Table of Contents Table of Contents
Previous Page  640 / 1082 Next Page
Information
Show Menu
Previous Page 640 / 1082 Next Page
Page Background

S624

ESTRO 36 2017

_______________________________________________________________________________________________

occurring during 90 days from the start of HWBI, overall

survival (OS), disease-free survival (DFS), ipsilateral-

breast relapse-free survival (IB-RFS), and the proportion

of breast cosmetic change. Early AEs and late ARs were

evaluated using CTCAE ver3.0. Survival time was

estimated by the Kaplan-Meier methods.

Results

Between 2010 and 2012, 312 women were registered. 306

patients received HWBI and 66 patients received HWBI

with BI, but six chose CWBI prior to the start of irradiation.

301 patients (96.5%; 95%CI: 93.8-98.2) were treated within

the recommended period. Evaluation of early AEs found

that 38 patients (12.4%) had grade 2, including 25 patients

(8.2%) with radiation dermatitis, and no patients had

grade 3/4. On 306 patients receiving HWBI, 3-years OS,

DFS and IB-RFS were 99.7% (95%CI: 97.7-100), 95.7%

(95%CI: 92.7-97.5) and 99.0% (95%CI: 97.0-99.7). Among

303 (97%) patients, evaluation of late ARs found that 13

patients (4.3%; 90%CI: 2.6-6.7) had grade 2/3, including

one of grade 3 pneumonitis. None had grade 4 or

treatment-related death.

Conclusion

Short-course HWBI is considered as one of the standard

treatments for Japanese women with margin-negative

invasive breast cancer after BCS. Further follow-up is

continued and cosmetic outcome will be analyzed.

EP-1157 Serial changes of post-lumpectomy seroma

during MRI-guided partial breast irradiation

S.H. Jeon

1

, K.H. Shin

1

, S.Y. Park

1

, J.M. Park

1

1

Seoul National University Hospital, Radiation Oncology,

Seoul, Korea Republic of

Purpose or Objective

After breast conserving surgery, the volume of post-

lumpectomy seroma changes by time. We analyzed serial

changes of seroma volume (SV) using magnetic resonance

image (MRI) to investigate the possible benefit of adaptive

radiation therapy during partial breast irradiation (PBI).

Material and Methods

From October 2015 to July 2016, 37 patients were

prospectively included in the study. A total dose of 38.5

Gy in 3.85 Gy fractions once daily was prescribed to the

planning target volume (PTV). The PTV was defined as

unequal margins of 1-1.5cm added according to the

directional safety margin status of each seroma.

Treatment was done using MRI-guided radiation therapy

(ViewRay system). During the 10 fractions of treatment,

MRI scans were acquired at the time of simulation, 1st,

6th and 10th fractions.

Results

The average time intervals of surgery-simulation,

simulation-1st, 1st-6th, and 6th-10th fractions were 23.1,

8.5, 7.2, and 5.9 days, respectively. SV was smaller during

treatment than at simulation in 34 patients. Mean SV

decreased from 100% at simulation to 65%, 55%, and 47%

at each MRI scan. Age, body mass index, tumor size,

seroma location, SV and delivery of radiotherapy did not

showed association with SV change (p>0.05, student’s t-

test). In 34 patients with decreased SV, mean PTVs were

84.7 cm

3

and 56.9 cm

3

at simulation and 6th fraction,

respectively, and their difference was proportional to SV

at simulation (r=0.832, p<0.001, pearson’s correlation

test).

Conclusion

During PBI, rate of SV change is associated with time

elapsed from surgery. Frequent monitoring of seroma

change with MRI seems helpful for all patients receiving

PBI.

EP-1158 Vmat radiation induced nausea/vomiting in

adjuvant breast cancer radiotherapy: dosimetrical

issues.

G. Lazzari

1

, A. Terlizzi

1

, B. Turi

1

, M.G. Leo

1

, D. Becci

1

, G.

