Hepatocellular CarcinomaNCT02899325
FDGal PET/CT to Detect Hepatocellular Carcinoma
An observational study of Hepatocellular Carcinoma and Liver Cirrhosis, run by British Columbia Cancer Agency at 1 site in Canada.
Trial summary
Liver cancer is one of the leading causes of cancer death among Asian men. If diagnosed early the disease is treatable with surgery. Current conventional imaging modalities have limitations to early detection. Read more about this study
- Who is it for?
- Ages 19 years and older
- Conditions the study is for
- Hepatocellular Carcinoma, Liver Cirrhosis, Chronic Liver Disease
- What is being tested?
- Diagnostic PET/CT scans
- How many people
- 0 participants
- Where
- 1 siteCanada
- Study dates
- Oct 2019to Oct 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
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 19 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: The purpose of this study is to evaluate the diagnostic utility of 18F-FDGal PET/CT in identifying sites of hepatocellular carcinoma where conventional imaging has not been as effective. Concordance with histology, imaging or follow up will be assessed.
Who may be able to join
- Male or female, age ≥ 19 years of age.
- Patient who accepts to enter the study by signing written informed consent.
- Patient with performance status ≤ 2 Eastern Cooperative Oncology Group (ECOG).
- Patient with cirrhosis or chronic liver disease suspected to have at least 1 hepatic nodule larger than 1 cm in diameter detected by conventional image (US, CT, MRI).
- Hepatic nodule is defined as any one of the following conditions: suspicious hepatocellular carcinoma, benign tumor such as hemangioma, adenoma or focal nodular hyperplasia, possible metastatic lesions from other primary malignancy.
Who cannot join
- Patient has serious allergic history or known allergy to 18F-FDGal or 18F-FDG.
- Patient has received therapy for aforementioned diagnosis before the PET scans
- Patient with known (proven) metastases from a prior malignancy
- Patient has been diagnosed with multiple malignancies.
- Female patient who is pregnant, lactating or planning to become pregnant during the study.
- Patient has participated in other investigational trials within 28 days prior to study enrollment.
Show all 9Show fewer
- Inability to lie supine for the duration of the imaging studies.
- Subject with active systemic infections, or medical conditions that may significantly affect adequate uptake and elimination of radiotracer.
- Subject with conditions judged by the investigator as unsuitable for the study.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Single-blind Study to Evaluate the Efficacy and Safety of 18F-Fluorodeoxygalactose (18F-FDGal) Compared to 18F-Fluorodeoxyglucose (18F-FDG) to Detect Hepatocellular Carcinoma Via PET/CT in Patients With Cirrhosis or Chronic Liver Disease
Liver cancer is one of the leading causes of cancer death among Asian men. If diagnosed early the disease is treatable with surgery. Current conventional imaging modalities have limitations to early detection. This study proposes to use 18F-FGal and 18F-FDG PET/CT scans to compare the clinical efficacy of diagnosing hepatocellular carcinoma (a type of liver cancer) using these PET/CT scans.
Read the detailed description
Screening Visit Patients will undergo screening procedures for determining eligibility prior to the first PET/CT examination. For practical reasons and to avoid unnecessary travel for research subjects, the initial screening can be conducted by phone, and completed on the day that the first PET/CT examination is performed. However, the PET/CT scan will only be done for subjects that meet all the eligibility criteria and sign the consent form prior to the examination. All patients should have received the consent form by mail, email or fax, at least 24 hours prior to the screening visit.
Demographics Demographic data including date of birth, gender, height and weight information will be obtained.
Medical History and Concomitant Medications The general medical history up to 3 months of study entry (screening visit) should be recorded at the screening visit. The medical history should include procedural and surgical history within the past year. Cancer history should be recorded on a lifetime basis. Previous medications should be recorded up to 28 days prior to screening visit and up to 1 year for cancer treatment if any. All concomitant medications starting from enrollment of subjects should be recorded on subsequent visits for the PET/CT examinations.
Vital Signs Patient's vital signs will be measured including blood pressure, pulse rate and oxygen saturation, within 60 minutes before and 5-15 minutes after administration of the investigational product at PET/CT visits.
