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S220

ESTRO 36 2017

_______________________________________________________________________________________________

Conclusion

The proposed method of analysis of isolated errors gives

the magnitude of errors. In general, the most important

are leaf gap width errors. Exception and further analysis

is required for VMAT patients with low DR. ArcCheck

positioning errors should not affect the gamma results

while being in specification tolerance.

PV-0421 In-magnet measurement setup for proof-of-

concept and commissioning of MR integrated proton

therapy

A. Lühr

1,2,3

, S. Gantz

1,3

, S. Schellhammer

1,3

, O. Zarini

4

, K.

Zeil

4

, U. Schramm

4

, A. Hoffmann

1,3,5

1

Helmholtz-Zentrum Dresden - Rossendorf, Institute of

Radiooncology, Dresden, Germany

2

German Cancer Consortium DKTK, Partner Site Dresden,

Dresden, Germany

3

OncoRay – National Center for Radiation Research in

Oncology, Medical Radiation Physics, Dresden, Germany

4

Helmholtz-Zentrum Dresden - Rossendorf, Institute of

Radiation Physics, Dresden, Germany

5

Faculty of Medicine and University Hospital Carl Gustav

Carus at the Technische Universität Dresden,

Department of Radiation Oncology, Dresden, Germany

Purpose or Objective

There is growing interest to explore the concept of

magnetic resonance integrated proton therapy (MRiPT).

However, no experimental proof-of-principle has been

established so far. The aim of this work was to develop an

in-magnet measurement setup that facilitates to

investigate the dosimetric feasibility of MRiPT and to

develop a commissioning procedure for future MRiPT

devices.

Material and Methods

A C-shaped 0.95 T permanent neodymium (NdFeB) dipole

magnet was used. The magnetic main and fringe fields

were characterized using 3D automated Hall probe

measurements. A method and procedure were established

to perform periodic quality assurance (QA) measurements

of the magnetic field’s constancy. A 3D vector field

representation for the magnetic flux density distribution

was calculated by finite-element modeling (FEM) using

COMSOL-Multiphysics®. For irradiation experiments,

proton beams of 80–225 MeV were collimated using brass

apertures having circular voids of either 5 or 10 mm

diameter. The beams entered a PMMA slab phantom being

placed inside the magnet’s horizontal air gap,

perpendicularly to the main field component. Proton

beam trajectories and depth-dose curves in the presence

of the magnetic field were measured with Gafchromic

EBT3 film, being placed between the two slabs of the

phantom. Reference trajectories were measured without

magnetic field. In transmission experiments without

phantom, beam deflections were measured with a 2D

scintillation detector (Lynx, IBA Dosimetry) positioned

perpendicular to the beam at 24 cm distally from the

magnet.

Results

Magnetometry results (Fig. 1) validated the 3D magnetic

flux density distribution as calculated by FEM. The

simulation tended to underestimate the measured

magnetic field strength in the plateau area by about 2%

(mean difference 20 mT). In repeated QA measurements,

field strength changes remained below a threshold of 3

mT. For all proton energies, the lateral beam deflection

due to the magnetic field increased with depth in the

phantom. Lateral displacement of the Bragg peak position

increased with initial energy, from 1.1 (±0.4) mm to 10.7

(±0.8) mm, for 80 and 180 MeV (Fig. 2), respectively. In

transmission measurements, only lateral deflections were

measurable, ranging from 56 (±0.5) to 30 (±0.5) mm for

beam energies between 80 and 225 MeV, which was in

excellent agreement with theoretical predictions.

Conclusion

An in-magnet measurement setup for first MRiPT proof-of-

principle experiments has been realized. Measurements of

the magnetic field and proton beam trajectory in tissue-

equivalent material proofed to be feasible and facilitate

the development of commissioning and QA procedures for

MRiPT. Ongoing experiments focus on the impact of

realistic treatment fields as well as the effect of

inhomogeneous media on the dose distribution. The data