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S514

ESTRO 36 2017

_______________________________________________________________________________________________

applicators were inserted, cone beam computed

tomography (CT) images were obtained. Rectal gas was

observed in 11 brachytherapy fractions from 8 patients.

After draining rectal gas with a Nelaton catheter, cone

beam CT images were obtained again. Brachytherapy was

prescribed to point A using standard two-dimensional

dosimetry and planning. To quantify the dose delivered to

the rectum and urinary bladder, three-dimensional dose

distributions were calculated using the images from

before and after draining rectal gas. The dose to the

rectum and urinary bladder was evaluated based on dose-

volume histograms. The influence of the volume of

discharging rectal gas (pre-draining rectal volume – post-

draining rectal volume) on the rectal dose was

investigated. The minimum doses to the maximum

exposed 0.1, 1 and 2 cc (D

0.1cc

, D

1cc

and D

2cc

) volumes were

evaluated using the dose from point A. Statistical analyses

were conducted using the paired t-test and a linear

regression model.

Results

The mean rectal dose after draining rectal gas was

significantly lower than that before draining. The rectal

doses (D

0.1cc

, D

1cc

and D

2cc

) relative to point A at post-

draining vs. pre-draining were as follows: 106.9% vs.

121.2%, 88.3% vs. 98.6% and 81.5% vs. 90.9%, respectively

(p<0.05). The mean urinary bladder dose was not

significantly different after draining rectal gas from

before. The urinary bladder doses (D

0.1cc

, D

1cc

and D

2cc

)

relative to point A at post-draining vs. pre-draining were

as follows: 136.0% vs. 133.2%, 112.3% vs. 111.8% and

103.3% vs. 102.4%, respectively. The volume of

discharging rectal gas slightly correlated with the rectal

dose at D

0.1cc

(R2=0.45); however, no significant

correlation was found for D

1cc

or D

2cc

(R2=0.10 and -0.01,

respectively).

Conclusion

Our data suggested that draining rectal gas is useful for

reducing the rectal dose in high-dose-rate brachytherapy

for gynecological cancer.

PO-0937 HDR image-guided interstitial brachytherapy

for postoperative local recurrent uterine cancer

K. Yoshida

1

, H. Yamazaki

2

, T. Takenaka

2

, T. Kotsuma

3

, K.

Masui

2

, T. Komori

1

, T. Shimbo

1

, N. Yoshikawa

1

, H.

Yoshioka

1

, Y. Uesugi

4

, T. Hamada

1

, M. Nakata

1

, H.

Matsutani

1

, M.M. Ueda

3

, Y. Tsujimoto

3

, E. Tanaka

3

, Y.

Narumi

1

1

Osaka Medical College, Radiology, Takatsuki, Japan

2

Kyoto Prefectural University of Medicine, Radiology,

Kyoto, Japan

3

National Hospital Organization Osaka National Hospital,

Radiation Oncology, Osaka, Japan

4

Kansai University of Welfare Sciences, Rehabilitation

Sciences, Kashiwara, Japan

Purpose or Objective

In order to evaluate the usefulness of high-dose-rate (HDR)

image-guided interstitial brachytherapy (ISBT) for

postoperative local recurrent uterine cancer, we analyzed

our clinical experience.

Material and Methods

We investigated 48 patients treated with HDR-ISBT at

National Hospital Organization Osaka National Hospital

and Osaka Medical College between May 2003 and January

2014. All patients received radical surgery and 10 patients

also received post-operative radiotherapy as previous

treatments. Histologic finding was squamous cell

carcinoma (SCC), endometrioid adenocarcinoma (AD),

mucinous adenocarcinoma (MAD) and the others

(serous/adenosquamous/endocrine/undifferentiated) for

20, 17, 5 and 6 patients. The median maximum tumor

diameter was 25 mm (range; 5-79 mm). In 38 patients who

had non-irradiation history, 23 patients also received

external beam radiotherapy (EBRT). The median ISBT

doses were 54 Gy in 9 fractions as monotherapy and 30 Gy

in 5 fractions as combination of EBRT. In 10 patients who

had irradiation history, lower doses (36 to 48 Gy in 6 to 8

fractions) were selected. We implanted 7–16 (median, 13)

applicators under transrectal ultrasonography guidance.

We used free-hand implantation with ambulatory

technique for later 42 patients. Magnetic resonance

imaging (MRI)-assisted image-based treatment planning

was also performed. Clinical target volumes (CTV) were

the gloss tumor volume with or without 10 mm of vaginal

margin for patients with or without non-irradiation

history.

Results

The median follow-up time was 41 months (range; 4-115

months). The median D90(CTV)s were 91.3 Gy and 75.6 Gy

for patients with or without non-irradiation history. The 4-

year local control and overall survival rates were 78% and

67% for all patients. The 4-year local control rates were

83% and 60% for patients with or without non-irradiation

history (p=0.02). Tumor diameter, primary site and

histology were not significant prognostic factors of local

control. The 4-year overall survival rates were 73, 65, 100

and 20% for SCC, AD, MAD and the others (P=0.06). The

D90(CTV)s were 93.5±24.3 Gy and 81.4±9.2 Gy for local

control and failure patients (p=0.1). Grade ≥3 late

complications occurred in 11 patients (23%). Ileus was only

observed for patients receiving EBRT.

Conclusion

Our treatment result of image-guided HDR-ISBT showed

good local control result. However, previous irradiation

history was a worse prognostic factor of local control.

Dose-volume histogram seems to be useful for dose

prescription.

PO-0938 Should we use point A dose for image-guided

adaptive brachytherapy reporting in cervix cancer?

R. Mazeron

1

, I. Dumas

2

, A. Escande

1

, W. Bacorro

1

, R.

Sun

1

, C. Haie-Meder

1

, C. Chargari

1

1

Institut Gustave Roussy, Radiation Oncology, Villejuif,

France

2

Institut Gustave Roussy, Medical Physics, Villejuif,

France

Purpose or Objective

The recent ICRU report 89 recommends continuing the

reporting of point A dose in the era of Image-guided

adaptive brachytherapy (IGABT). The study aim was to

evaluate the interest of such recommendation by testing

the value of point A as a surrogate of volumetric

dosimetric parameters and as a predicting factor of local

control.

Material and Methods

The dosimetric data from patients treated with a

combination of chemoradiation and intracavitory image-

guided adaptive brachytherapy were confronted to their

outcomes. Prescribing followed the GEC-ESTRO

recommendations. Point A was used for reporting, without

specific planning aim. All doses were converted in 2-Gy

equivalent, summing brachytherapy and EBRT doses. The

relationships between the D

90

CTV

HR

and CTV

IR

and point A

doses were studied. Dose-effect relationships based on the

probit model and log-rank tests were assessed using the

different dosimetric parameters.

Results

Two hundred and twelve patients were included with a

median follow-up of 53.0 months. MRI guidance was used

in 89.6% of the cases. A total of 28 local relapses were

reported resulting in a local control rate of 86.6% at 3

years. Mean D

90

CTV

HR

, D

90

CTV

IR

and point A doses were

respectively: 79.7±10.4 Gy, 67.4±5.8 Gy and 66.4±5.6 Gy.

The mean D

90

CTV

HR

and CTV

IR

were significantly different

from the mean point A dose (p=p<0.0001, and 0.022

respectively). Both D

90

CTV were independent from point

A doses, even in bulky (width >5cm) tumors at diagnosis or

in large CTV

HR

lesions (≥ 30cm

3

) Whereas significant

relationships between the probability of achieving local