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S91

ESTRO 36 2017

_______________________________________________________________________________________________

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

in 8 (6%) and unknown in 3 (2,5%) patients. Late skin

toxicity was registered in 29 (23,4%) patients, grade 1-2 in

28 (22,5%), grade 3 in 1 (0,8%). Late toxicity was

significantly related to the skin administered doses (≤ 55%

vs. > 55%,

P

< 0.05).

Conclusion

PBI delivered with

192

Ir HDR-BRT in selected breast cancer

patients was associated to high local control and survival

with excellent cosmetic outcomes. An appropriate

patient selection and skin dose ≤ 55% provided optimal

clinical outcomes.

OC-0182 2nd breast conserving therapy with

interstitial BT vs mastectomy for treatment of local

recurrences

V. Smanykó

1

, N. Mészáros

1

, M. Ujhelyi

2

, G. Stelczer

1

, T.

Major

1

, Z. Mátrai

2

, C. Polgár

1

1

National Institute of Oncology, Center of Radiotherapy,

Budapest, Hungary

2

National Institute of Oncology, Center of Surgery,

Budapest, Hungary

Purpose or Objective

To compare the clinical outcomes of second breast

conserving therapy (BCT) with perioperative high-dose-

rate (HDR) interstitial brachytherapy (iBT) versus salvage

mastectomy (sMT) for the treatment of ipsilateral breast

tumor recurrences (IBTRs).

Material and Methods

Between 1999 and 2016, 92 patients who presented with

an IBTR after previous BCT were salvaged either with

reexcision and perioperative HDR multi-catheter iBT

(n=35) or sMT (n=57). In the BCT + HDR iBT group a median

of 7 (range: 4-23) catheters were implanted

intraoperatively. A total dose of 22 Gy in 5 fractions of 4.4

Gy was delivered to the tumor bed with a margin of 1-2

cm perioperatively on 3 consecutive days. Similar

proportion of patients received adjuvant chemotherapy in

the two groups (17% after BCT + HDR iBT vs 21% after sMT)

and/or hormonal treatments (71% vs 70%, respectively).

Five-year oncologic outcomes (including ultimate local

tumor control, regional tumor control, disease-free

survival [DFS], cancer specific survival [CSS], and overall

survival [OS]) were estimated by the Kaplan-Meier

method. Survival curves were compared with the log-rank

test.

Results

Mean follow up time was 63 months (range: 2-183) in the

BCT + HDR iBT group vs 30 months (range: 4-164) in the

sMT group. The mean diameter of IBTRs was 16.8 mm

(range: 2-70) vs 24.5 mm (range: 2-60), respectively.

There was no significant difference in any other patient

(e.g. age, menopausal status) or IBTR related (e.g. grade,

vascular invasion, margin status, receptor status)

parameters between the two groups. Three out of 35

(8.6%) and 7 out of 57 (12.3%) second local recurrences

occurred in the BCT + HDR iBT and the sMT group,

respectively. The 5-year actuarial rate of second local

recurrence was 7.4% after BCT + HDR iBT vs 17.5% after

sMT (p=0.11). The respective 5-year rates of regional

recurrence were 7.2% vs 5.3% (p=0.17). The 5-year

probability of DFS, CSS, and OS were 69.7% vs 73.5%

(p=0.79), 74.9% vs 80.5% (p=0.72), and 74.9% vs 69.6%

(p=0.73), respectively. At the time of analysis data on

cosmetic results were available for 31 patients (88.6%) in

the BCT + HDR iBT group. Among these, 3 (9.7%), 16

(51.6%), 5 (16.1%), and 7 (22.6 %) patients had excellent,

good, fair, and poor cosmetic results. Grade 2 and 3 late

skin toxicity occurred in 2 (5.7%) and 1 (2.9%) patients,

while grade 2 and 3 fibrosis developed in 9 (25.7%) and 1

(2.9%) patients. Asymptomatic fat necrosis was detected

in 11 (31.4%) women.

Conclusion

Second BCT + HDR iBT is a safe and feasible option for the

management of IBTRs resulting similar 5-year oncologic

outcomes compared to standard sMT. HDR iBT may