This bill mandates that a percentage of federal cancer research funds, based on the proportion of the US population under 18, must be dedicated to pediatric cancer research starting in fiscal year 2026.
Brian Fitzpatrick
Representative
PA-1
The Fairness to Kids with Cancer Act of 2025 mandates that a specific, population-based percentage of total Federal cancer research funds must be dedicated to pediatric cancer research each fiscal year starting in 2026. This required percentage will be calculated annually based on the ratio of the U.S. population under age 18 to the total U.S. population. This ensures federal research funding reflects the proportion of children affected by cancer.
If you’ve ever felt like childhood cancer research gets the short end of the stick compared to adult cancers, the Fairness to Kids with Cancer Act of 2025 is trying to change that with a hard rule on federal spending. Starting in fiscal year 2026, this bill mandates that a specific, non-negotiable percentage of all federal cancer research funding must be dedicated solely to pediatric cancer research (SEC. 2).
This isn't a fixed dollar amount; it's a dynamic percentage tied directly to population data. The bill sets up a formula where the required percentage is calculated annually by dividing the total number of individuals under the age of 18 in the U.S. by the total U.S. population. The Bureau of the Census will provide these population figures, essentially making the proportion of kids in the country the floor for pediatric cancer research funding. For example, if 22% of the U.S. population is under 18, then 22% of all federal cancer research dollars must go to kids’ cancer research.
For families dealing with childhood cancer, this bill ensures a baseline of dedicated funding. Historically, pediatric cancer has been viewed as rare, sometimes leading to slower research progress and fewer treatment options compared to common adult cancers. This mandate aims to stabilize and increase the resources flowing into finding cures and better treatments for kids, which is a major win for parents and pediatric oncologists.
However, this approach introduces a few real-world complexities. The most immediate impact will be felt by the agencies that manage the overall cancer research budget—like the National Cancer Institute (NCI). They will now have a hard constraint on how they allocate funds. While the goal is beneficial, using a simple population ratio to determine the research budget floor is a bit blunt. The incidence, severity, and research complexity of pediatric cancer might not perfectly align with the population ratio. For instance, if the population ratio dictates 20% of the funds go to pediatric research, but adult cancers currently account for 90% of the deaths and 85% of the cases, this reallocation could potentially squeeze funding for critical adult cancer research programs.
The bill requires the President to "make sure" this percentage is met every year, starting in FY 2026. This puts the onus directly on the executive branch's budget process. While the intent is clear—to guarantee a minimum share for pediatric research—the bill doesn't detail the mechanism for enforcement or what happens if the Census data results in a massive shift in allocation that the research community isn't prepared for. Federal agencies will need clear guidance on how to implement this mandate without disrupting ongoing, multi-year research grants. Essentially, this guarantees a seat at the funding table for pediatric cancer research, but the practical challenge will be balancing this new minimum requirement against all the other vital research needs in the cancer fight.