Pros | Cons | |
---|---|---|
Detection and localisation | Gain in sensitivity for cancers located in hypovascular and fibrous zones (anterior fibromuscular stroma, central zone) or showing challenging appearance such as non-nodular infiltrating lesions in the peripheral zone | Gain in sensitivity compared to T2WI alone, but no added value compared to T2WI and DWI |
Gain in specificity (up to 17%) in differentiating cancer from atrophy, necrosis, haemorrhage, prostatitis, calcifications | Variable enhancement patterns in cancer, overlapping with benign conditions | |
Problem solver in PI-RADS version 2 for peripheral zone lesions | – | |
Rescue of examinations with inadequate or absent T2WI and/or DWI | – | |
Primary role in detecting recurrence after treatment | – | |
Research: prediction of tumour volume, prediction of biological aggressiveness (microvessel tissue density or Gleason score) | – | |
Staging | Gain in accuracy in less experienced readers (“first localise, then stage” approach), especially for seminal vesicle invasion | Conflicting results in literature |
Gain in assessing extraprostatic extension by detecting extraprostatic contrast enhancement | False positives related to inflammation | |
Patient-centred care | Negligible extra time in magnet | Extra time in magnet reducing patient comfort and compliance |
Adverse reactions to gadolinium-based contrast agents are rare and usually of limited clinical significance | Safety issues related to gadolinium-based contrast agents, including adverse reactions and gadolinium deposition in the brain | |
Costs | – | Increased costs (up to 20–30% of the whole examination). |