CholangiocarcinomaPhase 2/3FAPICholNCT06355427
The Effect of [18F] F-FAPI PET-CT on Management in Patients With Proximal Cholangiocarcinoma
A Phase 2/3 study testing [18F]F-FAPI PET-CT in people with Cholangiocarcinoma, run by Mara Veenstra, MD at 3 sites in Netherlands.
Trial summary
Background Bile duct cancer (cholangiocarcinoma) represents the second most common type of hepatobiliary cancer worldwide with an incidence of 0.35 to 2 per 100.000 annually. Currently, surgical resection is the only curative option. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cholangiocarcinoma
- What is being tested?
- [18F]F-FAPI PET-CT
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 81 participants
- Where
- 3 sitesNetherlands
- Study dates
- 29 Nov 2024to 1 Feb 2028
- Phase
- Phase 2/3
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patient is scheduled for explorative laparoscopy or laparotomy for suspicion of proximal cholangiocarcinoma (perihilar, intrahepatic and gall bladder cholangiocarcinoma)
- Tumor is regarded as resectable based on preoperative CT and MRI
- Patient is 18 years or older and is able to give informed consent
Who cannot join
- Previous abdominal surgery or chemotherapy
- Patient had FDG PET-CT in addition to preoperative CT and MRI
- Contra-indication for performing PET-CT
- Indication for FDG PET-CT
- Pregnancy or lactation, for the latter, temporary discontinuation may be considered.
- Known allergic reaction to therapeutic radiopharmaceuticals
Show all 9Show fewer
- Inability to lie still on the back for the duration of PET-CT
- Impaired renal function, defined as eGFR (MDRD) \<25 ml/min/1,73 m2. An exception can be made in consultation with the treating physician.
- Any (other) condition, disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding that may affect the interpretation of the results, or which might contribute substantially to the patient\'s experience of study burden (such as non-suppressible claustrophobia)
Trial locations and contacts
3 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Netherlands3 sites, 3 recruiting
- Recruiting
Amsterdam UMC
Amsterdam
Mara Veenstra, M.D., +31 (0)10 704 2006, m.m.k.veenstra@erasmusmc.nl
Rutger-Jan Swijnenburg, M.D., PhD
- Recruiting
Erasmus MC
Rotterdam
Mara Veenstra, M.D., +31 (0)10 704 2006, m.m.k.veenstra@erasmusmc.nl
Maarten Thomeer, M.D., PhD
- Not yet recruiting
UMC Utrecht
Utrecht
Mara Veenstra, M.D., +31 (0)10 704 2006, m.m.k.veenstra@erasmusmc.nl
Jeroen Hagendoorn, M.D., PhD
About this study
Official title: The Effect of [18F] F-FAPI PET-CT on Management in Patients With Potentially Resectable Biliary Tract Cancers: Prospective Multicenter Study and Cost-effectivity Analysis
Background
Bile duct cancer (cholangiocarcinoma) represents the second most common type of hepatobiliary cancer worldwide with an incidence of 0.35 to 2 per 100.000 annually. Currently, surgical resection is the only curative option. However, patients are not eligible for surgery if the tumor cannot be resected or the cancer has spread. For this group of patients, palliative chemotherapy is the most suited treatment option. To find out if a patient is suited for surgery, CT and MRI are performed. These imaging techniques, however, struggle to correctly identify small cancer spreads that are smaller than 1 cm. Therefore, cancer that has already spread can be found during surgery. In these cases, the tumor cannot be removed and the surgery therefore has not been of any benefit for the patient. These surgeries could be avoided by implementing a diagnostic tool with significantly higher accuracy than those currently used. Single center studies have shown that fibroblast activation protein inhibitor (FAPI) PET-CT is a very promising technique for determining metastases in tumors with prominent desmoplastic reactions, like cholangiocarcinoma. The investigators predict that implementation of preoperative FAPI PET-CT could prevent futile surgery for at least half of patients in whom intra-operative metastasized disease is found using the current work-up.
Read more
Patient population
Patients ≥18 years with potentially curable proximal cholangiocarcinoma (perihilar, intrahepatic and gall bladder cholangiocarcinoma) who are planned to undergo surgery based on imaging using CT thorax/abdomen and MRI of the upper abdomen. Exclusion criteria are previous abdominal surgery or chemotherapy, known pregnancy or lactation and indication for FDG PET-CT.
