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S74

ESTRO 36

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and range deviations are quantified for two different

treatment sites.

Material and Methods

Based on a database of more than 1000 clinical DECT scans

acquired with a single-source DECT scanner (Siemens

Somatom Definition AS), 10 prostate cancer and 54 head

tumor patients were selected to assess intra- and

interpatient tissue diversity and its impact on SPR

prediction. To evaluate age- and sex-dependent

variability, the head tumor cohort was divided in children,

women and men. DECT scans were converted in 79 keV

pseudo-monoenergetic CT scans (MonoCTs) and SPR

datasets derived by voxelwise calculations of electron

density and effective atomic number using syngo.via

(Siemens Healthineers). In XiO (Elekta) clinical proton

treatment plans were recalculated (a) on MonoCTs using

the clinical HLUT and (b) on SPR datasets to quantify range

and dose differences.

Results

The voxelwise correlation of SPR and CT number is similar

for men and women, but differs considerably between

adults and children in bony tissue, likely due to the

amount of calcium embedded in bones, which increases

with age. Based on voxelwise SPR comparisons, the clinical

HLUT predicts on average (2.2 ± 0.6) % larger SPRs for head

tumor patients and (1.7 ± 0.3) % larger SPRs for prostate

cases. The impact of both approaches on dose

distributions is shown in Fig. 1 and 2 for an exemplary head

tumor and prostate cancer patient. In the head case, the

HLUT predicts a 1.7 % shorter range (2.4 mm) resulting

from a 0.7 mm range underestimation in water-filled

ventricles (not precisely predicted by the HLUT) and

different SPR predictions for brain. A range deviation of

up to 3.0 % (7.1 mm) is obtained in the prostate case,

which is mainly caused by different SPR predictions for

bone marrow and muscle. These range differences in

single beams are not compensated in the overall

treatment plan.

Conclusion

In contrast to a generic HLUT, a DECT-based SPR

prediction can individually consider age- and sex-

dependent tissue variability in proton treatment planning.

This diversity information can also provide suggestions for

subgroup-specific improvements of the heuristic CT

calibration. The assessment of relative SPR and dose