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Patient-derived Xenograft Models of Tumor From Patients With Head and Neck Cancer

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02572778
Acronym
UCL-Xenog
Enrollment
40
Registered
2015-10-09
Start date
2015-09-30
Completion date
2025-12-31
Last updated
2024-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Squamous Cell Carcinoma of the Head and Neck

Brief summary

The investigators want to have a collection of fresh primary or recurrent tumor tissue for establishment of patients-derived xenografts in order to: generate a biobank of in vivo patient xenografts representing the different subgroups of tumors for head and neck cancer * perform genetic and transcriptional profiling of the primary, metastatic tumors and xenograft tumors * evaluate the efficacy of new targeted agents, whether or not in combination with standard treatment options * evaluate biomarkers of drug sensitivity * study primary and secondary (acquired) resistance in these models

Interventions

PROCEDURELocal biopsy in the tumor

A tumor biopsy of 0.5 cm2 or more will be collected from every patient during surgery or endoscopy after informed consent and if there is enough material after review by the pathologist.

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Identification of the biomarkers of new cancer therapies for head and neck cancer on the patient-derived xenografts with immunohistochemistry (KI67) on FFPE (fixation followed by paraffin embedding) slides10 yearsIdentification of the biomarkers of new cancer therapies for head and neck

Secondary

MeasureTime frameDescription
Characterization of the biomarkers of new cancer therapies for head and neck cancer on the patient-derived xenografts with genetic techniques10 yearsCharacterization of the biomarkers of new cancer therapies for head and neck cancer on the patient-derived xenografts with genetic techniques

Countries

Belgium

Contacts

Primary ContactAline Gillain, MedSciences
aline.gillain@uclouvain.be00322764
Backup ContactSandra Schmitz, MD, PhD
sandra.schmitz@uclouvain.be00322764

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026