Participation in this study
Participation would mean to undergo FAPI PET-CT prior to the scheduled surgery. This will take up about half a day of the participant's time. Afterwards, participants receive questionnaires about quality of life and use of healthcare services over a period of six months in order for the researchers to be able to calculate the cost-effectiveness of additional FAPI PET-CT.
Risks and benefits of participation
Patients may benefit directly from [18F]F-FAPI PET-CT by allowing for more targeted treatment, possibly avoiding futile surgery and receiving chemotherapy or best clinical support instead, minimizing treatment delay. Avoiding futile surgery will also prevent patients from being exposed to the risks and discomfort associated with surgery: hospital stay, possibility of intraoperative or postoperative complications, postoperative pain and recovery, and mortality.
Potential risks and burdens associated with this study are an extra hospital visit and a time burden of approximately half a day. Risks associated with administering FAPI are (re)bleed and infection. Both risks have a minimal probability of onset and can usually easily be treated. As [18F]F-FAPI is a sub-pharmacologically micro-dosed diagnostic tracer, the risk of allergic reactions is expected to be minimal and no tissue damage is expected. The burden associated with undergoing a PET-CT may be laying still for a certain time, and possible experience of claustrophobia. Possible metastases of the cancer will have to be confirmed when suspicious findings are seen on FAPI PET-CT. This could mean that participants will have to undergo additional testing such as imaging (CT or MRI) or biopsy. Undergoing FAPI PET-CT prior to surgery will result in a surgical delay when compared with the current clinical practice. The investigators do not expect this delay to influence the patient's prognosis. Follow-up will result in a time burden for patients to answer questionnaires on a two-weekly or monthly basis.
Read the detailed description
Rationale
Bile duct cancer (cholangiocarcinoma) represents the second most common type of hepatobiliary cancer worldwide with an incidence of 0.35 to 2 per 100.000 annually. Currently, surgical resection is the only curative option. However, patients are not eligible for surgery if vascular invasion, distant tumor positive lymph nodes, peritoneal metastases or organ metastases are found on preoperative imaging. For this group of patients, palliative chemotherapy is the most suited treatment option. The preoperative imaging currently includes CT, MRI and FDG PET-CT. In around 29 % of potentially resectable tumors (based on preoperative imaging) metastases are found during subsequent surgery. These explorations could be avoided by implementing a diagnostic tool with significantly higher accuracy than those currently used. Single center studies have shown that fibroblast activation protein inhibitor (FAPI) PET-CT is a very promising technique for determining metastases in tumors with prominent desmoplastic reactions, like cholangiocarcinoma. Our systematic review has shown it is superior to the commonly used FDG PET-CT for this indication. The investigators predict that implementation of preoperative FAPI PET-CT could alter treatment course for at least half (13%) of patients in whom intra-operative metastasized disease is found using the current work-up.
Objective
The primary aim of this study is to assess whether preoperative [18F]F-FAPI PET-CT in addition to standard preoperative imaging can successfully identify metastasized disease and change treatment plan in patients with potentially resectable proximal bile duct cancer (intrahepatic, perihilar and gall bladder cholangiocarcinoma). This study also aims to evaluate if adding [18F]F-FAPI PET-CT to preoperative imaging is cost-effective.
Main trial endpoints
The main endpoint is the diagnostic accuracy (sensitivity, specificity, positive predictive value, negative predictive value) of [18F]F-FAPI PET-CT.
Secondary trial endpoints
- Diagnostic accuracy of [18F]F-FAPI PET-CT per abdominal region and per lesion
- The number of additional significant findings on [18F]F-FAPI PET-CT
- Change of treatment: true change and virtual change
- The number of times readers' conclusions differed and why
- Cost-effectiveness analysis, budget impact analysis (BIA), sector costs, societal costs, health-related quality of life (HRQoL)
- The number of additional significant findings on [18F]F-FAPI PET-CT
- Number of days between date of first imaging (CT/MRI) and starting date of chemotherapy, palliative therapy or surgical resection
- The incidence and severity of AEs and SAEs according to CTCAEv5
- VOI, TTP, K1 and k2, SUV and TBR (in a subgroup of patients)
Trial design
Prospective multicenter observational cohort study, expected total duration 4 years. Participants will be participating for at least six months.
