
Health Equity & Access Weekly Roundup: July 10, 2026
Key Takeaways
- Financial toxicity is shifting toward commercially insured patients as PBM designs increase cost sharing, even as Medicare Part D reforms reduce out-of-pocket exposure for oral targeted therapies.
- Pharmacists and technicians can preempt denials by aligning formulary selections, strengthening prior-authorization documentation, and routing patients to manufacturer copay programs, foundations, and grants.
Pharmacy eases lung cancer costs; pediatric cancer erases 40% income; BTKis widen CLL access; hospitals lag on translated aid; MN mandate ends NGS denials.
Pharmacists Help Navigate Precision Lung Cancer Care: Stefanie Houseknecht, PharmD
Financial toxicity for patients on long-term targeted therapies for lung cancer has shifted from Medicare beneficiaries to commercially insured patients, according to Stefanie Houseknecht, PharmD, a clinical pharmacy specialist at Johns Hopkins Hospital speaking at the
Pediatric Cancer Creates Long-Term Financial Challenges for Patients, Families: Cherie Daly, MD
Financial toxicity in pediatric cancer extends well beyond the cost of medicine, according to Cherie Daly, MD, director of scientific affairs at the Pediatric Cancer Research Foundation. While institutions such as St. Jude Children's Research Hospital help cover treatment costs, Daly said nearly 40% of household income is typically lost when a parent leaves the workforce to care for a child with cancer full time, on top of costs tied to fertility preservation, sibling care, and mental health support, with long-term survivors, particularly those with brain tumors, facing lifelong disability, chronic organ damage, and lost future earning potential. She said financial hardship directly threatens treatment adherence, since pediatric cancer protocols often include extended maintenance phases that patients may abandon under financial strain, raising the risk of relapse and, in turn, greater long-term costs; she described the cumulative toll on families as a "snowball" and called for greater recognition of these nonmedical costs earlier in the treatment journey.
Easing Barriers to BTK Inhibitors in CLL: Kerry Rogers, MD
Financial toxicity tied to long-term Bruton tyrosine kinase (BTK) inhibitor therapy in chronic lymphocytic leukemia (CLL) is as much psychological as it is fiscal, Kerry Rogers, MD, of The Ohio State University Comprehensive Cancer Center—The James, said in an interview, noting that even patients with minimal out-of-pocket costs have questioned whether they are "worth" the price of therapy. She called financial toxicity a health system-level problem spanning drug pricing negotiation, government regulation, and reimbursement practices rather than something hematologists can solve alone, pointing to the American Society of Clinical Oncology's value framework, which found ibrutinib's efficacy and quality-of-life benefits made it the higher-value option despite its higher price than bendamustine/rituximab. On access, Rogers said oral BTK inhibitors, which can be mailed directly to patients, reduce geographic barriers compared with infusional regimens like venetoclax and obinutuzumab, and that manufacturer programs and Medicaid coverage have kept them financially accessible, sometimes more so than for commercially insured or Medicare patients; she also noted CLL trials underrepresent non-White populations relative to disease demographics and often exclude frail patients, citing new trials designed around higher comorbidity scores and a first-line pirtobrutinib study built to limit clinic visits for elderly enrollees.
Nonprofit, System-Affiliated Hospitals Lead in Multilingual Financial Assistance Access: Erin L. Duffy, PhD, MPH
Nonprofit and system-affiliated hospitals provide better access to financial assistance information in languages other than English compared with other hospital types, according to a study by Erin L. Duffy, PhD, MPH, a health policy researcher at the University of Southern California's Schaeffer Center for Health Policy & Economics, discussed on
Reducing Coverage Barriers, Testing Delays Could Further Improve Lung Cancer Outcomes: Robert Kratzke, MD
Coverage denials for genomic testing in lung cancer have "essentially disappeared" at the University of Minnesota, according to Robert Kratzke, MD, a professor of medicine there, speaking with AJMC following a Minneapolis Institute for Value-Based Medicine event. Kratzke attributed much of the decline to Minnesota's biomarker testing mandate, effective January 2025, which requires state Medicaid to cover necessary genomic testing for patients with cancer; he has not seen a Medicare denial in about 5 years, and none in the past 2, and called for CMS to adopt a similar nationwide policy so that access to next-generation sequencing (NGS) does not depend on geography, comparing withheld biomarker testing to denying an X-ray for a broken bone. He also flagged turnaround time as a persistent barrier, noting nanopore microfluidic sequencing could return results in 24 to 48 hours, yet patients often wait 7 to 14 days, with Medicare's 14-day inpatient testing rule a particular obstacle, though his institution's reflex-testing model helps ensure sequencing data is ready by a patient's first oncology visit; he closed on an optimistic note, citing gains in stage 4 lung cancer survival from about 1 year historically to commonly 3 to 5 years today.




