Literature DB >> 18253858

Clinical implications of introducing a new PSA assay.

Ramachandran Venkitaraman1, Andrew R Norman, Jhangir Iqbal, David P Dearnaley, Alan Horwich, Robert A Huddart, Chris C Parker.   

Abstract

BACKGROUND: A number of different prostate-specific antigen (PSA) assays are in common use. There has been little consideration of the possible clinical implications of interassay variation. The availability of two assays in the same laboratory provided an opportunity to audit the clinical implications of the interassay variation in PSA levels.
METHODS: The same serum samples from patients with prostate cancer on follow-up were analyzed for PSA by the Abbott AxSYM assay and by the Abbott ARCHITECT assays. To assess within-patient reproducibility of the interassay variation, repeat analysis of PSA by both assays was conducted in a second sample obtained at least 1 month after the first.
RESULTS: Samples from 156 cases were analyzed. The mean ratio of serum PSA values by the two assays (AxSYM assay/ARCHITECT assay) was 0.89 (range 0.5-2.27). The interassay coefficient of variation was 20%. In a subgroup of 50 cases with repeat samples available, the correlation coefficient, r, of the interassay variation in PSA between the first and second samples was 0.441.
CONCLUSIONS: Interassay variation in serum PSA is clinically significant, both between patients and on repeated measurement within the same patient. Clinicians should be aware that simple correction factors may not accurately control for variation between PSA assays. Ideally, patients on follow-up for prostate cancer should be monitored using a single PSA assay.

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Year:  2008        PMID: 18253858     DOI: 10.1007/s11255-007-9330-7

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN: 0301-1623            Impact factor:   2.370


  5 in total

1.  Comparison of a polyclonal and monoclonal immunoassay for PSA: need for an international antigen standard.

Authors:  H C Graves; N Wehner; T A Stamey
Journal:  J Urol       Date:  1990-12       Impact factor: 7.450

2.  Comparability of serum prostate-specific antigen measurement between the hybritech Tandem-R and Abbott AxSYM assays.

Authors:  S Leewansangtong; S Goktas; R Lepoff; K Holthaus; E D Crawford
Journal:  Urology       Date:  1998-09       Impact factor: 2.649

3.  Comparison of 6 automated assays for total and free prostate-specific antigen with special reference to their reactivity toward the WHO 96/670 reference preparation.

Authors:  Sheila A R Kort; Frans Martens; Hilde Vanpoucke; Hans L van Duijnhoven; Marinus A Blankenstein
Journal:  Clin Chem       Date:  2006-06-08       Impact factor: 8.327

4.  Comparability of serum prostate-specific antigen measurement between the Roche Diagnostics Elecsys 2010 and the Abbott Architect i2000.

Authors:  Marion A Gray; Russell R Cooke; Philip Weinstein; John N Nacey
Journal:  Ann Clin Biochem       Date:  2004-05       Impact factor: 2.057

5.  Comparison of 3 investigational assays for the free form of prostate specific antigen.

Authors:  R G Nixon; G E Meyer; A B Blase; M H Gold; M K Brawer
Journal:  J Urol       Date:  1998-08       Impact factor: 7.450

  5 in total

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