Solitary Pulmonary NodulesNCT07087080
Plasma Metabolomics as a Tool to Distinguish PET-positive Malignant From PET-positive Benign Nodules
A study testing Blood sampling in people with Solitary Pulmonary Nodules and Lung Cancer, run by Hasselt University at 1 site in Belgium.
Trial summary
Positron emission tomography-computed tomography (PET-CT) is an important technique in lung cancer staging, where almost no lung lesion goes undetected. However, PET-CT often fails to discriminate between malignant and non-malignant PET-positive solitary pulmonary nodules (SPNs) with a specificity of only 23%. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Solitary Pulmonary Nodules, Lung Cancer
- What is being tested?
- Blood sampling
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 350 participants
- Where
- 1 siteBelgium
- Study dates
- 2 Mar 2022to 1 Nov 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- patients who undergo a PET-CT scan at ZOL for a lung nodule, who are willing to provide written informed consent
Who cannot join
- no fasting starting 6h prior to blood sampling;
- medication intake on the morning of blood sampling;
- fasting blood glucose concentration is higher than 200 mg/dL in the morning of blood sampling;
- history of cancer during the past five years;
- treatment for cancer during the past five years.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Liesbet Mesotten, prof. dr. contact
Belgium1 site, 1 recruiting
- Recruiting
Ziekenhuis Oost-Limburg
Genk, Limburg, 3600
Jill Meynen, 003289804034, jill.meynen@uhasselt.be
Liesbet Mesotten, prof. dr.
About this study
Official title: Combining PET-CT With a Glutamate-based Blood Test Improves Cancer Diagnosis in Solitary Pulmonary Nodules
Positron emission tomography-computed tomography (PET-CT) is an important technique in lung cancer staging, where almost no lung lesion goes undetected. However, PET-CT often fails to discriminate between malignant and non-malignant PET-positive solitary pulmonary nodules (SPNs) with a specificity of only 23%. 40-50% of those patients are advised to repeat their CT after three to six months to follow up on their lesions' progression, delaying a clear and correct cancer diagnosis and subsequent therapy. In more than 10% of the patients with an SPN on the PET-CT scan, an uncertain lung cancer diagnosis based on the PET-positive lesion leads to surgery that appears to be unnecessary.
This project aims to use the plasma glutamate concentration as a biomarker to complement PET-CT in the discrimination between malignant and non-malignant PET-positive SPNs. The investigators will validate a plasma glutamate determination by high- performance liquid chromatography (HPLC) since this test needs to be rapid, cheap, minimally invasive, and available in every hospital. In addition to the analysis of plasma glutamate, other plasma metabolites will be screened to check for other potential biomarkers to discriminate between malignant and non-malignant PET-positive SPNs. Together with the PET-CTs' basic parameters, a quick measurement of fasted plasma glutamate and potentially other biomarker levels right before undergoing a PET-CT scan will support a more rapid lung cancer diagnosis and treatment, resulting in less risk for disease progression. In conclusion, our approach will improve the accuracy of lung cancer diagnosis, and avoid unnecessary surgery.
Read the detailed description
PET-CT is an indispensable technique in lung cancer staging, where almost no lung lesion goes undetected since its sensitivity reaches 96%. However, PET-CT often fails to discriminate between malignant and non-malignant PET-positive SPNs with a specificity of only 23%. 40-50% of those patients are advised to repeat their CT after three to six months to follow up on their lesions' progression, delaying a clear and correct cancer diagnosis and subsequent therapy. More than 10% of the patients with a non-metastasized SPN on the PET-CT scan receive an unnecessary surgery due to this diagnostic uncertainty.
Due to these current challenges, the investigators will be searching for metabolite biomarkers that allow discrimination between benign and malignant SPNs. Biomarkers are defined as "characteristics that are objectively measured and evaluated as indicators of normal biological processes, pathological processes, or pharmacological responses to therapeutic interventions". This research will focus on metabolomics-based/metabolite biomarkers, as metabolic reprogramming is one of the hallmarks of cancer cells. As soon as the disease arises, cancer cells will reprogram their metabolism in order to meet the increased proliferation rate and energy consumption. Changes in metabolism result in changes in the concentration of metabolic end-products, metabolites, both intra- and extracellular. This principle allows for the detection of malignant SPNs by measuring metabolite concentrations in plasma.
The clinical applicability of metabolite biomarkers became clear from previously published work. Using proton nuclear magnetic resonance (1H-NMR) based metabolomics, a prior study of our research group demonstrated that a single plasma glutamate analysis could increase the PET-CT scans' discriminative specificity from 23% to 81% in a PET-positive patient population. However, further development and optimization are still needed to reach a clinical phase.
