Collection of Plasma Samples for Squamous Cell Carcinoma of the Head and Neck Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain

About this trial

The investigators will collect plasma samples at baseline, during treatment, and at progression.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients treated with radiation therapy and cetuximab according to Bonner et al

patients treated with cetuximab in combination with chemotherapy according to Vermorken et al.

patients treated with a molecular targeted agent as a part of a clinical study

Disqualifiers

patients with another type of head and neck cancer

patients non treated with targeted therapies

Trial population

PATIENTS TREATED WITH MOLECULAR TARGETED THERAPIES FOR SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Plasma samples

    Other intervention

    Plasma samples at baseline (and one whole blood sample) and at every radiological evaluations

Treatment groups

400 Participants
are divided into 1 treatment group
Group A: No treatment1 intervention

Trial outcomes

Primary outcomes

1

Prospective storage of plasma samples of patients treated with cetuximab or other targeted agents

All the analyses will be done when we have enough of collected samples

Time frame
one year after the collection

Secondary outcomes

Other outcomes

Sponsors and contacts

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