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S386

ESTRO 36 2017

_______________________________________________________________________________________________

Conclusion

Our experience suggests that the combination of

Ipi+SRS/SRT in MBMs pts can obtain a better survival with

a low toxicity profile related to combined treatment. The

high precision of treatment with Cyberknife allows to

reduce radiation of organs at risk. The optimal timing of

combination Ipi+RT is not clear, but from our experience

it would seem to be a benefit of using the Ipi before

SRS/SRT on LC. The recruitment of a greater number of

pts and a longer follow-up are needed to demonstrate the

role of Ipi also in the treatment of melanoma pts with BMs

and the better sequence with RT.

Poster: Clinical track: Sarcoma

PO-0742 Target delineation conformity in extremity

STS within the UK phase II multi-centre IMRiS trial

H. Yang

1

, R. Simões

1

, F. Le Grange

2

, S. Forsyth

3

, D.

Eaton

1

, B. Seddon

2

1

Mount Vernon Cancer Centre, National Radiotherapy

Trials Quality Assurance Group, Northwood, United

Kingdom

2

University College Hospital, Sarcoma Unit, London,

United Kingdom

3

University College London, Cancer Research UK &

University College London Cancer Trials Centre, London,

United Kingdom

Purpose or Objective

Accurate target volume delineation is essential in the use

of intensity-modulated radiotherapy, where its role in the

treatment of bone and soft tissue sarcoma (STS) is being

investigated for the first time within the UK in IMRiS, a

prospective multi-centre phase II trial.

As part of radiotherapy trials quality assurance, we

determined the conformity of volume delineation of an

extremity STS benchmark training case in the post-

operative setting, and report target outlining variation in

relation to the trial protocol.

Material and Methods

The clinical history, operation/histology reports, pre-

operative magnetic resonance imaging and planning scans

of the training case were made available to participating

clinicians, who submitted outlines based on the protocol.

Both first and re-submissions were evaluated by two

clinicians, where GTV, CTV_6000 and CTV_5220 were

compared to the reference contours. The volumes were

quantitatively assessed using Dice Similarity Coefficient

(DSC) as:

, where A and B represent

regions of interest. Individual feedback based on trial

protocol variations was provided for all submissions.

Results

There was a total of 25 submissions from 23 centres.

Delineation of GTV, CTV_6000 and CTV_5220 were

deemed unacceptable according to the protocol in 5(20%),

10(40%) and 5(20%) submissions respectively.

The table details the unacceptable variations from the

protocol. All unacceptable GTV contours failed to

reconstruct the pre-operative disease in its entirety.

Incorrect margin expansion constituted the majority of the

unacceptable submissions for both CTVs.

The mean DSCs were systematically lower for the

unacceptable contours compared to accepted contours for

GTV [0.61 (range 0.55–0.66) vs 0.77 (range 0.60–0.81),

p<0.001], CTV_6000 [0.75 (range 0.53–0.82) vs 0.82 (range

0.77–0.89), p=0.036] and CTV_5220 [0.15 (range 0.02–

0.36) vs 0.43 (range 0.11–0.64), p=0.002].

CTV_5220 was incorrectly positioned in 5 submissions due

to the contouring inaccuracies of GTV/CTV_6000. Other

variations in the inclusion of the scar/seroma were seen

where it was not fully encompassed axially (CTV_6000: 8

submissions, CTV_5220: 6 submissions), and wh ere

CTV_6000 was extended beyond margins longitudinally to

include it (5 submissions). In addition, some volumes were

tapered where the anatomical planes were not followed

lengthwise (CTV_6000: 5 submissions, CTV_5220: 13

submissions).

There were five re-submissions after feedback, for which

all target volumes had either acceptable, or no variation

from the protocol (mean DSC GTV: 0.75, CTV_6000: 0.83,

CTV_5220: 0.48).

Conclusion

High numbers of unacceptable variations from the trial

protocol were seen in the first submission of the training

case; the adherence to the protocol improved following

individualised feedback. As the outlining of both CTVs is

dependent on the accuracy of the reconstructed GTV in

the post-operative setting, this should be done with