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ePoster Display

456P - Prognostic and predictive value of tumor-infiltrating lymphocytes in combination with systemic inflammatory markers in colon cancer

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Colon and Rectal Cancer

Presenters

Safa Can Efil

Citation

Annals of Oncology (2021) 32 (suppl_5): S530-S582. 10.1016/annonc/annonc698

Authors

S.C. Efil1, G. Güner2, D.C. Guven3, B. Çelikten4, E. Çelebiyev4, H. Taban5, A. Akyol2, S. Kilickap5, Ş. Yalcin6, Ö. Dizdar7

Author affiliations

  • 1 İnternal Medicine, Hacettepe University - Faculty of Medicine, 06100 - Ankara/TR
  • 2 Pathology, Hacettepe University - Faculty of Medicine, 06230 - Ankara/TR
  • 3 Medical Oncology, Hacettepe University Oncology Hospital, 06230 - Ankara/TR
  • 4 İnternal Medicine, Hacettepe University - Faculty of Medicine, 06230 - Ankara/TR
  • 5 Medical Oncology, Hacettepe University - Faculty of Medicine, 06100 - Ankara/TR
  • 6 Medical Oncology, Hacettepe University Cancer Institute, Ankara/TR
  • 7 Medical Oncology, Hacettepe University - Faculty of Medicine, Ankara/TR

Resources

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Abstract 456P

Background

Tumor lymphocyte infiltrates (e.g. Immunoscore) and systemic inflammatory indices (SII) are highly prognostic in colon cancer but combined assessment is less well studied. The aim of this study was to investigate the prognostic and predictive value of CD8 + tumor-infiltrating lymphocytes (TIL) in combination with SII in patients with resected stage II-III colon cancer (CC).

Methods

Patients with stage II-III CC (n=304) diagnosed between 2008-2016 in our hospital were included. Pan-immune inflammation value (PIV) was calculated as; (neutrophil count × platelet count × monocyte count)/lymphocyte count. The mean density of CD8 + TILs in the periphery and center of the tumor was assessed and dichotomized at the 75th percentile. Combined inflammation score (CIS) was classified as “high” in patients with high PIV (>median) and low mean CD8 + TIL density, and “low” in the remaining patients.

Results

Five year DFS was 71% (78% in stage II, 64% in stage III). CD8 + TIL density was lower in node positive tumors and higher in mismatch repair deficient tumors, no association was observed with age, tumor sidedness or systemic inflammation indices. High PIV (>491), low CD8 + (<46 /mm2) and high CIS were associated with shorter disease-free survival (DFS). In multivariate analysis; age > 65 (vs <65) years (HR: 3.12 95% CI 1.78-5.48 p <0.001), stage 3 (vs. 2) disease (HR: 1.82 95% CI 1.06 3.12 p = 0.029) and high (vs low) CIS (HR: 3.82 95% CI 2.21-6.61 p <0.001) were associated with shorter DFS. Among patients with stage II disease, 78 patients (52%) received adjuvant chemotherapy. Patients with high CIS derived significant benefit from adjuvant chemotherapy (5 yr DFS 100% vs 60%, p=0.008) while those with low CIS derived no benefit (5 yr DFS 88 vs 89% p=0,94). (Table) Table: 456P

Predictors of DFS in multivariate analysis

HR %95 CI p
Age ≥ 65 (vs <65) 3,12 1,78-5,48 <0,001
Stage III (vs II) 1,82 1,06-3,12 0,029
Combined inflammation score High (vs low) 3,82 2,21-6,61 <0,001

Conclusions

Combined inflammation score may represent a new prognostic factor for localized colon cancer and predictor of chemotherapy response in patients with stage II disease.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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