Laboratory findings have set the stage for a clinical trial investigating a drug for pancreatic cancer that has spread to the liver.

Pancreatic cancer is tricky to manage because it spreads easily and early, and the tumors have a unique biological makeup. But, researchers made a breakthrough by learning about the genetic changes that occur during tumor migration—and also found a drug that can obstruct the process.

The next step is a groundbreaking clinical trial at Wilmot Cancer Institute, planned for early in 2024, to test the drug from their laboratory discovery, says senior investigator Darren Carpizo, co-leader of Wilmot’s genetics, epigenetics, and metabolism research program, and chief of surgical oncology at the University of Rochester Medical Center.

“We will be the first institution in the US to study the safety and effectiveness of the experimental drug, known as NP137, on pancreatic cancer that has spread to the liver,” Carpizo says.

Carpizo and several collaborators recently published the results of their bench science investigation in the journal Cell Reports , and Carpizo will lead the clinical trial with Aram Hezel, chief of hematology/oncology, and Nabeel Badri, a medical oncologist.

The five-year survival rate for pancreatic cancer is only 12%, which is a slight increase in 2023 compared to previous years. The number of cases is rising worldwide, however, and by 2030, pancreatic cancer is predicted to be the second leading cause of cancer deaths.

Why is pancreatic cancer deadly?

First, because it spreads (metastasizes) very early during its development. In 85% of patients, the cancer has already spread outside of the pancreas at diagnosis . Even when the cancer is localized to the pancreas and surgical removal is possible, the majority of patients face a recurrence of their cancer. The metastasis causes these patients to eventually succumb to the disease, which is why researchers are focused on understanding the biology of metastatic pancreatic cancer.

Second, although pancreatic cancer cells do not have to travel far to reach the liver, along the way they genetically reprogram themselves and become stronger. The result: newly seeded cancer cells in the liver have a distinctly different biology from the primary tumor in the pancreas, and are able to resist standard treatment, Carpizo says.

In their latest work, Wilmot researchers built on what was already known about a key gene, Netrin-1, involved in pancreas, breast, and colon cancers. They discovered, for the first time, the complex mechanisms that allow Netrin-1 to drive the lethal, genetic changes as pancreatic cancer cells migrate to the liver. They also showed how Netrin-1 activates hepatic stellate cells, which are involved in liver fibrosis, a serious chronic disease, priming the liver as a host for cancer.

In mice and in tissue studies, when researchers suppressed Netrin-1 with the anti-cancer drug (NP137), cancer was less likely to spread and cancer cell death occurred. The team includes scientists from Rutgers University, Fox Chase Cancer Center in Philadelphia, and a laboratory in France.

The clinical trial will likely require eligible patients to take two cycles of NP137 before surgery, undergo surgery to remove the cancer, and then take more of the experimental medication along with chemotherapy after surgery for up to six months, Carpizo says. He notes that NP137 is made by Netris Pharma, of Lyon, France, and is currently being tested in clinical trials in that country.

The Pancreatic Cancer Action Network (PanCAN) funded much of the work through a grant to Carpizo; Wilmot also provided pilot funding. PanCAN has emphasized that the recent, small uptick in survivorship rates for pancreatic cancer is due to transformative research and clinical trials, and strongly recommends that patients talk to their oncologists about clinical trials at every stage of their disease.

Source: University of Rochester

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