18F-Fluciclovine (Axumin) PET/CT for Detecting True- versus Pseudo-Progression of Brain Metastases in Patients Receiving Immunotherapy

Inclusion Criteria

• Age ≥ 18 years * Because no dosing or adverse event data are currently available on the use of Axumin in pediatric patients, patients < 18 years of age are excluded from this study
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥ 60%)
• Willingness to participate in the study and ability to provide written informed consent
• Patients must have documented brain metastatic lesion(s) in the medical record
• On active immunotherapy for the diagnosed malignancy. Concurrent other treatment is allowed. Immunotherapy and other treatment regimens are determined by treating physicians as per standard clinical practice
• Patients with at least one metastatic brain lesion showing suspected pseudoprogression on SoC imaging modality (such as CT, or MRI, or fludeoxyglucose F-18 [FDG] PET-CT, or dodecanetetraacetic acid Tyr3-octreotate [DOTATATE] PET/CT, or prostate specific membrane antigen [PSMA] PET/CT)
• The suspected pseudoprogression can be determined by imaging physician (such as neuroradiologists and/or nuclear medicine physicians) and/or treating physicians (usually are oncologists). Ideally, the target/index lesion should be measurable (at discretion of investigator imaging physicians) and feasible for series follow up and comparison at imaging physician’s discretion
• Ability and willingness to undergo another follow up fluciclovine PET/CT, usually within 60 days of SoC follow up imaging modality
• Ability and willingness to undergo biopsy if needed per standard of care
• Estimated life expectancy of at least 3 months as determined by the investigator or treating physician

Exclusion Criteria

• Pregnant or breastfeeding during participation in the study are excluded because: There is no information on the risk of adverse developmental outcomes in pregnant women or animals with the use of fluciclovine F18. All radiopharmaceuticals, including Axumin, have the potential to cause fetal harm depending on the fetal stage of development and the magnitude of the radiation dose; There is no information on the presence of fluciclovine F18 in human milk, the effect on the breastfed infant, or the effect on milk production
• History of severe allergic reactions to Axumin PET radiopharmaceuticals. Mild to moderate reactions that can be controlled by medications prior to the scheduled PET/CT are acceptable
• Patients with psychiatric illness/social situations that would limit compliance with study requirements
• Unable to lie flat during or tolerate PET-CT
• Contraindications to Axumin injection have not been established in humans. None are known or have been observed in nonclinical or clinical studies performed to date
• Subjects with any medical condition or circumstance that the investigator believes may compromise the safety or compliance of the subject to produce reliable data or completing the study