Ki-67 Labeling Index in Pulmonary Carcinoid Tumors

Ki-67 labeling index is incorporated into the 3-tiered grading system for neuroendocrine neoplasms of the gastrointestinal and pancreaticobiliary tract (grade 1 tumors have Ki-67 <3% by hot spot method; grade 2 tumors have Ki-67 between 3% and 20%; grade 3 neoplasms have Ki-67 >20%).8 Although...

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Bibliographic Details
Published inArchives of pathology & laboratory medicine (1976) Vol. 144; no. 8; pp. 982 - 990
Main Authors Boland, Jennifer M, Kroneman, Trynda N, Jenkins, Sarah M, Terra, Simone B S P, Xie, Hao, Molina, Julian, Mounajjed, Taofic, Roden, Anja C
Format Journal Article
LanguageEnglish
Published Northfield College of American Pathologists 01.08.2020
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Summary:Ki-67 labeling index is incorporated into the 3-tiered grading system for neuroendocrine neoplasms of the gastrointestinal and pancreaticobiliary tract (grade 1 tumors have Ki-67 <3% by hot spot method; grade 2 tumors have Ki-67 between 3% and 20%; grade 3 neoplasms have Ki-67 >20%).8 Although Ki-67 is not currently used in the WHO grading scheme for pulmonary carcinoids, many studies have shown that ACTs have increased Ki-67, and that increased Ki-67 is generally associated with poorer prognosis.2,9-24 However, the use of Ki-67 labeling index in the evaluation of pulmonary carcinoid tumors is controversial and not standardized, because there are conflicting data regarding the added value to the current WHO system. Ki-67 immunostaining (clone MIB1, Dako, Carpintería, California) was performed on formalin-fixed, paraffin-embedded tissue sections from both biopsy/cell block and resection specimens (1 representative whole tissue section was stained for resection specimens to include any areas of increased mitotic activity, if applicable). Ki-67 labeling index was determined via digital image analysis by an experienced technologist, using both hot spot and tumor tracing methods. Manual assessment of Ki-67 was performed in 10% of cases by a pathologist as a quality control measure, which included verification of placement of hot spot boxes, confirmation of excluded nontumor areas/cells, and counting of at least 5 high-power fields for a manual estimate of Ki-67 both in hot spot areas and at random; no discrepancies were identified from the automated reads.
ISSN:0003-9985
1543-2165
DOI:10.5858/arpa.2019-0374-OA