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Poster Display session

54P - Survival outcomes and clinicopathological features of rectal neuroendocrine tumors: A retrospective analysis from a Latin American cohort

Date

21 Mar 2025

Session

Poster Display session

Presenters

Wagner Cruz Diaz

Citation

Annals of Oncology (2025) 10 (suppl_3): 1-7. 10.1016/esmoop/esmoop104347

Authors

W.E. Cruz Diaz, A.D. Leonardo Carbajal, V.R. Paitan Amaro, J.C. Haro Varas, J.G. Macetas, E.C. Veramendi Cabana, C. Pacheco, M.J. Calderon Anticona, V. Castro Oliden

Author affiliations

  • Department Of Medical Oncology, INEN - Instituto Nacional de Enfermedades Neoplasicas, 15038 - Lima/PE

Resources

This content is available to ESMO members and event participants.

Abstract 54P

Background

Rectal neuroendocrine tumors (rNETs) represent approximately 20% of gastrointestinal neuroendocrine tumors, with a rising incidence over recent decades. However, data from Latin America remain limited.

Methods

This retrospective study included patients diagnosed with rNETs at the Instituto Nacional de Enfermedades Neoplásicas (INEN) between September 2009 and February 2024. Clinicopathological characteristics were analyzed, and overall survival (OS) was estimated using the Kaplan-Meier method. Survival differences were assessed with the log-rank test.

Results

57 patients were included, with a median age of 54 years (27–74); 66.7% were female. Advanced disease was observed in 40.4% (n=23), 59.6% (n=34) had localized disease. All tumors were well-differentiated, with 56.1% (n=32) classified as G1 and 43.9% (n=25) as G2. Among advanced cases, 87% (n=20) were G2, whereas 85.3% (n=29) of localized tumors were G1. Nodal involvement (N+) was present in 78.3% (n=18) of advanced cases, while 90.6% (n=29) of localized tumors had no nodal involvement (N-). Surgical resection of the primary tumor was performed in 21.1% (n=12), while endoscopic resection in 50.9% (n=29). Median tumor size was 1.1 cm (0.2–7.8 cm). Tumors >2 cm were observed in 78.3% (18/23) of advanced cases but were absent in localized disease. Median OS for all patients was 112.3 months (95% CI: 48.8–175.8), with a median follow-up of 25.4 months. Median OS in advanced disease was 48.4 months (95% CI: 29.6–66.9; p=0.001), while it was not reached for localized disease. G2 tumors had a median OS of 46.4 months, compared to an unreached median OS in G1 tumors (p < 0.001).

Conclusions

Tumor size >2 cm, G2 tumors, and N+ were strongly associated with advanced disease and worse survival outcomes. Early detection and resection of localized rNETs significantly improved survival, emphasizing the need for timely diagnosis and personalized treatment strategies.

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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