Direct tumour-adipocyte contact / Stroma AReactive Invasion Front Area (TAC/SARIFA) predicts adverse outcome in colorectal cancer: a focused evidence synthesis and meta-analysis.

HistopathologyJul 16, 2026 (epub)
Clinical ResearchOncology (Medical)

Nic G Reitsam, Bruno Märkl, Iris D Nagtegaal et al.

✦ AI-curated · Sources linked

In 30 seconds

This focused evidence synthesis and meta-analysis assessed whether direct tumour-adipocyte contact, termed TAC/SARIFA, is associated with survival in colorectal cancer. It included retrospective observational cohorts reporting multivariable-adjusted hazard ratios. Seven cohorts comprising 5,932 patients contributed cancer-specific survival data, and five cohorts comprising 4,545 patients contributed overall survival data. TAC/SARIFA positivity was associated with inferior cancer-specific survival (pooled HR 1.77, 95% confidence interval [CI] 1.55-2.01) and overall survival (pooled HR 1.53, 95% CI 1.39-1.68), with no relevant heterogeneity detected.

Key findings

  • TAC/SARIFA positivity was associated with inferior cancer-specific survival (pooled HR 1.77, 95% CI 1.55-2.01).
  • TAC/SARIFA positivity was associated with inferior overall survival (pooled HR 1.53, 95% CI 1.39-1.68).
  • Seven cohorts (5,932 patients) contributed cancer-specific survival data; five cohorts (4,545 patients) contributed overall survival data.

Why it matters

The findings suggest that a histological feature visible on H&E sections may provide prognostic information in colorectal cancer. Its association with both cancer-specific and overall survival supports further evaluation as a risk-stratification marker, while the observational evidence does not establish that TAC/SARIFA causes poorer outcomes or that using the marker improves patient care.

What to keep in mind

All included studies were retrospective observational cohorts; the authors state that prospective validation is warranted.

Source

Published in Histopathology. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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