Biomarkers in Oncology – Access & Reimbursement – Detailed, Expanded Analysis (US) Biomarkers in Oncology
Biomarkers have become an integral component of the treatment landscape for an increasing number of oncology indications. Patients’ biomarker status often directs prescription choice in malignant melanoma, colorectal cancer, and ovarian cancer. When incorporated into standard clinical care, biomarker-driven therapies offer specific subpopulations of patients the potential for higher response rates and improved survival, albeit often at a high price. We explore the drivers of and barriers to the use of biomarker-based therapies and the impact of reimbursement policies on the use of these therapies. We also evaluate surveyed medical oncologists’ and surveyed payers’ prescriptions of emerging biomarker-driven therapies to treat these solid-tumor indications.
QUESTIONS ANSWERED
· What factors largely influence payers’ reimbursement decisions for biomarker-driven therapies in malignant melanoma, colorectal cancer, and ovarian cancer? What restrictions do they impose?
· Do access and reimbursement challenges differ by indication, and how well established are biomarkers in each indication?
· What impact do reimbursement and access have on oncologists’ decisions to prescribe biomarker-driven therapies?
· What are payer opinions of emerging agents, and how will oncologists’ prescribing patterns change with the launch of new therapies?
GEOGRAPHY: United States.
PRIMARY RESEARCH: Survey of 101 U.S. medical oncologists and 31 U.S. managed care organization (MCO) pharmacy directors and medical directors (PDs/MDs).
KEY DRUGS COVERED: Avastin, Erbitux, Vectibix, Opdivo, Keytruda, Yervoy, Zelboraf, Tafinlar, Mekinist, Cotellic, Braftovi, Mektovi, Lynparza, Zejula, Rubraca
CONTENT HIGHLIGHTS:
- Executive Summary
- Reimbursement
- Access and prescribing.
- Special topic: Market Access Outlook for biomarkers testing
- Opportunities and challenges for emerging therapies.
Table of contents
- Biomarkers in Oncology - Access & Reimbursement - Detailed, Expanded Analysis (US) Biomarkers in Oncology
- Access & Reimbursement | Biomarkers in Oncology | US | December 2020
- Biomarker-Driven Prescribing in Malignant Melanoma, Colorectal Cancer, and Ovarian Cancer | Access and Reimbursement | US
- Biomarker-Driven Prescribing in Malignant Melanoma, Colorectal Cancer, and Ovarian Cancer | Access and Reimbursement | US-1608212073
Neela Rambaruth, M.Sc., Ph.D., is an analyst on the Oncology team at DRG, part of Clarivate. She has authored content on non-small-cell lung cancer and hepatocellular carcinoma. Prior to joining DRG, she was a postdoctoral scientist at University College London, where she investigated the interaction of novel drugs with a therapeutic receptor involved in cardiovascular disease. She also held a postdoctoral position at Imperial College London, where she studied host-pathogen interaction in tuberculosis. She received her Ph.D. in breast oncology from the University of Westminster. Her doctorate focused on the identification of novel biomarkers associated with metastatic breast cancer. She has also published several peer-reviewed articles on oncology and therapeutic drug discovery.