Table of Contents Table of Contents
Previous Page  468 / 1096 Next Page
Information
Show Menu
Previous Page 468 / 1096 Next Page
Page Background

S453

ESTRO 36

_______________________________________________________________________________________________

Conclusion

This study demonstrates the ability of creating high-

quality MRL treatment plans for rectum cancer. Given the

differences in machine characteristics, some plan quality

differences were found between MRL treatment plans and

current clinical practice. These results support a well-

prepared clinical introduction of the MRL.

PO-0839 Personalized VMAT optimization for

pancreatic SBRT

I. Mihaylov

1

, L. Portelance

1

1

University of Miami, Radiation Oncology, Miami, USA

Purpose or Objective

Inverse IMRT planning is a very labor intensive, trial-and-

error process, aiming to find a middle ground between the

conflicting objectives of adequate tumor coverage and

sparing nearby healthy tissues. Even if a plan is clinically

acceptable, that plan is unlikely to be the best solution,

where the healthy tissue is spared as much as possible. To

a large extent the optimization process is user and

treatment planning system specific, where more

experienced users generate better quality radiotherapy

plans. This work introduces a fully automated inverse

optimization approach and its application to pancreatic

SBRT.

Material and Methods

Ten cases, treated breath-hold, were retrospectively

studied. The outlined anatomical structures consisted of a

PTV, and OARs including duodenum, stomach, bowel,

spinal cord, liver, and kidneys. In each case the

prescription was set to 35 Gy (to 95% of the PTV) in 5

fractions. The treatment plans were created by

experienced dosimetrists, following national and

international clinical protocols. Those treatment plans

were generated for VMAT delivery. For each case an

additional plan was generated with the newly proposed

automated inverse optimization. This optimization is

based on unattended step-wise reduction of DVHs, where

several DVH objectives were specified for each OAR. The

automated plans utilized the same number of arcs, with

the same parameters as the treatment plans. The

treatment and the automated plans (Treatment and Auto

hereafter) were compared on commonly used clinical

dosimetric parameters. Those parameters included D

PTV

95%

(dose to 95% of the PTV), D

Duodenum

1%

, D

Bowel

1%

, D

Stomach

1%

,

D

Cord

1%

, D

Liver

mean

, D

rt_kidney

mean

, and D

lt_kidney

mean

. The doses to

1% of the volumes of duodenum, bowel, stomach, and

spinal cord were used as surrogates for maximum doses.

The prescriptions for the Auto plans matched the

prescriptions of the Treatment plans.

Results

The first row in the table below summarizes the average

values of the tallied quantities (over the ten patients) as

derived from the treatment plans. The second row

outlines the average differences (in per-cent) between the

dosimetric endpoints as well as the range of the

differences between the Treatment and the Auto-

optimized plans. The negative differences indicate that

the Auto plans result in lower absolute doses and vice-

versa. The figure outlines the normalized (with respect to

the Treatment plans) tallied quantities on patient-by-

patient basis. In 8 out of the 40 maximum doses the

Treatment plans demonstrated lower absolute doses. For

none of the 30 tallied average (or mean) doses the

Treatment plans were better than the Auto plans. The

average differences over the patient cohort range from -

7% to +36%.

Conclusion

Unattended inverse optimization holds great potential for

further personalization and tailoring of radiotherapy to

particular patient anatomies. It utilizes minimum user

time and it can be used at the very minimum as a good

starting point for personalized precision radiotherapy.

PO-0840 Hypofractionated intensity modulated

radiotherapy in patients with immediate breast

reconstruction

D.P. Rojas

1

, R. Ricotti

2

, M.C. Leonardi

2

, A. Viola

1

, S.

Dicuonzo

1

, D. Ciardo

2

, R. Cambria

3

, R. Luraschi

3

, F.

Cattani

3

, C. Fodor

2

, A. Morra

2

, V. Dell'Acqua

2

, V.

Galimberti

4

, R. Orecchia

5

, B.A. Jereczek-Fossa

1

1

European Institute of Oncology - University of Milan,

Department of Radiation Oncology - Department of

Oncology and Hemato-oncology, MIlan, Italy

2

European Institute of Oncology, Department of

Radiation Oncology, MIlan, Italy

3

European Institute of Oncology, Department of Medical

Physics, MIlan, Italy

4

European Institute of Oncology, Department of Surgery,

MIlan, Italy

5

European Institute of Oncology - University of Milan,

Department of Medical Imaging and Radiation Sciences -