This prospective study will not only study plasma glutamate levels, but also the plasma levels of 61 additional metabolites. These 61 additional metabolites were identified in plasma in a previous study performed by our research group using 1H-NMR. Several of these metabolites, including lactate, acetate, cysteine, and asparagine, have already been shown to significantly contribute to malignant processes. Besides including more metabolites compared to the previously performed glutamate study, a technique other than 1H-NMR will be used. Even though 1H-NMR is characterized by its non-destructive and fast sample preparation and quantitative nature, it is a very costly technique that is usually unavailable in most hospitals. As this study aims to find plasma metabolites that can serve as clinical biomarkers for the distinction between benign and malignant SPNs, a more widely available technique will be used, called high-performance liquid chromatography (HPLC).
As the 61 metabolites of interest can be categorized into multiple chemical classes, such as amino acids and organic acids, different HPLC methods will be required. After the development of a suitable method for metabolite identification and quantification, plasma samples will be measured and metabolites will be quantified. By comparing metabolite concentrations in plasma samples derived from patients with a benign SPN and a malignant SPN, the investigators aim to find significant differences in metabolite concentrations between these two groups. Significantly altered metabolites could then potentially serve as plasma biomarkers for the distinction of benign and malignant SPNs, thereby improving diagnostic accuracy.
- Conditions
- Solitary Pulmonary Nodules, Lung Cancer
- Being tested
- Blood sampling
- Keywords
- Pulmonary nodules, Lung cancer, Plasma metabolomics, 1H-NMR, HPLC
- Medical subject headings
- Solitary Pulmonary Nodule, Lung Neoplasms, Multiple Pulmonary Nodules
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Blood samplingOther
Single blood sampling (16 ml) after study inclusion before undergoing the PET-CT scan
| Study group | Role | What they receive |
|---|---|---|
| Blood sampling | Other | Blood sampling Receives: Other: Blood sampling |
What is being measured
The primary outcome is the main question the study is designed to answer.
Fasted glutamate concentration
Fasted glutamate, measured by High-Performance Liquid Chromatography (HPLC), will serve as metabolic biomarker in distinguishing between malignancy and non-malignancy in positron-emission tomography (PET) positive solitary pulmonary nodules (SPNs). To this end, fasted plasma glutamate concentration will be compared between patients with a final diagnosis of malignant and non-malignant PET-positive SPNs. Based on this, plasma glutamate cut-off values will be determined between the two groups of patients. Combining these cut-off values with PET-parameters can eventually increase the specificity of PET-CT.
Measured: baseline
Secondary outcomes (2)
Screening of 61 measurable plasma metabolites
Screening 61 measurable plasma metabolites via multivariate statistics to find other potential biomarkers to differentiate between malignant and benign PET-positive SPNs. By analyzing more metabolites than glutamate, the investigators aim to increase the specificity even more. When significant differences in one or more metabolites are found, cut-off values will again be determined between the two groups of patients.
Measured: baseline
Combine metabolite values to radiomics features
HPLC metabolite values will be combined with advanced PET-CT features (radiomics study). SPNs of the included patients will be segmented using the ACCURATE tool. Radiomic features will eventually be extracted from all segmented lesions using the RADIOMICS tool, yielding a total of about 500 features per lesion. In the case of overfitting, several feature reduction methods might be explored, such as LASSO, pairwise feature elimination, or random forest. The obtained radiomic features will first be analyzed individually and afterward analyzed in combination with the obtained metabolomic data. The investigators aim to determine whether a combination of radiomic and metabolomic data improves the specificity of SPN diagnosis compared to the use of these methods individually.
Measured: baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Jul 2025
- Study start2 Mar 2022
- Primary completion1 Apr 2027 (estimated)
- Study completion1 Nov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Solitary Pulmonary NodulesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- 16 mL blood will be sampled from each participant before undergoing the PET/CT scan.
- Masking
- None (open label)
- Enrolment
- 350 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hasselt University
- Sponsor type
- University, hospital or other
- Collaborators
- Ziekenhuis Oost-Limburg
- Responsible party
- Principal investigator, Prof. dr. Liesbet Mesotten, Hasselt University
- Investigators
- Liesbet Mesotten, prof. dr., Principal investigator, Ziekenhuis Oost-LimburgJill Meynen, Study chair, Hasselt UniversityElien Derveaux, dr., Study chair, Hasselt UniversityWouter Marchal, prof. dr., Study chair, Hasselt University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07087080
- Sponsor's protocol ID
- 2020/12375/1
- Status last verified
- Jul 2025
- First submitted
- 20 May 2025
- Last updated
- 31 Jul 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Vanhove K, Giesen P, Owokotomo OE, Mesotten L, Louis E, Shkedy Z, Thomeer M, Adriaensens P. The plasma glutamate concentration as a complementary tool to differentiate benign PET-positive lung lesions from lung cancer. BMC Cancer. 2018 Sep 3;18(1):868. doi: 10.1186/s12885-018-4755-1.
