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S997

ESTRO 36

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differences were noted in the first three contoured cases:

the Z-axis deviation exceeded 5 mm in more than half of

hippocampus contours and hippocampal volume were

larger than in later defined seven cases. The volume of LH

in more than half hippocampus contours was slightly

bigger than the RH (1.9 cm

3

vs. 1.8 cm

3

). Most differences

in contouring of hippocampus ware observed in the area

of posterior horn of the lateral ventricle. Contrary, a large

number of hippocampal outlines overlapped with each

other near brainstem and anterior horn of the lateral

ventricle. The average dimension of the hippocampus

were 1.7 cm and 0.9 cm in the Z and X axes, respectively.

Conclusion

The proper contouring of hippocampus is difficult for the

beginner’s physicians. The training in delineating this

organ at risk under the supervision of experienced

radiation oncologist is strongly needed to achieve optimal

results in hippocampus sparing procedure, which in

consequence would result in improving QoL of the

patients.

EP-1819 EORTC RTT Delineation Project: improving

volume definition of OAR within the EORTC Lungtech

trial

M. Van Os

1

, M. Rossi

2

, C. Hurkmans

3

1

Erasmus MC Cancer Institute, Department of Radiation

Oncology, Rotterdam, The Netherlands

2

Netherlands Cancer Institute, Radiation Oncology

Department, Amsterdam, The Netherlands

3

Catharina Ziekenhuis EIndhoven, Radiation Oncology,

Eindhoven, The Netherlands

Purpose or Objective

To accurately evaluate toxicity within a trial, it is

important that the delineation of the Organs at risk (OAR)

is performed

consistently.

The aim of the EORTC ROG/RTT delineation project is to

reduce variability in OAR delineation to allow better

comparison of toxicity in EORTC trials between institutes.

Within the EORTC LungTech trial we evaluated whether

provided delineation guidelines are explicit enough to

avoid misinterpretation in volume definition of OAR and

whether a hands-on delineation workshop adds to this.

Material and Methods

A questionnaire was developed and distributed amongst

participating institutes requesting feedback after they had

completed their benchmark delineation for the EORTC

LungTech trial. Difficult areas could be identified.

Subsequently two groups were defined: Group A to

perform delineation of OAR according to protocol

guidelines and with additional visual guidelines. Group B

was invited to a delineation workshop where an expert

teacher addressed the difficult areas provided from the

benchmark cases. The consequent delineations were then

evaluated per organ at risk between group A and B and

also compared to the benchmark cases. The volume of

agreement

was

calculated.

Our hypothesis is that a delineation workshop prior to

launching a trial improves consistent volume definition.

Results

Introducing visual guidelines as an extra aid to the written

guidelines significantly reduced misinterpretation and

greatly improves the consensus of delineation. Although

not specifically tested between the groups the RTT’s

performance in delineating the OARs was deemed as

consistent as the clinicians. We aim to demonstrate the

additional value of teaching by means of a delineation

workshop, but this analysis is still ongoing.

Conclusion

The EORTC ROG advised to involve RTTs in future EORTC

trials for volume definition of

OAR.

In future EORTC trials, a kick-off including a delineation

workshop for participating institutes is planned to achieve

more consistent delineation of OAR.

Electronic Poster: RTT track: Treatment planning and

dose calculation / QC and QA

EP-1820 RapidArc vs IMRT in adjuvant gastric cancer

irradiation: any dosimetric advantage?

K. Mashhour

1

, W. Hashem

1

, R. Fawzy

1

, H. Abdelghany

2

1

Kasr el ainy school of medicine-Cairo university, clinical

oncology, cairo, Egypt

2

Kasr el ainy school of medicine-Cairo university,

radiation physics, cairo, Egypt

Purpose or Objective

The outcome of intensity modulated radiation therapy

(IMRT) plans depends on the choice of number of fields,

beam orientations, optimization algorithms & planner

experience. The RapidArc has the characteristics of both

good plan quality as well as high delivery efficiency. The

purpose of this work was to compare dosimetric endpoints

between IMRT & RapidArc techniques for gastric

carcinoma patients in the adjuvant setting.

Material and Methods

Twenty gastric cancer patients who had a radical

gastrectomy with D2 dissection were eligible. The clinical

target volume (CTV) included the gastric bed, anastomosis

with 2-cm proximal/distal margins & regional LN areas.

The planning target volume (PTV) consisted of CTV plus a

10 mm margin.All plans were created in the Eclipse

treatment planning system (v8.6 Varian Medical System).

For IMRT, a coplanar seven-field plan was performed.

Regarding the RapidArc, plans were done using a double

arc plan consisting of 2 co-planar arcs of 360° in clockwise

& counter clockwise direction. Dose prescribed was 45 Gy

to the PTV in 25 fractions using 6MV photons. The PTV dose

coverage criteria were as follows: at least 95% of PTV

received 45Gy; The conformity index (CI) & homogeneity

index (HI) were calculated. The organs at risk (OAR) were

the spinal cord, both kidneys and liver.

Results

Target coverage was similar for both techniques. The

mean V95 was found to be 94.7% & 94.8% for the IMRT and

RapidArc respectively (p = 0.32). The CI for IMRT and

RapidArc were 0.93 ± 0.01 & 0.94 ± 0.01, respectively;

while the HI was 1.15 ± 0.01 for IMRT & 1.14 ± 0.02 for

RapidArc (both p > 0.04).All the plans met the required

dose limitations. The maximum spinal cord dose for IMRT

and RapidArc was 37.87 Gy vs 36.42 Gy (p = 0.34). For the

right kidney, IMRT had significantly lower mean V20

(volume that receives 20 Gy) compared to RapidArc (23.2

vs. 30.3, p = 0.01). The mean V20 to the left kidney were

28.4 and 27.4 in the IMRT and RapidArc respectively (p =

0.01). The IMRT produced a similar liver mean V30 (volume

that receives 30 Gy) (24.3 vs. 23.1, p = 0.52) to RapidArc.

The treatment delivery time was 193.5 ± 25.0 s (range 157–

230 s) to IMRT and 66.0 ± 8.7 s (range 55–77 s) to RapidArc

(p = 0.00). The total monitor units (MU) for IMRT and

RapidArc were

343.0 ± 94.0 & 363.0 ± 44.0 (p = 0.07),

respectively.

Conclusion

RapidArc obtained similar dosimetric outcomes to IMRT

plans regarding target coverage & OAR sparing with an

advantage of shorter delivery time & lower number of MU.