Preclinical evidence for cytokine-based immunotherapy in pancreatic cancer treatment: A systematic review.

Int J Biol MacromolJul 10, 2026 (epub)
Clinical ResearchOncology (Medical)

Jorge Rodríguez-Criado, Alfonso J Corona-Castro, Francisco Quiñonero et al.

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In 30 seconds

This systematic review assessed cytokine-based immunotherapy for pancreatic cancer, analyzing 46 preclinical studies. It found that targeting cytokines like TGF-β and IL-6 improved stromal remodeling, while pro-inflammatory cytokines enhanced T-cell persistence. The review highlights the potential of combining cytokine modulation with chemotherapy or checkpoint inhibitors to improve treatment outcomes.

Key findings

  • Blocking TGF-β and IL-6 led to significant stromal remodeling and fibrosis reduction.
  • Pro-inflammatory cytokines like IL-2, IL-12, and IL-15 enhanced T-cell persistence.
  • Cytokine modulation alone was rarely sufficient but showed robust responses when combined with other therapies.

Why it matters

Understanding the role of cytokines in pancreatic cancer treatment could help clinicians develop more effective immunotherapy strategies, particularly in overcoming the challenges posed by the tumor microenvironment.

What to keep in mind

The review is limited by the use of subcutaneous and xenograft models that do not fully replicate human pancreatic stroma and varying risk of bias in studies.

Source

Published in Int J Biol Macromol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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