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Related Concept Videos

  1. Home
  2. Research Domains
  3. Biomedical And Clinical Sciences
  4. Oncology And Carcinogenesis
  5. Predictive And Prognostic Markers
  6. Molecular And Nutritional Markers In Head And Neck Cancer.
  1. Home
  2. Research Domains
  3. Biomedical And Clinical Sciences
  4. Oncology And Carcinogenesis
  5. Predictive And Prognostic Markers
  6. Molecular And Nutritional Markers In Head And Neck Cancer.

Related Experiment Video

Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma
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Published on: April 20, 2018

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Molecular and nutritional markers in head and neck cancer.

Gerard Milano1, Jocelyn Gal2, René-Jean Bensadoun3

  • 1University Côte d'Azur, Centre Antoine Lacassagne, Scientific Valorisation Department.

Current Opinion in Oncology
|March 5, 2024

View abstract on PubMed

Summary
This summary is machine-generated.

Biomarkers for squamous cell carcinoma of the head and neck (SCCHN) are needed. Liquid biopsies, including circulating tumor cells (CTCs), show promise for predicting patient outcomes in SCCHN management.

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Area of Science:

  • Oncology
  • Biomarker Research
  • Head and Neck Cancer

Background:

  • Squamous cell carcinoma of the head and neck (SCCHN) management requires reliable predictive and prognostic biomarkers, particularly in induction and neoadjuvant settings.
  • Current biomarkers like p16 (human papilloma virus [HPV] positivity) indicate favorable prognosis but show variability in disease progression.
  • The correlation between immunohistochemistry (IHC) for epidermal growth factor receptors (EGFRs) and response to targeted therapies remains unclear due to quantification issues.

Approach:

  • This review synthesizes current knowledge on predictive and prognostic biomarkers for SCCHN.
  • It examines the utility of established markers and emerging technologies like circulating tumor cells (CTCs).
  • The focus is on biomarkers relevant to clinical decision-making in SCCHN treatment.

Key Points:

  • HPV positivity, indicated by p16, is associated with a better prognosis in SCCHN, though outcomes can vary.
  • EGFR expression measured by IHC does not consistently predict response to EGFR-targeted therapies.
  • Circulating tumor cells (CTCs) may offer insights into primary tumor mutations and have potential for outcome prediction via single-cell analysis.

Conclusions:

  • No definitive biological marker for clinical use in SCCHN outcome prediction has emerged yet.
  • Liquid biopsies, specifically circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA), represent a promising future direction.
  • Further research into liquid biopsy applications could significantly advance SCCHN patient management.