Silvano

1

1

Azienda Ospedaliera SS. Annunziata Presidio Osped,

Radiology, Taranto, Italy

Purpose or Objective

Breast radiotherapy is associated with a minimal

emetogenic risk in MASCC/ESMO guidelines. Although the

emetogenic potential risk is estimated < 30%, VMAT

adjuvant radiotherapy may induce an unexpected acute

toxicity defined radiation induced nausea and vomiting

(RINV) as we observed in our experience. Aim of our report

is to find a correlation between dosimetrical factors and

RINV occurrence in our patients (pts).

Material and Methods

In our institutionfrom January 2013 to May 2016 106 breast

cancer pts were treated with adjuvant radiotherapy (RT)

in VMAT modality. Al pts had surgery ( conservative or

radical). Mean age was 54 years. Neoadjuvant or adjuvant

chemotherapy was given in 6 pts and 68 pts respectively

(62 pts had high risk emetogenic agents combination, 12

pts had CMF). Left side breasts were treated with in 95

pts, right breast RT occurred in 11 pts. CT planning

included all the chest from C6 to D12-L3 vertebrae. PTV

consisted of residual breast or chest wall and nodal sites.

According ICRU 83 , the prescribed dose was 50 Gy total

dose (2 Gy/25) to breast-chest wall and internal mammary

chain (10 pts). Supraclavicular nodes (36 pts) were treated

simultaneously , 1.92 Gy/25 fractions to 48 Gy total dose.

VMAT was planned on treatment planning system Oncentra

Masterplan® (collapsed cone algorithm) or Monaco®

(Monte Carlo photon algorithm) and consisted of dual arc

plan (170°/340° for left breast; 190°/20° for right breast)

and 6 MV photons beams. In all the pts we retrospectively

contoured on CT planning a volume containing the

anatomical structures of emetic vagal-simpatical

afferental pathways as the celiac plexus and

gastroesophageal junction (GEJCPs). This area was

identified as an organ at risk (OAR) for which the total

volume, Dmax, Dmean and D1cc were calculated.

Univariate analysis with χ

2

, t-test and Pearson covariance

were used for statistical analysis.

Results

On 106 pts, 68 (64%) patients complained acute RINV

according CTCAE v.3 criteria G1 nausea in 46 pts (43%), G2

nausea in 13 pts (12%), G1 vomiting in 8 pts (7 %) were

recorded. Symptoms occurred at 34 Gy delivered dose

(mean 30 Gy, range 20-34). In right side irradiated breasts

RINV occurred in 3 pts (27%), in left side RT in 65 pts (60%).

RINV was related to a Dmax >10 Gy on GEJCPs (p < 0.005).

G1 vomiting and G2 nausea were related to a Dmax > 17

Gy (p < 0.005) and to a Dmax > 15 Gy (p < 0.005)

respectively. Radiation breast side, age, systemic

therapy, nodal radiation and PTVs volume values were not

statistically significant for RINV.

Conclusion

RINV in breast radiation is not a common acute side effect.

VMAT in breast radiation is responsible for a low dose bath

to nearest structures as the GEJCPs and this may explain

RINV in our cases. A useful constraint as Dmax < 10 Gy on

GEJCPs like a serial structure may be considered in VMAT

breast planning to avoid RINV.

EP-1159 Hypofractionated adjuvant radiotherapy and

concomitant trastuzumab for breast cancer: 5-year

results

M. Pasetti

1

, A. Fodor

1

, C. Sini

2

, F. Zerbetto

1

, P. Mangili

2

,

P. Signorotto

2

, I. Dell'Oca

1

, C. Gumina

1

, M. Azizi

1

, A.M.

Deli

1

, P. Passoni

1

, N. Slim

1

, C.L. Deantoni

1

, B. Noris

Chiorda

1

, S. Foti

1

, A. Chiara

1

, G. Rossi

1

, C. Fiorino

2

, A.

Bolognesi

1

, N.G. Di Muzio

1

1

San Raffaele Scientific Institute, Department of

Radiotherapy, Milano, Italy

2

San Raffaele Scientific Institute, Medical Physics,

Milano, Italy

Purpose or Objective