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S979

ESTRO 36

_______________________________________________________________________________________________

Purpose or Objective

To retrospectively evaluate the incidence, magnitude,

and dosimetric impact of any air pockets between the

vaginal cylinders and the vaginal mucosa using CT-scan

images.

Material and Methods

120 postoperative vaginal cuff brachytherapy cases were

analyzed for receiving the prescribed dose to 5 mm depth

from the cylinder wall. CT-Based treatment planning was

performed in each fraction. The incidence, vaginal

mucosa displacement and air volume were assessed in

each treatment. A Monte Carlo study has also been done

to evaluate the dosimetric effect of air pockets around the

vaginal cylinder.

Results

In 50 patients, a total of 90 air pockets were observed in

150 procedures. Four patients had pocket free insertion

during the whole treatment sessions. The volume of air

pockets ranged between 0.01 cm3 and 4.5 cm3 with

average value of 2.5cm3, and the maximum displacement

of vaginal mucosa from cylinder surface was between 0.2

and 2 cm with average value of 0.8cm. Thirty patients had

no air pockets on their first fraction but in subsequent

fractions. Twenty patients had incorrect applicator

insertion as they have an air gap between applicator tip

and cylinder dome ranged between 0.3 cm and 1.1 cm with

average value of 0.8 cm. The Monte Carlo dosimetry also

shows that the average dose reduction to the vaginal

surface and 5mm-depth, at the air pocket, is respectively

about 9.2% and 7.3% per 1 mm of the air thickness.

Conclusion

Air pockets between vaginal cylinder and the vaginal

mucosa are observed in the majority of treatment

fractions, and the probability of occurrence varies from

patient to patient and procedure to procedure. The dose

reduction effect of air pockets needs to be considered

especially around the vaginal cuff using imaged based

treatment planning in each fraction and the effect on the

clinical outcome should be put under more investigation.

EP-1782 Effect of the amount of bladder filling on

normal tissue doses in 3D-HDR vaginal vault

brachytherapy

I. Er

1

, S. Kınay

1

, R. Kandemir

1

, F. Obuz

2

, A.N. Demiral

1

1

Dokuz Eylul Univ. Health Sciences Institute, Radiation

Oncology, IZMIR, Turkey

2

Dokuz Eylul Univ. Health Sciences Institute, Radiology,

IZMIR, Turkey

Purpose or Objective

In this retrospective study, it was aimed to compare the

dose volume parameters of organs at risk for the bladder

filling of 50 cc versus 150 cc in high dose rate (HDR) three-

dimensional (3-D) vaginal cuff (VC) brachytherapy (BRT).

Material and Methods

The dosimetric data of the 8 hysterectomized patients

with

gynecological

malignancy

who

received

postoperative pelvic external radiotherapy (RT) + 3-D HDR

VC-BRT between March 2015 and August 2015 were

analyzed. Computerized tomography (CT) sectional

images obtained for VC BRT treatment planning were used

for the study. The proximal 1/3 portion of vagina, drawn

as a layer of 0.5 cm thickness from the vaginal mucosa

(cylinder surface), had been delineated as clinical target

volume (CTV). A total dose of 18 Gy (3x6Gy) had been

prescribed to the CTV. For the study, bladder, rectum,

sigmoid, bowel and CTV were recontoured in a 3-D manner

by the same radiation oncology resident. Then the

contours were controlled and corrected first by a staff

radiation oncologist and then a staff radiologist.

Afterwards, treatment planning was performed by the

medical physicist using BRT treatment planning system.

Mean CTV dose-volume parameters (D90%, D100%,

D50%/D90%, V100%, V150%) for all patients were similar in

the treatment plans for two different bladder fillings.

Bladder V50%, D50% and D2cc, rectum D2cc, sigmoid D2cc,

bowel D50% and D2cc were recorded from the dose-

volume histograms obtained in the treatment planning

system. Paired comparisons were made for the parameters

above for the bladder filling of 50 cc versus 150 cc.

Different bladder fillings were compared using Wilcoxon

Signed-Rank Test in the SPSS 15.0 statistics program.

Results

It was observed that as the amount of bladder filling

increases, bowel is displaced cranially from the

applicator. Bladder D50% decreases (p=0.012) while

bladder D2cc increases (p=0.025) in case of 150 cc bladder

filling instead of 50 cc. Rectum D2cc shows a statistical

trend for increase (p=0.05), however bowel D50%

decreases (p=0.012) in 150 cc bladder filling compared to

50cc.

Conclusion

The statistically significant decrease in bladder and

especially bowel D50% parameters supports filling bladder

with 150 cc instead of 50 cc in 3D VC-BRT.

EP-1783 Acute toxicity with Xoft Axxent Electronic

Brachytherapy (XB) in endometrial or cervical cancer

A. Mendez Villamon

1

, A. Miranda Burgos

1

, M. Gascón

Ferrer

1

, M. Puertas Valiño

1

, S. Lozares Cordero

2

, A.

Gandia Martinez

2

, J. Font Gomez

2

, M. Tejedor Gutierrez

1

1

H.U. Miguel Servet, RADIATION ONCOLOGY, Zaragoza,

Spain

2

H.U. Miguel Servet, MEDICAL PHYSICIST, Zaragoza, Spain

Purpose or Objective

To analyze acute toxicity outcomes after treatment with

Xoft Axxent Electronic Brachytherapy (XB) in postsurgical

endometrial or cervical cancer patients treated at our

medical centre.

Material and Methods

Prospective study in which we selected 29 patients that

received treatment with Xoft Axxent Electronic

Brachytherapy (XB) administered twice a week after

endometrial or cervical cancer surgery, with 3D

planification. The patients were selected from September

2015 to September 2016. They were divided in two groups:

Group 1 (15/29) considered high risk and group 2 (14/29)

considered intermediate risk. Group 1 received external

beam radiotherapy (46Gy) followed by XB (15Gy in 5Gy

fractions) and group 2 received exclusive XB (25Gy in 5Gy

fractions). We analyzed the median dose in bladder,

rectum and sigmoid D2cc, V50, V35 with XB comparing the

doses with Ir-192. The vaginal mucosa, gastrointestinal

(GI) and genitourinary (GU) toxicities were analyzed with

the Common Terminology Criteria for Adverse Events

(CTCAE 4.0) scale.

Results

The median dose in bladder with XB vs. Ir-192 was: 2cc

66,4% vs. 71.6%, V50 7,2 vs. 11.9 Gy, V35 14.8 vs. 26,6. In

rectum XB vs. Ir-192 was: D 2cc 68,4% vs. 73.5% , V50 9.9

vs. 16.7 Gy, V35 19.9 vs. 36. In sigmoid XB vs. Ir-192 was:

D 51.4%vs. 59.8%, V50 12.9 vs. 21.3 Gy, V35 28.8 vs. 41.5.

The median follow-up was six and a half months (range 3-

12 months).

In group 1, acute vaginal mucositis (G1) was observed in

40% of the patients, GI toxicity (G1) occurred in 13% and

GU toxicity (G1, G2, G3) was not present.

In group 2, we observed acute vaginal mucositis (G1 and

G2) in 57% of the patients, GI toxicity (G1) occurred in 7%

and GU toxicity (G1) was present in 29%. There was no

grade 3 or greater toxicity in any of the groups. At 3

months follow-up, all of the patients were asymptomatic.

Conclusion

The dose received by the organs at risk with the Xoft

Axxent Electronic Brachytherapy is less compared to Ir-