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Updated: Jul 2, 2026

Multianimal Magnetic Resonance Imaging for Tumor Measurements in Pancreatic Cancer Mouse Models
Published on: February 3, 2026
Molecular targeted therapies for pancreatic cancer
Daniel Borja-Cacho1, Eric Hans Jensen, Ashok Kumar Saluja
1Department of Surgery, University of Minnesota, Minneapolis, MN, USA.
Background:
Pancreatic cancer cells express different mutations that increase the aggressiveness and confer resistance to conventional chemotherapy and radiotherapy. Molecules that selectively bind and inhibit these mutations are effective in other solid tumors and are now emerging as a complementary therapy in pancreatic cancer. The objective of this review is to describe the effect of drugs that inhibit specific mutations present in pancreatic cancer with special emphasis on clinical trials.
Data Sources:
We reviewed the English-language literature (MedLine) addressing the role of drugs that target mutations present in pancreatic cancer. Both preclinical and clinical studies were included.
Conclusions:
Preclinical evidence supports the combination of conventional approved therapies plus drugs that block epidermal growth factor receptor and vascular growth endothelial factor or induce apoptosis. However, most of the current clinical evidence is limited to small phase I trials evaluating the toxicity and safety of these regimens. The results of additional randomized trials that are still undergoing will clarify the role of these drugs in pancreatic cancer.
Insights
Targeted therapies inhibiting specific mutations show promise in pancreatic cancer treatment. While preclinical data are encouraging, further clinical trials are needed to confirm their efficacy and role alongside conventional treatments.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Pancreatic cancer exhibits mutations conferring chemo- and radio-resistance.
- Targeted therapies are effective in other solid tumors and are emerging for pancreatic cancer.
- Investigating drugs that inhibit specific pancreatic cancer mutations is crucial.
Purpose of the Study:
- To review the impact of drugs targeting specific mutations in pancreatic cancer.
- To emphasize the role of these targeted drugs in ongoing clinical trials.
Main Methods:
- Comprehensive literature review of English-language studies (MedLine).
- Inclusion of both preclinical and clinical research on targeted mutation inhibitors.
- Focus on drugs targeting specific mutations in pancreatic cancer.
Main Results:
- Preclinical studies support combining targeted therapies (EGFR, VEGF inhibitors, apoptosis inducers) with conventional treatments.
- Current clinical evidence is primarily from small Phase I trials assessing safety and toxicity.
- Ongoing randomized trials are essential for definitive results.
Conclusions:
- Targeted therapies hold potential as complementary treatments for pancreatic cancer.
- Further randomized clinical trials are necessary to establish the definitive role of these agents.
- The safety and efficacy of targeted agents in combination regimens require continued investigation.
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