# Intraperitoneal nivolumab for malignant ascites in patients with advanced gastrointestinal or pancreaticobiliary tract cancer

**Authors:** Hsiu-Tzu Wang, Yung-Luen Yu, Wen-Jyi Lo, Mei-Chen Lin, Chien-Lun Chu, Chia-Yu Chen, Sing-Ting Wang, Chang-Fang Chiu, En-Jia Bai, Li-Yuan Bai

PMC · DOI: 10.1007/s10147-025-02930-y · International Journal of Clinical Oncology · 2025-12-10

## TL;DR

This study shows that intraperitoneal nivolumab can effectively reduce malignant ascites in patients with advanced gastrointestinal or pancreaticobiliary cancer.

## Contribution

The study introduces intraperitoneal nivolumab as a novel treatment for malignant ascites with minimal side effects.

## Key findings

- Seven out of nine patients showed clinical improvement with reduced ascites and longer intervals between paracenteses.
- Increased vascular endothelial growth factor A and decreased interleukin-1α levels were observed in responders.
- The treatment was well-tolerated with only grade 1 tenderness at puncture sites reported.

## Abstract

Malignant ascites occur in 10–15% of patients with gastrointestinal tract cancers. The abundance of immune cells in the peritoneum and ascitic fluid, along with the immunosuppressive environment created by cancer cells, suggests the potential utility of intraperitoneal (IP) immune checkpoint inhibitors for controlling malignant ascites.

Patients with gastrointestinal or pancreaticobiliary tract cancer and cytologically confirmed malignant ascites received IP nivolumab. Twenty mg of nivolumab diluted in 100 mL of saline was infused into the peritoneal cavity over 10 min following paracentesis. IP treatment was repeated after each subsequent paracentesis until deemed ineffective by the treating physician, upon the occurrence of unacceptable toxicity, or discontinued at the patient’s request. This study was registered at ClinicalTrials.gov (NCT05745233).

The median age of the nine enrolled patients was 55 years. Underlying malignancies included pancreatic (n = 4), biliary tract (n = 3), and gastric cancers (n = 2). After a median of 3 (range: 2–5) treatment cycles, seven patients (77.8%) showed a clinical response, as evidenced by reduced ascitic fluid and prolonged intervals between paracenteses. The only adverse effect observed was grade 1 tenderness at the puncture sites. Reduction in tumor cell count in ascites, rather than changes in the total lymphocyte count or lymphocyte subpopulations, correlated with clinical response. Responders consistently exhibited increased vascular endothelial growth factor A and decreased interleukin-1α levels following nivolumab administration.

Intraperitoneal administration of nivolumab effectively controlled malignant ascites with minimal adverse effects. However, further validation in a larger cohort is required.

The online version contains supplementary material available at 10.1007/s10147-025-02930-y.

## Linked entities

- **Diseases:** pancreatic cancer (MONDO:0005192), biliary tract cancer (MONDO:0003060), gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** toxicity (MESH:D064420), gastric cancers (MESH:D013274), gastrointestinal or pancreaticobiliary tract cancer (MESH:D005770), tenderness (MESH:D063806), cancer (MESH:D009369), Malignant ascites (MESH:D001201)
- **Chemicals:** nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12847151