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S945

ESTRO 36 2017

_______________________________________________________________________________________________

Results

The

basic

characteristics

of

couch-bending,

reproducibility and stability were within 0.10mm within

the treatment volume (see Fig.2 a, b).

The relative spatial deviation was smaller than 0.40mm

for rotations ranging up to 200° (see Fig.2 c). For different

vertical positions, the couch drifted less than 0.25mm for

2 different loads and rotations.

The differences between the prescribed and measured

absolute position were evaluated in terms of histograms

showing the overall 3D deviation. In 95% of all

measurement points the 3D accuracy was better than 0.63

mm (see Fig.2 d).

Regarding the weight-induced couch-bending no

correlation between the accuracy and payload could be

found.

Conclusion

The results show that the important spatial properties of

the patient positioning system are well within the

acceptable clinical tolerances. The very high

reproducibility of the PPS allows further optimization of

the absolute position. The measured datasets serve as

new input for a high accuracy calibration.

EP-1742 Optimisation and implementation of brain

CBCT templates; an institutional pilot study.

S. Petkar

1

, N. Lalli

2

, F. Solda'

1

, C. Gillies

2

, S. Moinuddin

1

,

N. Fersht

1

1

UCLH NHS Foundation Trust, Radiotherapy, London,

United Kingdom

2

UCLH NHS Foundation Trust, Radiotherapy Physics,

London, United Kingdom

Purpose or Objective

Volumetric imaging (CBCT) in brain has facilitated the use

of volumetric delivery techniques and reduction of

uncertainty margins by quantifying bone set-up variation,

and, by inference, OAR position.

The aim of this work is to optimise the current imaging

practice on a Truebeam Linac STx(2.5) for adult brain

tumour patients by investigating the relationship between

CBCT parameters, patient dose and image quality for both

bone and soft tissue.

Material and Methods

In our institution we currently image this cohort with daily

kV imaging and weekly CBCT. A daily ‘shift to zero’ is

applied for set-up variations of less than 3mm with

residual error evaluated on a weekly basis via a standard

Full-Fan, partial arc CBCT template (Table 1-Template 1)

The CBCT image quality was evaluated by comparing three

progressive dose-reduction trial imaging templates +/-

length reduction (Table1-Templates 2, 3, 4) with the

standard CBCT template.

Initial tests were carried on Catphan

®

and Rando

®

phantoms to assess image quality and scan artefact

limitations. Three consecutive skull-base meningioma

patients were then imaged with the four templates on

sequential weekly imaging sessions during treatment.

Each CBCT was reviewed by an expert group of a clinician,

two radiographers and two physicists to evaluate, by

consensus, the discernibility of the optic nerves,

ventricles, cranial bones, temporalis muscle, and the

external contour. In addition, the fidelity of the co-

registration to the skull-base anatomy (ROI) was assessed.

A standard threshold was applied throughout the

investigation.

Results

A total of 15 CBCT images were acquired and reviewed.

All structures were visible for each template except for

the ventricles which were assessed as indistinct with

templates 3 and 4 (Figure 1).

The fidelity of registration was satisfactory for each

template.

Conclusion

A length-reduction template can be utilised in brain

tumours providing the skull-base is included in the CBCT

ROI. In cases where the PTV is distant to the skull base,

length reduction should be used with care.

A concomitant dose reduction is also feasible unless the

discernibility of the ventricles is essential, such as when

changes in ventricular volume/position are of concern.

In our institution we will adopt a new imaging strategy for

brain tumour patients employing template 4 for all benign

skull based tumours and retaining template 1 (standard)

for all other lesions.

Further similar work will be carried out to optimise the

CBCT protocols in other cohorts of patients (e.g.

paediatrics).

EP-1743 Evaluation of proton grid therapy in

challenging clinical cases

T. Henry

1

, A. Valdman

2

, A. Siegbahn

1

1

Stockholm University, Department of Medical Physics,

Stockholm, Sweden