Relating to health benefit plan coverage for chimeric antigen receptor T-cell therapy.
ModeratePlan for compliance
Medium Cost
Effective:2025-06-20
Enforcing Agencies
Texas Department of Insurance
01
Compliance Analysis
Key implementation requirements and action items for compliance with this legislation
Implementation Timeline
Effective Date: June 20, 2025 (Legal effect due to supermajority vote).
Compliance Deadline:January 1, 2026. The requirements apply to health benefit plans delivered, issued for delivery, or renewed on or after this date.
Agency Rulemaking: The Texas Department of Insurance (TDI) is required to adopt rules necessary to administer Subchapter E-2 prior to January 1, 2026. Watch the Texas Register in Q3/Q4 2025 for definitions regarding "medical necessity" documentation.
Immediate Action Plan
1.Audit Network: Cross-reference your current in-network hospitals against the FDA’s list of certified CAR T facilities.
2.Update Plan Documents: Revise Summary Plan Descriptions (SPDs) and policies for 2026 renewals to remove "Center of Excellence" exclusivity language regarding CAR T.
3.Reprogram Claims Logic: Ensure claims systems do not auto-deny CAR T codes from general in-network hospitals starting Jan 1, 2026.
4.Engage Stop-Loss: Discuss the impact of network expansion on your attachment points and premiums for the upcoming plan year.
Operational Changes Required
Contracts
Provider Agreements: Review all hospital and cancer center contracts immediately. Exclusivity clauses or "carve-outs" that restrict CAR T therapy to specific facilities are unenforceable as of the 2026 plan year if the facility is otherwise in-network.
Fee Schedules: If your current master agreements with general hospitals exclude CAR T codes (anticipating they would go to a Center of Excellence), you must negotiate fee schedules for these services immediately to avoid defaulting to higher out-of-network or chargemaster rates.
Reinsurance/Stop-Loss: Notify your stop-loss carriers immediately. The removal of steering mechanisms increases the probability of high-dollar claims at higher-cost facilities.
Hiring/Training
Utilization Review (UR) Teams: Update clinical guidelines and decision trees. Staff must be trained that they cannot deny pre-authorization based on facility network status if the facility is in-network for other services.
Credentialing: Staff must verify facility certifications against FDA lists specifically for the CAR T product requested (e.g., Yescarta vs. Kymriah).
Reporting & Record-Keeping
FDA Verification: Implement a workflow to document that the treating facility held a valid FDA certification for the specific product *at the time of service*. This will be your primary defense in a bad-faith claim or audit.
Medical Necessity: Ensure clinical denials are strictly based on patient medical status, not provider location. Documentation must be robust to survive TDI scrutiny.
Fees & Costs
Premium Adjustments: Based on the Fiscal Note regarding TRS (projected $3.4M+ annual increase), carriers and PEOs must factor increased utilization and unit costs into 2026 premium renewals.
Medicaid Exclusion: Do not apply these cost assumptions or operational changes to Medicaid or CHIP lines of business; they are statutorily exempt.
Strategic Ambiguities & Considerations
"Any Other Service": The statute compels coverage if a provider is participating "with respect to *any other service*." This is legally broad. If a hospital system is in-network for maternity or orthopedics but carved out for oncology, the strict reading of the law implies they are now in-network for CAR T. Expect TDI rulemaking to potentially narrow this, but plan for the broadest interpretation.
Product Specificity: The law ties coverage to FDA certification. It is unclear how plans should handle a facility certified for *one* CAR T product but requesting authorization for a *different* one. Until rules are issued, strictly adhere to the specific FDA certification held by the facility.
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The bill author has informed the committee that Chimeric Antigen Receptor T-cell (CAR T) therapy is a transformational treatment that harnesses the T-cells in a person's immune system to target and destroy cancer cells and may hold the potential to be curative for severely ill patients and eliminate rounds of less effective treatments. However, the bill author has also informed the committee that because timely patient access is required to enable the greatest chance of survival, patients must be accompanied by a caregiver for preparation visits to an authorized treatment center for testing, with a weeklong inpatient stay followed by monitoring at a nearby health care facility for 28 to 30 days. The bill author has further informed the committee that some commercial payers are preventing the expansion of CAR T therapy to qualified community centers despite proven safety and efficacy outside of academic centers by requiring the completion of the treatment to take place at accredited facilities that currently only exist in Texas in Houston, Dallas, San Antonio, Austin, and Belton, leaving people in other parts of the state to travel to one of these cities for 28-30 days to complete the therapy. C.S.H.B. 3057 seeks to increase access to CAR T therapy by requiring a health benefit plan that provides coverage for the therapy to provide coverage that is medically necessary and administered by certain certified health care facilities enrolled in an approved risk evaluation and mitigation strategy for the therapy.
CRIMINAL JUSTICE IMPACT
It is the committee's opinion that this bill does not expressly create a criminal offense, increase the punishment for an existing criminal offense or category of offenses, or change the eligibility of a person for community supervision, parole, or mandatory supervision.
RULEMAKING AUTHORITY
It is the committee's opinion that rulemaking authority is expressly granted to the commissioner of insurance in SECTION 1 of this bill.
ANALYSIS
C.S.H.B. 3057 amends the Insurance Code to require a health benefit plan that provides coverage for chimeric antigen receptor T-cell therapy to provide coverage for such therapy that is medically necessary and administered by a health care provider that meets the following criteria:
·is a certified health care facility enrolled in an approved risk evaluation and mitigation strategy under applicable federal law for the therapy being administered; and
·is participating in the health benefit plan's network.
