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Related Concept Videos

Tumor Progression02:07

Tumor Progression

6.2K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
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Comparison of Five Pathological Tumor Regression Grading Systems for Rectal Cancer Following Chemoradiation:

Sahaphol Anannamcharoen1, Chinakrit Boonya-Ussadorn1, K Satayasoontorn2

  • 1Department of Surgery, Phramongkutklao Hospital, Thailand.

Asian Pacific Journal of Cancer Prevention : APJCP
|January 28, 2025
PubMed
Summary
This summary is machine-generated.

Tumor regression grading (TRG) systems assessing fibrosis and residual tumor show strong correlations. The modified Ryan TRG system, focusing only on residual cancer cells, demonstrated lower reliability in this rectal adenocarcinoma study.

Keywords:
Correlation coefficientTest-Retestchemoradiotherapyrectal cancertumor regression grade

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Area of Science:

  • Oncology
  • Pathology
  • Medical Imaging

Background:

  • Accurate tumor regression grading (TRG) is crucial for evaluating neoadjuvant therapy response in rectal adenocarcinoma.
  • Standardized TRG systems are essential for consistent clinical interpretation and research.

Purpose of the Study:

  • To evaluate the correlation among five distinct tumor regression grading systems.
  • To assess the test-retest reliability and internal validity of these TRG systems in rectal cancer specimens.

Main Methods:

  • A test-retest reliability study was conducted on 34 rectal adenocarcinoma specimens post-neoadjuvant chemoradiotherapy (CRT).
  • Pathologists assessed each specimen twice, 3 weeks apart, using five TRG systems: Dworak, Mandard, Ryan, AJCC, and modified Ryan.
  • Intra-rater reliability was analyzed to determine consistency.

Main Results:

  • TRG systems evaluating both residual tumor and therapy-induced fibrosis demonstrated very strong correlations (0.964–1.0).
  • The modified Ryan system, based solely on residual viable cancer cells, showed lower correlations (0.549–0.617).
  • Excellent intra-rater correlation coefficients were observed for Mandard (0.947), Dworak (0.947), Ryan (0.918), AJCC (0.957), and modified Ryan (0.934) systems.

Conclusions:

  • TRG systems incorporating both residual tumor and fibrosis exhibit high inter-system correlation.
  • The modified Ryan TRG system may lead to interpretation discrepancies due to its sole reliance on residual cancer cell quantity.
  • The study confirms excellent intra-rater reliability for most TRG systems, indicating high internal validity.