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S861

ESTRO 36 2017

_______________________________________________________________________________________________

Physics, Aarhus C, Denmark

3

Heidelberg University Hospital, Department of

Radiooncology, Heidelberg, Germany

Purpose or Objective

Dose planning constraints, such as the volume receiving

xGy (V

x

), are often extracted from clinical outcome data.

These data are tainted by uncertainties in dose- and

output recording, large patient heterogeneity, small

sample size and -variability. Our study is dedicated to the

investigation of the fundamental uncertainty with which

dose planning constraints can be extracted from clinical

radiation pneumonitis data and how this relates to patient

number and complication incidence rate.

Material and Methods

In order to measure the reliability of a V

x

logistic

regression model, the dose-response mechanism

generating the complication events needs to be known.

For this reason, we generated cohorts of patients using

real-life dose distributions of patients treated for

advanced lung cancer, combined with a postulated V

x

logistic dose-response model. In each of the 1000 cohorts,

the patients were randomly assigned complication/no-

complication based on the individual risks given by the

postulated model. Thus, “alternative reality” cohorts

comprised of the same patients, but with different

outcomes from the same dose distributions were created.

Each cohort thus represented a possible result of a clinical

study. They were analyzed with a number of logistic V

x

models, and the best fitting model was selected. This was

matched to the postulated model to determine its

recognition rate. The postulated model was varied to

produce low, intermediate and high incidence rates.

Results

For a patient cohort of 100 individuals, a postulated model

with an incidence rate of 15/100 was recognized in 31% of

the cohorts. For a cohort size of 500, the correct-

recognition rates increased to 75%. For a lower incidence

model (7/100), these recognition frequencies dropped to

20% and 56%,

respectively.

To ensure a recognition rate >90%, large cohorts of

between 500 and 2000 patients were required, see Figure

1(a). Figure 1(b) shows that the distribution width for the

15/100 incidence rate model decreased from a standard

deviation of 10Gy for 100 patients to 1Gy for 2000

patients.

Conclusion

For realistic dose distributions and cohort sizes, a state-

of-the-art analysis failed to identify the postulated dose-

response in about 2-in-3 cases for the low incidence of the

large-volume effect complication radiation pneumonitis.

Very large patient cohorts were required to ensure

recognition rates above 90%. This fundamentally low

success rate could explain the persistent difficulties to

derive dose constraints from clinical data for

complications in large-volume effect, “parallel” organs.

EP-1615 Second cancer risk after radiation of localized

prostate cancer with and without flattening filter

M. Treutwein

1

, M. Hipp

2

, R. Loeschel

3

, O. Koelbl

1

, B.

Dobler

1

1

Klinik und Poliklinik für Strahlentherapie- Unive,

Regensburg University Medical Center- Department of

Radiation Oncology, Regensburg, Germany

2

Klinkum St. Marien, Department of Radiotherapy,

Amberg, Germany

3

Ostbayerische Technische Hochschule, Faculty of

Computer Science and Mathematics, Regensburg,

Germany

Purpose or Objective

Radiotherapy is a standard treatment modality with

curative intent for localized prostate cancer. Prostate

cancer is a disease of elderly men. Nevertheless these

patients have a remaining life span of ten years or more.

Radiotherapy compared to surgery may increase the risk

for second cancer. Minimizing this risk can be one criterion

in deciding for a specific technique. Therefore we

compared the organ equivalent dose (OED) and excess

absolute risk (EAR) for second cancer for different

treatment techniques.

Material and Methods

For ten patients four different plans were calculated,

using a seven field intensity modulated radiotherapy

(IMRT) and a single arc volumetric modulated arc therapy

(VMAT) with and without flattening filter. The