Trial population
Patients ≥18 years with potentially curable proximal cholangiocarcinoma (perihilar, intrahepatic and gall bladder cholangiocarcinoma) who are planned to undergo surgery based on imaging using CT thorax/abdomen and MRI of the upper abdomen. Exclusion criteria are previous abdominal surgery or chemotherapy, known pregnancy or lactation and indication for FDG PET-CT.
Interventions
If patients are deemed eligible for surgery (laparoscopy or laparotomy) by the weekly organ-specific multidisciplinary team (MDT) including an abdominal nuclear medicine specialist, radiologist, surgeon, gastroenterologist/hepatologist, oncologist and, optionally, pathologist, patients will be asked to participate in the study. After inclusion, patients will receive additional [18F]F-FAPI PET-CT. Patients who underwent [18F]F-FAPI PET-CT will undergo follow-up for at least six months, if clinically advisable. Follow-up includes information regarding additional imaging, surgery or complications. To determine cost-effectiveness, patients' medical consumption will be elicited using two questionnaires. Patients will be asked to fill out the 'institute for Medical Technology Assessment (iMTA) Medical Consumption Questionnaire (iMCQ)' at three and six months after their initial CT/MRI imaging (before [18F]F-FAPI PET-CT or surgery). Patients will also be asked to fill out the European Organisation for Research and Treatment of Cancer (EORTC) group's QLQ-C30 and QLQ-BIL21 questionnaires and the EuroQol (EQ) Group's EQ-5D-5L questionnaire once every two weeks during the first two months after [18F]F-FAPI PET-CT and then once every four weeks until six months follow-up.
Risks and benefits
Patients may benefit directly from [18F]F-FAPI PET-CT by allowing for more targeted treatment, possibly avoiding futile surgery and receiving chemotherapy or best clinical support instead, minimizing treatment delay. Avoiding futile surgery will also prevent patients from being exposed to the risks and discomfort associated with surgery: hospital stay, possibility of intraoperative or postoperative complications, postoperative pain and recovery, and mortality.
Potential risks and burdens associated with this study are an extra site visit and a time burden of approximately half a day. Risks associated with vena puncture are (re)bleed and infection. Both risks have a minimal probability of onset, and when anticipated upon, are not expected to have significant clinical consequences. Risks associated with the administration of the study agent are allergic reactions and radiation burden. [18F]F-FAPI is a sub-pharmacologically micro-dosed diagnostic tracer, which is why the risk of allergic reactions is expected to be minimal and no tissue damage is expected. The burden associated with undergoing a PET-CT may be laying still for a certain time, and possible experience of claustrophobia. Metastases will have to be confirmed when suspicious findings are seen on [18F]F-FAPI PET-CT. This could mean subjects will have to undergo additional testing such as imaging (CT or MRI) or biopsy. If these additional tests are negative for metastases, the subject's exploratory surgery will have been needlessly delayed. Having to undergo [18F]F-FAPI PET-CT prior to surgery will also result in a surgical delay when compared with the current clinical practice. The investigators do not expect this delay to influence the subject's prognosis. Follow-up will result in a time burden for patients to answer questionnaires on a two-weekly or monthly basis.
- Conditions
- Cholangiocarcinoma
- Being tested
- [18F]F-FAPI PET-CT
- Keywords
- FAPI, Cholangiocarcinoma, FAPI PET/CT, Fibroblast Activation Protein Inhibitor, Proximal cholangiocarcinoma, FAPIChol, PET/CT, 18F-FAPI-74
- Medical subject headings
- Cholangiocarcinoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
[18F]F-FAPI PET-CTDrug
[18F]F-FAPI PET-CT in addition to regular CT and MRI, prior to participants undergoing surgery
| Study group | Role | What they receive |
|---|---|---|
| FAPI PET-CT | Experimental | Participants will undergo additional FAPI PET-CT prior to scheduled surgery. Receives: Drug: [18F]F-FAPI PET-CT |
What is being measured
The primary outcome is the main question the study is designed to answer.
