The American Society of Clinical Oncology (ASCO) has raised concerns that utilization management strategies, especially for high-cost prescription drugs, could reduce patient access.
Health plans often experiment with different models to identify optimal strategies on utilization management, especially high-cost prescription drugs. In its new policy statement, the American Society of Clinical Oncology (ASCO) has raised concerns that these strategies could reduce patient access.
Prior authorization (PA), clinical pathways, step-therapy protocols, restrictive formularies, and specialty tiers are some of the ways in which health insurance companies restrict use of prescription drugs. Such restrictions can prove problematic for patients being treated for cancer, because often there is a lack of interchangeable clinical options in oncology. Ensuring compliance with the different health plan policies is also a huge administrative investment for clinics, and to avoid this, ASCO, in collaboration with the American Medical Association, developed resource utilization principles to bring about reform with the process.
“Utilization management strategies, when implemented without appropriate patient safeguards, can impede patient access to high-value, clinically appropriate care,” said ASCO President Daniel F. Hayes, MD, FASCO, FACP. “Payer policies must reflect the current requirements of contemporary cancer care and be evidence-based on what constitutes high-quality care.”
The new policy statement provides the following recommendations:
The policy statment recommends following ASCO’s criteria, “which promote patient protections for clinical pathway development, implementation and use, and analytics.”
Exploring Racial, Ethnic Disparities in Cancer Care Prior Authorization Decisions
October 24th 2024On this episode of Managed Care Cast, we're talking with the author of a study published in the October 2024 issue of The American Journal of Managed Care® that explored prior authorization decisions in cancer care by race and ethnicity for commercially insured patients.
Listen
FDA Approves Danziten for Chronic Myeloid Leukemia Without Mealtime Restrictions
November 14th 2024The FDA has granted approval to Azurity Pharmaceuticals' nilotinib tablets (Danziten), a novel version of the tyrosine kinase inhibitor for chronic myeloid leukemia that can be taken without mealtime restrictions.
Read More
Bridging Cancer Care Gaps and Overcoming Medical Mistrust
November 13th 2024In this clip from our interview with Oscar B. Lahoud, MD, cochair of our Institute for Value-Based Medicine® evening hosted with NYU Langone Health, he addressed medical mistrust in underrepresented communities.
Read More