Current and Future Therapies for Pancreatic Ductal Adenocarcinoma

Áine Sally, Ryan McGowan, Karen Finn, Brian Michael Moran

Research output: Contribution to journalReview articlepeer-review

12 Citations (Scopus)

Abstract

Pancreatic cancer is one of the leading causes of cancer-related death worldwide. This is due to delayed diagnosis and resistance to traditional chemotherapy. Delayed diagnosis is often due to the broad range of non-specific symptoms that are associated with the disease. Resistance to current chemotherapies, such as gemcitabine, develops due to genetic mutations that are either intrinsic or acquired. This has resulted in poor patient prognosis and, therefore, justifies the requirement for new targeted therapies. A synthetic lethality approach, that targets specific loss-of-function mutations in cancer cells, has shown great potential in pancreatic ductal adenocarcinoma (PDAC). Immunotherapies have also yielded promising results in the development of new treatment options, with several currently undergoing clinical trials. The utilisation of monoclonal antibodies, immune checkpoint inhibitors, adoptive cell transfer, and vaccines have shown success in several neoplasms such as breast cancer and B-cell malignancies and, therefore, could hold the same potential in PDAC treatment. These therapeutic strategies could have the potential to be at the forefront of pancreatic cancer therapy in the future. This review focuses on currently approved therapies for PDAC, the challenges associated with them, and future directions of therapy including synthetically lethal approaches, immunotherapy, and current clinical trials.

Original languageEnglish
Article number2417
JournalCancers
Volume14
Issue number10
DOIs
Publication statusPublished - 1 May 2022

Keywords

  • chemoresistance
  • chemotherapy
  • clinical trials
  • immunotherapy
  • pancreatic ductal adenocarcinoma
  • synthetic lethality

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