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January 14, 2026Journal of Clinical Oncology0 citations

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

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CDC. DiazDRDiana Alejandra Rubio-DelgadoDCDennis Cerrato-Izaguirre

Key Points

  • This research aimed to develop a prognostic nomogram for 12-month overall survival in metastatic gastric cancer.
  • Retrospective analysis of 1,323 patients with metastatic gastric cancer
  • Collected demographic, clinical, biochemical, and histologic data
  • Utilized Kaplan–Meier method for survival estimation
  • Performed multivariate Cox regression and developed a nomogram
  • Median overall survival was 6.04 months
  • Independent adverse prognostic factors included hepatic metastases and ascites
  • The nomogram effectively stratified patients into risk groups with varying 12-month survival probabilities

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.

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Cite This Study

Diaz et al. (2026) studied this question.

synapsesocial.com/papers/6966f31d13bf7a6f02c00d3ahttps://doi.org/10.1200/jco.2026.44.2_suppl.325
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