Hyperpolarized 13C Pyruvate MRI for Early Immune Evaluation in Cervical Cancer Patients at Baseline and CCRT Therapy
Primary Purpose
Cervical Cancer
Status
Recruiting
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
Hyperpolarized 13C Pyruvate
Sponsored by
About this trial
This is an interventional diagnostic trial for Cervical Cancer focused on measuring Hyperpolarized 13C pyruvate, Dynamic nuclear polarization, Artificial intelligence, Cervical cancer, Magnetic resonance fingerprinting, Precision medicine, Radiomics
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed carcinoma of the uterine cervix.
- Age ≥ 20 years.
- Clinical International Federation of Gynecology and Obstetrics (FIGO) stage IB2-IV.
- Tumor diameter ≥ 4 cm, verified by MRI or CT.
- Scheduled curative-intent non-surgical treatment.
Exclusion Criteria:
- Contraindication to MRI study (e.g. claustrophobia, cardiac pacemaker, metal implants in pelvis).
- Inadequate marrow, liver and renal functions.
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- Pregnant or breast-feeding women.
Sites / Locations
- Chang Gung Memorial HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Hyperpolarized 13C pyruvate DNP-MRI scan
Arm Description
Patients receive hyperpolarized 13C pyruvate through IV injection less than 1-2 minute then undergo MRI over 3-5 minutes at baseline and 2 weeks after CCRT treatment. Total 2 times of MRI scan.
Outcomes
Primary Outcome Measures
MRI size measurement of the primary tumor
Tumor size measurement by regular MRI
Secondary Outcome Measures
Recurrent rate
Follow-up recurrent rate
Full Information
NCT ID
NCT04951921
First Posted
June 21, 2021
Last Updated
March 2, 2023
Sponsor
Chang Gung Memorial Hospital
Collaborators
Ministry of Science and Technology, Taiwan
1. Study Identification
Unique Protocol Identification Number
NCT04951921
Brief Title
Hyperpolarized 13C Pyruvate MRI for Early Immune Evaluation in Cervical Cancer Patients at Baseline and CCRT Therapy
Official Title
Precision Medicine Imaging for Cervical Cancer: Integrating MR Fingerprinting, Dynamic Nuclear Polarization (DNP)-MRI and Artificial Intelligence Radiomics
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 15, 2021 (Actual)
Primary Completion Date
July 31, 2024 (Anticipated)
Study Completion Date
July 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chang Gung Memorial Hospital
Collaborators
Ministry of Science and Technology, Taiwan
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In this single armed, single-center, case-controlled study, the investigators will conduct a prospective trial and integrate the most advanced imaging technology to medical practice, attempting to solve the problem detected by radiomics approach. The investigators plan a 3-year project with non-randomized, single group assignment observational study design. Thirty participants with diagnosed LACC that are to receive CCRT are to be recruited for this prospective single institutional study from Chang Gung Memorial Hospital at Linkou (CGMH). Standard-of-care MRI/CT that is required for staging will be the first line screening method. A tumor biopsy and routine blood test will be obtained at the time of the initial clinic visit. Participants eligible for this study will receive two investigative exams-MRF, CEST, DNP-MRI MRI and Metabolomics, at baseline and the 2-week during CCRT.
The new imaging methods being tested are MRF and CEST without contrast enhancement, and DNP-MRI which provides quantitative measurement of the metabolism occurring within cancer cells. It also involves injection of a contrast agent-Hyperpolarized pyruvate (13C) Injection. The participants will be injected with the study drug at a dose of 0.43 ml/kg and then receive MRI scan.
Detailed Description
Primary objective
Bridging the Gap between Imaging and Biology. DNP is the only technology that can measure real-time flux of pyruvate to lactate conversion and mitochondria metabolism. DNP-MRI will combine the strength of MRI (anatomy, tissue contrast via MRF, CEST and DWI) and DNP (biochemistry measurement), and the blood/urine metabolomics approach, to noninvasively bring more insightful information for clinical application.
