Development of a prognostic nomogram to guide clinical decision-making in metastatic gastric cancer: A Latin American cohort study.

C Consuelo Diaz (Gastrointestinal Oncology Unit, Instituto Nacional de Cancerologia, Mexico City, Mexico) D Diana Alejandra Rubio-Delgado (Instituto Nacional de Cancerología, Mexico City, Mexico) D Dennis Cerrato-Izaguirre M Marytere Herrera (Instituto Nacional de Cancerología, Mexico City, Mexico) M Mariana Sayako Miyagui (Instituto Nacional de Cancerología, Mexico City, Mexico) G German Caderillo-Ruiz (Instituto Nacional de Cancerología, Mexico City, Mexico) J Jairo Rubio (Instituto Nacional de Cancerología, Mexico City, Mexico) E Erika Ruiz (Instituto Nacional de Cancerología, Mexico City, Mexico) E Estefania Soto-Rangel (Instituto Nacional de Cancerologia, Mexico City, Mexico) L Luis Angel Medel-Alarcon (Instituto Nacional de Cancerologia, Mexico City, Mexico)

Abstract

325 Background: Metastatic gastric cancer (mGC) is associated with dismal outcomes, and most patients eventually receive only palliative care. Accurate prognostic models are urgently needed to individualize survival estimates, optimize therapeutic decisions, and inform trial design. Data from Latin American populations are scarce. We aimed to develop and internally validate a prognostic nomogram for 12-month overall survival (OS) in patients with mGC. Methods: We retrospectively analyzed 1,323 patients with histologically confirmed mGC treated at the Instituto Nacional de Cancerología (Mexico) between 2010 and 2022. Demographic, clinical, biochemical, and histologic data were collected. OS was estimated using the Kaplan–Meier method. Multivariate Cox regression was performed in R Studio, and independent prognostic factors were incorporated into a nomogram predicting 12-month OS. Discrimination and calibration were assessed Results: Median age was 54 years (±13.5), with 63.4% younger than 50 years; 52.5% were male. ECOG performance status was 0–1 in 71.2% of patients. Median weight loss at diagnosis was 10 kg. Anemia grade ≥2 occurred in 27.7% and hypoalbuminemia (<3.5 g/dL) in 29.3%. Peritoneal carcinomatosis (58.1%), ascites (28.4%), and hepatic metastases (20.8%) were the most frequent metastatic sites. Median OS was 6.04 months (95% CI, 5.61–6.47). Independent adverse prognostic factors included hepatic metastases, ascites, peritoneal carcinomatosis, retroperitoneal involvement, anemia grade 2–3, and low serum albumin. The nomogram demonstrated strong discrimination and calibration, stratifying patients into clinically meaningful risk groups with differential 12-month OS probabilities. Conclusions: This is the first prognostic nomogram for mGC developed in a Latin American cohort, integrating both clinical and nutritional parameters. The tool provides individualized prediction of 12-month OS, offering oncologists an evidence-based resource to identify patients who may benefit from systemic therapy versus those more likely to transition early to supportive care. External validation is needed, but this nomogram has the potential to shift decision-making in a setting where most patients face limited therapeutic opportunities.

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 325-325
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

C

Consuelo Diaz

Gastrointestinal Oncology Unit, Instituto Nacional de Cancerologia, Mexico City, Mexico

D

Diana Alejandra Rubio-Delgado

Instituto Nacional de Cancerología, Mexico City, Mexico

D

Dennis Cerrato-Izaguirre

M

Marytere Herrera

Instituto Nacional de Cancerología, Mexico City, Mexico

M

Mariana Sayako Miyagui

Instituto Nacional de Cancerología, Mexico City, Mexico

G

German Caderillo-Ruiz

Instituto Nacional de Cancerología, Mexico City, Mexico

J

Jairo Rubio

Instituto Nacional de Cancerología, Mexico City, Mexico

E

Erika Ruiz

Instituto Nacional de Cancerología, Mexico City, Mexico

E

Estefania Soto-Rangel

Instituto Nacional de Cancerologia, Mexico City, Mexico

L

Luis Angel Medel-Alarcon

Instituto Nacional de Cancerologia, Mexico City, Mexico