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S235

ESTRO 36

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Conclusion

Robust CTV-based VMAT optimization in head and neck

patients resulted in improved estimated actual given dose

distributions with lower normal tissue dose and equal

target coverage compared to non-robustly optimized

plans. This is the first study to compare robustly optimized

photon plans to non-robustly optimized photon plans in

terms of dose accumulation using daily CBCT images. The

differences in dose are deemed clinically relevant and are

expected to lead to an improved method of patient

selection for proton therapy.

OC-0444 Pareto-optimal plans as ground truth to

validate a commercial knowledge-based DVH-

prediction system

E. Cagni

1

, A. Botti

1

, Y. Wang

2

, M. Iori

1

, S.F. Petit

2

, B.J.

Heijmen

2

1

Arcispedale S. Maria Nuova - IRCCS, Medical Physics

Unit, Reggio Emilia, Italy

2

Erasmus MC Cancer Institute, Department of Radiation

Oncology, Rotterdam, The Netherlands

Purpose or Objective

The purpose of the current study was two fold. First, to

evaluate the DVH prediction accuracy of RapidPlan (Varian

Medical Systems, Palo Alto) using a large database of

Pareto optimal treatment plans. These were consistently

generated with automated prioritized multi-criterial

treatment plan optimization, independent of RapidPlan,

and therefore can be considered as an unbiased, ground

truth of achievable plan quality. Second, to determine the

importance of the size/variability of the plan database on

the accuracy of the RapidPlan DVH predictions. Using the

automatically generated plans, the prediction accuracy of

RapidPlan could be investigated without an impact of

unavoidable plan quality variations related to manual

planning.

Material and Methods

A previously published database of 115 Pareto-optimal

prostate VMAT plans, consistently generated with

automatic prioritized planning, was used in this study

[Wang et al, PMB, 2016]. Separate Rapidplan prediction

models were generated for training groups consisting of

20, 30, 45, 55, or 114 randomly selected plans, the latter

using a leave-one-out technique. In a second experiment,

Model-20 was also built for 4 other groups of randomly

selected training patients. Prediction accuracy of all

models was assessed using a fixed, independent validation

group of 60 plans and comparing predicted dose

parameters (rectum Dmean, V65, and V75, anus Dmean,

and bladder Dmean) with the achieved values of the

Pareto optimal plans.

Results

For Model-114, the absolute (relative) prediction errors

(mean±SD), for rectum Dmean, V65, and V75 were

1.8±1.4Gy (6.9±5.6%), 1.0±0.9% (8.9±13.4%), and 1.6±1.4%

(36.3±62.2%), respectively. For anus and bladder Dmean,

these errors were 2.2±1.7Gy (18.3±21.3%) and 1.8±1.3Gy

(4.9±4.2%), respectively. For 63.3% of the validation plans,

Model-114 predicted a lower rectum V65 than could

actually be achieved. Because of the prioritized

optimization used for generating the input Pareto-optimal

plans, this can only be realized by underdosing the target.

In 36.7% of plans, the predicted V65 was higher than

obtained in the input plan, possibly losing an opportunity

for lower rectum dose.

Table 1

demonstrates equal

prediction accuracies for model-114 and the smaller

models (only first Model-20 included).

Table 2

compares

Model-114 with all 5 investigated Models-20, showing

significant differences in performance of the Models-20.