PET/CT Scans Patients who meet all eligibility requirements for entry into the study will undergo both an 18F-FDGal and 18F-FDG PET/CT examinations at the BCCA - Vancouver Centre's Functional Imaging Department. The two scans are to be performed on separate days and must be performed between 1 and 15 calendar days of each other. Each PET/CT scan will require approximately 3 hours of additional time from the subject above standard of care. The screening visit and informed consent, can be performed on the same day as the first PET/CT scan (and before the examination), will take approximately one hour.
Prior to the PET/CT scans, subjects will be instructed to take their usual medications as prescribed by their family physician. Subjects will also be instructed to drink 3 to 4 glasses of water within two hours prior to their scan appointment in order to promote hydration and facilitate urinary clearance of background 18F-FDGal/18F-FDG. Subjects must fast for 6 hours prior to 18F-FDGal and 18F-FDG injection, but can drink water at will.
Upon arrival at the PET Imaging department, all subjects will have their weight recorded prior to 18F-FDGal/18F-FDG injection. A baseline blood pressure, heart rate, and oxygen saturation levels will be recorded within 60 minutes prior to 18F-FDGal/18F-FDG injection, and 5 - 15 minutes after injection.
Each study subject will have an intravenous catheter inserted. The subject will receive a bolus intravenous dose of 18F-FDGal/18F-FDG from the BCCA, at a dose of 237 - 521 MBq for 18F-FDG and 119 - 261 MBq MBq for 18F-FDGal, followed by a 5 - 20 mL normal saline flush. The subject will rest in a comfortable chair for 60 minutes.
Upon completion of the scan, subjects will be free to leave the department and will be encouraged to drink 3-4 extra glasses of water by the end of the day to promote further clearance of the remaining tracer in the urinary tract. Overall, the study will take approximately 3 hours of subject time.
Each patient will be monitored on vital signs, adverse events before and after the intravenously 18F-FDGal/18F-FDG administration. Concomitant medication(s) will also be recorded. All of the 18F-FDGal/18F-FDG PET/CT imaging obtained at all study will be sent to a centralized location in DVD sets for re-labeling purpose to mask the patients' identifiers from readers.
- Being tested
- Diagnostic PET/CT scans
- Medical subject headings
- Carcinoma, Hepatocellular, Liver Cirrhosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Diagnostic PET/CT scansDrug
Also called 18F-FDG and 18F-FDGal PET/CT scans
These PET/CT scans will be performed for diagnostic purposes of hepatocellular carcinoma.
What is being measured
The primary outcome is the main question the study is designed to answer.
Sensitivity of 18F-FDGal in the diagnosis of HCC on per-patient basis
Determination of sensitivity of both exams when compared with pathology reports (if available) and compared with routine imaging (CT, MRI, US) if available. The treatment group will be declared superior if the lower limit of the 95% two-sided confidence interval of the difference of these two proportions is greater than 0.
Measured: 6 months
Secondary outcomes (3)
Number of participants with 18F-FDGal-related adverse events as assessed by abnormal vital sign measurement
Vital signs (blood pressure, heart rate and pulse oximetry) will be measured at three time points (before and after injection, and 1 hour after the injection). All values that fall outside of the normal parameters will be assessed by a physician and reported as an adverse event.
Measured: 1 hour
Sensitivity of 18F-FDGal in the diagnosis of HCC on per-site basis
Determination of sensitivity of both exams when compared with pathology reports (if available) and compared with routine imaging (CT, MRI, US) if available. The treatment group will be declared superior if the lower limit of the 95% two-sided confidence interval of the difference of these two proportions is greater than 0.
Measured: 6 months
Specificity of 18F-FDGal in the diagnosis of HCC
Specificity of 18F-FDGal and 18F-FDG PET/CT are calculated on per-patient and per-site basis (site=lesion).
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Sep 2016 (estimated)
- Study startOct 2019 (estimated)
- Primary completionOct 2020 (estimated)
- Study completionOct 2021 (estimated)
Why it stopped: PIs will not pursue trial due to staff and time constraints
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hepatocellular CarcinomaStudies of the same condition, open and under way.
- More trials run by British Columbia Cancer AgencyThe sponsor's other registered studies.
