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S94

ESTRO 36

_______________________________________________________________________________________________

Conclusion

A new form of BT, MBT, has been proposed, as well as a

promising method of generating optimal treatment plans.

It can be seen that the treatment plans proposed by the

optimiser (NSGA2) deliver satisfactory absorbed dose

distributions to the tumour, whilst sparing surrounding

tissue, which in turn spares more OARs. This method can

be used in real time during clinical treatment of MBT.

References

[1] K. Deb, A. Pratap, S. Agarwal, and T. Meyarivan, “A

fast and elitist multiobjective genetic algorithm: NSGA-

II,”

IEEE Trans. Evol. Comput.

, vol. 6, no. 2, pp. 182–197,

2002.

PV-0184 Quantitative study on position margin in

Intraluminal Brachytherapy Planning for lung

treatment

C.W. Kong

1

, H. Geng

1

, Y.W. Ho

1

, W.W. Lam

1

, K.Y.

Cheung

1

, S.K. Yu

1

1

Hong Kong Sanatorium & Hospital, Medical Physics and

Research Department, Happy Valley, Hong Kong SAR

China

Purpose or Objective

In Intraluminal Brachytherapy for lung treatment, a

Lumincath applicator, normally 5F flexible nylon catheter,

is inserted through the Trachea and Bronchus. High

activity radioactive source is loaded through the catheter

for treating the tumor site. Unlike external radiotherapy,

there is no motion control technique for afterloading

brachytherapy treatment. Breathing motion should affect

the position accuracy of Intraluminal Brachytherapy as

both Trachea and Bronchus move with the breathing

motion of the patient. It is not practical for the patient to

do breath-hold during treatment since the whole

treatment can last for several cycles of breathing

depending on the source activity. The additional margin

for treatment length should be considered in Intraluminal

Brachytherapy to compensate such effect. The objective

of this study is to investigate the position margin of

treatment planning on intraluminal brachytherapy for lung

treatment.

Material and Methods

We

applied

two-dimensional

(2D)

projection

reconstruction methods to measure the movement of

catheter due to the breathing motion. In 2D projection

reconstruction an orthogonal pair of isocentric

radiographs were taken on the patient inserted with the

Lumincath catheter. By localizing difference position

markers on the catheter in two separate projections, the

catheter can be reconstructed in three-dimensional (3D)

space for the planning calculation. The average position

difference of reconstructed points between two

projections reflects the accuracy of 2D reconstruction

method. By comparing the reconstruction accuracy

between two scenarios: patient doing free breathing and

breath-hold, the impact of breathing motion on the

position of catheter can be derived. In the study an

orthogonal pair of radiographs were done on patients with

free breathing and breath-hold; The discrepancy in the

average position difference between 2D projection

reconstructions with free breathing and breath-hold was

calculated. Such comparsion was done for 12 times on

different patients.

Results

The average position difference between two radiographs

in the breath-hold reconstruction was 1.3 ± 0.5 mm among

different patients. Such difference was greatly increased

to 6.5 ± 2.5 mm in free-breathing reconstruction. Assume

the position difference in the reconstruction due to

breathing motion was independent from other factors such

as isocenter precision and reconstruction calculation

accuracy, the derived average position error of catheter

in the reconstructions due to breathing motion was 6.4 ±

2.5 mm.

Conclusion

Our study showed that in Intraluminal Brachytherapy for

lung treatment, the breathing motion can significantly

affect the catheter position by 6.4 ± 2.5 mm on average.

Position margin of such value should be added in the

treatment length during Intraluminal Brachytherapy

planning to compensate such effect.

PV-0185 Retina dose as risk factor for worse visual

outcome in 106Ru plaque brachytherapy of uveal

melanoma

G. Heilemann

1

, L. Fetty

1

, M. Blaickner

2

, N. Nesvacil

3

, D.

Georg

3

, R. Dunavoelgyi

4

1

Medical University of Vienna/AKH Vienna, Department

of Radiotherapy, Vienna, Austria

2

Austrian Institute of Technology GmbH, Health and

Environment Department Biomedical Systems, Vienna,

Austria

3

Medical University of Vienna/AKH Vienna, Department

of Radiotherapy/Christian Doppler Laboratory for

Medical Radiation Research for Radiation Oncology,

Vienna, Austria

4

Medical University of Vienna/ AKH Vienna, Department

for Ophthalmology and Optometry, Vienna, Austria

Purpose or Objective

Visual acuity is a common side effect in

106

Ru plaque

brachytherapy. The purpose of this study was to evaluate

the retina dose as a risk factor associated with visual

outcome.

Material and Methods

45 Patients treated with

106

Ru plaque brachytherapy were

included in this retrospective study. A minimum of 100 Gy

was prescribed to the tumor apex using one of two

available plaque (types CCB, CCA) manufactured by BEBIG

(Eckert & Ziegler, Germany). Treatment planning and dose

calculation was performed using an in-house developed 3D

treatment planning system with Monte Carlo based dose

calculation. Dose volume histograms (DVH) were

generated for both physical absorbed dose and biological

equivalent dose (BED), according to the definition

introduced by Dale and Jones [1]. Visual acuity was

reported using Snellen charts. To analyze potential

predictors in anterior tumor locations, a subgroup of 20

patients was selected presenting with a minimum distance

of 5 mm between tumor and macula. Statistical

calculations were performed in SPSS (version 21, IBM). Risk

factors associated with loss of visual acuity were

evaluated using the Cox proportional hazards models. The

loss of visual acuity was correlated to risk factors using

Pearson correlation coefficients. Statistical significance

was assumed to be p ≤ 0.05.

Results

Median follow-up time was 29.5 months (IQR, 15.0-29.8).

A median apex dose of 131 Gy (IQR, 113.0-150.4) was

delivered to tumors with median apex heights of 4.6 mm

(IQR, 3.5-6.0)), largest basal diameters of 10.8 mm (IQR,

8.3-12.6) and smallest diameter of 9.3 mm (IQR, 7.9-

11.4). The baseline visual acuity (Snellen 0.82 ± 0.23 SD)

was significantly higher (p < 0.001) than the mean visual

acuity at last individual follow-up (0.59 ± 028 SD). The

Pearson Correlation analysis showed a significant