Diagnostic accuracy of [18F]F-FAPI PET-CT
Diagnostic accuracy will be expressed using sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV)
Measured: Six months following PET-CT
Secondary outcomes (12)
Change of treatment
Change of treatment is based on a combination of true change during work-up and virtual change based on [18F]F-FAPI PET-CT findings, with proof during further exploration (laparoscopy or laparotomy), resection or follow-up. True change is defined as a positive finding that changes the intent of treatment, i.e. no explorative laparoscopy/laparotomy and no resection. Virtual change of therapy is defined as a positive finding with FAPI PET-CT, which should preclude explorative laparoscopy and resection but where the latter is still performed.
Measured: Within one month following PET-CT
Cost-effectiveness
Determining the value of introducing [18F]F-FAPI PET-CT in terms of quality-adjusted life years (QALY) and costs compared to the current standard of care (SoC).
Measured: Six months following PET-CT
Number of additional significant findings using [18F]F-FAPI PET-CT
Additional significant findings include other primary tumors (albeit benign or malignant) and other relevant findings such as infectious and inflammatory processes.
Measured: Within one week after PET-CT
Number of times nuclear medicine specialists' [18F]F-FAPI PET-CT conclusions differed from one another
To assess the inter-reader variability between nuclear medicine specialists. Consensus regarding the presence of metastases, lymph node involvement, and the location of possible metastases and/or suspicious lymph nodes will be assessed.
Measured: Within one week after PET-CT
Number of lesions found on [18F]F-FAPI PET-CT
The amount of suspicious findings on [18F]F-FAPI PET-CT
Measured: Within one week after PET-CT
Number of days between [18F]F-FAPI PET-CT and exploratory surgery
Differences in treatment delay between patients with and without significant findings on [18F]F-FAPI PET-CT will be assessed. Treatment delay is defined as the time in days from the first multidisciplinary team meeting to exploratory surgery.
Measured: Six months following PET-CT
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Measured by the incidence and severity of AEs and SAEs according to CTCAE v5.0
Measured: Six months following PET-CT
Number of participants in which dynamic [18F]F-FAPI PET-CT followed by conventional [18F]F-FAPI PET-CT was able to distinguish benign lesions from malignant lesions
Subgroup analysis. As part of the subgroup analysis participants undergo dynamic [18F]F-FAPI PET-CT followed by conventional PET-CT at one hour post-injection.
Measured: Six months following PET-CT
Change in volume of interest (cm3) using dynamic [18F]F-FAPI PET-CT
Subgroup analysis. As part of the subgroup analysis participants undergo dynamic [18F]F-FAPI PET-CT followed by conventional PET-CT at one hour post-injection.
Measured: Within one week after PET-CT
Difference in SUVmax between dynamic and conventional [18F]F-FAPI PET-CT
Subgroup analysis. As part of the subgroup analysis participants undergo dynamic [18F]F-FAPI PET-CT followed by conventional PET-CT at one hour post-injection.
Measured: Within one week after PET-CT
Difference in SUVmean between dynamic and conventional [18F]F-FAPI PET-CT
Subgroup analysis. As part of the subgroup analysis participants undergo dynamic [18F]F-FAPI PET-CT followed by conventional PET-CT at one hour post-injection.
Measured: Within one week after PET-CT
Difference in transport rate (k1 to k2) on dynamic [18F]F-FAPI PET-CT between participants with malignant lesions and particpants with benign lesions
Subgroup analysis. As part of the subgroup analysis participants undergo dynamic [18F]F-FAPI PET-CT followed by conventional PET-CT at one hour post-injection.
Measured: Six months following PET-CT
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Apr 2024
- Study start29 Nov 2024
- Primary completion1 Sep 2027 (estimated)
- Study completion1 Feb 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for CholangiocarcinomaStudies 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 2/3
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 81 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Mara Veenstra, MD
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Mara Veenstra, MD, Erasmus Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06355427
- Sponsor's protocol ID
- 2023-507938-24-00
- Other IDs
- 2023
- Acronym
- FAPIChol
- Status last verified
- Apr 2025
- First submitted
- 15 Mar 2024
- Last updated
- 11 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 11 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of [18F] F-FAPI PET-CT on Management in Patients With Potentially Resectable Biliary Tract Cancers: Prospective Multicenter Study and Cost-effectivity Analysis
- ClinicalTrials.gov ID
- NCT06355427
- Acronym / sponsor ID
- FAPIChol / 2023-507938-24-00
- Conditions
- Cholangiocarcinoma
- Keywords
- FAPI, Cholangiocarcinoma, FAPI PET/CT, Fibroblast Activation Protein Inhibitor, Proximal cholangiocarcinoma, FAPIChol, PET/CT, 18F-FAPI-74
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 81 participants (estimated)
- Lead sponsor
- Mara Veenstra, MDUniversity, hospital or other
- Collaborators
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), UMC Utrecht
- Study start
- 29 Nov 2024 (actual)
- Primary completion
- 1 Sep 2027 (estimated)
- Study completion
- 1 Feb 2028 (estimated)
- First posted
- 9 Apr 2024 (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.
