
Preclinical Study: Three-Step Treatment Strategy for Pancreatic Cancer
Cedars-Sinai cancer study shows novel strategy disrupts the difficult-to-treat tumor microenvironment, preventing cancer from spreading.
Research led by investigators at
The preclinical study, published in the peer-reviewed journal
“These three drugs, used in combination in a laboratory setting, prevented disease metastasis,” said
The three-step combinatorial strategy combined an anti-PD-1 immunotherapy antibody and a protein known as FAKi with a novel pathway called CXCR4. This combination destroyed the tumor’s outer microenvironment, attacked the tumor itself, and bolstered the immune system of the laboratory mice.
“The combined therapy prevented disease metastasis and extended life,” said Osipov, also a medical oncologist and researcher in the Gastrointestinal Research Group at the Samuel Oschin Cancer Center. “This is an important step for a disease that is extremely challenging to treat and has very low survival rates.”
The tumor microenvironment in pancreatic ductal adenocarcinoma—the most common form of pancreatic cancer—has long been resistant to therapeutics, including immunotherapy.
Pancreas tumors tend to be aggressive and often become resistant to traditional treatments like chemotherapy. While immunotherapies have proven successful in many other forms of cancer—like melanoma and lung cancer—benefits have been limited in pancreatic cancer.
This difficulty to treat the disease has made pancreatic cancer one of the deadliest cancers, with a five-year survival rate of just 11%.
More than 62,000 Americans are expected to be diagnosed with pancreatic cancer in 2022. And, by the year 2030,
“Our teams of investigators are exploring novel methods to target the tumor microenvironment with the hope of improving survival and treatment options for patients,” said
As a next step, Osipov and team plan to develop a clinical trial to further explore the treatment potential of the CXCR4 pathway.



