- 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- British Columbia Cancer Agency
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Francois Benard, MD, Principal investigator, British Columbia Cancer Agency
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02899325
- Sponsor's protocol ID
- H16-01905
- Status last verified
- Dec 2019
- First submitted
- 9 Sep 2016
- Last updated
- 21 Feb 2023
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- No: There is no plan to share individual participant data.
Study at a glance
From the registry record, last updated by the sponsor on 21 Feb 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Single-blind Study to Evaluate the Efficacy and Safety of 18F-Fluorodeoxygalactose (18F-FDGal) Compared to 18F-Fluorodeoxyglucose (18F-FDG) to Detect Hepatocellular Carcinoma Via PET/CT in Patients With Cirrhosis or Chronic Liver Disease
- ClinicalTrials.gov ID
- NCT02899325
- Acronym / sponsor ID
- H16-01905
- Study type
- Observational
- Recruitment status
- WithdrawnReason stopped: PIs will not pursue trial due to staff and time constraints
- Enrolment
- 0 participants (actual)
- Lead sponsor
- British Columbia Cancer AgencyUniversity, hospital or other
- Study start
- Oct 2019 (estimated)
- Primary completion
- Oct 2020 (estimated)
- Study completion
- Oct 2021 (estimated)
- First posted
- 14 Sep 2016 (estimated)
- 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.
Liver cancer is one of the leading causes of cancer death among Asian men. If diagnosed early the disease is treatable with surgery. Current conventional imaging modalities have limitations to early detection. This study proposes to use 18F-FGal and 18F-FDG PET/CT scans to compare the clinical efficacy of diagnosing hepatocellular carcinoma (a type of liver cancer) using these PET/CT scans.
Detailed description
Screening Visit Patients will undergo screening procedures for determining eligibility prior to the first PET/CT examination. For practical reasons and to avoid unnecessary travel for research subjects, the initial screening can be conducted by phone, and completed on the day that the first PET/CT examination is performed. However, the PET/CT scan will only be done for subjects that meet all the eligibility criteria and sign the consent form prior to the examination. All patients should have received the consent form by mail, email or fax, at least 24 hours prior to the screening visit.
Demographics Demographic data including date of birth, gender, height and weight information will be obtained.
Medical History and Concomitant Medications The general medical history up to 3 months of study entry (screening visit) should be recorded at the screening visit. The medical history should include procedural and surgical history within the past year. Cancer history should be recorded on a lifetime basis. Previous medications should be recorded up to 28 days prior to screening visit and up to 1 year for cancer treatment if any. All concomitant medications starting from enrollment of subjects should be recorded on subsequent visits for the PET/CT examinations.
Vital Signs Patient's vital signs will be measured including blood pressure, pulse rate and oxygen saturation, within 60 minutes before and 5-15 minutes after administration of the investigational product at PET/CT visits.
PET/CT Scans Patients who meet all eligibility requirements for entry into the study will undergo both an 18F-FDGal and 18F-FDG PET/CT examinations at the BCCA - Vancouver Centre's Functional Imaging Department. The two scans are to be performed on separate days and must be performed between 1 and 15 calendar days of each other. Each PET/CT scan will require approximately 3 hours of additional time from the subject above standard of care. The screening visit and informed consent, can be performed on the same day as the first PET/CT scan (and before the examination), will take approximately one hour.
Prior to the PET/CT scans, subjects will be instructed to take their usual medications as prescribed by their family physician. Subjects will also be instructed to drink 3 to 4 glasses of water within two hours prior to their scan appointment in order to promote hydration and facilitate urinary clearance of background 18F-FDGal/18F-FDG. Subjects must fast for 6 hours prior to 18F-FDGal and 18F-FDG injection, but can drink water at will.
Upon arrival at the PET Imaging department, all subjects will have their weight recorded prior to 18F-FDGal/18F-FDG injection. A baseline blood pressure, heart rate, and oxygen saturation levels will be recorded within 60 minutes prior to 18F-FDGal/18F-FDG injection, and 5 - 15 minutes after injection.
Each study subject will have an intravenous catheter inserted. The subject will receive a bolus intravenous dose of 18F-FDGal/18F-FDG from the BCCA, at a dose of 237 - 521 MBq for 18F-FDG and 119 - 261 MBq MBq for 18F-FDGal, followed by a 5 - 20 mL normal saline flush. The subject will rest in a comfortable chair for 60 minutes.
