4.4 Article

Prognostic Utility of the Ki-67 Labeling Index in Follicular Thyroid Tumors: a 20-Year Experience from a Tertiary Thyroid Center

Journal

ENDOCRINE PATHOLOGY
Volume 33, Issue 2, Pages 231-242

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12022-022-09714-4

Keywords

Follicular thyroid adenoma; Follicular thyroid carcinoma; Ki-67; Immunohistochemistry; Prognosis

Funding

  1. Karolinska Institutet
  2. Swedish Cancer Society
  3. Swedish Society for Medical Research
  4. Stockholm City Council

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The study aimed to assess the potential value of Ki-67 as an adjunct tool for distinguishing between follicular thyroid carcinoma (FTC) and adenoma (FTA) and predicting prognosis. The findings suggest that the Ki-67 labeling index can be used to separate FTC from FTA and identify high-risk FTCs. This marker has the potential to be beneficial in the histopathological assessment of follicular thyroid tumors if reproduced in international series.
Follicular thyroid tumors pose a diagnostic challenge on the preoperative level, as the discrimination between follicular thyroid carcinoma (FTC) and adenoma (FTA) demands careful histopathological investigation. Moreover, prognostication of FTCs is mostly based on tumor size and extent of invasive properties, while immunohistochemical markers pinpointing high-risk cases are lacking. We have routinely established a Ki-67 labeling index for follicular thyroid tumors since 1999. To assess the potential value of Ki-67 as an adjunct tool to (1) correctly separate FTCs from FTAs and (2) help identify poor-prognosis FTCs, we collected histopathological and clinical data from 818 follicular thyroid tumors with a histological Ki-67 labeling index established in clinical routine practice (516 FTAs, 252 FTCs, and 50 follicular thyroid tumors of uncertain malignant potential (FT-UMPs)). The Ki-67 labeling index was higher in FTCs (mean 5.8%) than in FTAs (mean 2.6%) (P < 0.001), and a receiver operating characteristic curve analysis revealed a cut-off value of 4% to separate FTC from FTA with a sensitivity and specificity of 65% and 83%, respectively. Similarly, a Ki-67 labeling index above 4% was found to identify FTCs that later metastasized from clinically indolent FTCs with a sensitivity and specificity of 80% and 48%, respectively. Ki-67 constituted an independent predictor of future FTC metastases/recurrence and death of disease, and a value > 4% was a reliable prognostic marker within individual pT staging groups. We conclude that Ki-67 is a potentially valuable marker for the prognostication of FTCs, and future implementation in the histopathological assessments of follicular thyroid tumors could be beneficial if reproduced in international series.

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