Abstract

Pancreatic cancer is one of the most aggressive cancers with a high mortality rate even among patients with early-stage disease. Although recent studies with novel therapeutic approaches have led to modest improvement in survival outcomes, limited progress is achieved for the use of immunotherapeutics in this challenging cancer. Immune checkpoint inhibitors, thus far, single-agent or in combination, have not yielded significant improvement in survival outcomes except in mismatch repair-deficient pancreatic cancer. The tumor microenvironment of pancreatic cancer has been considered as an attractive target for over a decade based on preclinical studies that suggested it may adversely affect drug delivery and antitumor immunity. In this review article, we elaborate on the biology of pancreatic cancer microenvironment, its highly complicated interaction with cancer cells, and the immune system. We also discuss plausible explanations that led to the failure of immune checkpoint inhibitors as therapeutic agents and the potential impacts of pancreatic cancer stroma on these negative studies.

Highlights

  • Pancreatic adenocarcinoma is one of the most challenging cancers among solid tumors with limited progress in therapeutic options in advanced-stage disease leading to dismal outcomes[1]

  • We review possible therapeutic approaches to combat the adverse effects of tumor microenvironment on the anti-cancer immune response

  • Colony-stimulating factor1-receptor (CSF-1R) signaling, which promotes macrophage recruitment to tumor microenvironment to fuel cancer growth, is being targeted in a clinical trial in combination with pembrolizumab and GVAX to reverse the inhibitory signals in patients with borderline resectable pancreatic cancer (NCT03153410)

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Summary

Introduction

Pancreatic adenocarcinoma is one of the most challenging cancers among solid tumors with limited progress in therapeutic options in advanced-stage disease leading to dismal outcomes[1]. Tumor-associated macrophages are another group of negative regulators of effector T cell function in pancreatic cancer and the inhibition of these cells results in improved antitumor immune response in preclinical studies[38]. Ipilimumab, one of the first immune checkpoint inhibitors targeting CTLA4, has been investigated as a single agent in pancreatic adenocarcinoma patients .[41] This phase II trial enrolled 27 patients with advanced-stage disease and no objective response was reported by the authors[41].

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