Table of Contents Table of Contents
Previous Page  955 / 1082 Next Page
Information
Show Menu
Previous Page 955 / 1082 Next Page
Page Background

S939

ESTRO 36 2017

_______________________________________________________________________________________________

Figure 1: Planning Study target doses

Material and Methods

Eight clinical cases were identified as part of the initial

planning study and independently re-planned per the RT

trial protocol with and without dose escalation by two

experienced IMRT planners. A single (female) case was

then selected representative of a typical yet challenging

case and used as the planning benchmark.

Ten of the fifteen centres participating in the pilot phase

of the trial completed the benchmark planning case,

planning with dose escalation only. All pilot centre data

was processed with CERR

[1]

software enabling dose

distribution and dose volume histograms to be assessed.

Results

Dose escalated plans for the initial eight cases showed no

statistically significant increase in dose to the OAR with

dose escalation (p-value>0.1) whilst maintaining PTV

coverage (D95%>95%).

Ten centres participating in the pilot phase completed the

pre-trial exercise. A range of plan beam configurations

were used: 1x 2arc 6 flattening filter free (FFF) MV, 2x

3arc 6MV, 2x 7-field IMRT 6MV, 2x2arc 6MV, 2x

Tomotherapy and 1x 4arc 6MV.

All centres met all trial mandatory dose objectives for the

benchmark planning case and the vast majority of optimal

constraints, see table 1

.

Table 1: Optimal and mandatory dose constraints

Conclusion

Two sequential planning excercises have demonstrated

dose escalation in anal cancer patients is achievable

without sacrifice of OAR sparing. This shows OAR sparing

is achievable across multiple centres using a variety of

planning techniques, giving expectation of consistent

quality plans for trial patients.

Over 30 sites will join the trial in the next phase and will

complete the same RTQA process.

References

[1]

A Computational Environment for Radiotherapy

Research, CERR; Online:

http://www.cerr.info/about.php

EP-1733 Proton grid therapy (PGT): a parameter study

T. Henry

1

, A. Valdman

2

, A. Siegbahn

1

1

Stockholm University, Department of Medical Physics,

Stockholm, Sweden

2

Karolinska Institutet, Department of Oncology and

Pathology, Stockholm, Sweden

Purpose or Objective

Proton grid therapy (PGT) with the use of crossfired and

interlaced proton pencil beams has recently been

proposed by our research group. A clear potential for

clinical applications has been demonstrated. The beam

sizes used in our proof-of-concept study were in the range

7-12 mm, full-width at half maximum (FWHM),

representing the typical range of available proton pencil-

beam widths at a modern proton therapy facility.

However, to further take advantage of the dose-volume

effect, on which the grid therapy approach is based, and

thereby improve the overall outcome of such treatment,

smaller beams are desirable. In this present study, Monte-

Carlo (MC) simulations of a simple PGT treatment were

performed with varying beam sizes and center-to-center

(c-t-c) distances between the beams. The aim was to

determine which combinations of those two parameters

would produce the most therapeutically desirable dose

distributions (high target dose and low valley dose outside

of the target).

Material and Methods

MC calculations were performed using TOPAS version 2.0

in a 20x20x20 cm

3

water tank. The beam grids were aimed

towards a 2x2x2 cm

3

cubic target at the tank center. Two

opposing (or 2x2 opposing) grids were used. The target was

cross-fired in an interlaced manner. Grids containing

planar beams (1-D grids) or circular beams (2-D grids) were

considered. Three beam widths (1, 2 and 3 mm FWHM) and