PET Helps Quantify Cancer Immunotherapy Target Engagement

Using the peptide radiotracer [64Cu]WL12 and PET imaging demonstrated that variable PD-L1 expression and its saturation by antibody therapeutics can be quantified. Next, they used the radiotracer to evaluate the impact of time and dose on the unoccupied fraction of tumor PD-L1; using mathematical modeling, they calculated the antibody therapeutic doses needed to achieve therapeutically effective occupancy (defined as over 90%). The study was published in the February 2019 issue of the Journal of Clinical Investigation.

“This approach offers a vital step toward directly measuring how well immunotherapy drugs are able to engage a tumor in any given person, and give us some insight about how to optimize further treatments by increasing the dose or substituting other drugs or therapies more quickly,” said senior author professor of radiology Sridhar Nimmagadda, PhD, of JHU-SOM. “Its use could streamline cancer therapy by enhancing doctors' ability to tailor therapy, help determine the therapeutic dose of a drug, and avoid or stop treatments that are not effective.”

Checkpoint inhibitors are designed to help the immune system recognize cancer cells as dangerous and target them for destruction. Tumors often hijack these natural protective systems, thus allowing them to masquerade as healthy tissues. PD-L1 is one such checkpoint target, and it is currently the backbone of immune checkpoint therapies.

Related Links:
Johns Hopkins University School of Medicine
Memorial Sloan-Kettering Cancer Center