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Imaging Brain Tumors With FACBC and Methionine

Imaging Brain Tumors With FACBC and Methionine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00597246
Enrollment
30
Registered
2008-01-18
Start date
2003-05-13
Completion date
2019-11-27
Last updated
2020-12-17

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

Conditions

Brain Cancer, CNS Cancer

Keywords

Brain, CNS, Central Nervous System

Brief summary

This research protocol makes pictures of brain tumors. The pictures are made with a positron emission tomography (PET) scanner. PET scans use radioactivity to see cancer cells. We are using a new kind of PET scan. The new PET scan is called \[18F\]-FACBC PET. We will compare this to the standard PET scan. The standard PET scan is called \[11C\]-methionine PET. We expect these pictures will give us information about your tumor. We also hope to collect information about the amount of radioactivity exposure. We will measure radioactivity exposure to your tumor, brain and other organs. The research study results will be used to support the submission of an investigational new drug (IND) application to the Food and Drug Administration (FDA).

Detailed description

The purpose of this research is to: 1) perform both 3-\[18F\]-FACBC and \[11C-methyl\]-Lmethionine brain tumor PET imaging studies in patients with primary brain tumors who have previously been treated and are now suspect for having recurrence or progression of disease (a pilot study, n=20); 2) perform only 3-\[18F\]-FACBC PET imaging studies on an additional set of patients with primary brain tumors who have previously been treated and are now suspect for having recurrence (n=10) . 3) obtain organ/tissue and body radiation dosimetry information following i.v. injection of 3-\[18F\]-FACBC; 4) look for potential correlations between the scan results obtained from those patients enrolled to 03-028 and the patients' past medical treatment; The first set of 20 patients will agree to two PET studies. One study will involve the i.v. administration of a fluorine-18 labeled amino acid analogue, 3-fluoro-aminocyclobutane carboxylic acid (3-\[18F\]-FACBC) with sequential brain and body PET imaging. The second study will involve i.v. administration of \[11C-methyl\]-L-methionine and head imaging only. The additional set of 10 patients will undergo one PET study which will consist of the i.v. administration of fluorine-18 labeled amino acid analogue, 3-fluoro-aminocyclobutane carboxylic acid (3-\[18F\]-FACBC) with one brain scan and one body scan only. The 3-\[18F\]-FACBC PET studies (n=30) will be performed under the Radioactive Drug Research Committee (RDRC) guidelines as defined and established by the Federal Drug Administration (FDA). \[11C-methyl\]-L-methionine is in the hospital formulary and is approved for imaging brain tumors at MSKCC. Our hypotheses include: 1) \[18F\]-FACBC has equal or better brain tumor imaging characteristics compared to \[11C\]-methionine; 2) \[18F\]-FACBC is not metabolized, and radiolabeled metabolites will not confound the interpretation of the images as can be the case with \[11C\]-methionine; 3) imaging recurrent brain tumors with \[18F\]-FACBC will be enhanced by lower brain (background) activity as compared to corresponding \[11C\]- methionine images; 4) the biodistribution of \[18F\]-FACBC and radiation dosimetry following i.v. administration of a 370 MBq (10 mCi) dose is safe and within FDA guidelines; 5) a 370 MBq (10 mCi) dose of \[18F\]-FACBC is sufficient for imaging brain tumors in a clinical setting; 6) the accumulation of \[18F\]-FACBC will correlate with the patients response to prior treatment and will provide prognostic information with respect to tumor progression and survival.

Interventions

DRUGFACBC, Methionine

F-18 labeled FACBC is prepared stereo-specifically in a semi-automated, NCA procedure utilizing the General Electric FDG MicroLab, a system employing a quaternary 4-aminopyridinium resin to effect F-18 fluorination. The triflate species is displaced with F-18 fluoride in the MicroLab, and then the 1-t-butyl carbamate-3- trifluoromethane sulfonoxy-1-cyclobutane-1-carboxylic acid methyl ester is hydrolyzed with 1 N HCl. The final product is isotonic and sterile, and has been utilized in animal experiments. The product was obtained in 30% radiochemical yield after 65 minutes from EOB. The radiochemical purity was greater than 95% and no preparative HPLC was required. The procedure could be considered routine, and is performed on the FDG synthetic module without changes either to the programming or to the cassettes.

OTHERPET Scan

GE Advance PET scanner for sequential body imaging

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Registered patient at MSKCC. * Child-bearing age females must be non-pregnant, non-lactating, and must be using adequate contraception or surgically sterile. * Karnofsky score of 60 or greater. * Children that can sit still for 60-90 minutes, without sedation, will be included in this protocol.

Exclusion criteria

* Patient cannot tolerate lying still for 90 minute sessions in the PET tomograph.

Design outcomes

Primary

MeasureTime frameDescription
Maximum Standardized Uptake Value of 3-[18F]-FACBCDuration of scan, an average of 1 hourDetermine clearance of 3-\[18F\]-FACBC in different tissues/organs of body.

Secondary

MeasureTime frameDescription
Rate of 18F-Fluciclovine Transport (k1) Into TumorsDuration of scan, an average of 1 hourLook for potential correlations bet subsequent MR & PET results obtained from patients enrolled and patients' subsequent medical treatment, progression of tumor & survival.

Countries

United States

Participant flow

Participants by arm

ArmCount
Participants With Brain Tumors
FACBC, Methionine: F-18 labeled FACBC is prepared stereo-specifically in a semi-automated, NCA procedure utilizing the General Electric FDG MicroLab, a system employing a quaternary 4-aminopyridinium resin to effect F-18 fluorination. The triflate species is displaced with F-18 fluoride in the MicroLab, and then the 1-t-butyl carbamate-3- trifluoromethane sulfonoxy-1-cyclobutane-1-carboxylic acid methyl ester is hydrolyzed with 1 N HCl. The final product is isotonic and sterile, and has been utilized in animal experiments. The product was obtained in 30% radiochemical yield after 65 minutes from EOB. The radiochemical purity was greater than 95% and no preparative HPLC was required. The procedure could be considered routine, and is performed on the FDG synthetic module without changes either to the programming or to the cassettes. PET Scan: GE Advance PET scanner for sequential body imaging
30
Total30

Baseline characteristics

CharacteristicParticipants With Brain Tumors
Age, Continuous54 years
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
29 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
1 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
2 Participants
Race (NIH/OMB)
White
27 Participants
Region of Enrollment
United States
30 Participants
Sex: Female, Male
Female
9 Participants
Sex: Female, Male
Male
21 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
29 / 30
other
Total, other adverse events
2 / 30
serious
Total, serious adverse events
0 / 30

Outcome results

Primary

Maximum Standardized Uptake Value of 3-[18F]-FACBC

Determine clearance of 3-\[18F\]-FACBC in different tissues/organs of body.

Time frame: Duration of scan, an average of 1 hour

Population: 3 participants did not receive 18F-Fluciclovine PET studies

ArmMeasureValue (MEAN)Dispersion
Participants With Brain TumorsMaximum Standardized Uptake Value of 3-[18F]-FACBC4.5 SUVmaxStandard Deviation 2.3
Secondary

Rate of 18F-Fluciclovine Transport (k1) Into Tumors

Look for potential correlations bet subsequent MR & PET results obtained from patients enrolled and patients' subsequent medical treatment, progression of tumor & survival.

Time frame: Duration of scan, an average of 1 hour

Population: 3 participants did not receive PET scans

ArmMeasureValue (MEAN)Dispersion
Participants With Brain TumorsRate of 18F-Fluciclovine Transport (k1) Into Tumors0.14 mL/min/gStandard Deviation 0.24

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026