Background
Bile duct cancer (cholangiocarcinoma) represents the second most common type of hepatobiliary cancer worldwide with an incidence of 0.35 to 2 per 100.000 annually. Currently, surgical resection is the only curative option. However, patients are not eligible for surgery if the tumor cannot be resected or the cancer has spread. For this group of patients, palliative chemotherapy is the most suited treatment option. To find out if a patient is suited for surgery, CT and MRI are performed. These imaging techniques, however, struggle to correctly identify small cancer spreads that are smaller than 1 cm. Therefore, cancer that has already spread can be found during surgery. In these cases, the tumor cannot be removed and the surgery therefore has not been of any benefit for the patient. These surgeries could be avoided by implementing a diagnostic tool with significantly higher accuracy than those currently used. Single center studies have shown that fibroblast activation protein inhibitor (FAPI) PET-CT is a very promising technique for determining metastases in tumors with prominent desmoplastic reactions, like cholangiocarcinoma. The investigators predict that implementation of preoperative FAPI PET-CT could prevent futile surgery for at least half of patients in whom intra-operative metastasized disease is found using the current work-up.
Patient population
Patients ≥18 years with potentially curable proximal cholangiocarcinoma (perihilar, intrahepatic and gall bladder cholangiocarcinoma) who are planned to undergo surgery based on imaging using CT thorax/abdomen and MRI of the upper abdomen. Exclusion criteria are previous abdominal surgery or chemotherapy, known pregnancy or lactation and indication for FDG PET-CT.
Participation in this study
Participation would mean to undergo FAPI PET-CT prior to the scheduled surgery. This will take up about half a day of the participant's time. Afterwards, participants receive questionnaires about quality of life and use of healthcare services over a period of six months in order for the researchers to be able to calculate the cost-effectiveness of additional FAPI PET-CT.
Risks and benefits of participation
Patients may benefit directly from [18F]F-FAPI PET-CT by allowing for more targeted treatment, possibly avoiding futile surgery and receiving chemotherapy or best clinical support instead, minimizing treatment delay. Avoiding futile surgery will also prevent patients from being exposed to the risks and discomfort associated with surgery: hospital stay, possibility of intraoperative or postoperative complications, postoperative pain and recovery, and mortality.
Potential risks and burdens associated with this study are an extra hospital visit and a time burden of approximately half a day. Risks associated with administering FAPI are (re)bleed and infection. Both risks have a minimal probability of onset and can usually easily be treated. As [18F]F-FAPI is a sub-pharmacologically micro-dosed diagnostic tracer, the risk of allergic reactions is expected to be minimal and no tissue damage is expected. The burden associated with undergoing a PET-CT may be laying still for a certain time, and possible experience of claustrophobia. Possible metastases of the cancer will have to be confirmed when suspicious findings are seen on FAPI PET-CT. This could mean that participants will have to undergo additional testing such as imaging (CT or MRI) or biopsy. Undergoing FAPI PET-CT prior to surgery will result in a surgical delay when compared with the current clinical practice. The investigators do not expect this delay to influence the patient's prognosis. Follow-up will result in a time burden for patients to answer questionnaires on a two-weekly or monthly basis.
