Purpose:
The standardization of small field dosimetry is fundamental to
ensure that different institutions deliver comparable and consistent radi-
ation doses. The current study presents a multicenter evaluation of MLC-
defined small field Tissue Phantom Ratio (TPR), dose profiles FWHM and
penumbra and output factors (OF), for the two major linear accelerator
manufacturers.
Materials and Methods:
The project initially enrolled 31 Italian centers,
15 equipped with Elekta Linacs and 16 equipped with Varian Linacs. Each
center performed TPR measurement, in-plane and cross-plane dose profile
of 0.8
×
0.8 cm
2
field and OFs measurements for field sizes ranging from
0.6
×
0.6 to 10
×
10 cm
2
defined by both secondary jaws and MLC. Set-up
conditions were 10 cm depth in water phantom at SSD 90 cm. Measure-
ments were performed using the new Exradin W1 plastic scintillator
detector. To take into account for the Cerenkov effect, a correction factor
for each detector was measured and then applied before any measure-
ment session.
Results:
The analysis of the measurements performed by 13 Varian and
13 Elekta centers was performed; 7 centers were excluded due to mea-
surements inaccuracy, probably due to detector’s instability. TPR
measurements showed standard deviations within 0.6%; penumbra values
of dose profiles showed standard deviations within 0.5 mm, while FWHM
measurements showed a greater variability. OF measurements showed stan-
dard deviations within 1.5% for field size greater than 2
×
2 cm
2
; for field
size less than 2
×
2 cm
2
measurements’ variability increases with decreas-
ing field size. OF values show no dependence from the effective field size.
Conclusions:
Results show that there is a relatively high degree of con-
sistency regarding TPR and penumbra values. FWHM and OF instead show
greater variability, also for Linac with the same model of the head. Mea-
surements confirmW1 PSD as a candidate for small field clinical radiation
dosimetry in advanced radiation therapy techniques.
http://dx.doi.org/10.1016/j.ejmp.2016.01.138A.135
STUDY ON THE DOSIMETRY OF LASER ACCELERATED BEAMS FOR FUTURE
CLINICAL APPLICATIONS
R. Manna
* , a ,G.A.P. Cirrone
a ,G. Cuttone
a ,F. Romano
a ,V. Scuderi
a , b ,A.G. Amico
a , c ,G. Candiano
a ,G. Larosa
a ,R. Leanza
a , c ,V. Marchese
a ,G. Milluzzo
a , c ,G. Petringa
a , c ,J. Pipek
a ,F. Schillaci
a ,N. Amato
a ,G. Gallo
a ,L. Allegra
a .a
Laboratori Nazionali del Sud, Istituto Nazionale di Fisica Nucleare,
Catania, Italy;
b
Department of Experimental Program at ELI-Beamlines, Institute
of Physics of the ASCR, Prague, Czech Republic;
c
Dipartimento di Fisica e
Astronomia, Università degli studi di Catania, Catania, Italy
Introduction:
Charged particle acceleration, based on the interaction of
ultra-intense and ultra-short laser with a solid target, can represent a future
alternative to conventional techniques, in many applications, from Nuclear
Physics to Radiobiology.
In this context, The ELIMED (MEDical and multidisciplinary applications
at ELI-Beamlines) project aims to realise transport, diagnostics and dosi-
metric elements able to make suitable laser-driven ion beams for
multidisciplinary applications, with particular interest in hadrontherapy.
Materials and Methods:
The detectors dedicated to dosimetry of laser-
accelerated beams must offer a response independent of dose rate and they
must be suitable to operate with a highly intense beam pulse and strong
electromagnetic noise (EMP), in order to obtain a precise knowledge of the
absolute dose delivered, which is mandatory for clinical applications.
For the absolute dosimetry system, an innovative Faraday Cup, optimised
for highly pulsed ion beams, has been developed within the ELIMED
collaboration.
The designed FC has a peculiar geometry, which has been inspired to similar
detectors already developed for ion beam dosimetry; it contains a second
bevelled electrode coaxial and internal to a traditional one that deter-
mines a special-shaped electric field.
Results:
Dosimetric tests, performed with conventional proton beam at
CATANA facility (INFN-LNS), show that the innovative design of FC optimises
the charge collection efficiency and reduces the uncertainties related to the
charge collection in agreement with simulations performed using SIMION
software.
Furthermore, preliminary tests have been performed during experimen-
tal campaigns at laser facility; the preliminary results will be presented.
