Clinical Chemistry · 1988 · 11 citations · 0 references
MedicineOncologyCancer ImmunologyEndocrine OncologyTumor PathologyBioanalytical Method ValidationTumor AntigensAntigen Detection ComparisonCancer DiagnosticsImmunoassay BiomarkersLaboratory Test EvaluationReference Interval Determination
Abstract Using 600 clinical specimens, we compared the concordance of four methods for carcinoembryonic antigen: the Roche RIA (I); the Roche EIA (II); Hybritech EIA (III); and Abbott EIA (IV). EDTA-treated plasma was used for Methods I and II and serum for Methods III and IV. However, no significant difference was found between results for serum and plasma in Method II. The normal reference interval (in micrograms/L) was I (222 specimens), 1.94 +/- 1.54; II (57 specimens), 0.8 +/- 0.5; III (100 specimens), 2.94 +/- 2.47; and IV (614 specimens), less than 5.0. The precision of all four methods was acceptable. Concordance among all of the methods exceeded 90%.