Treatment optimization of locally advanced and metastatic pancreatic cancer (Review)

Int J Oncol. 2021 Dec;59(6):110. doi: 10.3892/ijo.2021.5290. Epub 2021 Dec 3.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignant tumor types, being the sixth leading cause of mortality worldwide and the fourth in Europe. Globally, it has a mortality/incidence ratio of 98%, and the 5‑year survival rate in Europe is only 3%. Although risk factors, such as obesity, diabetes mellitus, smoking, alcohol consumption and genetic factors, have been identified, the causes of PDAC remain elusive. Additionally, the only curative treatment for PDAC is surgery with negative margins. However, upon diagnosis, ~30% of the patients already present with locally advanced disease. In these cases, a multidisciplinary approach is required to improve disease‑related symptoms and prolong patient survival. In the present article, a comprehensive review of PDAC epidemiology, physiology and treatment is provided. Moreover, guidelines on patient treatment are suggested. Among the different available therapeutic options for the treatment of advanced PDAC, results are modest, most likely due to the complexity of the disease, and so the prognostic remains poor. Molecular approaches based on multi‑omics research are promising and will contribute to groundbreaking personalized medicine. Thus, economic investment that promotes research of pancreatic cancer will be critical to the development of more efficient diagnostic and treatment strategies.

Keywords: clinical trials; epidemiology; palliative; pancreatic cancer; risk factors; treatment guidelines.

Publication types

  • Review

MeSH terms

  • Carcinoma, Pancreatic Ductal / secondary
  • Carcinoma, Pancreatic Ductal / therapy*
  • Combined Modality Therapy
  • Humans
  • Pancreatic Neoplasms / pathology
  • Pancreatic Neoplasms / therapy*
  • Precision Medicine / standards*
  • Risk Factors

Grants and funding

Editorial support, in the form of medical writing and editing assistance, in the development of this manuscript was provided by x2-Science Solutions, and was unconditionally funded by AstraZeneca plc. AstraZeneca plc had no role in the conduct of the research, in study design, in the collection, analysis and interpretation of data, in the writing of the report or in the decision to submit the article for publication.