The rationale for targeting nectin-4 in pancreatic cancer

Sarah Cronjaeger1, Lena Seifert2, Adrian M Seifert3

  • 1Department of Visceral, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; National Center for Tumor Diseases (NCT), Dresden, Germany; German Cancer Research Center (DKFZ), Heidelberg, Germany; Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Dresden, Germany.

Trends in Cancer
|March 11, 2026
PubMed

Insights

Nectin-4 promotes pancreatic cancer aggressiveness and immune evasion. Targeting nectin-4 with antibody-drug conjugates is a promising therapeutic strategy for pancreatic ductal adenocarcinoma (PDAC).

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Nectin-4 is an immunoglobulin-like cell adhesion molecule.
  • Nectin-4 contributes to tumor aggressiveness and immune evasion in pancreatic ductal adenocarcinoma (PDAC).

Purpose of the Study:

  • To establish nectin-4 as a therapeutic target in PDAC.
  • To evaluate the potential of nectin-4-targeted therapies for PDAC.

Main Methods:

  • Analysis of nectin-4 expression in PDAC.
  • Review of clinical efficacy of nectin-4-targeted antibody-drug conjugates in other solid tumors.

Main Results:

  • Nectin-4 is highly and selectively expressed on pancreatic cancer cells.
  • Nectin-4-targeted antibody-drug conjugates have shown clinical efficacy in other solid tumors.

Conclusions:

  • Nectin-4 is a compelling therapeutic target for PDAC due to its selective expression and the success of targeted therapies.
  • Targeting nectin-4 offers a promising strategy for treating pancreatic ductal adenocarcinoma.