# A Case of Recurrent Acute Pancreatitis After Gemcitabine + Nab-Paclitaxel and Modified FOLFIRINOX Therapy for Advanced Recurrent Pancreatic Cancer

**Authors:** Yusuke Inada, Haruna Sango, Noriki Kasuga, Hiroko Yukawa, Motohiko Sano

PMC · DOI: 10.7759/cureus.102865 · 2026-02-02

## TL;DR

A patient with advanced pancreatic cancer experienced repeated episodes of acute pancreatitis after two different chemotherapy treatments, raising concerns about drug-induced pancreatitis.

## Contribution

This case report highlights the potential risk of acute pancreatitis associated with specific chemotherapy regimens in pancreatic cancer.

## Key findings

- Acute pancreatitis occurred within 24 hours of starting both gemcitabine/nab-paclitaxel and modified FOLFIRINOX therapies.
- 5-HT3 receptor antagonists, common to both regimens, may have contributed to pancreatitis.
- The clinical course of pancreatitis was mild and consistent with drug-induced cases.

## Abstract

The incidence of drug-induced acute pancreatitis is an important consideration when developing treatment strategies for patients with pancreatic ductal adenocarcinoma. We report a case of recurrent acute pancreatitis that developed following both gemcitabine plus nab-paclitaxel (GnP) chemotherapy and modified FOLFIRINOX (mFFX) therapy. The clinical stage at initial diagnosis was cT3N1M0 stage IIB pancreatic cancer, with subsequent progression to metastatic disease over approximately 1.5 years. Treatment was prioritized at each stage of disease progression despite the occurrence of acute pancreatitis. Recurrent episodes of acute pancreatitis prompted a change in chemotherapy regimen from GnP to mFFX; however, a single causative agent could not be identified. For both chemotherapy regimens, the onset of acute pancreatitis occurred within 24 hours of treatment initiation, and the clinical course was mild, consistent with previous reports of drug-induced pancreatitis. Agents common to both regimens, specifically 5-hydroxytryptamine type 3 (5-HT3) receptor antagonists, may have contributed to the development of pancreatitis. Further accumulation of similar cases is required to better clarify the relationship between pancreatic cancer chemotherapy and the risk of acute pancreatitis.

## Linked entities

- **Chemicals:** gemcitabine (PubChem CID 60750), nab-paclitaxel (PubChem CID 36314), 5-hydroxytryptamine (PubChem CID 5202)
- **Diseases:** pancreatic ductal adenocarcinoma (MONDO:0005184), acute pancreatitis (MONDO:0006515)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), trauma (MESH:D014947), PDAC (MESH:D021441), Pancreatic Cancer (MESH:D010190), epigastric pain (MESH:D010146), gallstones (MESH:D042882), cancer (MESH:D009369), dilation of the common bile duct (MESH:D003137), Acute Pancreatitis (MESH:D010195), abdominal pain (MESH:D015746), pancreatic head tumor (MESH:D006258), biliary disease (MESH:D001660), skin rash (MESH:D005076), anastomotic stenosis (MESH:D003251), liver metastasis (MESH:D009362), infection (MESH:D007239), hypercalcemia (MESH:D006934), Drug Reaction (MESH:D004342), tenderness (MESH:D063806), necrosis (MESH:D009336), obstructive jaundice (MESH:D041781), hypertriglyceridemia (MESH:D015228)
- **Chemicals:** acetaminophen (MESH:D000082), irinotecan (MESH:D000077146), Paclitaxel (MESH:D017239), granisetron (MESH:D017829), 5-fluorouracil (MESH:D005472), leucovorin (MESH:D002955), oxaliplatin (MESH:D000077150), 5-HT3 receptor antagonist (-), lansoprazole (MESH:D064747), palonosetron (MESH:D000077924), dexamethasone (MESH:D003907), ampicillin/sulbactam (MESH:C035444), FOLFIRINOX (MESH:C000627770), magnesium oxide (MESH:D008277), alcohol (MESH:D000438), tramadol (MESH:D014147), Gemcitabine (MESH:D000093542)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12961556/full.md

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Source: https://tomesphere.com/paper/PMC12961556