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Updated: May 13, 2026

Reprogramming Pancreatic Ductal Adenocarcinoma to Pluripotency
Published on: February 2, 2024
Novel agents in the treatment of pancreatic adenocarcinoma
Anastasios Dimou1, Konstantinos N Syrigos, Muhammad Wasif Saif
1Department of Internal Medicine, Albert Einstein Medical Center, Philadelphia, PA, USA.
Abstract:
The development of new agents and treatment strategies against pancreatic adenocarcinoma is vital, given the poor prognosis of the patients with this particular type of cancer. Three novel compounds were tested at different phases of clinical research and the results were presented in the recent ASCO Gastrointestinal Cancers Symposium. FG-3019 inhibits the connective tissue growth factor which is important in the biology of pancreatic cancer and was shown to be relatively safe in a phase I study (Abstract #213). In addition, ASG-5ME, an antibody specific for SLC44A4 that is universally expressed in pancreatic cancer and also carries a conjugate chemotherapy particle was safe at the appropriate dosing in a phase I trial (Abstract #176). Last but not least, tanespimycin, a molecule that inhibits heat shock protein 90 was not effective in the first line treatment of patients with pancreatic cancer in a phase II study (Abstract #245). Further studying of FG-3019 and ASG-5ME will show the potential activity if any of these compounds in patients with pancreatic cancer.
Insights
Researchers evaluated novel pancreatic cancer treatments. FG-3019 and ASG-5ME showed promise in early trials, while tanespimycin was ineffective, warranting further investigation of the former two agents.
Area of Science:
- Oncology
- Gastroenterology
- Clinical Pharmacology
Background:
- Pancreatic adenocarcinoma has a poor patient prognosis, necessitating the development of novel therapeutic agents and strategies.
- Connective tissue growth factor (CTGF) and SLC44A4 are implicated in pancreatic cancer biology.
- Heat shock protein 90 (HSP90) is a target in cancer therapy.
Purpose of the Study:
- To present results from clinical trials of three novel compounds targeting pancreatic cancer.
- To evaluate the safety and potential efficacy of FG-3019, ASG-5ME, and tanespimycin in pancreatic cancer patients.
Main Methods:
- Phase I clinical trial of FG-3019, an inhibitor of connective tissue growth factor (CTGF).
- Phase I clinical trial of ASG-5ME, an antibody targeting SLC44A4 with a chemotherapy conjugate.
- Phase II clinical trial of tanespimycin, a heat shock protein 90 (HSP90) inhibitor, in first-line treatment.
Main Results:
- FG-3019 demonstrated relative safety in a Phase I study (Abstract #213).
- ASG-5ME was found to be safe at appropriate doses in a Phase I trial (Abstract #176).
- Tanespimycin showed no effectiveness as a first-line treatment in a Phase II study (Abstract #245).
Conclusions:
- FG-3019 and ASG-5ME warrant further investigation for potential activity in pancreatic cancer patients.
- Tanespimycin was not effective in the studied first-line treatment setting for pancreatic cancer.
- Ongoing research into novel agents is crucial for improving outcomes in pancreatic adenocarcinoma.
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