Insurance coverage policies are a major determinant of patient access to genomic tests. The objective of this study was to examine differences in coverage policies for guideline-recommended pharmacogenomic tests that inform cancer treatment. We analyzed coverage policies from eight Medicare contractors and 10 private payers for 23 biomarkers (e.g., HER2 and EGFR) and multi-gene tests. We extracted policy coverage and criteria, prior authorization requirements, and an evidence basis for coverage. We reviewed professional society guidelines and their recommendations for use of pharmacogenomic tests. Coverage for KRAS, EGFR, and BRAF tests were common across Medicare contractors and private payers, but few policies covered PML/RARA, CD25, or G...
Pre-emptive pharmacogenomic (PGx) testing of a panel of genes may be easier to implement and more co...
Pre-emptive pharmacogenomic (PGx) testing of a panel of genes may be easier to implement and more co...
Next-generation sequencing promises major advancements in precision medicine but faces considerable ...
Abstract: Insurance coverage policies are a major determinant of patient access to genomic tests. Th...
Background/Aims: Modern medicine is transitioning from empirical treatment to treatment on the basis...
Genomic tests are the fastest growing sector in medicine and medical science, yet there remains a de...
Recent advances in genomic medicine have led to the availability of genomic tests that have the pote...
BackgroundClinical adoption of the sequencing of circulating tumor DNA (ctDNA) for cancer has rapidl...
Background: Genomic tests are the fastest growing sector of medicine and medical science, yet there ...
OBJECTIVES:The aim of this study was to examine the evidence payers cited in their coverage policies...
Background: Genetic tests are the fastest growing sector of medicine and medical science, yet there ...
Class of 2018 AbstractSpecific Aims: To determine which Arizona health insurance companies provide c...
Exome sequencing (ES) is often a standard step in the genetic testing process for patients with rare...
Cancer has a large public health impact because it directly or indirectly affects all individuals, r...
PURPOSE: Given the likely proliferation of targeted testing and treatment strategies for cancer, a b...
Pre-emptive pharmacogenomic (PGx) testing of a panel of genes may be easier to implement and more co...
Pre-emptive pharmacogenomic (PGx) testing of a panel of genes may be easier to implement and more co...
Next-generation sequencing promises major advancements in precision medicine but faces considerable ...
Abstract: Insurance coverage policies are a major determinant of patient access to genomic tests. Th...
Background/Aims: Modern medicine is transitioning from empirical treatment to treatment on the basis...
Genomic tests are the fastest growing sector in medicine and medical science, yet there remains a de...
Recent advances in genomic medicine have led to the availability of genomic tests that have the pote...
BackgroundClinical adoption of the sequencing of circulating tumor DNA (ctDNA) for cancer has rapidl...
Background: Genomic tests are the fastest growing sector of medicine and medical science, yet there ...
OBJECTIVES:The aim of this study was to examine the evidence payers cited in their coverage policies...
Background: Genetic tests are the fastest growing sector of medicine and medical science, yet there ...
Class of 2018 AbstractSpecific Aims: To determine which Arizona health insurance companies provide c...
Exome sequencing (ES) is often a standard step in the genetic testing process for patients with rare...
Cancer has a large public health impact because it directly or indirectly affects all individuals, r...
PURPOSE: Given the likely proliferation of targeted testing and treatment strategies for cancer, a b...
Pre-emptive pharmacogenomic (PGx) testing of a panel of genes may be easier to implement and more co...
Pre-emptive pharmacogenomic (PGx) testing of a panel of genes may be easier to implement and more co...
Next-generation sequencing promises major advancements in precision medicine but faces considerable ...