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S513

ESTRO 36 2017

_______________________________________________________________________________________________

There is little existing data guiding urethral dose

constraint but study in peri-urethral cancer has

demonstrated a higher risk of urethral toxicity in patients

with a urethral EQD2 of >85Gy. Our median EQD2 was

below this level but with a wide range, indicating the

degree of adaptation using image guidance. Given the

poor correlation of applicator angle and length with dose

to OARs choice of applicator should remain dictated by the

patients’ anatomy.

PO-0934 Brachytherapy as part of the conservative

treatment for primary and recurrent vulvar carcinoma

C. Chargari

1,2

, P. Castelnau-Marchand

1

, A. Escande

1

, I.

Dumas

1

, R. Mazeron

1

, P. Maroun

1

, E. Bentivegna

3

, S.

Gouy

3

, A. Cavalcanti

3

, P. Morice

3

, C. Haie-Meder

1

1

Gustave Roussy Cancer Campus, Brachytherapy unit-

Radiation oncology, Villejuif, France

2

French Military Health Services Academy, French

Military Health Services Academy, Paris, France

3

Gustave Roussy Cancer Campus, Department of Surgery,

Villejuif, France

Purpose or Objective

There are only scarce data on the place of brachytherapy

(BT) for treatment of vulvar carcinoma. Our institutional

experience of interstitial BT for vulvar carcinoma patients

is reported.

Material and Methods

Clinical records of patients receiving low-dose rate (LDR)

or pulsed-dose rate (PDR) BT as part of the primary

treatment for primary/recurrent vulvar squamous cell

carcinoma or as part of adjuvant treatment between 2000

and 2015 were included. Patients, tumors and treatments

characteristics as well as clinical outcome were examined.

Results

A total of 26 patients treated with BT were identified. BT

was delivered as part of primary intent treatment for

locally advanced/recurrent cancer in 11 patients, and as

part of adjuvant treatment in 15 patients. Median age at

time of BT was 63 years (range: 41 – 88 years). PDR and

LDR were used in 15 patients and 11 patients,

respectively. BT was performed as a boost to the tumour

bed following EBRT (n=13) or as only irradiation modality

(n=13). Total median dose at the level of primary tumor

was 60 GyEQD2 (range: 55 – 60 GyEQD2). With mean

follow-up of 41 months (range: 5 months – 11.3 years), 11

patients experienced tumour relapse. Ten patients

experienced local relapse as first event, associated with

synchronous extra-vulvar events in 8/10 patients. Three-

year estimated disease-free survival and overall survival

rates were 57% (95%CI: 45–69%) and 81% (95%CI: 72-90%).

All toxicities were grade 2 or less.

Conclusion

Interstitial BT used as part of the primary or adjuvant

treatment of vulvar carcinoma is feasible with a

satisfactory toxicity profile. Prognosis remains however,

dismal, with a high frequency of local and distant failures

in patients with locally advanced tumors.

PO-0935 Modeling to compensate for intra-fractional

bladder dose variations in gynecological brachytherapy

Z. Siavashpour

1

, R. Jaberi

2

, M.R. Aghamiri

1

, C. Kirisits

3

1

Shahid Beheshti University, Medical Radiation

Engineering, Tehran, Iran Islamic Republic of

2

Tehran University of Medical Sciences, Radiotherapy,

Tehran, Iran Islamic Republic of

3

Comprehensive Cancer Center- Medical University of

Vienna, Department of Radiotherapy and Oncology,

Vienna, Austria

Purpose or Objective

Proposing a model to compensate for intra-fractional

bladder dose variations during gynecological (GYN)

brachytherapy.

Material and Methods

Thirty advanced cervical cancer patients treated with HDR

(

192

I source) intracavitary brachytherapy were selected.

Rotterdam applicators (tandem-ovoids) were used for

them. Patients pelvic CT scans were done twice; pre- and

post-treatment (about 30 min after dose delivery), with

applicator in situ. Flexiplan

®

(version 2.6, Isodose control,

the Netherlands) as a 3D treatment planning software was

used. Applicator reconstruction and organs delineation

were done by the same physicist /physician on both image

sets. Totally identical plans (dwell times/positions) were

applied to both image sets and DVH parameters were

recorded; planning aims: 80-90 Gy (EQD2) for D

90

of CTV

HR

and less than 85, 75, and 75 Gy for D

2cm³

of bladder,

rectum, and sigmoid, respectively.

RT-Structure files (in DICOM format) of the patients for

whom intra-fractional dose (D

2cm³

) variations were higher

than 5% were exported from planning system. Applicator-

organs distances along the active length of three

applicators were extracted by some in-house MATLAB

written codes. Source dwell times were extracted from

treatment planning report files (in xps format). A model

was design to propose new source dwell times to

compensate for the bladder wall to applicators walls

distances intra-fractional variations, considering the TG43

algorithm and inverse square law. Some dwell times

acceptance criteria were considered during modeling such

as: D

90

of CTV

HR

and CTV

IR

have not changed to be less than

85 Gy 70 Gy, respectively. New dwell times were applied

to the plans to test their influences on DVH parameters.

Also, the model was further optimized to reduce the

executing time by searching for the most impressive part

of the applicators lengths on bladder dose.

Results

For one third of the considered patients bladder dose

changes were higher than 5%. Mean ± SD of D

2cm³

intra-

fractional relative changes ((D

2cm³(before)

- D

2cm³(after)

)/

D

2cm³(before)

× 100) of these ten cases were 19.3 ± 18.0 %.

After correcting the plans these variations became 10.5 ±

14.5. More bladder dose correction would lead to a

significant decrease in dose to CTV

HR

and was

unjustifiable. Model runtime was about 3 minutes (Intel

corei7 laptop, RAM = 8 GB, CPU = 2 GHz).

Conclusion

A model was developed to correct the bladder dose to be

as similar as possible to the pre-treatment plan one. It is

a semi-online model that can be used in the routine

clinical workflow to reduce the GYN image-guided

adaptive brachytherapy uncertainties. The model can be

generalized to other organs at risk.

PO-0936 Dose effects of draining rectal gas in image-

guided brachytherapy for gynecological cancer

H. Takase

1

, N. Ii

2

, Y. Yamao

1

, T. Kawamura

2

, M. Naito

1

,

Y. Watanabe

2,3

, Y. Toyomasu

2

, A. Takada

2

, H. Tanaka

2

, T.

Yamada

1

, H. Maki

1

, H. Sakuma

4

, Y. Nomoto

5

1

Mie University Hospital, Department of Radiology, Tsu,

Japan

2

Mie University Hospital, Department of Radiation

Oncology, Tsu, Japan

3

Matsusaka central hospital, Department of Radiation

Oncology, Matsusaka, Japan

4

Mie University Graduate School of Medicine,

Department of Radiology, Tsu, Japan

5

Mie University Graduate School of Medicine,

Department of Radiation Oncology, Tsu, Japan

Purpose or Objective

To verify the usefulness of draining rectal gas in image-

guided high-dose-rate brachytherapy for gynecological

cancer, we quantified the dose delivered to the rectum

and urinary bladder with and without draining rectal gas.

Material and Methods

From October 2013 to July 2014, 116 brachytherapy

fractions from 34 patients were performed in our

department for gynecological cancer. After the