BackgroundNext-generation tumor sequencing (NGTS) panels, which include multiple established and novel targets across cancers, are emerging in oncology practice, but lack formal positive coverage by US payers. Lack of coverage may impact access and adoption. This study identified challenges of NGTS coverage by private payers.MethodsWe conducted semi-structured interviews with 14 NGTS experts on potential NGTS benefits, and with 10 major payers, representing more than 125,000,000 enrollees, on NGTS coverage considerations. We used the framework approach of qualitative research for study design and thematic analyses and simple frequencies to further describe findings.ResultsAll interviewed payers see potential NGTS benefits, but all noted cha...
BackgroundClinical adoption of the sequencing of circulating tumor DNA (ctDNA) for cancer has rapidl...
Single gene tests to predict whether cancers respond to specific targeted therapies are performed in...
PurposeThere is limited payer coverage for genome sequencing (GS) relative to exome sequencing (ES) ...
BackgroundNext-generation tumor sequencing (NGTS) panels, which include multiple established and nov...
Next-generation sequencing promises major advancements in precision medicine but faces considerable ...
Background: Hereditary cancer panels (HCPs), testing for multiple genes and syndromes, are rapidly t...
Public and private payers face complex decisions regarding whether, when, and how to cover and reimb...
ObjectivesTo examine the temporal trajectory of insurance coverage for next-generation tumor sequenc...
Background: Next Generation Sequencing (NGS) is expected to lift molecular diagnostics in clinical o...
AbstractThis research aims to inform policymakers by engaging expert stakeholders to identify, prior...
This research aims to inform policymakers by engaging expert stakeholders to identify, prioritize, a...
Large-panel genomic tumor testing (GTT) is an emerging technology that promises to make cancer treat...
International audienceNext-generation sequencing (NGS) may enable more focused and highly personaliz...
Precision medicine seeks to use genomic data to help provide the right treatment to the right patien...
Objective: Next generation sequencing (NGS) may aid in tumor classification and treatment. Barriers ...
BackgroundClinical adoption of the sequencing of circulating tumor DNA (ctDNA) for cancer has rapidl...
Single gene tests to predict whether cancers respond to specific targeted therapies are performed in...
PurposeThere is limited payer coverage for genome sequencing (GS) relative to exome sequencing (ES) ...
BackgroundNext-generation tumor sequencing (NGTS) panels, which include multiple established and nov...
Next-generation sequencing promises major advancements in precision medicine but faces considerable ...
Background: Hereditary cancer panels (HCPs), testing for multiple genes and syndromes, are rapidly t...
Public and private payers face complex decisions regarding whether, when, and how to cover and reimb...
ObjectivesTo examine the temporal trajectory of insurance coverage for next-generation tumor sequenc...
Background: Next Generation Sequencing (NGS) is expected to lift molecular diagnostics in clinical o...
AbstractThis research aims to inform policymakers by engaging expert stakeholders to identify, prior...
This research aims to inform policymakers by engaging expert stakeholders to identify, prioritize, a...
Large-panel genomic tumor testing (GTT) is an emerging technology that promises to make cancer treat...
International audienceNext-generation sequencing (NGS) may enable more focused and highly personaliz...
Precision medicine seeks to use genomic data to help provide the right treatment to the right patien...
Objective: Next generation sequencing (NGS) may aid in tumor classification and treatment. Barriers ...
BackgroundClinical adoption of the sequencing of circulating tumor DNA (ctDNA) for cancer has rapidl...
Single gene tests to predict whether cancers respond to specific targeted therapies are performed in...
PurposeThere is limited payer coverage for genome sequencing (GS) relative to exome sequencing (ES) ...