., April 1, 2000; 46(4): 474 - 482. [Abstract] [Full Text] [PDF] |
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