Background: An increasing number of multiparametric immuno-analysers for PS
A assays are available. As different immuno-assays may vary in their analyt
ical quality and their accuracy for the follow-up of patients, expertise is
necessary for each new assay. Methods: The PSA assay on the Vitros-ECi ana
lyser has been evaluated and compared with the PSA assay from the Kryptor a
nalyser. Results: Variation coefficients were 0.91 to 1.98% for within-run
assays, and 4.2% to 5.4% for inter-assay (PSA levels = 0.8 mug/L to 33.6 mu
g/L). Dilution tests showed 93 to 136% recovery until 70 mug/L PSA. Functio
nal sensitivity was estimated at 0.03 mug/L. Equimolarity of the test was c
onfirmed. Correlation of PSA levels measured with Vitros-ECi and Kryptor an
alysers displayed a correlation coefficient r(2) of 0.9716. The half-lives
and doubling times of PSA were similar using both methods. Conclusion: Vitr
os-ECi PSA assay meets the major criteria for the management of prostate ca
ncer patients.