Conclusion:
New technologies and innovative dosimeters must be devel-
oped and realised in order to achieve an accurate evaluation of the dose
delivered for the future use of these non-conventional beams in medical
applications.
http://dx.doi.org/10.1016/j.ejmp.2016.01.139A.136
EVALUATION OF SCATTERED RADIATION FROM ELECTRON APPLICATORS
IN PATIENT WITH IMPLANTED ELECTRONIC DEVICES
L. Mantovani
*
, M. Lamborizio, G. Daprati, R. Di Liberto.
IRCCS Fondazione
Policlinico San Matteo, Pavia, Italy
Introduction:
In this study, the out-of-field scattered dose from electron
beams was measured in patient with implanted defibrillator Medtronic.
Manufacturing company indicates 5 Gy as maximum dose to prevent damage
or malfunction, but threshold dose may vary depending on the model.
Materials and Methods:
The PTV was the left parotid region irradiated with
9 MeV electron beam. The prescribed dose was 60 Gy (2 Gy per fraction),
using 10
×
10cm
2
applicator and 0.5 cm bolus. The inferior margin of PTV
valuated with CT scan was about 8 cm from defibrillator in longitudinal di-
rection; the depth of measurements was 1 mm simulating subcutaneous
region. The total dose to defibrillator was considered as amount of scat-
tered dose in body from direct beam and scattered dose in air from electron
applicator. The Monte Carlo algorithm, with CT scan and water-equivalent
slab phantom with a Markus chamber, were used to measure and evalu-
ate the scattered dose in tissue and in air respectively. Two P-type silicon
diode detectors have been used to monitor the dose delivered to defibril-
lator during treatment sessions.
Results:
The dose amount is mainly due to primary beam scattered from
electron applicator. In the experimental setup (ionization chamber posi-
tioned at the side of applicator edge) the total measured dose for the
complete treatment was 1.6 Gy. Dose typically increases with decreasing
distance from the source and falls with depth. Dose measured in-vivo with
semiconductor detectors confirms the expected results (0.05 Gy for single
fraction) and drastic dose reduction is obtained applying a 2 cmwater equiv-
alent bolus on the top of defibrillator.
Conclusions:
The results show that it is very important to evaluate ap-
propriate shielding for patient with electronic device to prevent
malfunctions. The dose measured can be significant when the applicator
is close to the electronic implanted device. The use of water equivalent bolus
is a practical solution to reduce peripheral dose.
http://dx.doi.org/10.1016/j.ejmp.2016.01.140A.137
PROTOCOL IMPLEMENTATION OF TOTAL MARROW IRRADIATION (TMI)
PLUS TOTAL LYMPHOID IRRADIATION (TLI) USING HELICAL
TOMOTHERAPY (HT)
M. Marcantonini
*
, a ,V. Lancellotta
b ,G. Montesi
b ,L. Falcinelli
a ,C. Aristei
b ,R. Tarducci
a .a
Perugia General Hspital, Perugia, Italy;
b
University of Perugia
and Perugia General Hospital, Perugia, Italy
Introduction:
TBI plays an important role in patients undergoing stem-
cell-transplant for a wide variety of hematological malignancies, but is
associated with significant toxicities. TMI plus TLI delivered with HT may
overcome this problem. The protocol implemented in our department is
here described.
Materials and Methods:
Head and shoulders of patient are immobilized
by means a thermoplastic mask, with arms along the sides. Buns, legs and
feet are positioned in a vacuum cushion. Two CT scans 1 cm slice thick-
ness are collected, with head first (part I) and with feet first (part II) supine
orientation. The PTV (expansions 3–7 mm) consisted of whole body skel-
etal bone, spleen and major lymph node areas. The main OARs are lungs,
heart, liver, kidneys, small intestine, eyes. The plan is prescribed to ensure
90% PTV dose coverage with the 90% of 13.5 Gy prescribed dose (1.5 Gy BID)
and D50%
=
13.5 Gy. Dose limit for lungs, heart, liver, kidneys, small intes-
tine, eyes are maxD50%
=
7.5 Gy, 8 Gy, 7.5 Gy, 7.5 Gy, 9 Gy, 6 Gy respectively.
For each CT a treatment plan is elaborated, FW
=
5.0 cm, Pitch
=
0.430 and
0.287, MF
=
2 and 2.5 for parts I and II. The junction region is divided into
3 parts A, B, C with D50%
=
7.0 Gy, 3.5 Gy, 1.0 Gy in part I and D50%
=
6.5 Gy,
e40
Abstracts/Physica Medica 32 (2016) e1–e70




