Table of Contents Table of Contents
Previous Page  752 / 1082 Next Page
Information
Show Menu
Previous Page 752 / 1082 Next Page
Page Background

S736

ESTRO 36 2017

_______________________________________________________________________________________________

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.

EP-1391 Digestive toxicity after conformal

radiotherapy for palliative cervico-thoracic spinal

metastases

G. Peyraga

1

, D. Caron

1

, Y. Metayer

2

, Y. Pointreau

3

, F.

Denis

3

, G. Ganem

3

, C. Lafond

3

, S. Roche

3

, O. Dupuis

3

1

Institut de Cancérologie de l'Ouest, Radiation Therapy,

Angers, France

2

Centre Jean Bernard, Medical Physics, Le Mans, France

3

Centre Jean Bernard, Radiation Therapy, Le Mans,

France

Purpose or Objective

The palliative treatment of cervico-thoracic spinal

metastases is based on a conformal radiotherapy (CRT),

delivering 30 Gy in 10 fractions (5 days a week for 2

weeks). Digestive toxicities (esophagitis, nausea and

vomiting) are common after these radiations and cause a

clinical impact probably underestimated in patients. We

performed a retrospective monocentric study of early

digestive toxicities occurred secondarily to palliative CRT

of cervico-thoracic spinal metastases.

Material and Methods

All patients receiving palliative CRT at Jean Bernard

Center from January 2013 to December 2014 of spinal

metastases (all primitive tumors were included) between

the fifth cervical vertebra (C5) and 10th thoracic vertebra

(T10) for which clinical follow-up was available beyond 3

months were included. Re-irradiations were excluded.

CRT was delivered by a linear accelerator (CLINAC,

Varian). Premedication to prevent digestive toxicities was

not recommended. Adverse events (esophagitis and

nausea/vomiting < 3 months) were evaluated according

the NCI-CTCae (version 4).

Results

From January 2013 to December 2014, 128 patients met

the study criteria. The median age was 69.6 years [31.8;

88.6]. The majority (84.4%) patients received a dose of 30

Gy in 10 fractions. The median treatment duration was 13

days [3-33]. Forty patients (31.3%) experienced grade 2 or

3 of esophagitis (35 grade 2 (27.4%) and 5 grade 3 (3.9%)),

and 8 patients (6.3%) experienced grade 2 or 3 of nausea

or vomiting (6 grade 2 (4.7%), 1 grade 3 (0.8%) and 1 grade

4 (0.8%)). The risk of digestive toxicities seems to be

related to spinal localization of metastases (38.5% of

grade 2 or 3 esophagitis if radiation from C5 to T4 versus

31.2% if radiation from T5 to T10, and 87.5% of nausea and

vomiting concerned T9 or T10) and to the number of