clinical-application

FDG-PET / CT in Oncology

F-18 fluorodeoxyglucose (FDG) PET / CT is the dominant molecular imaging exam in oncology. FDG — a glucose analog — concentrates in metabolically active cells including most malignancies, and its 511 keV annihilation photons are detected by the PET ring. Combined with the CT for anatomic correlation and attenuation correction. The largest volume PET indication globally; the foundation oncology-imaging workflow that PET / CT installed-base economics depend on.

Clinical indications

Workflow

  1. Patient prep — NPO 4–6 hours, glucose < 200 mg/dL at injection.
  2. Injection — ~10 mCi F-18 FDG IV.
  3. Uptake — 60 min in a quiet shielded uptake room.
  4. CT — low-dose CT for attenuation correction + anatomic localization (sometimes diagnostic-quality contrast CT).
  5. PET acquisition — 6–8 bed positions skull base to mid-thigh, 2–3 min per bed (digital SiPM platforms shorter).
  6. Reconstruction — ToF + iterative (Q.Clear on GE, TrueX / OptisoHD on Siemens, AI-DR / equivalents).
  7. Read + report — SUV-max measurements, staging, comparison to priors, Deauville for lymphoma.

Typical systems

Throughput reality

Scanner throughput rarely limits real-world PET volume. Limits are:

Digital SiPM PET / CT shortens scanner time per patient meaningfully but does not address the upstream bottlenecks.

Equipment considerations that bite

Dose + regulatory

Patient dose ~7–15 mSv (CT + PET combined). Staff dose ALARA — shielded injection, pre-injection room, uptake rooms, control area. NRC or Agreement-State byproduct license required. RSO + Authorized User credentialing mandatory.

Operational reality

Related