Quantification: Why and How-to

Davide Poggiali

Outline:

  1. What is quantification in PET/SPECT (and why should I care)
  2. From visive/qualitative to quantitative assessment
  3. Conclusions

What is quantification in PET/SPECT

PET and SPECT already provide quantitative images in terms of tracer concentration [Bq/ml], corrected for radiotracer decaying.

\[ C(t) = C_0 e^{-\lambda (t-t_0)} \]

where \(\lambda=\frac{log 2}{T_{1/2}}\).

So what do we need more?

By quantification we actually mean the computation of a numerical value per Volume of Interest (VOI) which actually tells us something about the tracer's kinetics and deposition.

Absolute quantification:

  • Relies on mathematical modelling
  • Requires a timeframe 4D (list mode) image

PROs:

  • Accurate
  • Reliable

CONs:

  • Time consuming
  • A bit hard to explain

 Semi-quantification:

  • Normalized for infra-subject variability
  • Requires a static 3D image

PROs:

  • Faster
  • Easier to understand

CONs:

  • Less reliable
  • Tracer's kinetics ignored

2. From visive/qualitative to quantitative assessment.

What do we see?

Some low signal on frontal lobe....

  • I see that ...
  • I heard that ...
  • I imagine that ...

 

  • The measures tell me that...
  • Statistical analysis says that...

Measurements

Expertise

Experience

Some steps from visual to numerical assessment:

1. Mean per VOI

VOI Mean value
Frontal L 121.3
Frontal R 149.1
Occipital L 297.1
Occipital R 279.7
WM 98.1
Cerebellum GM 137.3

Some steps from visual to numerical assessment:

2. SUVr

VOI SUVr
Frontal L 0.88
Frontal R 1.08
Occipital L 2.16
Occipital R 2.04
WM 0.71
Cerebellum GM 1.0 (ref.)

Some steps from visual to numerical assessment:

3. Percentile or z-score of SUVr w/ respect to normal population

VOI z-score
Frontal L -3.01
Frontal R -1.45
Occipital L 0.43
Occipital R 0.23
WM 1.12
Cerebellum GM --- (ref.)

Conclusions:

Quantification allows to:

  1. Objectively compare radiotracer captation on VOIs
  2. Quantitatively compare subject's image with a reference cohort
  3. Make predictions, given the data (Machine/Deep Leaning)
  4. Reduce the grey zone in between diagnotypes for clinical evaluation

Thanks for the attention!

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