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Updated: Jul 22, 2026

Establishment and Analysis of Tumor Slice Explants As a Prerequisite for Diagnostic Testing
Published on: November 29, 2018
A semi-automated microscopic image analysis method for scoring Ki-67 nuclear immunostaining.
S M Fernezlian1, C M Baldavira1, M L F de Souza1
1Laboratório de Genômica e Histomorfometria, Departamento de Patologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.
Nuclear proliferation marker Ki-67 (MIB-1) nuclear gradient (NG) shows prognostic value in pulmonary typical carcinoid (PTC) tumors. This study introduces a method to assess Ki-67 NG, aiding in PTC diagnosis and prognosis.
Area of Science:
- Oncology
- Pathology
- Biomarker Research
Background:
- The diagnostic and prognostic significance of Ki-67 nuclear staining intensity and location (nuclear gradient, NG) remains underexplored in tumor pathology.
- Pulmonary typical carcinoid (PTC) tumors require refined prognostic markers for improved patient management.
Approach:
- A novel method was developed to classify Ki-67 NG, stratifying it into NG1, NG2, and NG3/4 categories.
- A semi-automated image analysis protocol was established to quantify Ki-67 NG in PTC, pulmonary adenocarcinoma (PAD), and breast ductal carcinoma (BDC).
- Intraobserver and interobserver agreement for Ki-67 NG determination were assessed in tumor specimens.
Key Points:
- Ki-67 NG1 and NG2 were observed at lower levels in PTC compared to PAD and BDC.
- Cox multivariate analysis revealed that Ki-67 NG1 and NG2 significantly predicted clinical outcomes in PTC, independent of age and lymph node status.
- The proposed semi-automated quantification method demonstrated high intraobserver consistency and moderate interobserver agreement.
Conclusions:
- Ki-67 nuclear gradient (NG) is a significant prognostic indicator in pulmonary typical carcinoid (PTC) tumors.
- The developed semi-automated image analysis protocol for Ki-67 NG quantification offers a valuable tool for PTC diagnosis and prognosis.
- Further validation of this method could enhance the clinical utility of Ki-67 immunohistochemistry in thoracic oncology.
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