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FDG PET/CT in Monitoring Very Early Therapy Response in Patients With Glioblastoma

Very Early Response Monitoring in Patients With Glioblastoma Undergoing Therapy Using FDG PET/CT

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02902757
Enrollment
7
Registered
2016-09-16
Start date
2015-08-25
Completion date
2025-01-29
Last updated
2026-07-17

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

Conditions

Glioblastoma

Keywords

FDG, PET/CT very early response (48 hrs)

Brief summary

This pilot clinical trial studies fluordeoxyglucose (fludeoxyglucose) F-18 (FDG) positron emission tomography (PET)/computed tomography (CT) in monitoring very early therapy response in patients with glioblastoma. Diagnostic procedures, such as FDG PET/CT, may help measure a patient's response to earlier treatment. Chemotherapy can induce very rapid changes to the tumor's glucose consumption which can be measured with imaging. FDG PET/CT shortly after the start of therapy may help identify very early therapy response in patients with glioblastoma.

Detailed description

PRIMARY OBJECTIVES: I. To assess very early response to therapy in glioblastoma patients using 18F-FDG PET/CT. II. Evaluate very early changes in FDG uptake within 48 hours of start of therapy and correlate them with objective response parameters such as Response Assessment in Neuro-Oncology (RANO) and survival. OUTLINE: Patients undergo standard FDG PET/CT scan 6-8 weeks before start of chemotherapy and one additional FDG PET/CT scan within 48 hours of the start of chemotherapy.

Interventions

PROCEDUREComputed Tomography

Undergo FDG PET/CT

RADIATIONFludeoxyglucose F-18

Undergo FDG PET/CT

PROCEDUREPositron Emission Tomography

Undergo FDG PET/CT

Sponsors

Jonsson Comprehensive Cancer Center
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH
National Institutes of Health (NIH)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Patients with histologically proven high grade glioma * Intention to start therapy

Exclusion criteria

* Severe psychiatric illness * Inability to give written consent * Breast feeding / pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Changes in glucose uptakeFrom baseline up to 48 hoursStandardized uptake values (SUV) will be calculated for different organs and for regions of tumor. Further, regional target to background count-activity ratios will be established.
Very early changes in tumor glucose uptake predictive for objective treatments response and survival assessed using RANO criteriaOne PET/CT 48 hours after start of therapySUV will be calculated for different organs and for regions of tumor. Further, regional target to background count-activity ratios will be established.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJohannes Czernin, MD

UCLA / Jonsson Comprehensive Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 18, 2026