Certain treatments have long served as stress tests for payer operations. That’s certainly true of transplants, which are not only expensive but require complex and careful coordination.
Success depends not only on the surgery itself, but on what happens before and after. A missed immunosuppressant refill or a follow-up appointment scheduled weeks too late can have serious consequences.
Now cell and gene therapies (CGTs) are placing additional pressure on health systems as even more complicated and expensive procedures. The price of chimeric antigen receptor (CAR) T-cell alone averages more than $500,000.1
Like transplants, CGTs are complex. They require careful quality control and coordination and specialized treatment facilities, which can add significant costs to treatment.
For payers, the challenge isn’t just about managing complex and costly treatments. It’s about whether the right systems are in place to identify risk and collaborate with care teams to support access to these treatments at scale.
Many payers say the U.S. isn’t there yet. In a 2025 survey of payers covering nearly 280 million lives, 95% reported that the American health system isn’t prepared for broad cell and gene therapy adoption. When asked about barriers, respondents cited:
- High upfront costs
- Uncertain long-term outcomes
- Multisite care logistics2
Fortunately, transplant care offers a practical blueprint that can be applied to CGT to answer some of those concerns.