Hidden advanced physiology in non-metastatic gastrointestinal cancer: Malnutrition/cachexia and in-patient failure-to-rescue.
Abstract
11102 Background: Cancer stage is often used as a proxy for inpatient risk, yet physiologic reserve may better determine outcomes. It was hypothesized that among gastrointestinal (GI) cancer hospitalizations without coded metastasis, malnutrition/cachexia identifies a vulnerable subgroup with complication burden, ICU escalation, and post-complication mortality approaching that of metastatic disease. Methods: A survey-weighted analysis of the National Inpatient Sample (NIS), 2016–2023, was conducted. Adult hospitalizations with any GI malignancy (ICD-10-CM C15–C20, C22–C25) were included; encounters with palliative care coding (Z51.5) were excluded. Metastatic disease was defined by C77–C79. Vulnerability was defined as malnutrition/cachexia (E43, E44, E46, R64). Major complications included sepsis, bleeding/transfusion, venous thromboembolism, acute kidney injury (AKI), bowel injury/peritonitis, and respiratory failure. ICU escalation proxies included mechanical ventilation and/or shock. Outcomes were compared across three groups: non-metastatic/no vulnerability, non-metastatic/vulnerable, and metastatic. Failure-to-rescue was defined among non-metastatic surgical hospitalizations as death following ≥1 major complication. Results: The cohort included 748,734 weighted hospitalizations; 39.6% had coded metastasis. Among non-metastatic admissions, vulnerability prevalence increased from 15.6% in 2016 to 21.9% in 2023. In-hospital mortality in the non-metastatic/vulnerable group (4.14% [95% CI, 4.00–4.29]) approximated metastatic mortality (3.96%) and exceeded non-metastatic/no vulnerability mortality (1.86% [95% CI, 1.81–1.91]). Compared with non-metastatic/no vulnerability, vulnerable admissions demonstrated higher ICU escalation (7.75% [95% CI, 7.56–7.94] vs 3.54%), AKI (27.30% [95% CI, 26.98–27.62] vs 17.25%), and any major complication (59.31% [95% CI, 58.95–59.67] vs 42.93%). Resource utilization was higher in the vulnerable group (LOS 9.33 vs 5.49 days; cost $33,156 vs $22,879). Among non-metastatic admissions with complications, mortality was higher with vulnerability (6.46% [95% CI, 6.24–6.69] vs 3.88%). In the non-metastatic surgical subcohort, failure-to-rescue mortality was 5.90% (95% CI, 5.59–6.22) with vulnerability versus 2.65%. Conclusions: Among U.S. GI cancer hospitalizations without coded metastasis, malnutrition/cachexia identifies a high-risk inpatient phenotype with complication burden, ICU escalation, and post-complication mortality closely resembling metastatic disease. These findings suggest physiologic vulnerability, rather than stage alone, drives inpatient risk and failure-to-rescue, supporting targeted inpatient risk stratification and earlier supportive interventions.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (9)
Wei Ju Lin
1University of California, Riverside School of Medicine, Internal Medicine, Riverside, United States
Ramaditya Srinivasmurthy
Mount Sinai Morningside, NY, New York, United States
Rishi Kumar Nanda
Touro University Nevada College of Osteopathic Medicine, Las Vegas, NV
Jason Ta
HCA Healthcare/USF Morsani GME Consortium, HCA Florida Citrus Hospital, Florida, Florida, United States
Riccesha Hattin
Kirk Kerkorian School of Medicine at UNLV, Las Vegas, Nevada, United States
Abbas Hussain
Kirk Kerkorian School of Medicine at UNLV, Las Vegas, Nevada, United States
Charles Abraham Joseph Larson
Trinity School of Medicine, Warner Robins, GA
Daniel Thomas Jones
HCA Sunrise Health GME Consortium - MountainView Hospital, Las Vegas, NV
Kyaw Zin Thein
3Comprehensive Cancer Centers of Nevada, Division of Hematology and Medical Oncology, Las Vegas, United States