somatom sessions 11
TRANSCRIPT
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Computed Tomography for
Oncology Care
Page 4
CASE 14:
Clinical Studies of CT with PET
Page 6
CASE 56:
Clinical Studies of CT with
Angiographic Interventions
Page 18
CASE 7:
Clinical Study of CT-guided
Radiation Therapy
Page 22
CASE 8:
Clinical Study of CT
in Therapy Planning
Page 24
Virtual Simulation
Page 26
Contents
SOMATOMSESSIONS
Is sue no.11
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SOMATOM SESSIONS 11
This is the eleventh issue of Siemens SOMATOM Sessions.
We feature CT in oncology care, namely clinical applications
in combination with the other modalities such as Angio-
graphy, Radiation Therapy (RT) and Positron Emission
Tomography (PET).
This issue also presents you with clinical case studies for
each application.
To order copies of the past issue or submit your registration
for receiving future issues, please visit our Web site at:
http://www.siemensmedical.com/somatomsessions
As always, we appreciate your suggestions and comments.
Xiaoyan Chen, M.D., MBA Roselle Anderson
Editor of SOMATOM Sessions Guest editor of this issue
The information in this document contains general descriptions of the tech-
nical options available, which do not always have to be present in individual
cases. The required features should therefore be specified in each individual
case at the time of closing the contract.
The information presented in the case report is for illustration only and is not
intended to be relied upon by the reader for instruction as to the practice of
medicine. Any health care practitioner reading this information is reminded
that they must use their own learning,training and expertise in dealing with
their individual patients.This material does not substitute for that duty and is
not intended by Siemens Medical Solutions Inc., to be used for any purpose
in that regard.
The drugs and doses mentioned herein were specified to the best of our
knowledge.We assume no responsibility whatsoever for the correctness of
this information.Variations may prove necessary for individual patients.
The treating physician bears the sole responsibility for all of the parameters
selected.
From the Editor
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Computed Tomography for Oncology Care Page 4
CASE 1:
Diagnosis of Gastrointestinal
Stromal Tumor with Multiple Metastases Page 6
CASE 2:
Diagnosis of Non-Small Cell Lung Cancer
with Multiple Metastases Page 10
CASE 3:
Therapy Monitoring in the Treatment
of Hepatic Metastasis with Radiofrequency
Ablation Page 14
CASE 4:
Diagnosis of Recurrent
Non-Hodgkins Lymphoma Page 16
CASE 5:
Diagnosis of Hepatocellular
Carcinoma Page 18
CASE 6:
Diagnosis and Interventions of
Bladder Cancer Page 20
CASE 7:
Image Guided Radiation Therapy of Prostate
Cancer Using a Novel Combination of
CT and Linear Accelerator, the PRIMATOM Page 22
CASE 8:
CT imaging in Radiation Therapy Page 24
Virtual Simulation Page 26
Contents
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SOMATOM SESSIONS 11
SINCE THE EARLY DAYS of Computed Tomography dat-
ing back to the early 1970s medical engineering has been
pushing the limits of this technology. Today, we boast
shorter scan times than ever before; increased detail reso-
lution; sophisticated image post-processing capabilities;
greater ease of use with the common syngo user interface;
and efficient networking solutions.
Routinely, much of the focus of clinical work with CT has
been for the visualization and staging of malignancy. In
fact, it is estimated today that over 50% of all examinations
are performed to help the physician either confirm the
presence or absence of lesions like tumors. Other applica-
tions such as low-dose CT exams for the early visualization
of pulmonary nodules and CT-guided interventions are also
performed clinically. The merging of CT and PET technolo-
gies brings oncology imaging to unprecedented levels,
helping to reduce the PET examination times and providing
functional images with morphological landmarks. And as
advanced techniques such as Intensity Modulated Radia-
tion Therapy (IMRT) become more widespread in the ther-
apy arena, CT is gaining presence as the modality of choicefor simulation of radiation treatments. In the following
brief overview, we would like to introduce you to some of
the clinical applications of CT as a crucial modality in the
continuum of oncology care.
biograph CT + PET
The biograph system combines two technologies Com-
puted Tomography and Positron Emission Tomography
(PET) [Fig. 1]. It provides both anatomical and functional
information by image acquisition and fusion from both
modalities. Please refer to cases 14 for clinical examples.
