Frontiers and future of immunotherapy for pancreatic cancer: from molecular mechanisms to clinical application

Front Immunol. 2024 May 2:15:1383978. doi: 10.3389/fimmu.2024.1383978. eCollection 2024.

Abstract

Pancreatic cancer is a highly aggressive malignant tumor, that is becoming increasingly common in recent years. Despite advances in intensive treatment modalities including surgery, radiotherapy, biological therapy, and targeted therapy, the overall survival rate has not significantly improved in patients with pancreatic cancer. This may be attributed to the insidious onset, unknown pathophysiology, and poor prognosis of the disease. It is therefore essential to identify and develop more effective and safer treatments for pancreatic cancer. Tumor immunotherapy is the new and fourth pillar of anti-tumor therapy after surgery, radiotherapy, and chemotherapy. Significant progress has made in the use of immunotherapy for a wide variety of malignant tumors in recent years; a breakthrough has also been made in the treatment of pancreatic cancer. This review describes the advances in immune checkpoint inhibitors, cancer vaccines, adoptive cell therapy, oncolytic virus, and matrix-depletion therapies for the treatment of pancreatic cancer. At the same time, some new potential biomarkers and potential immunotherapy combinations for pancreatic cancer are discussed. The molecular mechanisms of various immunotherapies have also been elucidated, and their clinical applications have been highlighted. The current challenges associated with immunotherapy and proposed strategies that hold promise in overcoming these limitations have also been discussed, with the aim of offering new insights into immunotherapy for pancreatic cancer.

Keywords: adoptive cell therapy; cancer vaccines; immune checkpoint inhibitors; immune therapy; pancreatic cancer.

Publication types

  • Review

MeSH terms

  • Animals
  • Biomarkers, Tumor
  • Cancer Vaccines* / immunology
  • Cancer Vaccines* / therapeutic use
  • Combined Modality Therapy
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Immunotherapy* / methods
  • Oncolytic Virotherapy / methods
  • Pancreatic Neoplasms* / immunology
  • Pancreatic Neoplasms* / therapy

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This review was supported by grants from the National Natural Science Foundation of China (No. 82260489, No. 22264023, and No. 82260530) the Shaanxi Science, the Shaanxi University Science and Technology Association Youth Lifting Project (No: 20240316) and Technology Department Project (No. 2022JQ-931) and Shaanxi Provincial Department of Education Project (No. 23JK0721).