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cDNA and Residual Disease After Chemoradiotherapy for Locally Advanced Head and Neck Squamous Cell Carcinomas

RecruitingNAAges 18 Years - 80 YearsAllCentre Jean Perrin
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In plain words

What the trial is, and whether it could suit you

The goal of this ancillary clinical trial is to evaluated circulating DNA as a biomarker of residual disease after chemoradiotherapy for locally advanced head and neck squamous cell carninoma. The main question it aims to answer is : \- Does circulating DNA (cDNA) be able to detect residual disease 3 months after the end of chemoradiotherapy ? Researchers will compare detection of cDNA at 3-months and objective response (clinical and radiological). Participants will : * be included in the main study (Neck-TAR) * have a blood sample 1 and 3-month after the end of treatment

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Selection Criteria: * Patient included in NeckTAR study * Written informed consent signed for NeckTAR-IN study * Affiliation to the French social security system
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What it tests

  • blood sampling
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Where

4 sites
CH Henri Mondor Aurillac
Aurillac, France
Centre Jean PERRIN
Clermont-Ferrand, France
Hôpital de la Croix-Rousse
Lyon, France
CHU de Saint-Étienne
Saint-Etienne, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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