Table of Contents Table of Contents
Previous Page  547 / 1082 Next Page
Information
Show Menu
Previous Page 547 / 1082 Next Page
Page Background

S532

ESTRO 36 2017

_______________________________________________________________________________________________

Conclusion

Our results show that a prompt increase in γH2AX foci at

24 hours post-implant relative to baseline may be a useful

measure to assess elevated risk of late RT related

toxicities for PPB patients. A subsequent investigation

recruiting a larger cohort of patients is warranted to verify

our findings.

Poster: Radiobiology track: Radiobiology of breast

cancer

PO-0971 Estimating second malignancy risk in IMRT and

VMAT in radiotherapy for carcinoma of left breast

J. Selvaraj

1

, V. Sakthivel

2

1

The Canberra Hospital, Medical Physics and Radiation

Engineering, Canberra, Australia

2

Advanced Medical Physics, Medical Physics, Houston-

Texas, USA

Purpose or Objective

IMRT and VMAT produce dose distributions with superior

target dose uniformity and normal tissue sparing.

However, this increases amount of volume receiving very

low doses substantially compared to conventional

techniques. This increases the risk of radiation-induced

second malignancy (SCR) as reported in the literature. The

aim of this study is to use a mechanistic radiobiological

model which is more accurate in predicting the dose-

response at low as well as high dose levels to estimate

SCR. Studies have shown patient age at exposure is

important in estimating SCR, thus patients’ age is also

accounted for in the SCR estimation. Moreover, the

mechanistic model also takes cell proliferation and dose

fractionation into account.

Material and Methods

Fifty IMRT and VMAT plans with similar dose-volume

objectives were selected for the study. The prescription

dose was 50 Gy in 25 fractions to the PTV. Monte Carlo

based dose calculation engine was the preferred choice as

it is more accurate at low dose levels which is more

relevant for estimating SCR. Appropriate model

parameters were taken from the literature for the

mechanistic model to calculate excess absolute risk (EAR),

lifetime attributable risk (LAR), integral dose and relative

risk (RR) for both lungs, contralateral breast, heart and

spinal cord.

Results

The mean MU in IMRT and VMAT plans were 751.1±133.3

and 1004.8±180 respectively for IMRT and VMAT. The mean

EAR values per 10,000 person years (PY) estimated for

IMRT and VMAT treatments including gender-specific

correction with and without age correction factor are

shown in figure 3. The mean EAR values with one standard

deviation without age correction were 42.4±11.3,

10.6±6.0, 12.3±6.7, 1.9±0.7 and 0.6±0.3 for left lung, right

lung, contralateral breast, heart and spinal cord

respectively for the IMRT plans. These values were

51.9±19.7, 28.7±11.4, 31.9±13.4, 2.3±0.8 and 1.5±0.8 for

the VMAT plans. However the values were reduced with

age correction, especially for the contralateral breast.

The values obtained with age correction were 44.6±11.9,

11.2±6.4, 5.4±4.0, 1.4±0.5 and 0.3±0.2 for left lung, right

lung, contralateral breast, heart and spinal cord

respectively for the IMRT treatments and 54.6±20.6,

30.2±12.0, 13.8±8.6, 1.6±0.6 and 0.9±0.5 for the VMAT

treatments.

Conclusion

Results showed VMAT plans had a higher risk of developing

second malignancy in lung, contralateral breast, heart and

cord compared to IMRT plans. However, the increase in

risk was found to be marginal. The increase in risk was

greater in both IMRT and VMAT for left lung and

contralateral breast compared to other organs included in

the study. Incorporating the age correction factor

decreased the risk of contralateral breast SCR. No strong

correlation was found between EAR and MU.

PO-0972 Breast cancer cell survival using flattening

filter-free beam compared to a standard flattened beam

M. Boccia

1

, L. Manti

2

, S. Clemente

3

, C. Oliviero

3

, F.

Perozziello

2

, R. Liuzzi

4

, M. Conson

1

, L. Cella

4

, R. Pacelli

1

1

Federico II University School of Medicine, Department of

Advanced Biomedical Sciences, Napoli, Italy