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S92

ESTRO 36

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derived DPs from treatment planning. In addition, the

maximal dose to the skin was determined. QC of EMT-

based dose distributions were normalized to the

corresponding values from treatment planning, so the

relative changes are reported.

Results

Without simulated errors, the maxim um dosimetric

deviations to the treatment plan were found on the 2

nd

treatment day in median -6.2% for the DNR and -4.3% for

the CI of the PTV.

For error simulation, 15,107 pairwise swaps of catheters

were analyzed. The reconstructed dose distributions

resulted in DNR changes form -22.7% to 38.9% (mean:

0.6%, SD: 5.5%) and CI changes from -63.5% to 11.4%

(mean: -7.4%, SD: 7.8%).

For each shift of single catheters, 2,264 combinations of

dose distributions were calculated. Relative dosimetric

changes for DNR ranged from -4.1% to 3.5%, from -6.8% to

6.2% and from -8.8% to 8.1% for catheter shifts of 5, 10

and 15 mm, respectively at mean values between 0.0% and

-0.3%. The CI for the PTV showed a mean change of -0.3%,

-1.3% and -2.8%, respectively. Increased catheter shifts

correlated with a higher local dose at the skin (see

figures). In addition, each 3D dose distribution was

analyzed to identify individual local dose deviations.

Conclusion

Statistically, the maximum dose deviation was found on

the 2

nd

day, what might impact boost treatments with two

fractions only. Based on EMT-determined dose

calculations adaptive treatment protocols and tests for

possible treatment delivery errors should be

implemented. Further work is required for the registration

method.

OC-0180 Prospective study of APBI With Multicatheter

Brachytherapy in Local Relapses of Breast Cancer

E. Villafranca Iturre

1

, L. Rubi

2

, M. Barrado

1

, A. Sola

1

, P.

Navarrete

1

, A. Manterola

1

, M. Dominguez

1

, G. Asin

1

, M.

Campo

1

, I. Visus

1

, G. Martinez

1

1

Hospital of Navarra, Radiation Oncology, Pamplona,

Spain

2

Hospital Juan Ramon Jimenez, Radiation Oncology,

Huelva, Spain

Purpose or Objective

To examine 5-year rates of local control for breast cancer

patients with local relapses after second conservative

surgery and accelerated partial breast irradiation (APBI).

Material and Methods

Eligibility included local relapses of breast cancer <3 cm

in size after lumpectomy with negative surgical margins.

The APBI dose delivered was 34 Gy in 10 twice-daily

fractions over 5 days for high-dose-rate. This analysis

focuses on ipsilateral breast recurrence(LBR), regional

recurrence (RR), and distant metastases (DM), disease-

free and overall survival.

Results

The median follow-up was 49.6 months (5-98m). Fithty

two patients (p) were accrued from Sep 2008 to August

2015.

Histology: Intraductal carcinoma 15 p, Ductal carcinoma

31 p, Lobulillar carcinoma: 5 p; Papilar carcinoma : 1p; 50

p had T1 tumors and 2 p had T2. Seventy-five percent were

estrogen receptor and/or progesterone receptor positive.

There have been 4 local breast recurrences, 1 regional

recurrence (RR), and 1 distant metastases (DM), The 5-

year Local Recurrence Disease Free rate was 91.6%. The

5-year Disease Free Survival and Overall Survival rates are

87 % and 100%, respectively.

Conclusion

This prospective trial studying APBI in local relapses of

Breast Cancer show a high local control, so this treatment

is an real option to Mastectomy in these patients

OC-0181 Long-term clinical and cosmetic outcomes of

high-dose-rate brachytherapy for early breast cancer

F. Arcidiacono

1

, L. Chirico

1

, M. Italiani

1

, P. Anselmo

1

, M.

Casale

1

, L. Draghini

1

, F. Trippa

1

, S. Fabiani

1

, M. Basagni

1

,

E. Maranzano

1

1

"S.Maria" Hospital, Radiotherapy Oncology Centre,

Terni, Italy

Purpose or Objective

To report long-term clinical and cosmetic outcomes of

partial breast irradiation (PBI) with

192

Ir high-dose-rate

brachytherapy (HDR-BRT) in early breast cancer patients.

Material and Methods

From May 2005 to February 2012, 124 patients undergoing

conservative surgery for early breast cancer were

recruited in a phase II trial of exclusive

192

Ir HDR-BRT.

Inclusion criteria were: age >40, PS 0-2, unifocal invasive

ductal cancer, intraductal cancer component <25%,

negative axillary nodes and tumor size ≤2.5 cm. Treatment

schedule was 4 Gy twice a day for 4-5 days, up to a total

dose of 32 Gy in 8 fractions with a minimum interval

between daily fractions of at least 6 hours. Late toxicity

was graded at each follow-up visit according to

RTOG/EORTC scoring criteria and cosmetic outcomes

according to Harvard criteria and scored as excellent,

good, fair and poor.

Results

Median age was 67 years (range, 42-85). There were 10

(8%) pT1a, 38 (31%) pT1b, 68 (55%) pT1c and 8 (6%) pT2.

Estrogenic and progestinic receptors were positive in 113

(91%) and 104 (85%) cases, respectively. 110 (88%) and 15

(12%) patients received adjuvant hormonal therapy and

chemotherapy, respectively. Median follow-up was 77

months (range, 8-132). 1 (0,8%) isolated out-field breast

relapse occurred 109 months after HDR-BRT. 1 (0,8%)

patient developed contralateral breast cancer

and another one (0,8%) regional relapse in axillary node.

13 (10,5%) patients reported a second primary cancer. 5-

and 10-year overall survival and cancer specific free

survival were 95% and 88%, 100% and 98%,

respectively. At last follow-up, 114 (92%) patients were

alive without disease and 3 (2,5%) with systemic disease.

10 (8%) patients died: 1 (0,8%) for breast cancer, 2 (1,6%)

for other cancers and 7 (5%) for other causes. Cosmetic

outcomes were excellent in 102 (82%), good in 11 (9%), fair