Clinical Trials Directory

Trials / Completed

CompletedNCT03540563

ctDNA as a Biomarker for Treatment Response in HNSCC

Prospective Study Evaluating ctDNA as a Biomarker for Treatment Response in Head and Neck Squamous Cell Carcinoma'

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
70 (actual)
Sponsor
The Netherlands Cancer Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Tumours continually shed DNA into the circulation, where it can be accessed. This circulating tumour DNA (ctDNA) directly reflects tumour burden and has great potential to be a sensitive biomarker for treatment recurrence. These "liquid biopsies" could give a more real-time picture of the genomic status and evolution of a tumour and can be easily assessed for measurement of different biomarkers. However, in head and neck squamous cell carcinoma (HNSCC) patients treated with primary curative radiotherapy, data regarding ctDNA kinetics and its correlation with outcome are scarce. A new or additional tool for response evaluation next to or instead of conventional imaging after treatment would be beneficial to detect recurrences in an earlier stage, thereby increasing the chances of success of salvage therapy. More importantly, an early response parameter during treatment could help to identify patients that have a good treatment response and might benefit from treatment adaptation. With this study, we aim to reveal ctDNA as an effective tool for future dose (de)-escalation trials in HNSCC.

Conditions

Interventions

TypeNameDescription
OTHERBlood drawBlood will be drawn to assess ctDNA

Timeline

Start date
2018-07-16
Primary completion
2023-08-01
Completion
2023-08-01
First posted
2018-05-30
Last updated
2024-02-01

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT03540563. Inclusion in this directory is not an endorsement.