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S153

ESTRO 36 2017

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irregularities. The limitation of CBCT for needing bony

landmarks, surrogates, the need for large tissue density

differences or the retrospective binning to assess motion

data will be solved when using MRI. So MRI is at the very

least a much better CBCT in the sense that it provides

direct visualization of target and surrounding structures.

CBCT guided proton therapy is lagging behind on the much

needed image guidance offered by MRI and hybrid MRI

radiotherapy systems will improve position verification.

On-line MRI will also enable on-line re-planning strategies

that are not, or only for some sites, feasible with CBCT as

an input. This on-line re-planning fits seamlessly into the

large research interest of the radiotherapy community to

adapt the dose more to the actual anatomy and deliver

more conformal dose distributions, currently being

implemented via library of plans or off-line re-planning

strategies.

Moreover, integrated MRI allows imaging during radiation

delivery. This way, assumptions on anatomical stability or

motion as determined on pre-treatment data can be

verified. Also, the intra-fraction volumetric imaging

provides the input for dose reconstruction, so even if the

pre-treatment assumptions are failing and the anatomy is

moving/deforming unexpectedly, one can reconstruct

exactly what the dose delivered is. This can be used for

off-line re-optimization for remaining fractions.

Additionally, as this dose reconstruction can be done in

near real-time, one can also built adaptation triggers on it

such as gating and ultimately intra-fraction re-planning

strategies. The latter would be truly interventional

radiosurgery where the dose distribution is continuously

adapted to the mobile anatomy.

Another advantage of integrated MRI radiotherapy systems

is the capability to assess functional parameters such as

perfusion or water diffusion, from the patient in

treatment position. This can provide great insight in

treatment response and temporal behavior during the

course of radiotherapy.

In summary

, there is a clear desire from the image guided

radiotherapy community to use more and better imaging

prior and during radiation delivery. MRI guided photon

therapy can fulfill this desire and will contribute to more

precise radiation delivery and to a more hypo-fractionated

approach. With that hybrid MRI radiotherapy systems will

become the first choice for radiotherapy and CBCT guided

proton therapy is mainly indicated in case the integral

dose is treatment limiting, e.g. for pediatrics.

SP-0299 Against the motion

A. Lomax

1

Paul Scherrer Institute PSI, CPT, Villigen PSI, Switzerland

Abstract not received

Proffered Papers: Intra-fraction motion management

OC-0300 Proof of tumor position during SBRT delivery

using (limited-arc) CBCT imaging

C. Hazelaar

1

, M. Dahele

1

, B. Slotman

1

, W. Verbakel

1

1

VU University Medical Center, Radiotherapy,

Amsterdam, The Netherlands

Purpose or Objective

SBRT requires accurate patient positioning and robust

positional verification during irradiation itself is desirable.

We investigated if CBCT scans reconstructed from

(collimated) fluoroscopic kV images acquired during

irradiation, including over a limited arc length, can

provide information on the average tumor position, for

spine and lung SBRT.

Material and Methods

In total, 38 fluoroscopy datasets (1 dataset/arc) of 16

patients treated with spine SBRT were used for full-arc

CBCT reconstruction. The kV images were continuously

acquired at 7, 11, or 15 frames/s with a field size ranging

from 10.5x9cm² to 26.6x20cm² (full field) during

flattening filter free VMAT delivery. For reconstruction, a

standard “spotlight” mode template was modified to suit

our data, i.e. full 360° trajectory, full fan, no filters, and

100 kV. The FDK filtered back projection algorithm was

used to reconstruct the CBCTs and the scans were

matched to the planning CT in Offline Review (Varian

Medical Systems, Palo Alto, CA). For validation purposes,

the resulting match values were compared to the average

spine offset values found using template matching +

triangulation of the individual kV images. For lung SBRT,

limited-arc CBCTs were reconstructed from fluoroscopic

images acquired during irradiation of a lung lesion

embedded in a 3D printed anthropomorphic thorax

phantom and of one patient treated in breath-hold. In

order to determine which arc length is required to obtain

sufficient image quality for reliable CBCT-CT matching,

multiple limited-arc CBCTs were reconstructed using arc

lengths from 180° down to 20° in steps of 20°.

Results

3D spine CBCT-CT registration revealed mean positional

offsets of -0.1±0.8 mm (range: -1.5–2.2) for the lateral, -

0.1±0.4 mm (range: -1.3–0.7) for the longitudinal, and -

0.1±0.5 mm (range: -1.1–1.3 mm) for the vertical

direction. Comparison of these match results to the

average spine offsets found using template matching +

triangulation showed mean differences of 0.1±0.1 mm for

all directions (range: 0.0–0.5 mm). For limited-arc CBCTs

of the lung phantom, the automatic CBCT-CT match

results were ≤1mm in all directions for arc lengths of 60-

180°, but in order to perform 3D visual verification, an arc

length of at least 80° was found to be desirable. 20° CBCT

reconstruction still allowed for positional verification in 2

dimensions. The figure illustrates a limited-arc CBCT over

80° for a phantom and 100° for a patient.

Conclusion

Using standard techniques, we have been able to obtain

CBCT reconstructions of planar kV images acquired during

VMAT irradiation. For treatments consisting of partial

arcs, e.g. lung breath-hold treatments, limited-arc CBCTs

can show the average tumor position during the actual

treatment delivery. It is anticipated that this capability

could be implemented clinically with few modifications to

current treatment platforms. This could substantially

improve positional verification during irradiation.

OC-0301 Target position uncertainty during visually

guided breathhold radiotherapy in locally advanced

NSCLC

J. Scherman Rydhög

1

, S. Riisgaard Mortensen

1

, M.

Josipovic

1

, R. Irming Jølck

2

, T. Andresen

3

, P. Rugaard

Poulsen

4

, G. Fredberg Persson

1

, P. Munck af Rosenschöld

1

1

Rigshospitalet, Department of Oncology- Section of

Radiotherapy, Copenhagen, Denmark

2

DTU Nanotech and Nanovi Radiotherapy A/S,

Department of Micro-and Nanotechnology- Center for

Nanomedicine and Theranostics, Lyngby, Denmark

3

DTU Nanotech, Department of Micro-and