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S799

ESTRO 36

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Conclusion

This 3-class density method can be used to monitor the

fraction dose in the PGs during oropharynx cancer IMRT.

Small significant differences are observed for the highest

dose received in the spinal cord, likely due to the bone

heterogeneity.

EP-1491 Verification of FFF VMAT plans with PDIP and

GLAaS algorithms by using the new imager of

TrueBeamSTx

T. Ercan

1

, A. Levent

2

, T. Cagin

3

, S.M. Igdem

1

1

Gayrettepe Florence Nightingale Hospital, Radiation

Oncology, Gayrettepe - Istanbul, Turkey

2

Medideal Medical Projects and Solutions Inc., Medical

Physics, Istanbul, Turkey

3

Liverpool School of Medicine, Department of

Biostatistics, Liverpool, United Kingdom

Purpose or Objective

Using flattenning filter free (FFF) beams shortens the

treatment time especially for stereotactic treatment

techniques when the high dose rate is used. It is not

possible to do quality assurance (QA) with all types of

amorphous silicon (aS) detectors because of their

saturation limit. In this study, verifications of volumetric

modulated arc therapy (VMAT) stereotactic treatment

plans were evaluated with PDIP and GLAaS algorithms by

using a new unsaturated aS detector and the results were

compared.

Material and Methods

aS1200 image detection unit (IDU) which has aS detector

integrated on a Varian TrueBeam STx linac was used

(Table 1). Portal Dosimetry (PD) (v.13.0.26) with PDIP

algorithm (Varian Medical Systems, Palo Alto) and Epiqa

(v.4.0.11) with GLAaS algorithm (Epidos s.r.o., Bratislava)

QA tools were configured at SDD: 100 cm with 2400

MU/min dose rate through the detector without saturation

issue to use for pre-treatment verification.10 MV FFF

VMAT treatment plans (2400 Dose Rate) of 35 patients with

in total 72 arcs were calculated by Anisotropic Analytical

Algorithm (AAA, ver.13.0.26) in Eclipse Treatment

Planning System. The verification plans were irradiated on

the aS1200 imager. The evaluations for both QA tools were

done with the technique of gamma analysis (GA). The GA

criterias for Distance to Agreement (DTA) and Dose

Difference (DD) were defined as 3%/3mm, 2%/2mm and

1%/1mm and applied for "field" (defined with jaws) and

"field+1cm" areas. The results were analysed with 2

sample T-test.

Table 1. Specifications of aS1200 IDU

Maximum active field size 43cm x 43cm

Maximum readout speed 20 frame/second

Matrix

1280 x1280

Resolution

0.0336 cm

Results

Epiqa had dramatically low GA (gamma<1.0) results; less

than 95% with the criterias DD:%1, DTA:1mm for field

(Average: 85,03, SD:±7,8) and field+1cm (Average: 93,30,

SD: ±2,4) comparison areas. There is no significant

difference (p>0,05) between PD and Epiqa for GA results

of DD:%3, DTA:3mm

criterias.

Table 2. Average and standard deviation (SD) results of

each method

Evaluated

field

Method,

DD, DTA

Average

value

Standard

deviation

p

value

Field+1cm PDIP, %3,

3mm

99.95

0.14

>0.06

GLAaS, %3,

3mm

99.98

0.05

PDIP, %2,

2mm

99.87

0.18

<0.05

GLAaS, %2,

2mm

99.72

0.30

PDIP, %1,

1mm

99.14

0.75

<0.05

GLAaS, %1,

1mm

93.30

2.44

Field

PDIP, %3,

3mm

99.92

0.16

>0.707

GLAaS, %3,

3mm

99.90

0.31

PDIP, %2,

2mm

99.59

0.50

<0.05

GLAaS, %2,

2mm

98.95

1.68

PDIP, %1,

1mm

97.03

2.08

<0.05

GLAaS, %1,

1mm

85.03

7.78

Conclusion

We could able to detect more errors with the hardest

criterias (DD:%1, DTA:1mm) as expected. Epiqa had better

performance for detecting the errors. It could be the

result of the differences in workflow. Epiqa compares the

dose calculated with clinical algorithm and irradiated

image, but PD compares the calculated dose with PDIP and

irradiated image. PD and Epiqa can be used for

stereotactic VMAT plans with aS1200 detector without

saturation problem at SSD: 100cm reliably. If the speed is

important for the clinics have high workload, PD could be

prefered through being an internal software.

EP-1492 Influence of induced accelerator’ errors on

dosimetric verification result and DVH of treatment

plan

M. Kruszyna

1

, K. Matuszewski

1

1

Greater Poland Cancer Centre, Medical Physics

Department, Poznan, Poland

Purpose or Objective

The commonly used gamma criteria of 3% dose difference

(global method) and 3 mm distance to agreement could

mask clinically relevant errors. The aim of this work was

to evaluate the influence of induced accelerator’s errors

on 3D gamma method results with the varies criteria and

on the patient’ dose distribution (DVHs).