Upon completion of the scan, subjects will be free to leave the department and will be encouraged to drink 3-4 extra glasses of water by the end of the day to promote further clearance of the remaining tracer in the urinary tract. Overall, the study will take approximately 3 hours of subject time.
Each patient will be monitored on vital signs, adverse events before and after the intravenously 18F-FDGal/18F-FDG administration. Concomitant medication(s) will also be recorded. All of the 18F-FDGal/18F-FDG PET/CT imaging obtained at all study will be sent to a centralized location in DVD sets for re-labeling purpose to mask the patients' identifiers from readers.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The purpose of this study is to evaluate the diagnostic utility of 18F-FDGal PET/CT in identifying sites of hepatocellular carcinoma where conventional imaging has not been as effective. Concordance with histology, imaging or follow up will be assessed.
Key inclusion criteria (5 listed)
- Male or female, age ≥ 19 years of age.
- Patient who accepts to enter the study by signing written informed consent.
- Patient with performance status ≤ 2 Eastern Cooperative Oncology Group (ECOG).
- Patient with cirrhosis or chronic liver disease suspected to have at least 1 hepatic nodule larger than 1 cm in diameter detected by conventional image (US, CT, MRI).
Key exclusion criteria (9 listed)
- Patient has serious allergic history or known allergy to 18F-FDGal or 18F-FDG.
- Patient has received therapy for aforementioned diagnosis before the PET scans
- Patient with known (proven) metastases from a prior malignancy
- Patient has been diagnosed with multiple malignancies.
- Female patient who is pregnant, lactating or planning to become pregnant during the study.
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 |
|---|---|---|
| Diagnostic PET/CT scansAlso: 18F-FDG and 18F-FDGal PET/CT scansThese PET/CT scans will be performed for diagnostic purposes of hepatocellular carcinoma. | Drug | – |
Primary outcome
Sensitivity of 18F-FDGal in the diagnosis of HCC on per-patient basis
Time frame: 6 months
Determination of sensitivity of both exams when compared with pathology reports (if available) and compared with routine imaging (CT, MRI, US) if available. The treatment group will be declared superior if the lower limit of the 95% two-sided confidence interval of the difference of these two proportions is greater than 0.
3 secondary outcomes
Number of participants with 18F-FDGal-related adverse events as assessed by abnormal vital sign measurement
Time frame: 1 hour
Sensitivity of 18F-FDGal in the diagnosis of HCC on per-site basis
Time frame: 6 months
Specificity of 18F-FDGal in the diagnosis of HCC
Time frame: 6 months
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Feb 2023.
- Individual participant dataSharing planned: No. There is no plan to share individual participant data.
Related trials for Hepatocellular Carcinoma
RecruitingObservational study
Real-world Evaluation of the HistoSonics Edison System for Treatment of Liver Tumors Across Multidisciplinary Users (BOOMBOX: Master Study)
Liver Neoplasms, Primary Liver Cancer
Recruiting
The Vanguard Study: Testing a New Way to Screen for Cancer
Bladder Carcinoma, Breast Carcinoma
Active, not recruitingPhase 1
Prospective Exploratory Study of FAPi PET/CT With Histopathology Validation in Patients With Various Cancers
Bladder Carcinoma, Cervical Carcinoma
RecruitingObservational study
A Study to Evaluate Patient-Reported Satisfaction, Effectiveness, and Safety of Atezolizumab in Participants Treated in Routine Clinical Practice
Lung Cancer, Hepatocellular Carcinoma
RecruitingPhase 2
At-Home Cancer Directed Therapy Versus in Clinic for the Treatment of Patients With Advanced Cancer
Advanced Anal Carcinoma, Advanced Biliary Tract Carcinoma
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. This study is not recruiting at the moment.
Francois Benard, MD principal investigator
British Columbia Cancer Agency
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hepatocellular Carcinoma and Liver Cirrhosis, run by British Columbia Cancer Agency at 1 site in Canada.
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 5 inclusion and 9 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: withdrawn, as of the sponsor's last update on 21 Feb 2023. 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 Canada. 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?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Sensitivity of 18F-FDGal in the diagnosis of HCC on per-patient basis (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 21 Feb 2023.