Detailed description
Rationale
Bile duct cancer (cholangiocarcinoma) represents the second most common type of hepatobiliary cancer worldwide with an incidence of 0.35 to 2 per 100.000 annually. Currently, surgical resection is the only curative option. However, patients are not eligible for surgery if vascular invasion, distant tumor positive lymph nodes, peritoneal metastases or organ metastases are found on preoperative imaging. For this group of patients, palliative chemotherapy is the most suited treatment option. The preoperative imaging currently includes CT, MRI and FDG PET-CT. In around 29 % of potentially resectable tumors (based on preoperative imaging) metastases are found during subsequent surgery. These explorations could be avoided by implementing a diagnostic tool with significantly higher accuracy than those currently used. Single center studies have shown that fibroblast activation protein inhibitor (FAPI) PET-CT is a very promising technique for determining metastases in tumors with prominent desmoplastic reactions, like cholangiocarcinoma. Our systematic review has shown it is superior to the commonly used FDG PET-CT for this indication. The investigators predict that implementation of preoperative FAPI PET-CT could alter treatment course for at least half (13%) of patients in whom intra-operative metastasized disease is found using the current work-up.
Objective
The primary aim of this study is to assess whether preoperative [18F]F-FAPI PET-CT in addition to standard preoperative imaging can successfully identify metastasized disease and change treatment plan in patients with potentially resectable proximal bile duct cancer (intrahepatic, perihilar and gall bladder cholangiocarcinoma). This study also aims to evaluate if adding [18F]F-FAPI PET-CT to preoperative imaging is cost-effective.
Main trial endpoints
The main endpoint is the diagnostic accuracy (sensitivity, specificity, positive predictive value, negative predictive value) of [18F]F-FAPI PET-CT.
Secondary trial endpoints
- Diagnostic accuracy of [18F]F-FAPI PET-CT per abdominal region and per lesion
- The number of additional significant findings on [18F]F-FAPI PET-CT
- Change of treatment: true change and virtual change
- The number of times readers' conclusions differed and why
- Cost-effectiveness analysis, budget impact analysis (BIA), sector costs, societal costs, health-related quality of life (HRQoL)
- The number of additional significant findings on [18F]F-FAPI PET-CT
- Number of days between date of first imaging (CT/MRI) and starting date of chemotherapy, palliative therapy or surgical resection
- The incidence and severity of AEs and SAEs according to CTCAEv5
- VOI, TTP, K1 and k2, SUV and TBR (in a subgroup of patients)
Trial design
Prospective multicenter observational cohort study, expected total duration 4 years. Participants will be participating for at least six months.
Trial population
Patients ≥18 years with potentially curable proximal cholangiocarcinoma (perihilar, intrahepatic and gall bladder cholangiocarcinoma) who are planned to undergo surgery based on imaging using CT thorax/abdomen and MRI of the upper abdomen. Exclusion criteria are previous abdominal surgery or chemotherapy, known pregnancy or lactation and indication for FDG PET-CT.
Interventions
If patients are deemed eligible for surgery (laparoscopy or laparotomy) by the weekly organ-specific multidisciplinary team (MDT) including an abdominal nuclear medicine specialist, radiologist, surgeon, gastroenterologist/hepatologist, oncologist and, optionally, pathologist, patients will be asked to participate in the study. After inclusion, patients will receive additional [18F]F-FAPI PET-CT. Patients who underwent [18F]F-FAPI PET-CT will undergo follow-up for at least six months, if clinically advisable. Follow-up includes information regarding additional imaging, surgery or complications. To determine cost-effectiveness, patients' medical consumption will be elicited using two questionnaires. Patients will be asked to fill out the 'institute for Medical Technology Assessment (iMTA) Medical Consumption Questionnaire (iMCQ)' at three and six months after their initial CT/MRI imaging (before [18F]F-FAPI PET-CT or surgery). Patients will also be asked to fill out the European Organisation for Research and Treatment of Cancer (EORTC) group's QLQ-C30 and QLQ-BIL21 questionnaires and the EuroQol (EQ) Group's EQ-5D-5L questionnaire once every two weeks during the first two months after [18F]F-FAPI PET-CT and then once every four weeks until six months follow-up.
Risks and benefits
Patients may benefit directly from [18F]F-FAPI PET-CT by allowing for more targeted treatment, possibly avoiding futile surgery and receiving chemotherapy or best clinical support instead, minimizing treatment delay. Avoiding futile surgery will also prevent patients from being exposed to the risks and discomfort associated with surgery: hospital stay, possibility of intraoperative or postoperative complications, postoperative pain and recovery, and mortality.
