Colon Rectal Cancer AdenocarcinomaNCT02624115
FAZA PET as Biomarker for Hypoxia in Rectal Cancer
An observational study of Colon Rectal Cancer Adenocarcinoma, run by University Health Network, Toronto at 1 site in Canada.
Trial summary
Colorectal cancer (CRC) is one of the leading causes of cancer mortality in Canada. Rectal cancers are now known to be hypoxic which is a negative prognostic factor and predictive of metastatic spread and poor responsiveness to treatment. This has also been shown in preclinical xenograft models. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Colon Rectal Cancer Adenocarcinoma
- How many people
- 8 participants
- Where
- 1 siteCanada
- Study dates
- 1 May 2016to 9 Jun 2019
- How long will I take part?
- 1 Month
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with rectal cancer undergoing neoadjuvant chemoradiotherapy
Who may be able to join
- Patients will be eligible for inclusion in this study if they meet all of the following criteria:
- Age ≥18 years
- Histologic proven locally advanced rectal cancer (T3-T4, or N1) based on clinical assessment and standard staging procedures.
- Intention to treat with neoadjuvant chemoradiotherapy prior to surgery, according to the current institutional treatment policies.
- A negative urine or serum pregnancy test within the two week interval immediately prior to imaging, in women of child-bearing age.
- Ability to provide written informed consent to participate in the study (for both components of the trial: imaging with FAZA-PET/MR and administration of Pimonidazole).
Who cannot join
- Patients will be ineligible to participate in this study if they meet any of the following criteria:
- Contraindication for MR as per current institutional guidelines.
- Inability to lie supine for at least 45 minutes.
- Contraindication for administration of pimonidazole (allergy)
- Any patient who is pregnant or breastfeeding.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: 18F-Fluoroazomycin Arabinoside (FAZA) Positron Emission Tomography/Magnetic Imaging Resonance (PET/MRI) as a Biomarker of Hypoxia in Rectal Cancer: A Pilot Study
Colorectal cancer (CRC) is one of the leading causes of cancer mortality in Canada. Rectal cancers are now known to be hypoxic which is a negative prognostic factor and predictive of metastatic spread and poor responsiveness to treatment. This has also been shown in preclinical xenograft models. Hence there is a need for identification of hypoxic rectal cancers.
In this pilot study the investigators intend to non-invasively assess the tumor and nodal metastasis using an integrated Positron Emission Tomography-Magnetic Resonance Imaging scanner (PET/MRI) with 18F-Fluoroazomycin Arabinoside (18F-FAZA) a radiopharmaceutical for assessing tumor hypoxia. The hypoxic rectal tumors will show an increased uptake of 18F-FAZA on PET which will have morphological correlation on MRI. The patient will then undergo neoadjuvant chemoradiation therapy (CRT) followed by repeat 18F-FAZA PET/MRI and rectal cancer surgery with pimonidazole staining. Pimonidazole is an extrinsic marker of hypoxia that is selectively reduced and covalently bound to intracellular macromolecules in areas of hypoxia within normal and tumor tissue with current approval for use in humans for research studies.
The primary goal of this pilot trial is to validate FAZA-PET as a biomarker of hypoxia by correlating its uptake in rectal tumors to pimonidazole staining in histopathology specimens. If the investigators pilot study successfully demonstrates the uptake and correlation of pimonidazole and FAZA-PET, the investigators would like to initiate a larger study examining hypoxia in rectal cancer. The investigators aims would be to image patients with locally advanced rectal cancer before CRT to ascertain whether high FAZA-PET uptake correlates with poor outcome to CRT. The ability to preoperatively predict the patient sub-population that will respond best to CRT, will help to identify the "complete pathological" responders and avoid unnecessary surgery. Furthermore, the FAZA-PET high subset of patients may benefit from other treatment strategies including clinical trials of anti-hypoxic agents.
Read the detailed description
Colorectal cancer (CRC) is one of the leading causes of cancer mortality in Canada. Rectal cancers are now known to be hypoxic which is a negative prognostic factor and predictive of metastatic spread and poor responsiveness to treatment. This has also been shown in preclinical xenograft models. Hence there is a need for identification of hypoxic rectal cancers.
