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S141

ESTRO 36 2017

_______________________________________________________________________________________________

HDR brachytherapy, using a phase-only cross correlation

localization method.

[1] Beld E. et al. 2015 Proc. Intl. Mag. Reson. Med. 24,

#4151.

[2] De Oliveira A. et al. 2008 MRM

59

1043-1050.

OC-0276 Toward adaptive MR-guided HDR prostate

brachytherapy – Simulation study based on anatomy

movements

M. Borot de Battisti

1

, B. Denis de Senneville

2

, G.

Hautvast

3

, D. Binnekamp

3

, M. Peters

1

, J. Van der Voort

van Zyp

1

, J.J.W. Lagendijk

1

, M. Maenhout

1

, M.A.

Moerland

1

1

University Medical Center Utrecht, Departement of

Radiotherapy, Utrecht, The Netherlands

2

UMR 5251 CNRS/University of Bordeaux, Mathematics,

Talence, France

3

Philips Group Innovation, Biomedical Systems,

Eindhoven, The Netherlands

Purpose or Objective

Dose delivery during a single needle, robotic MR-guided

HDR prostate brachytherapy may be impaired by: (1)

needle insertion errors caused by e.g. needle bending, (2)

unpredictable anatomy movements such as prostate

rotations (induced by the insertion or retraction of the

needle), prostate swelling or intra-procedural rectum or

bladder filling. In this study, a new adaptive dose planning

strategy is proposed to assess the second challenge. The

performance of this approach is evaluated by simulating

brachytherapy procedures using data of 10 patients

diagnosed with prostate cancer.

Material and Methods

Throughout HDR prostate brachytherapy, unpredictable

anatomy movements may cause errors in dose delivery and

potentially, this may result in failure to reach clinical

constraints (e.g. for single fraction monotherapy: D95%

PTV>19 Gy, D10% urethra<21 Gy, D1cc bladder<12 Gy and

D1cc rectum<12 Gy). In this study, a novel adaptive dose

planning pipeline for MR-guided HDR prostate

brachytherapy using a single needle robotic implant

device is proposed to address this issue (Figure 1a). The

dose plan (needle track positions, source positions and

dwell times) and needle insertion sequence are updated

after each needle insertion and retraction with MR–based

feedback on anatomy movements (cf. Figure 1b). The

pipeline was assessed on moving anatomy by simulating

MR-guided HDR prostate brachytherapy with varying

number of needle insertions (from 2 to 14) for 10 patients.

The initial anatomy of the patients was obtained using the

delineations of the prostate tumor and the OAR considered

(urethra, bladder and rectum) on MR images. Each needle

insertion and retraction induced anatomy movements

which were simulated in 2 steps: (1) a typical 3D rotation

of the prostate was imposed (2) a regularization of the

movement in space was then applied. The initial and final

dose parameters were compared in the situations with and

without update of dose plan and needle insertion

sequence.

Results

The computation time for re-planning was less than 90

seconds with a desktop PC. The actual delivered dose

improved with vs. without update of dose plan and needle

insertion sequence: On average, the dose coverage of the

PTV was higher in the situation with vs. without update

(Figure 1c). Moreover, the difference increased with the

number of needle insertions. The dose received by the PTV

in the situation with re-planning was not significantly

different compared to the initial dose plan. Finally, the

dose to the OAR’s was not significantly different between

the initial dose plan and the dose delivered in the situation

with and without update.

Conclusion

This study proposes a new adaptive workflow with

feedback on the anatomy movements for MR-guided HDR

prostate brachytherapy with a single needle robotic

implant device. The assessment of the pipeline showed

that the errors in the dose delivered due to movement of

anatomy can be compensated by updating the dose plan

and the needle insertion sequence based on MRI.