Potential risks and burdens associated with this study are an extra site visit and a time burden of approximately half a day. Risks associated with vena puncture are (re)bleed and infection. Both risks have a minimal probability of onset, and when anticipated upon, are not expected to have significant clinical consequences. Risks associated with the administration of the study agent are allergic reactions and radiation burden. [18F]F-FAPI is a sub-pharmacologically micro-dosed diagnostic tracer, which is why the risk of allergic reactions is expected to be minimal and no tissue damage is expected. The burden associated with undergoing a PET-CT may be laying still for a certain time, and possible experience of claustrophobia. Metastases will have to be confirmed when suspicious findings are seen on [18F]F-FAPI PET-CT. This could mean subjects will have to undergo additional testing such as imaging (CT or MRI) or biopsy. If these additional tests are negative for metastases, the subject's exploratory surgery will have been needlessly delayed. Having to undergo [18F]F-FAPI PET-CT prior to surgery will also result in a surgical delay when compared with the current clinical practice. The investigators do not expect this delay to influence the subject's prognosis. Follow-up will result in a time burden for patients to answer questionnaires on a two-weekly or monthly basis.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| FAPI PET-CT | Experimental | Drug: [18F]F-FAPI PET-CTParticipants will undergo additional FAPI PET-CT prior to scheduled surgery. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Patient is scheduled for explorative laparoscopy or laparotomy for suspicion of proximal cholangiocarcinoma (perihilar, intrahepatic and gall bladder cholangiocarcinoma)
- Tumor is regarded as resectable based on preoperative CT and MRI
- Patient is 18 years or older and is able to give informed consent
Key exclusion criteria (9 listed)
- Previous abdominal surgery or chemotherapy
- Patient had FDG PET-CT in addition to preoperative CT and MRI
- Contra-indication for performing PET-CT
- Indication for FDG PET-CT
- Pregnancy or lactation, for the latter, temporary discontinuation may be considered.
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 |
|---|---|---|
| [18F]F-FAPI PET-CT[18F]F-FAPI PET-CT in addition to regular CT and MRI, prior to participants undergoing surgery | Drug | FAPI PET-CT |
Primary outcome
Diagnostic accuracy of [18F]F-FAPI PET-CT
Time frame: Six months following PET-CT
Diagnostic accuracy will be expressed using sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV)
12 secondary outcomes
Change of treatment
Time frame: Within one month following PET-CT
Cost-effectiveness
Time frame: Six months following PET-CT
Number of additional significant findings using [18F]F-FAPI PET-CT
Time frame: Within one week after PET-CT
Number of times nuclear medicine specialists' [18F]F-FAPI PET-CT conclusions differed from one another
Time frame: Within one week after PET-CT
Number of lesions found on [18F]F-FAPI PET-CT
Time frame: Within one week after PET-CT
Number of days between [18F]F-FAPI PET-CT and exploratory surgery
Time frame: Six months following PET-CT
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: Six months following PET-CT
Number of participants in which dynamic [18F]F-FAPI PET-CT followed by conventional [18F]F-FAPI PET-CT was able to distinguish benign lesions from malignant lesions
Time frame: Six months following PET-CT
Change in volume of interest (cm3) using dynamic [18F]F-FAPI PET-CT
Time frame: Within one week after PET-CT
Difference in SUVmax between dynamic and conventional [18F]F-FAPI PET-CT
Time frame: Within one week after PET-CT
Difference in SUVmean between dynamic and conventional [18F]F-FAPI PET-CT
Time frame: Within one week after PET-CT
Difference in transport rate (k1 to k2) on dynamic [18F]F-FAPI PET-CT between participants with malignant lesions and particpants with benign lesions
Time frame: Six months following PET-CT
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 11 Apr 2025.
- Individual participant dataSharing planned: Undecided
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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.
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study testing [18F]F-FAPI PET-CT in people with Cholangiocarcinoma, run by Mara Veenstra, MD at 3 sites in Netherlands.
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 3 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: looking for participants now, as of the sponsor's last update on 11 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Netherlands. 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.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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 Mara Veenstra, M.D. (+31 (0)10 704 2006, m.m.k.veenstra@erasmusmc.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Diagnostic accuracy of [18F]F-FAPI PET-CT (time frame: Six months following PET-CT). 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 11 Apr 2025.