[18F]Fluciclovine and [18F]FLT PET/CT Assessment of Primary High-Grade Brain Tumors

The standard treatment approach for patients with high-grade primary brain tumors includes
maximum feasible surgical resection, followed by 6 weeks of concurrent cranial irradiation,
and daily low-dose temozolomide chemotherapy; followed by 12 cycles of high-dose temozolomide
administered for 5 consecutive days every 4 weeks (Stupp et al., 2005). Contrast-enhanced MRI
is the current standard for evaluating the success of therapy and monitoring for tumor
recurrence. MRI is typically obtained prior to initial surgery, within 24 hours after
surgery, at the conclusions of cranial irradiation, and then every 8 weeks during
temozolomide chemotherapy until evidence of recurrence. Despite this careful clinical and
radiographic surveillance, and despite decades of research into the histologic and molecular
classification of primary brain tumors, our ability to predict tumor behavior remains very
limited. Some gliomas will result in overall survival times of only months, whereas other
histologically-identical gliomas may yield survivals of years to decades (Curran et al.,
1993, Carson et al., 2007). Current assessment of tumor response to therapy is also poor.
Patients with complete radiographic response after cranial irradiation often progress rapidly
post-irradiation. In contrast, some patients with enhancing masses at the end of
chemoradiotherapy may respond dramatically to further chemotherapy alone; or the masses may
even disappear in the absence of further therapy, so called "tumor pseudoprogression"
(Chamberlain et al., 2007). This confounding situation demonstrates a need for better
assessment of tumor response.

Improvements in the ability to predict tumor behavior prior to the start of therapy would
allow more efficient and effective tumor surveillance; better prognostication; and more
appropriate assignment of patients to conventional, aggressive, or investigational therapies
early in their clinical courses. This would provide huge economic and social benefits, and
could afford decisive insights into brain tumor physiology and biology.

Similarly, the ability to identify, earlier and more accurately, whether individual patients
were responding to therapy would allow prompt discontinuation of ineffectual treatments and
institution of potentially more effective therapies.

Previous efforts using imaging for such tasks have generally been limited to a single
modality (e.g. MRI) and/or single-tracer (e.g. FDG-PET). However, there is a significant and
growing body of evidence that complementary imaging of multiple aspects of tumor physiology
(i.e. using multiple PET tracers) can provide greatly enhanced information over imaging with
a single modality or tracer alone. In solid tumors, complex interactions exist between blood
flow, metabolic activity, and oxygen status which affect metastatic and proliferative
activity. Heterogeneous tumors may contain both slow-growing and fast-growing regions that
present different profiles of proliferation rates and amino acid uptake.

Inclusion Criteria:

- Two adult patient groups will be eligible for inclusion in this study:

Group A: Patients where there is compelling evidence, based on the MRI and/or CT imaging,
that a high-grade primary brain tumor is present. Pathologic confirmation will occur with
biopsy or surgery.

Patients whose tumor is felt to be inoperable and a biopsy is performed but no surgery.

Patients with a newly diagnosed primary malignant brain tumor (WHO Grade III or IV) who
will be receiving chemoradiation and who either did not undergo surgical resection or
underwent incomplete resection with residual tumor > 1.0 cm in greatest diameter by
contrast MRI postoperatively.

Group B: Patients with pathologically proven malignant brain tumor (WHO Grade III or IV
glial-based tumors) who have undergone chemoradiation and have MRI-documented possible
recurrence/progression versus treatment effect (pseudoprogression) within 6 months from the
time of completion of chemoradiation.

- Patients must be 18 years or older for inclusion in this study. There is little
experience with the safety of [18F]FLT or [18F]Fluciclovine in children, and the risks
associated with radiation exposure may be increased for children under 18 years old as
well.

- Patients must document their willingness to be followed for at least 24 months after
recruitment by signing informed consent documenting their agreement to have clinical
endpoints and the results of histopathologic tissue analysis (when tissue becomes
available from routine care) entered into a research database.

- All patients, or their legal guardians, must sign a written informed consent and HIPAA
authorization in accordance with institutional guidelines.

- Determination of pregnancy status: Female patients who are not postmenopausal or
surgically sterile will undergo a serum pregnancy test prior to each set of [18F]FLT
and [18F]Fluciclovine PET scans. A negative test will be necessary for such patients
to undergo research PET imaging.

- Pre-imaging laboratory tests must be performed within 28 days prior to the [18F]FLT
imaging procedure. These must be less than 4.0 times below or above the upper or lower
limit range for the respective laboratory test for entry into the study (unless
clinically not relevant). In those instances where a laboratory value is outside of
this range, then such a patient will be ineligible for enrollment unless at the
discretion of the PI the abnormal lab value is of no clinical significance to the
safety or integrity of the study results. . For follow-up scanning sessions after
therapy has been instituted, laboratory testing will also be required due to the use
of [18F]FLT. The patients have brain tumors and will have received chemoradiation;
therefore, many routine laboratory tests may not be within the typical normal range.
As such, a factor of 4.0 times above or below the upper or lower value for the normal
range for any laboratory test will also be used to determine the acceptable range for
the 2nd and possibly 3rd imaging time points (unless clinically not relevant as
explained above). The baseline laboratory testing will include liver enzymes (ALT,
AST), bilirubin (total), serum electrolytes, CBC with platelets, prothrombin time,
partial thromboplastin time, BUN, and creatinine. For those patients receiving
coumadin or another anticoagulant the upper limit for prothrombin time or partial
thromboplastin time must not exceed 6 times the upper limit of the normal range.
(Appendix E, Laboratory Study Results).

Exclusion Criteria:

- Patients with clinically significant signs of uncal herniation, such as acute
pupillary enlargement, rapidly developing motor changes (over hours), or rapidly
decreasing level of consciousness, are not eligible.

- Patients with known allergic or hypersensitivity reactions to previously administered
radiopharmaceuticals. Patients with significant drug or other allergies or autoimmune
diseases may be enrolled at the Investigator's discretion.

- Patients who are pregnant or lactating or who suspect they might be pregnant. Serum
pregnancy tests will be obtained prior to each set of multi-tracer PET scans in female
patients that are not postmenopausal or surgically sterile.

- Adult patients who require monitored anesthesia for PET scanning.

- Patients who are too claustrophobic to undergo PET scanning.

- Known HIV positive patients due to the previous toxicity noted with [18F]FLT in this
patient group.