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Treating Pancreatic Ductal Adenocarcinoma: The Targeted Revolution is Here.

Drugs 2026 Vol.86(4) p. 507-532

May MS, Park W, O'Reilly EM

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Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies and is a rising cause of morbidity and mortality.

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BibTeX ↓ RIS ↓
APA May MS, Park W, O'Reilly EM (2026). Treating Pancreatic Ductal Adenocarcinoma: The Targeted Revolution is Here.. Drugs, 86(4), 507-532. https://doi.org/10.1007/s40265-026-02295-0
MLA May MS, et al.. "Treating Pancreatic Ductal Adenocarcinoma: The Targeted Revolution is Here.." Drugs, vol. 86, no. 4, 2026, pp. 507-532.
PMID 41731281

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies and is a rising cause of morbidity and mortality. An immunosuppressive, hostile tumor microenvironment, and KRAS-driven biology have contributed to poor outcomes in PDAC. Recent breakthroughs in targeting tumors with homologous repair deficiency, KRAS mutations, rare gene fusions, and other molecular abnormalities have improved outcomes in subsets of patients. KRAS inhibitors, both allele specific and pan(K)RAS, claudin-targeting biologics, and PRMT5 inhibitors have demonstrated single agent activity in pretreated, biomarker selected PDAC. An improved understanding of the tumor immune microenvironment has facilitated the development of promising cancer vaccines and immunomodulating agents. This review summarizes the current state of PDAC therapeutics and describes drug development targets that will transform outcomes in PDAC in the proximate future.

MeSH Terms

Humans; Carcinoma, Pancreatic Ductal; Pancreatic Neoplasms; Molecular Targeted Therapy; Tumor Microenvironment; Antineoplastic Agents; Proto-Oncogene Proteins p21(ras); Cancer Vaccines; Mutation

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