In-hospital outcomes of splanchnic vein thrombosis in patients with gastrointestinal malignancies.

R Rishi Bothara (1University of Illinois College of Medicine, Internal Medicine, Peoria, United States) M Manasa Kandula (1University of Illinois College of Medicine, Internal Medicine, Peoria, United States) N Nimarta Bheesham (University of Illlinois College of Medicine at Peoria, Peora, IL)

Abstract

853 Background: Splanchnic vein thrombosis (SVT) is an uncommon but important complication of GI malignancies. Evidence on in-hospital outcomes is limited. Methods: We performed a 10-year retrospective study at a tertiary hospital including adults (≥18 years) with active GI malignancy and radiologically confirmed SVT (portal, mesenteric, splenic, hepatic). Exclusions: non-malignant SVT, SVT predating cancer, cirrhosis, portal hypertension, prothrombotic disorders, recent pancreatitis, abscess, pregnancy, hormone therapy without malignancy, or recent trauma/surgery. Outcomes were limited to the index hospitalization. Results: 33 patients met criteria. Median age 70 (IQR 59–77), BMI 26.8 (22.6–34.9). Race: White 87.9%, Black 6.1%, Asian 3.0%, Other 3.0%. All had a smoking history. SVT sites: portal 66.7%, mesenteric 18.2%, splenic 15.2%, hepatic 0%. Cancer sites: pancreas 42.4%, liver 30.3%, colon 9.1%, stomach 6.1%, others 12.1%. Histology: adenocarcinoma 63.6%, hepatocellular carcinoma 30.3%, signet-ring 6.1%. Stage IV in 72.7%. Anticoagulation: LMWH 42.4%, UFH 24.2%, warfarin 3.0%, none 30.3%. At discharge, 42.4% received none (death, hospice, bleeding risk), 33.3% DOACs, 21.2% warfarin, 3.0% LMWH. 1 patient developed bleeding after anticoagulation. In-hospital outcomes: ICU admission 21.2%, mortality 12.1%, median LOS 6 days (2–11). By cancer type: pancreatic had poorest outcomes (ICU 35.7%, mortality 28.6%, LOS 2.5). Liver cancer (n=10) had no ICU or deaths, but longer LOS (11). Colon (n=3) and stomach (n=2) had no ICU/deaths (LOS 2–4.5). Rare cancers: appendix (LOS 1, no ICU/death), bile duct (ICU, survived, LOS 11), esophagus (ICU, survived, LOS 10), rectum (LOS 12, no ICU/death). By SVT type: portal (ICU 18.2%, mortality 9.1%, LOS 6.5), mesenteric (ICU 16.7%, mortality 16.7%, LOS 1.5), splenic (ICU 40.0%, mortality 20.0%, LOS 6). Conclusions: GI malignancy associated SVT carried 12.1% in-hospital mortality and 21.2% ICU admission. Nearly half were discharged without anticoagulation. LMWH was the most common initial therapy, while DOACs and warfarin predominated at discharge. Outcomes were poorest in pancreatic cancer and adenocarcinoma histology; liver cancer patients had prolonged LOS but no deaths. Splenic SVT showed the highest ICU use and mortality, though small numbers limit interpretation. Findings highlight the acute burden of SVT and the need for larger studies to guide long-term management. Group n ICU n (%) Mortality n (%) Median LOS, days (IQR) Overall 33 7 (21.2) 4 (12.1) 6 (2–11) Cancer  Pancreas 14 5 (35.7) 4 (28.6) 2.5 (1–7)  Liver 10 0 (0.0) 0 (0.0) 11 (6–12)  Colon 3 0 (0.0) 0 (0.0) 2 (0–3)  Stomach 2 0 (0.0) 0 (0.0) 4.5 (3–6)  Appendix 1 0 (0.0) 0 (0.0) 1 (1–1)  Bile duct 1 1 (100.0) 0 (0.0) 11 (11–11)  Esophagus 1 1 (100.0) 0 (0.0) 10 (10–10)  Rectum 1 0 (0.0) 0 (0.0) 12 (12–12) SVT  Portal 22 4 (18.2) 2 (9.1) 6.5 (2–11)  Mesenteric 6 1 (16.7) 1 (16.7) 1.5 (1–12)  Splenic 5 2 (40.0) 1 (20.0) 6 (2–7)

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 853-853
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (3)

R

Rishi Bothara

1University of Illinois College of Medicine, Internal Medicine, Peoria, United States

M

Manasa Kandula

1University of Illinois College of Medicine, Internal Medicine, Peoria, United States

N

Nimarta Bheesham

University of Illlinois College of Medicine at Peoria, Peora, IL