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New blood test could replace invasive cancer biopsies
NCT ID NCT04490564
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new blood test (liquid biopsy) to find cancer markers in 135 people with head and neck, lung, or skin cancer. The goal was to see if the blood test works as well as a standard tissue biopsy. The study did not provide treatment but aimed to improve how doctors monitor cancer.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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135 people
The number who actually took part.
- Started
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Jun 2019
- Finished
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Sep 2022
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
155 subjects as follows: 25 patients with metastatic/recurrent HNSCC 120 patients with metastatic NSCLC 10 patients with metastatic melanoma 30 healthy subjects
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male or female aged ≥ 18 years of age. 2. Patients with a diagnosis of 1. recurrent or metastatic head and neck squamous cell carcinoma (HNSCC), who are going to receive PD-1 inhibitor nivolumab OR 2. metastatic Non-Small Cell Lung Cancer (NSCLC), who are going to receive PD-1 inhibitor, e.g. nivolumab, pembrolizumab,OR 3. metastatic melanoma, who are going to receive to receive PD-1 inhibitor, e.g. nivolumab, pembrolizumab. 3. Available tumor tissue sample for immunohistochemical and molecular analysis. 4. Life expectancy ≥ 4 months. 5. Signed informed consent form. Exclusion Criteria: 1. Male or female younger than 18 years old. 2. History of another malignancy within 3 years or current 2nd primary malignancy. 3. Patients that have not signed the informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Aretaieio University Hospital of Athens
Athens, Attica, 11528, Greece
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Bioclinic
Thessaloniki, Thessaloniki, 546 22, Greece
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Metropolital Hospital
Piraeus, Piraeus, 18547, Greece
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Sotiria Thoracic Diseases Hospital of Athens
Athens, Attica, 11527, Greece
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University General Hospital of Alexandroupoli
Alexandroupoli, Alexandroupolis, 68100, Greece
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University General Hospital of Athens Attikon
Athens, Attica, 124 62, Greece
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