# Associations of corticosteroid therapy with weight change and appetite in patients with advanced pancreatic cancer – a post hoc analysis from the MISTRAL trial

**Authors:** Charlotte Goodrose-Flores, Stephanie E. Bonn, Linda Björkhem-Bergman, Kathrin Wode

PMC · DOI: 10.1007/s00520-026-10585-2 · 2026-03-28

## TL;DR

This study found that corticosteroid use in advanced pancreatic cancer patients is linked to greater weight loss and reduced appetite over time.

## Contribution

The study provides new evidence on the long-term effects of corticosteroids on weight and appetite in pancreatic cancer patients.

## Key findings

- Patients receiving corticosteroids experienced an average monthly weight loss of 1.48%.
- Corticosteroid users reported consistently poorer appetite compared to non-users.
- Corticosteroid-treated patients had lower BMI and performance status at baseline.

## Abstract

Loss of appetite and weight loss are major concerns in patients with pancreatic cancer. The aim of this study was to evaluate the associations of corticosteroid therapy with weight change and appetite in the long term, in patients with advanced pancreatic cancer.

This was a post hoc analysis of the previously performed randomized, controlled MISTRAL trial in patients with advanced pancreatic cancer. Data on weight and appetite at baseline and after approximately 1, 2, 3 and 4 months were used. The association between corticosteroid exposure and weight change was calculated using mixed linear regression, models adjusted for sex, age, randomization arm and performance status. Appetite was analyzed comparing those without and with corticosteroids during 3 days before appetite assessment.

Two hundred forty-four patients (121 women) were included. Patients who received corticosteroid therapy at any time during the 4 months had less appetite (p < 0.001), lower performance status (p < 0.001) and lower BMI (p < 0.05) compared to those not receiving corticosteroids. Patients receiving corticosteroids had a larger weight loss of on average 1.48% during a month of follow-up compared to those not receiving corticosteroids (β − 1.48, 95% CI =  − 2.11 to − 0.84). Patients exposed to corticosteroids reported poorer appetite at every time point than those not exposed.

In long-term follow-up, corticosteroid treatment was associated with greater weight loss and poorer appetite among patients with advanced pancreatic cancer. These findings may partly be explained by a higher symptom burden among patients receiving corticosteroids. Future prospective trials are warranted to clarify the effect of long-term corticosteroid treatment on weight and appetite.

## Linked entities

- **Diseases:** pancreatic cancer (MONDO:0005192)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, GDF15 (growth differentiation factor 15) [NCBI Gene 9518] {aka GDF-15, HG, MIC-1, MIC1, NAG-1, PDF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** weight gain (MESH:D015430), diseases of the musculoskeletal system and connective tissue (MESH:D003240), myopathy (MESH:D009135), peptic ulcers (MESH:D010437), fat (MESH:D004620), diseases of the circulatory system (MESH:D012769), loss of muscle mass (MESH:C536030), Weight loss (MESH:D015431), Cancer (MESH:D009369), insomnia (MESH:D007319), respiratory diseases (MESH:D012140), fatigue (MESH:D005221), hyperglycemia (MESH:D006943), increased (MESH:D000067251), Appetite (MESH:D001068), diseases of the digestive system (MESH:D004066), nausea (MESH:D009325), weight change (MESH:D001836), infection (MESH:D007239), Malnutrition (MESH:D044342), death (MESH:D003643), liver metastases (MESH:D009362), psychiatric disturbances (MESH:D001523), pain (MESH:D010146), exocrine pancreatic cancer (MESH:D010190), cachexia (MESH:D002100), endocrine diseases (MESH:D004700)
- **Chemicals:** steroid (MESH:D013256), gemcitabine (MESH:D000093542), FOLFIRINOX (MESH:C000627770), CST (-), betamethasone (MESH:D001623), prednisolone (MESH:D011239), dexamethasone (MESH:D003907)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13032967/full.md

---
Source: https://tomesphere.com/paper/PMC13032967