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Developing a New MRI Technique to Understand Changes in Brain Tumors After Treatment

Development of a Clinical CEST MR Fingerprinting Method for Treatment Response Assessment in Brain Metastases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05559853
Enrollment
119
Registered
2022-09-29
Start date
2022-09-22
Completion date
2027-09-22
Last updated
2026-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Metastases, Brain Metastases, Adult, Metastatic Brain Cancer, Metastatic Brain Tumor

Keywords

Brain Metastases, Healthy Volunteers, metastatic brain tumor, metastatic brain cancer, Brain Metastases, Adult, MRI, untreated brain metastasis, CEST-MRF, chemical exchange saturation transfer magnetic resonance fingerprinting, 22-191, Memorial Sloan Kettering Cancer Center

Brief summary

The purpose of this study is to develop and test a new magnetic resonance imaging (MRI) technique to see if it can be used to tell the difference between tumor growth from worsening of cancer and growth from the effects of treatment in participants who have brain tumors treated with radiation therapy called stereotactic radiosurgery (SRS).

Interventions

DIAGNOSTIC_TESTCEST-MRF

CEST-MRF enables accurate quantification of both proton exchange rates and volume fractions in a fraction of the time required by conventional pulse sequences will be developed and optimized.

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Healthy volunteers \[for Study Aim 1 (SA1) and Study Aim 2 (SA2)\] will be entered into the study if they meet the following criteria: * Age ≥ 18 years * Able to understand and give informed consent * No known cancer diagnosis Patients \[for Study Aim 1 (SA1)\] will be entered into the study if they meet the following criteria: * Age ≥ 18 years * Able to understand and give informed consent * At least one untreated brain metastasis \> 1cm (e.g., an enhancing lesion in the brain of a patient with known systemic cancer determined likely to represent metastasis by neuroradiologist) Patients \[for Study Aim 3 (SA3)\] will be entered into the study if they meet the following criteria: * Age ≥ 18 years * Able to understand and give informed consent * At least one untreated brain metastasis \> 1cm (e.g., an enhancing lesion in the brain of a patient with known systemic cancer determined likely to represent metastasis by neuroradiologist) * Planned SRS treatment

Exclusion criteria

Healthy volunteers (SA1 \& SA2) and patients (SA1 \& SA3)

Design outcomes

Primary

MeasureTime frameDescription
Change of Rapid chemical exchange saturation transfer (CEST) imaging with magnetic resonance fingerprinting (MRF)/CEST-MRF parameters with and without motionUp to 3 yearsDevelop a rapid and robust 3D CEST-MRF pulse sequence for clinical scanners using our preclinical CEST-MRF pulse sequence as a basis by evaluating the changes of the 6 CEST-MRF parameters with and without motion. These parameters include the water T1 and T2 relaxation (T1w,T2w), amide exchange rate (ksw) and volume fraction (fs) and the semi-solid exchange rate (kssw) and volume fraction (fss).

Secondary

MeasureTime frameDescription
Create CEST-MRF parameter mapsUp to 3 yearsDevelop an MRI physics-guided artificial intelligence approach to improve acquisition and reconstruction of multiparametric data
Measure longitudinal changes in CEST-MRF after SRSUp to 3 yearsEvaluate CEST-MRF changes before and after radiation therapy to assess potential role as predictive imaging biomarker for brain metastases

Countries

United States

Contacts

CONTACTOuri Cohen, PhD
coheno1@mskcc.org646-608-8259
CONTACTNelson Moss, MD
mossn@mskcc.org212-639-7075
PRINCIPAL_INVESTIGATOROuri Cohen, PhD

Memorial Sloan Kettering Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026