PubMed 30176828Derveaux E, Geubbelmans M, Criel M, Demedts I, Himpe U, Tournoy K, Vercauter P, Johansson E, Valkenborg D, Vanhove K, Mesotten L, Adriaensens P, Thomeer M. NMR-Metabolomics Reveals a Metabolic Shift after Surgical Resection of Non-Small Cell Lung Cancer. Cancers (Basel). 2023 Apr 3;15(7):2127. doi: 10.3390/cancers15072127.
PubMed 37046788
Study at a glance
From the registry record, last updated by the sponsor on 31 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Combining PET-CT With a Glutamate-based Blood Test Improves Cancer Diagnosis in Solitary Pulmonary Nodules
- ClinicalTrials.gov ID
- NCT07087080
- Acronym / sponsor ID
- 2020/12375/1
- Conditions
- Solitary Pulmonary Nodules, Lung Cancer
- Keywords
- Pulmonary nodules, Lung cancer, Plasma metabolomics, 1H-NMR, HPLC
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 350 participants (estimated)
- Lead sponsor
- Hasselt UniversityUniversity, hospital or other
- Collaborators
- Ziekenhuis Oost-Limburg
- Study start
- 2 Mar 2022 (actual)
- Primary completion
- 1 Apr 2027 (estimated)
- Study completion
- 1 Nov 2027 (estimated)
- First posted
- 25 Jul 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Positron emission tomography-computed tomography (PET-CT) is an important technique in lung cancer staging, where almost no lung lesion goes undetected. However, PET-CT often fails to discriminate between malignant and non-malignant PET-positive solitary pulmonary nodules (SPNs) with a specificity of only 23%. 40-50% of those patients are advised to repeat their CT after three to six months to follow up on their lesions' progression, delaying a clear and correct cancer diagnosis and subsequent therapy. In more than 10% of the patients with an SPN on the PET-CT scan, an uncertain lung cancer diagnosis based on the PET-positive lesion leads to surgery that appears to be unnecessary.
This project aims to use the plasma glutamate concentration as a biomarker to complement PET-CT in the discrimination between malignant and non-malignant PET-positive SPNs. The investigators will validate a plasma glutamate determination by high- performance liquid chromatography (HPLC) since this test needs to be rapid, cheap, minimally invasive, and available in every hospital. In addition to the analysis of plasma glutamate, other plasma metabolites will be screened to check for other potential biomarkers to discriminate between malignant and non-malignant PET-positive SPNs. Together with the PET-CTs' basic parameters, a quick measurement of fasted plasma glutamate and potentially other biomarker levels right before undergoing a PET-CT scan will support a more rapid lung cancer diagnosis and treatment, resulting in less risk for disease progression. In conclusion, our approach will improve the accuracy of lung cancer diagnosis, and avoid unnecessary surgery.
Detailed description
PET-CT is an indispensable technique in lung cancer staging, where almost no lung lesion goes undetected since its sensitivity reaches 96%. However, PET-CT often fails to discriminate between malignant and non-malignant PET-positive SPNs with a specificity of only 23%. 40-50% of those patients are advised to repeat their CT after three to six months to follow up on their lesions' progression, delaying a clear and correct cancer diagnosis and subsequent therapy. More than 10% of the patients with a non-metastasized SPN on the PET-CT scan receive an unnecessary surgery due to this diagnostic uncertainty.
Due to these current challenges, the investigators will be searching for metabolite biomarkers that allow discrimination between benign and malignant SPNs. Biomarkers are defined as "characteristics that are objectively measured and evaluated as indicators of normal biological processes, pathological processes, or pharmacological responses to therapeutic interventions". This research will focus on metabolomics-based/metabolite biomarkers, as metabolic reprogramming is one of the hallmarks of cancer cells. As soon as the disease arises, cancer cells will reprogram their metabolism in order to meet the increased proliferation rate and energy consumption. Changes in metabolism result in changes in the concentration of metabolic end-products, metabolites, both intra- and extracellular. This principle allows for the detection of malignant SPNs by measuring metabolite concentrations in plasma.
The clinical applicability of metabolite biomarkers became clear from previously published work. Using proton nuclear magnetic resonance (1H-NMR) based metabolomics, a prior study of our research group demonstrated that a single plasma glutamate analysis could increase the PET-CT scans' discriminative specificity from 23% to 81% in a PET-positive patient population. However, further development and optimization are still needed to reach a clinical phase.
This prospective study will not only study plasma glutamate levels, but also the plasma levels of 61 additional metabolites. These 61 additional metabolites were identified in plasma in a previous study performed by our research group using 1H-NMR. Several of these metabolites, including lactate, acetate, cysteine, and asparagine, have already been shown to significantly contribute to malignant processes. Besides including more metabolites compared to the previously performed glutamate study, a technique other than 1H-NMR will be used. Even though 1H-NMR is characterized by its non-destructive and fast sample preparation and quantitative nature, it is a very costly technique that is usually unavailable in most hospitals. As this study aims to find plasma metabolites that can serve as clinical biomarkers for the distinction between benign and malignant SPNs, a more widely available technique will be used, called high-performance liquid chromatography (HPLC).
