DENVER — A process of taking patients’ own cells and reprogramming them to fight cancer has been a last-ditch option for blood cancer patients when nothing else worked, but a new study underway in Aurora is trying to determine whether more patients could benefit from trying the procedure sooner.
Chimeric antigen receptor T cell therapy, known as CAR-T, is a type of immunotherapy that involves taking cells from the patient’s body and altering them to attack cancerous cells that have specific proteins on their surfaces. The patient then gets the altered cells by infusion.
A study at University of Colorado’s Gates Institute on the Anschutz Medical Campus is looking at CAR-T in adult patients with acute lymphocytic leukemia, a cancer of the blood and bone marrow, whose first round of chemotherapy either failed or gave a disappointing response that suggests it won’t work for long, executive director Dr. Terry Fry said. (The institute is named for rubber manufacturer Charles C. Gates.)
This specific study is looking for safety and will have preliminary results next year. Assuming it doesn’t find any problems, a larger study would test if patients do better when receiving CAR-T rather than another round of chemotherapy, Fry said.
When a cancer therapy is new and carries unknown risks, typically the first patients who receive it are those who are out of other options, Fry said. If it works well and doesn’t cause unacceptable side effects for patients whose cancer resisted treatment, then researchers start looking into whether offering it earlier could make sense, he said.
“When we see something is successful, we forget that someone had to be that first patient” and take risks, he said.
Generally, people with the type of leukemia CU is studying have two options: chemotherapy or a bone marrow transplant, both of which can be grueling, Fry said. The advantage of CAR-T, when it works, is that the patient only has to take it once, he said.
“It can be advantageous to take a single treatment, get on with their life and have done with it,” he said.
While nothing is certain, people who don’t go into remission after being treated with chemotherapy often don’t do much better with another round, so if studies find that giving them CAR-T earlier is effective, that could spare them another round of ineffective treatment, he said.
Immunotherapy carries its own risks, including secondary cancers, and a small number of patients have developed lymphoma after treatment with CAR-T for another blood cancer. Right now, it appears that developing lymphoma after CAR-T is “extremely rare,” and no one is sure if the CAR-T caused it or if the patients’ previous chemotherapy did, Fry said. Roughly 3% of patients who had one type of blood cancer develop a secondary cancer regardless of whether they received CAR-T, he said.
