NUCLEAR
Whole BodyDemonstration dataFDG PET-CT β Oncology
FDG PET-CT combines the glucose-analogue tracer F-18 FDG with anatomical CT to map tissue glucose metabolism across the body. Malignant cells overexpress GLUT transporters and hexokinase, trapping phosphorylated FDG (FDG-6-phosphate) intracellularly, producing high tumour-to-background contrast. It is central to staging, restaging, response assessment and radiotherapy planning across oncology, with the Deauville 5-point scale used for lymphoma response and PERCIST/EORTC frameworks for quantitative solid-tumour response.
Indications
- Staging and restaging of Hodgkin and aggressive non-Hodgkin lymphoma with interim and end-of-treatment Deauville scoring
- Staging, restaging and treatment response of solid tumours (lung, head and neck, oesophageal, colorectal, melanoma, cervical)
- Characterisation of the indeterminate solitary pulmonary nodule (>8-10 mm)
- Detection of recurrence in the setting of rising tumour markers (e.g. CEA, thyroglobulin) with negative conventional imaging
- Radiotherapy target-volume delineation and identification of an unknown primary with metastatic presentation
Contraindications & Cautions
- Pregnancy is a relative contraindication; defer or justify and minimise dose as FDG crosses the placenta
- Breastfeeding: FDG is minimally excreted in milk but close infant contact should be limited for ~12 h owing to external dose from the mother
- Uncontrolled hyperglycaemia (blood glucose typically >11 mmol/L / 200 mg/dL) reduces tumour uptake and degrades study quality β reschedule
- Recent chemotherapy, granulocyte colony-stimulating factor or radiotherapy cause reactive marrow and inflammatory uptake β allow adequate interval (chemo ~2-3 weeks, radiotherapy ~8-12 weeks)
- Inability to lie still or maintain the pre-scan resting/fasting protocol
Patient Preparation
- Fast 4-6 hours (water only); withhold food, sugary drinks and IV dextrose to lower serum insulin
- Check capillary blood glucose before injection; target <11 mmol/L (200 mg/dL)
- Diabetic patients: schedule early, adjust insulin/oral hypoglycaemics per protocol; avoid short-acting insulin close to injection
- Rest quietly in a warm room after injection to reduce muscle and brown-fat uptake; avoid talking, chewing and exertion for 24 h prior
- Ensure hydration and encourage voiding before imaging to reduce urinary tracer activity
Technique & Parameters
- Administer F-18 FDG ~3-4 MBq/kg (2.5-5 MBq/kg) intravenously after confirming glucose and hydration
- Uptake (incorporation) phase of ~60 minutes resting supine; standardise the interval to keep SUV reproducible
- Acquire integrated PET/CT from skull base to mid-thigh (extend to vertex and lower limbs for melanoma or where indicated)
- Low-dose CT for attenuation correction and localisation; add diagnostic contrast-enhanced CT when required
- Measure SUVmax/SUVpeak normalised to body weight or lean body mass; record uptake time and glucose for comparison studies
Systematic Review
- Confirm injected activity, uptake time and blood glucose β all affect SUV comparability
- Review PET, CT and fused images in three planes; correlate every focus with the CT substrate
- Assess the primary site, regional nodal stations and common metastatic sites (liver, lung, bone, adrenal)
- Recognise physiologic uptake: brain, myocardium, bowel, salivary/vocal, thymus, brown fat, and urinary excretion
- Compare with prior studies using matched SUV methodology; grade lymphoma response on the Deauville 5-point scale
- Screen the CT for incidental non-FDG-avid findings and radiation-relevant anatomy
Key Findings & Significance
- Focal uptake exceeding mediastinal blood pool and liver background suggests viable malignancy
- Deauville 1-2 (uptake at or below mediastinum/liver) is a complete metabolic response; Deauville 4-5 (above liver / markedly increased or new lesions) indicates inadequate response or progression
- Diffusely increased marrow and splenic uptake follows chemotherapy, G-CSF or anaemia β a reactive, not neoplastic, pattern
- Necrotic or mucinous tumours and small (<8-10 mm) or low-grade lesions may be falsely FDG-negative
- Inflammatory and infective processes (sarcoidosis, TB, abscess, post-radiation change) are FDG-avid and mimic tumour
Differential Considerations
- FDG-avid nodes: metastatic disease, lymphoma, reactive/infective adenopathy, sarcoidosis
- Solitary pulmonary nodule uptake: malignancy versus granuloma, infection or organising pneumonia
- Diffuse marrow uptake: G-CSF/chemotherapy effect, anaemia, myeloproliferative disease, marrow infiltration
- Bowel uptake: physiologic, metformin effect, inflammatory bowel disease, polyp or primary tumour
- Focal thyroid incidentaloma uptake: ~30% malignancy risk β recommend ultrasound and correlation
Pearls & Pitfalls
- Always record glucose and uptake time on the report β SUV is only comparable between studies with matched technique
- Metformin causes intense, often diffuse bowel uptake; a 48-72 h hold aids abdominal assessment when clinically appropriate
- Brown-fat uptake (neck, supraclavicular, paraspinal) is reduced by keeping the patient warm and, in some protocols, beta-blockade
- Post-treatment inflammation is FDG-avid β wait ~2-3 weeks after chemotherapy and 8-12 weeks after radiotherapy or surgery
- Deauville is scored visually against mediastinal blood pool and liver, not by an absolute SUV cut-off
Structured Report
- State tracer, injected activity, blood glucose, uptake time and scan extent
- Describe the primary lesion with SUVmax, size and CT correlate, then nodal and distant disease by station/organ
- For lymphoma give the Deauville score and compare with the baseline/interim study
- Summarise metabolic response (complete/partial/stable/progressive) using consistent methodology
- Provide TNM or disease extent, flag incidental CT findings, and give clear management recommendations
References
- Boellaard R, et al. FDG PET/CT: EANM procedure guidelines for tumour imaging version 2.0. Eur J Nucl Med Mol Imaging 2015
- SNMMI Procedure Standard / EANM Practice Guideline for FDG PET/CT (v2.0)
- Barrington SF, et al. Lugano Classification / Deauville criteria for response assessment in lymphoma. J Clin Oncol 2014
- Wahl RL, et al. From RECIST to PERCIST: evolving considerations for PET response criteria. J Nucl Med 2009
- Kapoor V, et al. An introduction to PET-CT imaging. RadioGraphics 2004
Educational clinical decision support only. Protocols vary by institution and equipment; always confirm with a qualified radiologist and local guidelines before clinical use.