Clinical trial Recruiting at 1 site Observational Ages 18 and up

Creating patient-derived tumor models for head and neck cancer

Official title: Establishment of Primary Patient-derived Xenograft Models of Tumor From Patients With Head and Neck Cancer for Preclinical Evaluation of Targeted Therapies.

Run by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · NCT02572778 · Data updated 2026-11-12

This study is trying to collect tumor samples from patients with head and neck cancer to create models that help test new treatments and understand how these tumors respond to them.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain
Academic / other
Locations1 site (Brussels)
StatusRecruiting
StartedSeptember 2015
Main results expectedDecember 2025
Study endsDecember 2025
Registry record updatedDecember 3, 2024
Trial IDNCT02572778 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients with primary or recurrent squamous cell carcinoma of the head and neck who can provide informed consent.

Probably not a fit

Patients with non-squamous cell carcinoma or those who are not eligible for biopsy may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to collect fresh tumor tissue from patients with primary or recurrent head and neck squamous cell carcinoma to establish patient-derived xenograft models. These models will be used to create a biobank representing various tumor subgroups, allowing for genetic and transcriptional profiling. The research will also evaluate the efficacy of new targeted therapies and biomarkers of drug sensitivity, as well as study resistance mechanisms in these tumors. The approach involves local biopsies to obtain the necessary tumor samples.

Why it matters

Potential benefit: If successful, this study could lead to more effective personalized treatment options for patients with head and neck cancer.

How similar studies have gone: Other studies utilizing patient-derived xenografts have shown promise in cancer research, indicating potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* In the first phase, all patients with primary or recurrent/ metastatic disease of head and neck cancer can be included pre-operatively or before a tumor biopsy after obtaining informed consent
* Data on stage, grade, histology, adjuvant treatment, responses, relapse should be available
* Follow-up data should be available
* Patients with recurrent disease are allowed
* Written informed consent

Where it's running

  • Cliniques universitaires Saint-Luc
    Brussels, Belgium
    Recruiting

Study contacts

  • Principal investigator: Jean-Pascal Machiels, MD, PhD — Cliniques universitaires Saint-Luc- Université Catholique de Louvain
  • Study coordinator: Aline Gillain, MedSciences
  • Email: aline.gillain@uclouvain.be
  • Phone: 00322764

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • MRG003 vs cetuximab/methotrexate for RM-SCCHN after prior therapies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.