Computed Tomography for Oncology Care
[ 1 ] biograph system
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Miyabi CT + Angiography
The Miyabi system combines two modalities a CT scanner
with sliding gantry and an Angiography system
[Fig. 2]. It can be used to aid the physician in the visualiza-
tion of lesions like tumors and also for performing safe and
effective interventional treatments. Please refer to cases
5 & 6 for clinical examples.
PRIMATOM CT +PRIMUS Linear Accelerator
The PRIMATOM system combines two modalities a CT
scanner with Sliding Gantry and a Radiation Therapy
delivery system [Fig. 3]. It is used for accurate verification
of tumor location prior to treatment delivery, as well as for
precise simulation on the therapy table. Please refer to case
7 for a clinical example.
In the pages that follow, we offer a glimpse of how
Siemens SOMATOM CT scanners are being used in
diverse applications and configurations in the oncology
arena today. We invite you to join us for an interesting
read.
[ 2 ] MIYABI system [ 3 ] PRIMATOM system
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PATIENT HISTORY
A 48-year-old male patient had been diagnosed with
hepatic metastases of an unknown primary tumor. Biopsy
of the hepatic lesions revealed metastases from a gastro-
intestinal stromal tumor. CT imaging of the abdomen as
well as endoscopy of the stomach and the colon had not
been able to define the primary lesion. A dual-modality
PET-CT examination was scheduled for further evaluation.
DIAGNOSIS
Examinations with a combined PET/ CT scanner, the bio-
graph, revealed a hypodense 2.5x2.5 cm lesion at the
lesser curvature of the stomach [Fig.1] with pathologically
increased tracer uptake (SUV 9.1). Adjacent to the gastric
lesion a pathologically enlarged lymph node (1.5 cm on CT)
was found to present with increased FDG utilization. Fur-
thermore, multiple hepatic metastases with pathologically
increased glucose metabolism (SUV 9.9) were verified
[Fig. 1 and 2]. On thoracic imaging bilateral pulmonarylesions of up to 0.7 cm in size were found, but no increased
tracer uptake was demonstrated [Fig. 3].
Diagnosis: Gastrointestinal stromal tumor of the stomachs
lesser curvature with local lymph node metastasis as well
as multiple hepatic and pulmonary metastases.
EXAMINATION PROTOCOLS
Case1: Diagnosis of Gastrointestinal Stromal Tumorwith Multiple Metastases
CT examination
Scanned body regions Thorax, abdomen, pelvis
Arm positioning Raised above head
mAs 140
kV 120
Slice width 5 mm
Table feed/rotation 8 mm
Pitch 1.6
Rotation time 800 msIncrement 2.5 mm
Scanning direction Craniocaudal
Oral contrast material 1000 ml barium(1.5 g/ 100 ml)
i.v. contrast material 1.80 ml at 3 ml/s
2.60 ml at 2 ml/ s
PET examination
Tracer 350 MBq FDG
Scanned body regions Thorax, abdomen, pelvis
Arm positioning Raised above headNumber of bed positions 5
Scan time/bed position 5 minutes
Reconstruction algorithms Iterative (FORE and AWOSEM),
2 iterations and 8 subsets;
Data filtered (FWHM 3.2 mm)Data scatter corrected
Reconstructed slice width 5 mm
Scanning direction Caudocranial
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[ 1 ] Axial images of the primary tumor (arrow) at the
lesser curvature of the stomach on CT (A), fused PET/ CT
(B), and PET images (C) with adjacent lymph node
metastasis and hepatic metastases.
7
A B
C
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SOMATOM SESSIONS 11
[ 2 ] Coronal view of CT (A), fused PET/CT (B), and PET
images (C) of the primary tumor and hepatic metastases.Evaluation of the PET images alone may have led to
misinterpretation of the primary tumor as just another
hepatic metastasis.
A B
C
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CASE 1: Clinical studies of CT with PET
COMMENTS
Dual-modality PET/CT was able to define a lesion at the
lesser curvature of the stomach as the primary tumor.
The diagnosis was verified on biopsy. Initially, the tumor of
the lesser curvature had not been visualized by CT orendoscopy. CT was negative because the hypodense lesion
may have been mistaken for parts of a bowel loop.
