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Next-Generation Sequencing Trends among Adult Patients with Select Advanced Tumor Types: A Real-World Evidence
Andrea Ferreira-Gonzalez1, Brian Hocum2, Gilbert Ko2
1Department of Pathology, Virginia Commonwealth University, Richmond, Virginia.
Abstract:
There are limited data on the prevalence of next-generation sequencing (NGS) in the United States, especially in light of the increasing importance of identifying actionable oncogenic variants due to molecular biomarker-based therapy approvals. This retrospective study of adult patients with select metastatic solid tumors and central nervous system tumors from the Optum Clinformatics Data Mart US health care claims database (January 1, 2014, to June 30, 2021; N = 63,209) examined NGS use trends over time. A modest increase in NGS was observed across tumor types from 2015 (0.0% to 1.5%) to 2021 (2.1% to 17.4%). A similar increase in NGS rates was also observed across key periods; however, rates in the final key period remained <10% for patients with breast, colorectal, head and neck, soft tissue sarcoma, and thyroid cancers, as well as central nervous system tumors. The median time to NGS from diagnosis was shortest among patients with non-small-cell lung cancer and longest for patients with breast cancer. Predictors of NGS varied by tumor type; test rates for minorities in select tumor types appeared comparable to the White population. Despite improving payer policies to expand coverage of NGS and molecular biomarker-based therapy approvals, NGS rates remained low across tumor types. Given the potential for improved patient outcomes with molecular biomarker-based therapy, further efforts to improve NGS rates are warranted.
Insights
Next-generation sequencing (NGS) use in cancer care increased modestly but remained low overall. Further efforts are needed to improve NGS adoption for molecular biomarker-based therapies.
Area of Science:
- Oncology
- Genomics
- Health Services Research
Background:
- Next-generation sequencing (NGS) is crucial for identifying actionable oncogenic variants to guide molecular biomarker-based therapies.
- Limited data exist on the prevalence and trends of NGS utilization in the United States across various cancer types.
- Increasing approvals of targeted therapies necessitate understanding current NGS adoption rates.
Purpose of the Study:
- To examine the trends in NGS utilization among adult patients with select metastatic solid tumors and central nervous system tumors in the US.
- To identify factors associated with NGS use and analyze time-to-test metrics.
- To assess the current landscape of NGS adoption in the context of evolving treatment paradigms.
Main Methods:
- Retrospective analysis of US health care claims data (Optum Clinformatics Data Mart) from January 1, 2014, to June 30, 2021.
- Inclusion of 63,209 adult patients diagnosed with specific metastatic solid tumors or central nervous system tumors.
- Examination of NGS use trends over time, time to NGS from diagnosis, and predictors of testing.
Main Results:
- NGS utilization showed a modest increase from 2015 (0.0%-1.5%) to 2021 (2.1%-17.4%) across tumor types.
- NGS rates remained below 10% in the final period for breast, colorectal, head and neck, soft tissue sarcoma, thyroid, and CNS cancers.
- Median time to NGS varied by cancer type, being shortest for non-small-cell lung cancer and longest for breast cancer. Predictors of NGS varied by tumor type, with comparable rates for minorities and White patients in select cancers.
Conclusions:
- Despite improvements in payer policies and therapy approvals, NGS rates remain low across many cancer types.
- The observed increase in NGS use is modest, highlighting a gap in adoption for molecular biomarker-based treatments.
- Further interventions are necessary to enhance NGS utilization and improve patient outcomes through precision oncology.
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