Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

507P - Oncology biomarker recommendations for gastrointestinal cancers as part of ONCOMARKR: The oncology biomarker review project

Date

27 Jun 2024

Session

Poster Display session

Presenters

Jennifer Hinkel

Citation

Annals of Oncology (2024) 35 (suppl_1): S205-S215. 10.1016/annonc/annonc1483

Authors

J. Hinkel1, J. Benton2, R. Kavade3, K. Kulig4, R. Fonseca5, K.B. Knopf6

Author affiliations

  • 1 University of Oxford - Kellogg College, Oxford/GB
  • 2 Independent Researcher, Larkspur/US
  • 3 LSE - The London School of Economics and Political Sciences, London/GB
  • 4 Kulig Consulting LLC, New York City/US
  • 5 Mayo Clinic Cancer Center, Phoenix/US
  • 6 UCSF Medical Center at Mission Bay, San Francisco/US

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 507P

Background

Oncology practice guidelines, including those from the National Comprehensive Cancer Network (NCCN), European Society for Medical Oncology (ESMO), and American Society of Clinical Oncology (ASCO), incorporate biomarker-related guidance. Guidelines inform clinical decision-making and influence reimbursement policies. Given the evolution of molecular science in diagnostic, predictive, and prognostic biomarkers, this study aims to systematically characterize biomarker recommendations within gastrointestinal (GI) tumor guidelines over the past 5 years.

Methods

Using systematic review methods, this study applied structured search, data extraction, pre-specified analysis, and quality assessment according to a protocol published on the Open Science Framework website. The review focused on variability and evolution of biomarker guidance across GI cancers.

Results

Biomarker guidance varies across GI tumors, with recommendations changing over time. Variability was noted in language used, patient care stage at which recommendations are made, technologies or approaches recommended, context of use, and specific biomarkers mentioned. Recommendations often lack consistent wording or detailed descriptions across both guidelines and tumors, and over time. Particularly in the NCCN Guidelines, specificity and detail have generally improved over time. Guidelines do not uniformly provide statements or evidence on clinical utility. The pace of new evidence appears to outstrip the frequency of some guideline updates.

Conclusions

The observed variability in biomarker recommendations across GI cancer guidelines may affect the uniformity and quality of care as well as patient access to recommended biomarker testing. As guideline recommendations impact reimbursement, patients may lack access to biomarker testing when language or context is vague. There is a pressing need for standardized, evidence-based approaches in biomarker recommendations to ensure they keep pace with rapid advancements in molecular science. Future directions should focus on enhancing the clarity and consistency of biomarker recommendations to optimize patient care outcomes.

Legal entity responsible for the study

J. Hinkel.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.