Cell therapies are growing in popularity
In recent years, cancer patients are being offered an additional option when chemotherapy and radiation treatments fail: chimeric antigen receptor (CAR) T-cell therapy. With CAR T-cell therapies, a type of ex vivo gene therapy, a patient’s T cells are genetically modified in a lab to better recognize and kill cancer cells.
The treatments are used for certain blood cancers such as leukemia, lymphoma and multiple myeloma.
Last year, the U.S. Food and Drug Administration (FDA) also approved1 the first cellular immunotherapies for treating solid tumors, adding to the host of previously approved CAR T-cell therapies.
Known commercially as AmtagviTM, a one-time treatment for patients with advanced melanoma, and TecelraTM,2 used to treat synovial sarcoma, these treatments leverage the body's own immune cells to recognize and attack cancer cells. But they come with a hefty price tag — roughly $515,000. That’s only slightly higher than existing CAR T-cell therapies for blood cancer patients, many of which cost upward of $400,000.3
These prices also don’t include the additional costs associated with these therapies, such as hospital and professional charges, invoice markups and other treatments for underlying conditions while a patient waits for cellular therapy.
Yet, the potential — and reality — of these therapies is undeniable. Since 2017, when the first CAR T-cell therapy was approved by the FDA, these therapies have become a key reason that survival rates of people with certain blood cancers have soared from 10–15% five years ago to 40% today.4 These results are the reason why payers must be prepared to manage the high costs of these treatments.