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S506

ESTRO 36 2017

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technique (orthogonal vs. CBCT and high vs. low quality)

on the doses to normal tissue was evaluated using Eclipse,

where the imaging doses were used as based plans in the

treatment planning process. For breast plans, doses to the

heart and lung were evaluated. For head/neck plans,

doses to all the normal tissues were compared.

Figure 1. Anthropomorphic phantom (CIRS) with dose

measurement points identified.

Results

Average imaging dose was measured as 1.3, 2.5, 3.7, and

7.6cGy for daily low dose MV pairs, high quality MV pairs,

low dose CBCT and high quality CBCT, respectively. Over

a 30 fraction treatment with daily IGRT, this equates to 38

- 227cGy. The average agreement between measured and

calculated tissue doses due to imaging was 0.4±0.4cGy.

The largest difference was 1.3cGy, found in the lung for

high quality CBCT imaging (~39cGy over a 30 fraction

treatment).

With imaging dose incorporated into the treatment

planning process, it was possible to create clinically

acceptable treatment plans for a range of treatment sites,

including breast, head and neck and prostate. The imaging

technique did, however, increase the heart and lung dose

for breast plans. For an example left breast treatment,

the mean heart dose in our original, clinically delivered

plan was 60cGy. With daily MV imaging included, this

increased to 140, 150, 190 and 260cGy for daily low dose

MV pairs, high quality MV pairs, low dose CBCT and high

quality CBCT, respectively. The corresponding values for

mean lung dose were 360cGy (original clinical) and 470,

490, 510 and 570cGy.

Table 1: Tissue doses(cGy/fraction) at different points in

the anthropomorphic phantom. M: Measured. C:

Calculated

Conclusion

Image-guided radiation therapy using MV imaging can be

incorporated into the treatment plan to give clinically

acceptable dose distributions. Dose to normal tissues is

increased, however, and depends on the imaging

technique, it is important to select the technique which

minimizes normal tissue dose while providing sufficient

image quality for patient setup.

Poster: Brachytherapy: Breast

PO-0922 Late toxicity and cosmetic outcome following

APBI using interstitial multicatheter HDR brachytherapy

T. Soror

1,2

, G. Kovács

2

, N. Seibold

2

, C. Melchert

2

, K.

Baumann

3

, E. Wenzel

4

, S. Stojanovic-Rundic

5

1

National Cancer Institute, Radiation Oncology

Department, Cairo, Egypt

2

Interdisciplinary Brachytherapy Unit, University of

Luebeck/UKSH-CL- Germany, Lübeck, Germany

3

Clinic for Gynecology and Obstetrics, University of

Luebeck/UKSH-CL- Germany, Lübeck, Germany

4

Clinic for Plastic Surgery, University of Luebeck/UKSH-

CL- Germany, Lübeck, Germany

5

5Institute for Oncology and Radiology IORS, Radiation

Oncology Department, Belgrad, Serbia

Purpose or Objective

Accelerated partial breast irradiation (APBI) has became a

valid option in treating patients with early stage breast

cancer following breast conservation surgery (BCS). This

work reports on the late toxicity and the cosmetic

outcome following APBI using interstitial multicatheter

HDR intensity modulated brachytherapy (HDR-IMBT).

Material and Methods

Between 2006 and 2014, 114 patients received adjuvant

APBI using interstitial multicatheter HDR-IMBT. Late

toxicities were reported according to both the

RTOG/EORTC score and the LENT/SOMA score. Cosmetic

changes were documented by taking digital photographs

before the APBI and during each follow-up visit. For each

patient, we assessed two photographs, the first was taken

after surgery and before APBI (baseline image), and the

second at the last available follow-up visit. The cosmesis

was assessed through a multidisciplinary team using the

Harvard breast cosmesis scale. The clinical and the

dosimetric parameters were investigated for any potential

correlations with the cosmetic results.

Results

The median follow-up period was 3.5 years (range 0.6 –

8.5). Late skin/soft tissue toxicities at the last follow-up

visit are listed in Table1. Ten patients had grade-3 toxicity

(8.8%) and no patients showed grade-4 toxicity. The most

common toxicities were fibrosis (56.2% by LENT/SOMA

score, and 47.4% by RTOG/EORTC score) followed by pain

(42.1%).

The final cosmetic scores were 81.5% excellent/good and

18.5% fair/poor. Comparing both the baseline and the last

follow-up cosmetic scores, 59.6% of the patients had the