The study, led by Dr. Antoni Ribas, director of the UCLA Jonsson Comprehensive Cancer Center Tumor Immunology Program, also found that JAK1 or JAK2 genetic mutations led to a loss of reactive PD-L1 expression. PD-L1 is an immune biomarker expressed on tumor cells and pembrolizumab requires an abundance of it to effectively attack cancer cells.
In previous findings published in the New England Journal of Medicine, UCLA researchers analyzed pairs of tumors before a person underwent immunotherapy treatment and after relapse. Ribas and colleagues discovered that one of the tumors lost a gene called B2M, which changed how the body’s immune system recognized the cancer. The loss of gene B2M caused JAK1 and JAK2 to function improperly by preventing the immune system from attacking the cancer.
In 2014, pembrolizumab, which is marketed as Keytruda, was approved by the U.S. Food and Drug Administration to treat advanced melanoma. Since then it has helped thousands of people live longer. The drug was also approved last year to treat people with advanced non-small-cell lung cancer. It works by blocking the interaction between two negative immune signals mediated by PD-1, a cell receptor expressed on immune cells, and its ligand PD-L1, a biomarker expressed on cancer cells.
The study was conducted over a two-year period and used biopsies from people with melanoma and colon cancer who received pembrolizumab. The researchers also studied the effects of genetic mutations in 48 previously studied melanoma cells lines.
UCLA researchers are currently studying animal models with JAK1 and JAK2 genetic mutations to help develop new and improved combination treatments for people who do not respond to anti-PD-1 treatment.