Development and Validation of Measurement Traceability for In Situ Immunoassays

• Published in: Clinical chemistry (Baltimore, Md.) Md.), 2021-05, Vol.67 (5), p.763-771
• Main Authors: Torlakovic, Emina E, Sompuram, Seshi R, Vani, Kodela, Wang, Lili, Schaedle, Anika K, DeRose, Paul C, Bogen, Steven A
• Format: Article
• Language: English
• Subjects: Analysis; Analytical chemistry; Arrays; Breast cancer; Cellular proteins; Estrogen receptors; Estrogens; Fluorescein; Fluoresceins; Humans; Immunoassay; Immunoassays; Immunohistochemistry; Laboratories; Laboratory tests; Mathematical analysis; Mensuration; Methods; Proteins; Quality assessment; Quality control; Receptors, Estrogen; Reference materials; Reference Standards; Sensitivity analysis; Standardization
• ISSN: 0009-9147; 1530-8561
• DOI: 10.1093/clinchem/hvab008

Abstract Background Immunoassays for protein analytes measured in situ support a $2 billion laboratory testing industry that suffers from significant interlaboratory disparities, affecting patient treatment. The root cause is that immunohistochemical testing lacks the generally accepted tools for analytic standardization, including reference standards and traceable units of measure. Until now, the creation of these tools has represented an insoluble technical hurdle. Methods We address the need with a new concept in metrology—that is, linked traceability. Rather than calculating analyte concentration directly, which has proven too variable, we calculate concentration by measuring an attached fluorescein, traceable to NIST Standard Reference Material 1934, a fluorescein standard. Results For validation, newly developed estrogen receptor (ER) calibrators were deployed in tandem with an array of 80 breast cancer tissue sections in a national external quality assessment program. Laboratory performance was assessed using both the ER standards and the tissue array. Similar to previous studies, the tissue array revealed substantial discrepancies in ER test results among the participating laboratories. The new ER calibrators revealed a broad range of analytic sensitivity, with the lower limits of detection ranging from 7310 to 74 790 molecules of ER. The data demonstrate, for the first time, that the variable test results correlate with analytic sensitivity, which can now be measured quantitatively. Conclusions The reference standard enables precise interlaboratory alignment of immunohistochemistry test sensitivity for measuring cellular proteins in situ. The introduction of a reference standard and traceable units of measure for protein expression marks an important milestone.