As the 61 metabolites of interest can be categorized into multiple chemical classes, such as amino acids and organic acids, different HPLC methods will be required. After the development of a suitable method for metabolite identification and quantification, plasma samples will be measured and metabolites will be quantified. By comparing metabolite concentrations in plasma samples derived from patients with a benign SPN and a malignant SPN, the investigators aim to find significant differences in metabolite concentrations between these two groups. Significantly altered metabolites could then potentially serve as plasma biomarkers for the distinction of benign and malignant SPNs, thereby improving diagnostic accuracy.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- 16 mL blood will be sampled from each participant before undergoing the PET/CT scan.
| Arm | Type | Receives |
|---|---|---|
| Blood sampling | Other | Other: Blood samplingBlood sampling |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- patients who undergo a PET-CT scan at ZOL for a lung nodule, who are willing to provide written informed consent
Key exclusion criteria (5 listed)
- no fasting starting 6h prior to blood sampling;
- medication intake on the morning of blood sampling;
- fasting blood glucose concentration is higher than 200 mg/dL in the morning of blood sampling;
- history of cancer during the past five years;
- treatment for cancer during the past five years.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Blood samplingSingle blood sampling (16 ml) after study inclusion before undergoing the PET-CT scan | Other | Blood sampling |
Primary outcome
Fasted glutamate concentration
Time frame: baseline
Fasted glutamate, measured by High-Performance Liquid Chromatography (HPLC), will serve as metabolic biomarker in distinguishing between malignancy and non-malignancy in positron-emission tomography (PET) positive solitary pulmonary nodules (SPNs). To this end, fasted plasma glutamate concentration will be compared between patients with a final diagnosis of malignant and non-malignant PET-positive SPNs. Based on this, plasma glutamate cut-off values will be determined between the two groups of patients. Combining these cut-off values with PET-parameters can eventually increase the specificity of PET-CT.
2 secondary outcomes
Screening of 61 measurable plasma metabolites
Time frame: baseline
Combine metabolite values to radiomics features
Time frame: baseline
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Jul 2025.
- Background: PubMed 30176828Vanhove K, Giesen P, Owokotomo OE, Mesotten L, Louis E, Shkedy Z, Thomeer M, Adriaensens P. The plasma glutamate concentration as a complementary tool to differentiate benign PET-positive lung lesions from lung cancer. BMC Cancer. 2018 Sep 3;18(1):868. doi: 10.1186/s12885-018-4755-1.
- Background: PubMed 37046788Derveaux E, Geubbelmans M, Criel M, Demedts I, Himpe U, Tournoy K, Vercauter P, Johansson E, Valkenborg D, Vanhove K, Mesotten L, Adriaensens P, Thomeer M. NMR-Metabolomics Reveals a Metabolic Shift after Surgical Resection of Non-Small Cell Lung Cancer. Cancers (Basel). 2023 Apr 3;15(7):2127. doi: 10.3390/cancers15072127.
Related trials for Solitary Pulmonary Nodules
RecruitingObservational study
Biomarkers for Risk Stratification in Lung Cancer
Nodule Solitary Pulmonary, Non-small Cell Lung Cancer
RecruitingObservational study
European Real-World Registry for Use of the Ion Endoluminal System
Pulmonary Nodule, Lung Cancer
Recruiting
Intraoperative Longitude-Latitude-Depth Localization Versus Preoperative CT-Guided Percutaneous Lung Puncture Localization for 0.8-2 cm Peripheral Pulmonary Nodules
Pulmonary Nodule, Solitary, Peripheral Pulmonary Nodules
Not yet recruitingObservational study
Radiomics for Distinguishing Benign and Malignant Lung Nodules
Solitary Pulmonary Nodule, Lung Neoplasms
Active, not recruiting
Teachable Moment to Opt-out of Tobacco: Interactive Voice Response Quit Line for Veteran Active Smokers With Lung Nodules
Solitary Pulmonary Nodule, Multiple Pulmonary Nodules
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Liesbet Mesotten, prof. dr. contact
Liesbet Mesotten, prof. dr. principal investigator
Ziekenhuis Oost-Limburg
Jill Meynen study chair
Hasselt University
Elien Derveaux, dr. study chair
Hasselt University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Blood sampling in people with Solitary Pulmonary Nodules and Lung Cancer, run by Hasselt University at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 31 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Jill Meynen, Master degree (003289804034, jill.meynen@uhasselt.be), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Fasted glutamate concentration (time frame: baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07087080, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Jul 2025.