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Empowering effective biomarker-driven precision oncology: A call to action
Mark Lawler1, Peter Keeling2, Olga Kholmanskikh3
1Patrick G Johnston Centre for Cancer Research, Queen's University Belfast, BT9 7AE, UK; Cancer Drug Development Forum, Clos Chapelle-aux-Champs 30, 1200 Brussels, Belgium.
Precision oncology utilizes biomarkers for better cancer diagnosis, prognosis, and treatment. Integrating genomic testing into routine care is crucial for effective, cost-efficient cancer treatment and improved patient outcomes.
Area of Science:
- Oncology
- Genomics
- Biomarker Discovery
Background:
- Precision oncology relies on biomarkers for cancer diagnosis, prognosis, and treatment prediction.
- Genomic testing advances are not fully integrated into clinical practice, hindering optimal patient care.
- Delays in biomarker testing availability and implementation limit access to life-saving therapies.
Purpose of the Study:
- To highlight the critical role of biomarkers in precision oncology.
- To identify barriers impeding the routine adoption of biomarker testing.
- To advocate for the integration of precision genomic testing into standard oncology care.
Main Methods:
- Review of current challenges in biomarker testing implementation.
- Analysis of factors hindering diagnostic pathways.
- Synthesis of evidence supporting cost-effectiveness of precision oncology.
Main Results:
- Genomic testing is underutilized in clinical practice, leading to missed treatment opportunities.
- Barriers include cost, reimbursement issues, limited access, regulatory hurdles, and assay validation needs.
- Precision oncology can be cost-effective, even in resource-limited settings.
Conclusions:
- Biomarker testing is essential for personalized cancer care and drug development.
- Routine integration of precision genomic testing is necessary for improved patient outcomes.
- Recommendations and a call to action are needed to mainstream biomarker-informed oncology.
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