In this pilot study, the investigators intend to non-invasively assess the tumor and nodal metastasis using an integrated PET/MRI with a radiopharmaceutical for assessing tumor hypoxia. The hypoxic rectal tumors will show increased uptake of 18F-FAZA on PET which will have morphological correlation on MRI. The patient will then undergo neoadjuvant chemoradiation therapy (CRT) followed by repeat 18F-FAZA PET/MRI and rectal cancer surgery with pimonidazole staining. Pimonidazole is an extrinsic marker of hypoxia that is selectively reduced and covalently bound to intracellular macromolecules in areas of hypoxia within normal and tumor tissue with current approval for use in humans for research studies.
The primary goal of this pilot trial is to validate FAZA-PET as a biomarker of hypoxia by correlating its uptake in rectal tumors to pimonidazole staining in histopathology specimens. If this pilot study successfully demonstrates the uptake and correlation of pimonidazole and FAZA-PET, the investigators would like to initiate a larger study examining hypoxia in rectal cancer. The aim would be to image patients with locally advanced rectal cancer before CRT to ascertain whether high FAZA-PET uptake correlates with poor outcome to CRT. The ability to preoperatively predict the patient subpopulation that will respond best to CRT, will help to identify the "complete pathological" responders and avoid unnecessary surgery. Furthermore, the FAZA-PET high subset of patients may benefit from other treatment strategies including clinical trials of anti-hypoxic agents.
Project Synopsis: STUDY OVERVIEW:
OBJECTIVES:
Primary Objective
- To determine the feasibility of using the FAZA-PET to image primary tumor hypoxia in patients with rectal cancer prior to treatment with chemoradiotherapy Secondary Objectives
- To optimize FAZA PET/MRI imaging protocol for use in patients with rectal cancer.
- To determine whether there is correlation between FAZA-PET, blood oxygen level-dependent MRI and Pimonidazole staining in primary rectal tumors before and after CRT.
- To correlate hypoxia defined by FAZA PET uptake and blood oxygen level-dependent MRI in rectal cancer with (pathologic) response to neoadjuvant chemoradiotherapy.
Study design: Single arm feasibility pilot study Study scheme: (see below)
Details on Tumor Microscopy and Pimonidazole Image analysis:
The initial assessment of pimonidazole-detected hypoxia in tumor sections from surgical specimens will be immunohistochemical which allows for both qualitative and quantitative assessment of pimonidazole staining in the context of histopathological morphology. To account for heterogeneity of pimonidazole staining, analysis will be performed in multiple surgical sections for each patient tumor (as previously published by the investigators own group). All staining, handling and processing of tissue specimens will done by the pathology department.
STUDY SCHEMA:
Target Population:
- Age ≥ 18 years
- Histological diagnosis of rectal cancer
- Intent to treat with neoadjuvant chemoradiotherapy and surgery
- Negative pregnancy test (for females in child bearing age)
- Informed Consent
- FAZA-PET/MRI
- Void bladder
- FAZA injection
- Dynamic PET acquisition with MRI Dixon sequences for attenuation correction (60 min; optional )
- 60 minute uptake time (rest)
- Void bladder
- Static PET/MRI pelvis (approximately 45 min)
- Standard treatment (neoadjuvant chemoradiotherapy
- Oral Pimonidazole on day prior to surgery
- Surgery
- Conditions
- Colon Rectal Cancer Adenocarcinoma
What is being measured
The primary outcome is the main question the study is designed to answer.
FAZA PET uptake in locally advanced rectal cancers prior to and after chemoradiotherapy
FAZA uptake will be measured by Semiquantitative Uptake Value measurements as well as against a standard of reference (blood pool activity, physiological muscle uptake).
Measured: 1.5 years
Secondary outcomes (1)
Correlation of FAZA-PET and blood oxygen level-dependent MRI to Pimonidazole staining in locally advanced rectal cancer
Measured: 1.5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Dec 2015 (estimated)
- Study start1 May 2016
- Primary completion9 Jun 2019
- Study completion9 Jun 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Colon Rectal Cancer AdenocarcinomaStudies of the same condition, open and under way.
