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Data analytics improves the diagnostic accuracy of serum free light chain results for detecting monoclonal gammopathy.
Treger, Rebecca S; Mathias, Patrick C; Cowan, Andrew J; Green, Damian; Hutchinson, Kathleen; Bryan, Andrew; Chaudhary, Anu; Fink, Susan L; Wener, Mark H; Morishima, Chihiro.
Affiliation
  • Treger RS; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, US.
  • Mathias PC; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, US.
  • Cowan AJ; Division of Medical Oncology, University of Washington, Seattle, WA, US.
  • Green D; Clinical Research Division, Fred Hutch Cancer Center, Seattle, WA, US.
  • Hutchinson K; Division of Medical Oncology, University of Washington, Seattle, WA, US.
  • Bryan A; Clinical Research Division, Fred Hutch Cancer Center, Seattle, WA, US.
  • Chaudhary A; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, US.
  • Fink SL; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, US.
  • Wener MH; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, US.
  • Morishima C; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, US.
Am J Clin Pathol ; 161(3): 216-231, 2024 Mar 01.
Article in En | MEDLINE | ID: mdl-37936261
OBJECTIVES: To evaluate the real-world performance and reference intervals of the Binding Site Freelite serum free light chain (SFLC) assay (Thermo Fisher Scientific), a global standard for diagnosis, prognostication, and response assessment for monoclonal gammopathies. METHODS: An informatics-based approach was used to retrospectively evaluate concordance between SFLC and the orthogonal Sebia HYDRASYS immunofixation assay results in a large clinical data set consecutively reported between 2010 and 2020. RESULTS: Among patients with monoclonal-negative results by both SFLC and Sebia HYDRASYS immunofixation assays, 25% (1226/5057) had κ/λ ratios (KLRs) outside the manufacturer-defined and International Myeloma Working Group-cited normal reference interval of 0.26 to 1.65. These results were consistent over the study period and were not affected by sex, age, impaired kidney function, or assay antisera lot variation. Assay drift, in addition to other potential factors, affected the KLR distribution. Using International Statistical Classification of Diseases (ICD) codes, kidney function data, and the central 95% of KLR values generated on the Optilite platform (Thermo Fisher Scientific), we derived a new reference interval of 0.67 to 2.13, reducing the KLR false-positive rate to 8%. However, normal KLR persisted among 16% (14/85) of samples with free λ chains by immunofixation, warranting caution during interpretation. CONCLUSIONS: Our analysis indicated that revision of Freelite SFLC reference intervals improves assay interpretation and should prompt reconsideration of Freelite reference intervals worldwide.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Monoclonal Gammopathy of Undetermined Significance / Data Science Limits: Humans Language: En Journal: Am J Clin Pathol Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Monoclonal Gammopathy of Undetermined Significance / Data Science Limits: Humans Language: En Journal: Am J Clin Pathol Year: 2024 Document type: Article Country of publication: