Table of Contents Table of Contents
Previous Page  933 / 1096 Next Page
Information
Show Menu
Previous Page 933 / 1096 Next Page
Page Background

S917

ESTRO 36

_______________________________________________________________________________________________

Z

eff

presented a 84.0% sensitivity and 81.8% specificity for

a threshold of 8.96 in ROC curves.

Conclusion

DECT imaging gives information on tumour necrosis.

Quantitative parameters (ρ

I

and Z

eff

) showed better

sensibility and specificity compared to standard HU

imaging. Mean Z

eff

showed better correlation with necrosis

status, due to necrotic core absorbs less iodine contrast.

Our approach has some advantages. Whole tumour semi-

automatic contouring had excellent reproducibility. No

cases were excluded due to geometry or mediastinal

contact.

This method could be a solid approach to assess necrosis

condition. However, we have not studied relationship

with the actual location of necrosis, so it would not be

useful for dose-painting protocols at necrotic core.

EP-1681 [C11]Choline PET/MRI for Prostate Cancer:

Identify Imaging Characteristics Predicting Metastasis

J.R. Tseng

1

, L.Y. Yang

2

, H.Y. Chang

2

, T.C. Yen

1

1

Chang Gung Memorial Hospital at Linkou, Nuclear

Medicine and Molecular Imaging Center, Kwei-Shan-

Taoyuan City, Taiwan

2

Chang Gung Memorial Hospital at Linkou, Biostatistics

Unit- Clinical Trial Center of Chang Gung Memorial

Hospital, Kwei-Shan- Taoyuan City, Taiwan

Purpose or Objective

Intergraded PET/MRI is a powerful imaging modality for

prostate cancer (Pca) in several aspects, from cancer

detection, primary staging, to staging of recurrent Pca.

The goal of primary staging is to detect metastatic spread

from the main tumor. In high risk Pca patients (PSA >20

ng/ml, or Gleason score of 8–10, or clinical stage T3a),

intergraded PET/MRI imaging may have great potential to

change clinical management. In the current study, we

aimed to identify imaging characteristics of main tumor

which can significantly predict distant metastasis.

Material and Methods

This prospective clinical study was approved by the Ethics

Committee (approval 102-3271A and 103-4561C). Since

January 2015 to June 2016, total 30 Pca patients

committed high risk criteria were enrolled to conduct

whole body integrated [C11]Choline PET/MRI (biograph

mMR, Simens). The PET and MRI imaging was interpreted

independently by one clinically-experienced nuclear

medicine physician and radiologist. In the PET imaging

analysis, main tumors were segmented using PMOD 3.3

software package. The borders of volumes of interest were

set by manual adjustment to avoid physiological

[C11]Choline uptake in the urine or intestine. The tumor

boundaries were automatically contoured based on the

thresholds of SUV 2.65. The gray-level run length encoding

matrix (GLRLM) was used for assessing the regional texture

features. In the MRI imaging analysis, anatomic (T2-

weighted MRI) and functional (diffusion-weighted MRI)

imaging features were documented. Multivariate

classification and regression tree analysis was used to

determine the best combination of variables and the

related cutoffs to predict risk for distant metastasis.

Results

The mean age is 70.1±6.2 years, and the mean PSA level

is 91.6 ± 139.4 ng/ml. In these 30 patients, 26 (87%) are

categorized as clinical stage IV, 4 (13%) as stage III. Fifteen

(50%) patients have distant metastasis, including 7 (23%)

non-regional lymph nodes metastasis, 11 (36%) bone

metastasis, 1 (3%) visceral organ metastasis. The

individual clinical risk factors (PSA >20 ng/ml, or Gleason

score of 8–10, or clinical stage T3a) are not significantly

associated with distant metastasis (P-value is 0.493,

0.087, 0.109, respectively). In the multivariate forward

analysis, imaging characteristics of main tumor side wall

invasion by anatomical T2 MRI is the only significant risk

factor predicting distant metastasis (odds ratio 42.25,

confidence interval 5.1-346.5, P-value <0.001). The PET

regional tumor texture features can further divide

patients into with or without distant metastasis by using

high intensity long run emphasis value > -0.40 and low

intensity run emphasis value <0.26 (Figure 1). The

Sensitivity and specificity of the multivariate tree model

was 80% and 80%, respectively.

Conclusion

By providing excellent anatomical, functional, and

metabolic information, integrated PET/MR enhances the

staging of metastatic disease in high risk Pca. Imaging

characteristics including pelvic side wall invasion and

tumor metabolic heterogeneity may have crucial role in

patient management.

EP-1682 Comparison of SUV based on different ROIs and

VOIs definitions: a multi-center 4D phantom study

M. Lambrecht

1

, K. Ortega Marin

1

, M. La Fontaine

2

, J.J.

Sonke

2

, R. Boellaard

3

, M. Verheij

2

, C.W. Hurkmans

1

1

Catharina Ziekenhuis, Physics/Radiotherapy, Eindhoven,

The Netherlands

2

Netherlands cancer institute, Radiotherapy,

Amsterdam, The Netherlands

3

University medical center- university of Groningen,

Nuclear medicine, Groningen, The Netherlands

Purpose or Objective

In the context of the EORTC LungTech trial, a QA

procedure including a PET/CT credentialing has been

developed. This procedure will ultimately allow us to pool

data from 23 institutions with the overall goal of

investigating the impact of tumour motion on

quantification. As no standardised procedure exists under

respiratory conditions, we investigated the variability of

14 SUV metrics to assess their robustness over respiratory

noise.

Material and Methods

The customized CIRS-008A phantom was scanned at 13

institutions. This phantom consists of a 18 cm long body,

a rod attached to a motion actuator, and a sphere of

either 1.5 or 2.5cm diameters. Body, rods and spheres

were filled with homogeneous 18FDG solutions

representative of activity concentrations in mediastinum,

lung and tumour for a 70kg patient. Three respiratory

patterns with peak-to-peak amplitudes and periods of

15mm/3sec, 15mm/6sec and 25mm/4sec were tested.

Prior to scanning in respiratory condition, a 3D static

PET/CT was acquired as reference. During motion, images