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S181

ESTRO 36 2017

_______________________________________________________________________________________________

lungs, intestine and stomach; smaller than 5Gy for scalp

and kidneys (Figure 2). Moreover, protons provide the

smallest non-PTV integral doses (V1Gy: 53% 3D-CRT, 69%

photons MT, 15% PBS; V5Gy: 23% 3D-CRT, 43% photons MT,

12% PBS). A considerable variation in PTV and OAR

dosimetry was observed within a certain technique.

Conclusion

Modern radiotherapy techniques demonstrate superior

conformity and homogeneity, and reduced mean dose the

OARs compared to 3D-CRT.

PBS produced the case with the lowest mean dose for each

OAR and integral doses. However, the variability among

centres using the same technique means it is not possible

to clearly identify the best technique from this

data. Efforts should be made to improve inter-centre

consistency for each technique.

OC-0346 Multicentre audit of SBRT oligometastases

plan quality

J. Lee

1

, R. Patel

1

, C. Dean

2

, G. Webster

3

, D.J. Eaton

1

1

Mount Vernon Cancer Centre, National Radiotherapy

Trials QA RTTQA Group, Northwood, United Kingdom

2

Barts Health NHS Trust, Radiotherapy Physics, London,

United Kingdom

3

Worcestershire Oncology Centre, Radiotherapy Physics,

Worcester, United Kingdom

Purpose or Objective

SBRT for oligometastases is currently being used to treat

patients at 17 centres in England, as part of the NHS

England “Commissioning through Evaluation” programme.

The national trials QA group conducted QA for the

programme, which included establishing appropriate

clinical plan quality metrics for auditing submitted SBRT

plans. The purpose of the audit was to inform future

guidance on plan quality metric tolerances and help

centres determine whether a given plan is optimal.

Material and Methods

Plans included were either benchmark plans using pre-

delineated CT images planned by all cen tres prior to

patient recruitment; or plans of initial patients reviewed

prior to treatment. VODCA software (Medical Software

Solutions) was used for independent plan review. Lung

plans were analysed separately due to the inherent

differences in scatter conditions around the tumour.

Initial analysis showed a high proportion of plans where

PTV coverage was compromised. Plan quality metrics were

therefore developed which were independent of PTV

coverage. These metrics are defined in eqn1 and eqn2:

where V

100%

and V

50%

are the volumes covered by 100% and

50% of the prescription dose (the dose intended to cover

the target) respectively. The mean, median and standard

deviation are reported for both metrics, split into PTV

V

100%

volume ranges of 0-20cc, 20-40cc and >40cc.

Results

38 lung and 77 non-lung (lymph node, liver, adrenal and

bone) plans were reviewed, produced for treatment using

Cyberknife (29), Tomotherapy (7), VMAT (71), fixed gantry

angle IMRT (5) or 3D conformal (3) modalities. 11% of lung

patients and 29% of non-lung patients had significantly

compromised PTV coverage (PTV V

100%

< 90%). The spillage

results for lung and non-lung sites were similar. Modified

Gradient Index (MGI) values were higher for lung than non-

lung sites and decreased with increased treated volume

(see table 1). No clinically significant differences were

seen between treatment platform or modality.

Table 1. The mean, median and standard deviation of the

“Spillage” and “Modified Gradient Index” plan quality

metrics for lung and non-lung oligometastatic SBRT plans.

Conclusion

The high proportion of non-lung patient plans with

compromised target coverage suggests that future

guidance documents should use plan quality metrics which

are independent of coverage, such as those proposed

here. The similar spillage results for lung and non-lung

sites suggest that for this metric, site specific tolerances

are not required. The MGI is higher for lung plans, as

expected with the increased scatter in low density

surroundings. MGI lung and non-lung results are similar in

absolute terms and so equivalent planning tolerances

could be applied to both groups. These data provide

evidence of what plan quality is achievable across multiple

treatment platforms, modalities and clinical sites. These

are particularly useful for non-lung oligometastatic SBRT

plans where there is currently a lack of data in the

literature.

OC-0347 Key factors for SBRT planning of spinal

metastasis: Indications from a large scale multicentre

study

M. Esposito

1

, L. Masi

2

, M. Zani

3

, R. Doro

2

, D. Fedele

3

, S.

Clemente

4

, C. Fiandra

5

, F.R. Giglioli

6

, C. Marino

7

, S.

Russo

1

, M. Stasi

8

, L. Strigari

9

, E. Villaggi

10

, P. Mancosu

11

1

Azienda Sanitaria USL centro, S.C. Fisica Sanitaria,

Firenze, Italy

2

Centro CyberKnife IFCA, Medical Physics, Firenze, Italy

3

Casa di cura San Rossore, Radioterapia, Pisa, Italy

4

Azienda Ospedaliera Universitaria Federico II, Medical

Physics, Napoli, Italy

5

Università degli Studi di Torino, Medical Physìcs,

Torino, Italy