- More trials run by University Health Network, TorontoThe 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
- 8 participants (actual)
- Target duration
- 1 Month
Sponsor and investigators
- Lead sponsor
- University Health Network, Toronto
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Catherine O'Brien, MD, Principal investigator, University Health Network, TorontoUr Metser, MD, Principal investigator, University Health Network, Toronto
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02624115
- Sponsor's protocol ID
- 15-9741
- Status last verified
- Aug 2019
- First submitted
- 25 Nov 2015
- Last updated
- 16 Aug 2019
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 16 Aug 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- 18F-Fluoroazomycin Arabinoside (FAZA) Positron Emission Tomography/Magnetic Imaging Resonance (PET/MRI) as a Biomarker of Hypoxia in Rectal Cancer: A Pilot Study
- ClinicalTrials.gov ID
- NCT02624115
- Acronym / sponsor ID
- 15-9741
- Conditions
- Colon Rectal Cancer Adenocarcinoma
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 8 participants (actual)
- Lead sponsor
- University Health Network, TorontoUniversity, hospital or other
- Study start
- 1 May 2016 (actual)
- Primary completion
- 9 Jun 2019 (actual)
- Study completion
- 9 Jun 2019 (actual)
- First posted
- 8 Dec 2015 (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.
Colorectal cancer (CRC) is one of the leading causes of cancer mortality in Canada. Rectal cancers are now known to be hypoxic which is a negative prognostic factor and predictive of metastatic spread and poor responsiveness to treatment. This has also been shown in preclinical xenograft models. Hence there is a need for identification of hypoxic rectal cancers.
In this pilot study the investigators intend to non-invasively assess the tumor and nodal metastasis using an integrated Positron Emission Tomography-Magnetic Resonance Imaging scanner (PET/MRI) with 18F-Fluoroazomycin Arabinoside (18F-FAZA) a radiopharmaceutical for assessing tumor hypoxia. The hypoxic rectal tumors will show an increased uptake of 18F-FAZA on PET which will have morphological correlation on MRI. The patient will then undergo neoadjuvant chemoradiation therapy (CRT) followed by repeat 18F-FAZA PET/MRI and rectal cancer surgery with pimonidazole staining. Pimonidazole is an extrinsic marker of hypoxia that is selectively reduced and covalently bound to intracellular macromolecules in areas of hypoxia within normal and tumor tissue with current approval for use in humans for research studies.
The primary goal of this pilot trial is to validate FAZA-PET as a biomarker of hypoxia by correlating its uptake in rectal tumors to pimonidazole staining in histopathology specimens. If the investigators pilot study successfully demonstrates the uptake and correlation of pimonidazole and FAZA-PET, the investigators would like to initiate a larger study examining hypoxia in rectal cancer. The investigators aims would be to image patients with locally advanced rectal cancer before CRT to ascertain whether high FAZA-PET uptake correlates with poor outcome to CRT. The ability to preoperatively predict the patient sub-population that will respond best to CRT, will help to identify the "complete pathological" responders and avoid unnecessary surgery. Furthermore, the FAZA-PET high subset of patients may benefit from other treatment strategies including clinical trials of anti-hypoxic agents.
Detailed description
Colorectal cancer (CRC) is one of the leading causes of cancer mortality in Canada. Rectal cancers are now known to be hypoxic which is a negative prognostic factor and predictive of metastatic spread and poor responsiveness to treatment. This has also been shown in preclinical xenograft models. Hence there is a need for identification of hypoxic rectal cancers.
In this pilot study, the investigators intend to non-invasively assess the tumor and nodal metastasis using an integrated PET/MRI with a radiopharmaceutical for assessing tumor hypoxia. The hypoxic rectal tumors will show increased uptake of 18F-FAZA on PET which will have morphological correlation on MRI. The patient will then undergo neoadjuvant chemoradiation therapy (CRT) followed by repeat 18F-FAZA PET/MRI and rectal cancer surgery with pimonidazole staining. Pimonidazole is an extrinsic marker of hypoxia that is selectively reduced and covalently bound to intracellular macromolecules in areas of hypoxia within normal and tumor tissue with current approval for use in humans for research studies.
The primary goal of this pilot trial is to validate FAZA-PET as a biomarker of hypoxia by correlating its uptake in rectal tumors to pimonidazole staining in histopathology specimens. If this pilot study successfully demonstrates the uptake and correlation of pimonidazole and FAZA-PET, the investigators would like to initiate a larger study examining hypoxia in rectal cancer. The aim would be to image patients with locally advanced rectal cancer before CRT to ascertain whether high FAZA-PET uptake correlates with poor outcome to CRT. The ability to preoperatively predict the patient subpopulation that will respond best to CRT, will help to identify the "complete pathological" responders and avoid unnecessary surgery. Furthermore, the FAZA-PET high subset of patients may benefit from other treatment strategies including clinical trials of anti-hypoxic agents.
Project Synopsis: STUDY OVERVIEW:
OBJECTIVES:
Primary Objective
- To determine the feasibility of using the FAZA-PET to image primary tumor hypoxia in patients with rectal cancer prior to treatment with chemoradiotherapy Secondary Objectives
- To optimize FAZA PET/MRI imaging protocol for use in patients with rectal cancer.
