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S744

ESTRO 36

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G2 thereafter. The mean follow-up was 12 months (range

1-50 months). The Local control rate was: 87%, 72%, 65%

and 53%, 63% and 75% at 1 , 3 , 6 , 12, 24, 36 months

respectively. The time to local progression was ranged

between 1 and 12 months (mean: 6 months). The detailed

results are reported in Table 1. Five patients are dead (4

for disease and one for vascular accident). Univariate

analysis showed that Tmean, Tmax, Tmin, T90 parameters

were not associated with local control rate

follow-up (months) CR (%) PR (%) SD (%) PD (%)

1

20

48

19

13

3

22

28

22

28

6

26

4

35

35

12

20

6

27

47

24

37.5 -

25

37.5

36

25

-

50

25

TABLE 1: response rate in the time (months)

Conclusion

RT-HT is useful combined treatment with a good local

control rate and patient compliance. The clinical outcome

and the time duration of the follow-up is affected by the

advanced stage of diseases. A larger pool and a more

detailed patient stratification are needed to evaluate the

outcome data in the time

Acknowledgments

This work was supported by “5 per Mille 2009 Ministero

della Salute-FPRC Onlus”.

EP-1390 Superior target delineation of renal cell

carcinoma bone metastases on MRI vs CT

F.M. Prins

1

, J.M. Van der Velden

1

, A.S. Gerlich

1

, A.N.T.J.

Kotte

1

, W.S.C. Eppinga

1

, N. Kasperts

1

, L.G.W. Kerkmeijer

1

1

UMC Utrecht, Radiation oncology, Utrecht, The

Netherlands

Purpose or Objective

In metastatic RCC (mRCC) there has been a treatment shift

towards targeted therapy, which has resulted in a 50%

increase in overall survival. Therefore, there is a need for

better local control of the tumor and its metastases.

Image-guided SBRT in bone metastases provides improved

symptom palliation and local control. After SBRT for

mRCC, local control rates have been improved from 50%

to 85% when compared to conventional fractionation

schemes. With the use of SBRT there is also a need for

accurate target delineation. The hypothesis is that MRI

allows for better visualization of the extend of bone

metastases in mRCC for contouring in the context of

stereotactic treatment planning.

Material and Methods

From 2013 to 2016, nine consecutive patients who

underwent SBRT for RCC bone metastases at our center

were included. A planning CT and MRI were performed in

radiotherapy position according to our clinical protocol.

CT images were performed at 1 mm slice thickness on a

large bore CT scanner (Philips, The Netherlands). In

addition, all patients underwent a 1.5 Tesla MRI scan

(Philips Ingenia, The Netherlands) at 1.1 – 4 mm slice

thickness. For every patient, T1-weighted images were

acquired in transversal and sagittal direction, including a

transversal mDIXON scan, as well as T2-weighted images

in transversal and sagittal direction, and diffusion

weighted images (DWI) according to our clinical MRI

protocol. Gross tumor volumes (GTV) in both CT and MRI

were delineated. Contouring was performed by a

specialized radiation oncologist, based on local consensus

contouring guidelines (T1 images were used for target

delineation aided by the information derived from the T2

and

DWI

sequences).

In both CT and MRI the GTV volumes, conformity index (CI)

and distance between the centers of mass (dCOM) were

compared. Statistical differences in volumes between CT

and MRI were tested with Wilcoxon rank sum test.

Results

Nine patients with 11 RCC bone metastases were

evaluated. The volumes of the lesions on MRI were larger

compared to the CT, for all but one lesion (Table 1). This

lesion was comparable in size on MRI and CT. Two visual

examples of the difference in delineation are shown in

Figure 1. The median GTV volume on MRI was 33.39mL

(range 0.2mL – 247.6mL), compared to 14.87mL on CT

(range 0.2mL – 179.4mL). The difference in volume as

delineated on CT and MRI was statistically significant

(p=0.005). The CI in the different lesions varied between

0.08 and 0.75. The dCOM varied between 0.78 and 13.34

mm.

Conclusion

Contouring of RCC bone metastases on MRI resulted in both

clinically and statistically significant larger lesions

compared with CT. MRI seems to represent the extend of

the GTV in RCC bone metastases more accurately, possibly

due to improved visualization of bone marrow infiltration.

Contouring based on CT-only could result in an

underestimation of the actual tumor volume, which may

cause an under dosage of the GTV in SBRT treatment

plans.