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Poster Display session

21P - The impact of adjuvant chemotherapy duration on progression-free survival in low-risk stage III colon cancer with N1a-b and N1c disease: A retrospective, single-center analysis

Date

27 Jun 2024

Session

Poster Display session

Presenters

Beliz Karaoglan

Citation

Annals of Oncology (2024) 35 (suppl_1): S1-S74. 10.1016/annonc/annonc1477

Authors

B.B. Karaoglan1, I. Oztürk2, C. Akyol2, B. Savas2, G. Utkan3

Author affiliations

  • 1 Ankara University Medical School - Cebeci Hastaneleri Tibbi Onkoloji, Ankara/TR
  • 2 Ankara University Faculty of Medicine, Ankara/TR
  • 3 Ankara University Faculty of Medicine, 06530 - Ankara/TR

Resources

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Abstract 21P

Background

Colorectal cancer (CRC) ranks among the most prevalent cancers globally. In Stage III colon cancer, high-risk patients (pT4 or pN2) receive 6 months of adjuvant chemotherapy, while low-risk patients (pT-3 and N1) are recommended either 3 or 6 months of CAPOX (capecitabine and oxaliplatin) or 6 months of FOLFOX therapy. Tumor deposits (TDs) are known to have a poor prognosis independent of lymph node (LN) involvement and are considered equivalent to LN metastases in the latest staging system. However, the optimal chemotherapy duration for patients classified as pN1c remains unknown. The aim of this study is to investigate the impact of adjuvant chemotherapy duration (3 months vs. 6 months) on survival in pN1a-b and pN1c patient groups.

Methods

We retrospectively analyzed patients with stage III colon cancer who underwent surgery between January 2014 and February 2024. Demographic and pathological data of patients were retrospectively collected. The primary outcome was progression-free survival (PFS).

Results

A total of 144 patients were included. 116 were pT1-3N1a-b and 28 were pT1-3N1c. Local (21.4% vs. 3.4%, P=0.001) and total recurrences (39.3% vs 14.6%, P=0.001) were significantly higher in the pN1c group. Univariate and multivariate analyses revealed no significant impact of adjuvant chemotherapy duration on PFS in the pN1a-b group (P=0.121), whereas in the pN1c group, 3-month chemotherapy resulted in significantly poorer PFS (HR: 2.13, 95% CI, 0.999-4.546, p=0.043). Table: 21P

Univariate and multivariate analysis of factors affecting progression-free survival

pN1a-b, n (%) n=116 pN1c, n (%) n=28
Univariate analysis Multivariate analysis Univariate analysis Multivariate analysis
P value HR 95% CI P value P value HR 95% CI P value
Age ≤50 >50 0.243 0.488
Sex Male Female 0.836 0.938
Tumor location Right sided Left sided 0.044 3.31 1 1.240-8.947 0.017 0.819
pT stage pT1-2 pT3 0.369 0.684
Tumor grade Low grade High grade 0.006 1 5.29 1.455-19.243 0.011 NA
Lymphovascular invasion No Yes 0.777 0.254
Perineural invasion No Yes 0.961 0.156
Tumor budding No Yes 0.271 0.095
Microsatellite instability MSS MSI-H 0.274 0.841
Adjuvant chemotherapy regimen XELOX FOLFOX Capecitabine 0.205 0.763
Duration of adjuvant chemotherapy 3 months 6 months 0.121 0.043

Abbreviations: CI: confidence interval, MSI-H: microsatellite instability high, MSS: microsatellite stable, PFS: progression-free survival.

Conclusions

In conclusion, our study suggests that 6-month chemotherapy is more suitable for patients with pT1-3N1c disease. Further research is needed for personalized treatment guidance.

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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