Diagnostic interobserver agreement for thyroid fine-needle aspirates: Effects of reviewer experience and molecular diagnostics

Am J Clin Pathol. 2024 Sep 3;162(3):302-313. doi: 10.1093/ajcp/aqae043.

Abstract

Objectives: Few cytologically indeterminate thyroid fine-needle aspirations (FNAs) harbor BRAF V600E. Here, we assess interobserver agreement for The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC) category III (atypia of undetermined significance [AUS]) FNAs harboring BRAF V600E and contrast their features with those harboring non-BRAF V600E alterations, with attention to cytopathology experience.

Methods: Seven reviewers evaluated 5 AUS thyroid FNAs harboring BRAF V600E. To blind reviewers, cases were intermixed with 19 FNAs falling within other TBSRTC categories and in which genetic alterations other than BRAF V600E had been identified (24 FNAs total). Interobserver agreement against both "index" and most popular ("mode") diagnoses was calculated. Four additional BRAF V600E cases were independently reviewed.

Results: Reviewers included 3 trainees and 3 American Board of Pathology (board)-certified cytopathologists. Board-certified cytopathologists, whose experience ranged from 2 to more than 15 subspecialty practice years, had known AUS rates. BRAF V600E was identified in 5 of 260 (2%) AUS FNAs. Interobserver agreement was higher among cytopathologists with more experience. Mode diagnosis differed from index diagnosis in 6 of 11 cases harboring RAS-like alterations; mode diagnosis was AUS in 4 of 5 BRAF V600E FNAs.

Conclusions: Atypia of undetermined significance of thyroid FNAs harboring BRAF V600E is uncommon yet relatively reproducible, particularly among pathologists with experience. It is advisable to sequence BRAF across V600 in such cases.

Keywords: The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC); fine-needle aspiration (FNA); health care quality assurance; interobserver agreement; molecular testing; thyroid nodule.

MeSH terms

  • Biopsy, Fine-Needle
  • Humans
  • Mutation
  • Observer Variation*
  • Pathology, Molecular
  • Proto-Oncogene Proteins B-raf* / genetics
  • Thyroid Gland* / pathology
  • Thyroid Neoplasms* / diagnosis
  • Thyroid Neoplasms* / genetics
  • Thyroid Neoplasms* / pathology
  • Thyroid Nodule / diagnosis
  • Thyroid Nodule / genetics
  • Thyroid Nodule / pathology

Substances

  • Proto-Oncogene Proteins B-raf
  • BRAF protein, human