Oncology State Societies Advocacy Resources

Advocacy Aimed at Improving Access and Outcomes in Cancer Care: To address policies and practices that affect patient care and access, the Oncology State Societies (OSS) leads a policy and advocacy program focused on legislation and regulations impacting patient care and provider access. OSS has expanded its reach by collaborating with local and national organizations and state lobbyists to prioritize key legislative issues.

The OSS policy program has helped establish a policy communication and learning infrastructure in 15 participating states with over 130 engaged multidisciplinary providers across the US, demonstrating the collective power available to drive meaningful change. By collaborating to address key policy issues, OSS members can have a tangible impact on improving patient care and quality of life for both patients and caregivers.

To learn more about your state’s policy committee, email Lu Anne Bankert at lbankert@accc-cancer.org.

Town Hall Executive Summary

OSS Policy Town Hall

In September 2024, the Oncology State Societies held a Policy Committee Town Hall Meeting that brought together oncology professionals, lobbyists, and state society leaders to discuss key legislative and advocacy priorities impacting oncology care across the US. There were 83 total attendees, including the ACCC President-Elect and 55 members across 18 State Societies.

Discussions focused on:

  • Bipartisan support for cancer initiatives
  • Challenges with Medicaid and pharmacy benefit manager (PBM) reforms
  • State-level advocacy efforts such as prior authorization and biomarker testing
  • Patient and provider story collections
  • Strategies for effective lobbying and coalition-building

Gain strategies to utilize local lobbyists, build effective coalitions, and collaborate with other states to advance key federal- and state-level legislation and advocacy priorities.

Download Summary

The Advocacy Engagement Report provides OSS members with comprehensive case studies on issues that galvanized state societies to act. The report documents the specific actions taken by different state policy committees to affect change.

Read the report to:

  • Unlock the 6 keys to successful grassroots advocacy as found in this effort.
  • Learn how states without governmental affairs resources leveraged the power of their membership and their committee expertise.
  • Benefit from lessons learned.
  • Gain inspiration from a nationwide effort across OSS members to effect change.

Download Report

Engaging in advocacy through our state societies is one of the most direct ways we can have a voice in healthcare policies impacting the care of our patients.

Haley M. Simpson, MD, PhD
Chair, Policy Committee, Rocky Mountain Oncology Society

Cancer Buzz Podcasts

CMS Finalizes Rule to Improve the Prior Authorization Process

By Monique J. Marino
February 22, 2024

On January 17, 2024, more than 1 year after it was initially proposed, the Centers for Medicare & Medicaid Services (CMS) finalized the CMS Interoperabil­ity and Prior Authorization Final Rule (CMS- 0057-F), establishing requirements for certain payers to streamline the prior authorization process. Specifically, “the rule sets require­ments for Medicare Advantage (MA) organiza­tions, Medicaid and the Children’s Health Insurance Program (CHIP) fee-for-service (FFS) programs, Medicaid managed care plans, CHIP managed care entities, and issuers of Qualified Health Plans (QHPs) offered on the Federally-Facilitated Exchanges (collectively ‘impacted payers’) to improve the electronic exchange of health information and prior authorization processes for medical items and services.” As a whole, the agency estimates these policies will improve prior authorization processes and reduce burden on patients, providers, and payers, resulting in approximately $15 billion of estimated savings over 10 years.

Beginning primarily in 2026, impacted payers will be required to send prior authorization decisions within 72 hours for expedited (ie, urgent) requests and 7 calendar days for standard (ie, non-urgent) requests for medical items and services. For some payers, this new timeframe for standard requests cuts current decision timeframes in half. To help facilitate resubmission of requests or appeals, the rule also requires all impacted payers to include a specific reason for denying a prior authoriza­tion request. Finally, impacted payers will be required to publicly report prior authoriza­tion metrics.

In addition, the rule requires impacted payers to implement an electronic prior authorization application programming interface (API) to establish a more efficient electronic prior authorization process between providers and payers by automating the end-to-end prior authorization process. It is expected that this new requirement “will reduce administrative burden on the healthcare workforce, empower clinicians to spend more time providing direct care to their patients, and prevent avoidable delays in care for patients.” A fact sheet for this final rule is available on the CMS website.

While the Assocation of Cancer Care Centers (ACCC) supports these efforts, the association is concerned that this rule only applies to payers in the federal programs outlined above and does not apply to the “approximately 158 million Americans who are insured through their employment—the most common kind of coverage in the United States.”

Prior authorization remains one of the most discussed barriers to timely quality cancer care delivery among health care providers. The burden placed on the multidisciplinary care team to submit authorizations, complete peer-to-peer interviews, and fight appeals is extraordinary. In a 2022 survey of American Society of Clinical Oncology (ASCO) members, nearly all participants reported that a patient they had treated had experienced harm as a result of late or denied prior authorizations, including disease progression (80%) and loss of life (36%). ASCO survey findings identified the items below as the most widely cited challenges for patients:

  • Treatment delays (96%)
  • Delays in diagnostic imaging (94%)
  • Patients being forced into using a second-choice therapy (93%)
  • Patients denied therapy (87%)
  • Increased patient out-of-pocket costs (88%)

How ACCC is Helping

ACCC has developed tools and resources to help its provider members, including a virtual Prior Authorization Clinic. This educational program seeks to help providers:

  • Reduce the administrative burden of prior authorization processes by sharing best practices
  • Address key components of prior authoriza­tion, including new technologies or areas where there are high errors in billing and coding that result in high denials
  • Provide examples of standardized criteria for ordering and prescribing services that align with evidence-based guidelines
  • Develop a series of case-based prior authorization scenarios that cancer programs can utilize when advocating for change, locally and nationally, at their cancer program
  • Highlight successful methods to track prior authorizations and results for pertinent members of the multidisciplinary cancer care team. 

As ACCC continues to advocate for long-term solutions to prior authorization challenges, including those instituted by private payers, we would love to hear from you about the impact that prior authorizations continue to have on your cancer program or practice, providers and staff, and the patients and families you treat. Contact us at rhodzic@accc-cancer.org.

Monique J. Marino is senior director, Editorial Content and Strategy, Association of Cancer Care Centers, Rockville, Maryland.

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