New Triple-Drug Treatment Eliminates Pancreatic Tumors in Mice, Study Finds

  A groundbreaking triple-drug therapy has shown remarkable success in eliminating pancreatic cancer tumors and preventing their recurrence in multiple mouse models. By simultaneously blocking three key growth pathways, 

A microscopic image showing pancreatic cancer cells (in purple) surrounded by healthy tissue (in pink).

The non-toxic treatment represents a promising new strategy to overcome the disease's notorious treatment resistance.

Targeting the Cancer's Survival Network

The research, published in PNAS, addresses a critical weakness of current treatments: cancer's ability to find "another door" for survival when one pathway is blocked. Senior author Carmen Guerra and her team identified that when major growth drivers like KRAS (mutated in nearly all pancreatic cancers) are inhibited, a backup protein called STAT3 becomes highly active. The new therapy strategically combines drugs to block KRAS, a related pathway, and STAT3 all at once.

The Three-Drug Cocktail & Stunning Results

A scientist in a lab coat examines data on a screen showing tumor regression charts.

The therapy uses:

  1. Afatinib: An FDA-approved lung cancer drug.
  2. Daraxonrasib: A drug currently in clinical trials.
  3. A novel STAT3 inhibitor.

Tested across three rigorous mouse models—including one using human tumor samples—the combination completely eliminated pancreatic tumors. “You couldn't even see where the tumor was. The pancreas was completely healthy,” Guerra reported. Critically, the cancer did not return for at least 200 days post-treatment, and the therapy showed no debilitating side effects in the mice.

Why This Breakthrough Matters

A conceptual graphic showing three different colored arrows blocking a path toward a cancer cell

Pancreatic ductal adenocarcinoma, the most common form, has a five-year survival rate of just 13%, dropping to 1% in late stages. Standard chemotherapy attacks all fast-dividing cells, causing severe side effects, and tumors rapidly develop resistance. This targeted approach aims to outmaneuver the cancer's adaptability by shutting down its primary and emergency survival routes simultaneously.

The Path Ahead: Cautious Optimism

While the mouse results are exceptional, researchers acknowledge the leap to human patients. Some drugs in the cocktail, like afatinib, are known to cause side effects (skin and GI issues) in people. The team is now working to develop better-tolerated drugs that target the same pathways. Further testing in mouse models with diverse genetic mutations is also planned to ensure broad effectiveness.

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Source Information:


This report is based on the peer-reviewed study in Proceedings of the National Academy of Sciences (PNAS).


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