C.S.H.B. 3057 specifies the types of plans to which its provisions apply and establishes exceptions to that applicability. The bill requires the commissioner of insurance to adopt rules as necessary to administer the bill's provisions. The bill applies to any health benefit plan that is delivered, issued for delivery, or renewed on or after January 1, 2026.
EFFECTIVE DATE
September 1, 2025.
COMPARISON OF INTRODUCED AND SUBSTITUTE
While C.S.H.B. 3057 may differ from the introduced in minor or nonsubstantive ways, the following summarizes the substantial differences between the introduced and committee substitute versions of the bill.
The substitute omits the following provisions from the introduced:
·a prohibition against a health benefit plan in Texas that provides coverage for chimeric antigen receptor T-cell (CAR T) therapy refusing to contract for the administration of any CAR T therapy by any provider that qualifies as a certified healthcare facility in accordance with approved procedure under the CAR-T product license by the FDA; and
·a prohibition against a health benefit plan in Texas that covers such therapy denying coverage for the administration of the therapy by any such provider.
The substitute instead includes a requirement absent from the introduced for a health benefit plan that provides coverage for chimeric antigen receptor T-cell therapy to provide coverage for such therapy that is medically necessary and administered by a health care provider that meets the following criteria:
·is a certified health care facility enrolled in an approved risk evaluation and mitigation strategy under applicable federal law for the therapy being administered; and
·is participating in the health benefit plan's network.
The substitute establishes exceptions to the applicability of its provisions, whereas the introduced did not establish those exceptions. The substitute omits the introduced version's provision establishing the purpose of the bill's provisions.
Honorable Jay Dean, Chair, House Committee on Insurance
FROM:
Jerry McGinty, Director, Legislative Budget Board
IN RE:
HB3057 by Landgraf (Relating to network standards for Chimeric Antigen Receptor T-Cell (CAR T) therapy.), As Introduced
Estimated Two-year Net Impact to General Revenue Related Funds for HB3057, As Introduced: an impact of $0 through the biennium ending August 31, 2027.
The bill would make no appropriation but could provide the legal basis for an appropriation of funds to implement the provisions of the bill.
General Revenue-Related Funds, Five- Year Impact:
Fiscal Year
Probable Net Positive/(Negative) Impact to General Revenue Related Funds
2026
$0
2027
$0
2028
$0
2029
$0
2030
$0
All Funds, Five-Year Impact:
Fiscal Year
Probable Savings/(Cost) from RETIRED SCHOOL EMP GROUP INSURANCE 989
Probable (Cost) from School Employees UGIP Trust Fund 855
2026
($3,415,467)
$0
2027
($3,644,303)
($3,374,592)
2028
($3,888,472)
($3,509,576)
2029
($4,148,999)
($3,649,959)
2030
($4,426,982)
($3,795,957)
Fiscal Analysis
The bill would expand access to Chimeric Antigen Receptor T-Cell (CAR T) therapy. Health benefit plans that cover CAR T therapy would be required to allow CAR T to be provided at any treatment center that qualifies as a certified healthcare facility in accordance with Food and Drug Administration standards.
The bill would take effect on September 1, 2025, and apply to health care plans issued or renewed on or after January 1, 2026.
Methodology
The Teacher Retirement System (TRS) indicates that the cost to TRS-Care, the retired school employee group insurance program, would be $3.4 million in fiscal year 2026, $3.6 million in fiscal year 2027, increasing to $4.4 million in fiscal year 2030. TRS estimates the cost to TRS-ActiveCare, the school employees uniform group insurance program, would be $3.4 million beginning in fiscal year 2027, increasing to $3.8 million in fiscal year 2030. Estimated annual cost increases are based on current medical trends.
According to the Health and Human Services Commission (HHSC), Medicaid managed care organizations (MCOs) are required to provide access to all medically necessary Medicaid covered services through an adequate provider network. MCOs are also responsible for negotiating contracts with providers for all covered services. HHSC has not indicated an expected cost to implement the provisions of the bill.
Other state agencies and institutions of higher education are already in compliance with the provisions of the bill, and their costs could be absorbed using existing resources.
Local Government Impact
No fiscal implication to units of local government is anticipated.
Source Agencies: b > td >
323 Teacher Retirement System, 327 Employees Retirement System, 454 Department of Insurance, 529 Health and Human Services Commission, 710 Texas A&M University System Administrative and General Offices, 720 The University of Texas System Administration
LBB Staff: b > td >
JMc, AAL, ASA, ENA
Related Legislation
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HB3057 effectively bans "narrow networks" for CAR T-cell therapy within commercial health plans and public employee plans (TRS/ERS/UT). If a medical facility is in your network for any service and holds the required FDA certification for a specific CAR T product, you must cover the treatment at that facility. This removes the ability to steer patients exclusively to designated "Centers of Excellence" for cost control.
Q
Who authored HB3057?
HB3057 was authored by Texas Representative Brooks Landgraf during the Regular Session.
Q
When was HB3057 signed into law?
HB3057 was signed into law by Governor Greg Abbott on June 20, 2025.
Q
Which agencies enforce HB3057?
HB3057 is enforced by Texas Department of Insurance.
Q
How urgent is compliance with HB3057?
The compliance urgency for HB3057 is rated as "moderate". Businesses and organizations should review the requirements and timeline to ensure timely compliance.
Q
What is the cost impact of HB3057?
The cost impact of HB3057 is estimated as "medium". This may vary based on industry and implementation requirements.
Q
What topics does HB3057 address?
HB3057 addresses topics including health, health--other diseases & medical conditions, insurance, insurance--health & accident and cancer.
Legislative data provided by LegiScanLast updated: November 25, 2025
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