Precision Medicine for Precision Response Prediction. Although AI or deep learning can identify high-risk patient for particularly treatment (CCRT in this project), the predictive model is based on prior database rather than this particular patient. The investigators urgently need a non-invasive precise measurement to monitor the response in a real-world situation, to reduce the treatment uncertainty, to select the most cost-effective treatment. This is of paramount importance for the more advanced treatment i.e. target therapy, immunotherapy etc. The investigators did not intend to change the standard-of-care but the information provided by this study will help to investigate the fundamental mechanisms hence providing hopes for alternative treatments.
Infrastructures for MR Fingerprinting and Dynamic Nuclear Polarization (DNP)-MRI Research for Taiwanese researchers. The investigators are very grateful to be able to install the first DNP system dedicated to human research in Asia and would like to introduce this novel technology to Taiwan. Currently, human DNP study has only been conducted in the USA (UCSF, MD Anderson Cancer Center and Memorial Sloan-Kettering Cancer Center) and the UK (University College of London, Oxford and Cambridge) and Canada (Toronto University). Based on our preliminary efforts of tracer preparation, multi-nuclei scanning equipment and dedicated pulse sequences, the investigators aim to build infrastructures for MR Fingerprinting and DNP-MRI Research for Taiwanese research groups.
Secondary objective
Translate technical advancements to clinically applicable tools
Converge integrated information to construct the prediction model
Establish the delta radiomics prediction model with biological meaningfulness
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer
Keywords
Hyperpolarized 13C pyruvate, Dynamic nuclear polarization, Artificial intelligence, Cervical cancer, Magnetic resonance fingerprinting, Precision medicine, Radiomics
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Hyperpolarized 13C pyruvate DNP-MRI scan
Arm Type
Experimental
Arm Description
Patients receive hyperpolarized 13C pyruvate through IV injection less than 1-2 minute then undergo MRI over 3-5 minutes at baseline and 2 weeks after CCRT treatment. Total 2 times of MRI scan.
Intervention Type
Drug
Intervention Name(s)
Hyperpolarized 13C Pyruvate
Other Intervention Name(s)
Hyperpolarized Carbon C 13 Pyruvate, Hyperpolarized Pyruvate (13C)
Intervention Description
Procedure: Magnetic Resonance Imaging Undergo 1H-MRI of DWI/MRF/CEST for tumor cite following by 13C DNP-MRI for spleen for 3-5 minutes after hyperpolarized 13C pyruvate injection
Primary Outcome Measure Information:
Title
MRI size measurement of the primary tumor
Description
Tumor size measurement by regular MRI
Time Frame
Change from baseline in tumor size at 3 months
Secondary Outcome Measure Information:
Title
Recurrent rate
Description
Follow-up recurrent rate
Time Frame
Follow-up for 5 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed carcinoma of the uterine cervix.
Age ≥ 20 years.
Clinical International Federation of Gynecology and Obstetrics (FIGO) stage IB2-IV.
Tumor diameter ≥ 4 cm, verified by MRI or CT.
Scheduled curative-intent non-surgical treatment.
Exclusion Criteria:
Contraindication to MRI study (e.g. claustrophobia, cardiac pacemaker, metal implants in pelvis).
Inadequate marrow, liver and renal functions.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Pregnant or breast-feeding women.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gigin Lin, MD, PhD
Phone
886-3-3281200
Ext
2575
Email
giginlin@cgmh.org.tw
First Name & Middle Initial & Last Name or Official Title & Degree
Kuan-Ying Lu, MS
Phone
886-3-3281200
Ext
2602
Email
fantacy52317@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gigin Lin, MD, PhD
Organizational Affiliation
Chang Gung Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chang Gung Memorial Hospital
City
Taoyuan City
State/Province
Guishan District
ZIP/Postal Code
333
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gigin Lin, MD, PhD
Phone
886-3-3281200
Ext
2575
Email
giginlin@cgmh.org.tw
First Name & Middle Initial & Last Name & Degree
Kuan-Ying Lu, MS
Phone
886-3-3281200
Ext
2602
Email
fantacy52317@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Hyperpolarized 13C Pyruvate MRI for Early Immune Evaluation in Cervical Cancer Patients at Baseline and CCRT Therapy
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