- To determine whether there is correlation between FAZA-PET, blood oxygen level-dependent MRI and Pimonidazole staining in primary rectal tumors before and after CRT.
- To correlate hypoxia defined by FAZA PET uptake and blood oxygen level-dependent MRI in rectal cancer with (pathologic) response to neoadjuvant chemoradiotherapy.
Study design: Single arm feasibility pilot study Study scheme: (see below)
Details on Tumor Microscopy and Pimonidazole Image analysis:
The initial assessment of pimonidazole-detected hypoxia in tumor sections from surgical specimens will be immunohistochemical which allows for both qualitative and quantitative assessment of pimonidazole staining in the context of histopathological morphology. To account for heterogeneity of pimonidazole staining, analysis will be performed in multiple surgical sections for each patient tumor (as previously published by the investigators own group). All staining, handling and processing of tissue specimens will done by the pathology department.
STUDY SCHEMA:
Target Population:
- Age ≥ 18 years
- Histological diagnosis of rectal cancer
- Intent to treat with neoadjuvant chemoradiotherapy and surgery
- Negative pregnancy test (for females in child bearing age)
- Informed Consent
- FAZA-PET/MRI
- Void bladder
- FAZA injection
- Dynamic PET acquisition with MRI Dixon sequences for attenuation correction (60 min; optional )
- 60 minute uptake time (rest)
- Void bladder
- Static PET/MRI pelvis (approximately 45 min)
- Standard treatment (neoadjuvant chemoradiotherapy
- Oral Pimonidazole on day prior to surgery
- Surgery
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Month
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with rectal cancer undergoing neoadjuvant chemoradiotherapy
Key inclusion criteria (6 listed)
- Patients will be eligible for inclusion in this study if they meet all of the following criteria:
- Age ≥18 years
- Histologic proven locally advanced rectal cancer (T3-T4, or N1) based on clinical assessment and standard staging procedures.
- Intention to treat with neoadjuvant chemoradiotherapy prior to surgery, according to the current institutional treatment policies.
- A negative urine or serum pregnancy test within the two week interval immediately prior to imaging, in women of child-bearing age.
Key exclusion criteria (5 listed)
- Patients will be ineligible to participate in this study if they meet any of the following criteria:
- Contraindication for MR as per current institutional guidelines.
- Inability to lie supine for at least 45 minutes.
- Contraindication for administration of pimonidazole (allergy)
- Any patient who is pregnant or breastfeeding.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
FAZA PET uptake in locally advanced rectal cancers prior to and after chemoradiotherapy
Time frame: 1.5 years
FAZA uptake will be measured by Semiquantitative Uptake Value measurements as well as against a standard of reference (blood pool activity, physiological muscle uptake).
1 secondary outcome
Correlation of FAZA-PET and blood oxygen level-dependent MRI to Pimonidazole staining in locally advanced rectal cancer
Time frame: 1.5 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Aug 2019.
- Individual participant dataSharing planned: Undecided
Related trials for Colon Rectal Cancer Adenocarcinoma
Not yet recruitingPhase 1
Hepatic Artery Infusion of Carfilzomib in Participants With Liver Metastatic Disease Previously Treated With Hepatic Artery Infusion Pump Therapy
Colorectal Neoplasms, Neoplasms
Recruiting
The Vanguard Study: Testing a New Way to Screen for Cancer
Bladder Carcinoma, Breast Carcinoma
RecruitingPhase 1
A Study of ERAS-0015 in Patients With Advanced or Metastatic Solid Tumors
Metastatic Solid Tumors
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
Active, not recruitingPhase 2
Perioperative Cadonilimab (AK104) in Locally Advanced MSI-H/dMMR Gastric or Gastroesophageal Junction and Colorectal Adenocarcinoma
MSI-H/dMMR Gastric Carcinoma and Colorectal Cancer
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.
Catherine O'Brien, MD principal investigator
University Health Network, Toronto
Ur Metser, MD principal investigator
University Health Network, Toronto
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 Colon Rectal Cancer Adenocarcinoma, run by University Health Network, Toronto 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 6 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: finished, as of the sponsor's last update on 16 Aug 2019. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
FAZA PET uptake in locally advanced rectal cancers prior to and after chemoradiotherapy (time frame: 1.5 years). 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 16 Aug 2019.