Endoscopy was negative because the tumor originated
from the outer parts of the gastric wall and was there-
fore not visible from inside the stomach. Compared to CT
alone, PET/ CT was able to define the primary tumor. Com-
pared to PET alone, the area of focal tracer uptake in the
epigastrium could accurately be attributed to a lesion at
the stomachs lesser curvature and an adjacent lymph
node. On plain PET imaging the primary tumor with the
adjacent lymph node metastasis would, probably, have
been mistaken for just another hepatic metastasis [see
Fig. 2]. Considering the pulmonary lesions another benefit
of combined PET/ CT over PET imaging becomes obvious.Small pulmonary lesions may not demonstrate tracer
uptake as PET images are acquired in shallow breathing
which leads to smearing in visualization of FDG uptake.
The integration of CT accurately demonstrated pulmonary
metastases and, therefore, increased diagnostic yield over
PET alone.
[ 3 ] Pulmonary metastasis without signs of FDG uptake.
PET image (C) was acquired in shallow breathing.(A) shows axial view of CT image and (B) shows fused
PET/CT image.
A B
C
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PATIENT HISTORY
45-year-old male patient with histologically proven non-
small cell lung cancer (NSCLC) in the apex of the left upper
pulmonary lobe. CT imaging of the thorax had revealed
mediastinal lesions suspected of lymph node metastases
as well as pulmonary lesions of up to 2.5 cm in diameter in
the right lung. PET/ CT imaging was carried out for tumor
staging.
EXPLANATION FORSPLIT PROTOCOL
To improve image quality by minimizing artefacts from the
arms in the field of view, combined PET/ CT was acquired in
two steps in this patient. First a PET/ CT of the thorax, ab-
domen and pelvis was carried out followed by another PET/
CT covering the head and neck. Between examinations the
patients arms were repositioned to be outside the field of
view.
DIAGNOSIS
The primary tumor in the left apex of the lung was clearly
visible on FDG-PET/CT as a region of inhomogeneous
contrast enhancement on CT with pathologically increased
tracer uptake on PET [SUV 8.0; Fig. 1]. In addition focal FDG
uptake could be demonstrated in mediastinal lymph nodes
[Fig. 2] as well as in the pulmonary lesions on the right side
[Fig. 3]. An area of focal tracer uptake was, furthermore,
demonstrated in projection on the pelvis. This hot spot
could be accurately attributed to the right pubic bone. Thecorresponding CT images revealed only mild sclerosis of
the bone without typical signs of osseous destruction
[Fig.4]. Diagnosis: NSCLC of the left pulmonary apex with
mediastinal lymph node metastases, pulmonary metas-
tases and a right pubic bone metastasis.
Case 2: Diagnosis of Non-Small Cell Lung Cancerwith Multiple Metastases
EXAMINATION PROTOCOLS
CT examination
Scanned body regions Head, neck, thorax,
abdomen, pelvis
Arm positioning Split protocol:
1. Beside trunk for head
and neck2. Raised above head for thorax
to pelvis
mAs 140
kV 120Slice width 5 mm
Table feed/rotation 8 mm
Pitch 1.6
Rotation time 800 ms
Increment 2,5 mm
Scanning direction Craniocaudal
Oral contrast material 1000 ml barium
(1,5 g/100 ml)
i.v. contrast material Head /neck: 70 ml at 2 ml /s
Thorax pelvis: 50 ml at
3 ml/s; 50 ml at 2 ml/s
PET examination
Tracer 350 MBq FDG
Scanned body regions Head, neck, thorax,
abdomen, pelvis
Arm positioning Split protocol:1. Beside trunk for head
and neck
2. Raised above head for thorax
to pelvis
Number of bed positions 7
Scan time/bed position 4 minutes
Reconstruction algorithms Iterative (FORE and AWOSEM)
2 iterations and 8 subsetsData filtered (FWHM 3.2 mm);
Data scatter corrected
Reconstructed slice width 5 mm
Scanning direction Caudocranial in both
examinations
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[ 1] Partially necrotic non-small cell lung cancer
of the left pulmonary apex as demonstrated on CT (A),
fused (B), and PET (C) images.
[ 2 ] CT (A), PET/CT (B), and PET (C) images of an
infracarinal lymph node metastasis from NSCLC.
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A
B
C
A
B
C
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[ 3 ] Right pulmonary metastasis from NSCLC.
Only mild FDG uptake is mainly attributed to smearing
due to respiratory motion.
Also note a mediastinal lymph node metastasis.
[ 4 ] Bone metastasis in the right pubic bone.
CT (A) demonstrated only mild sclerosis while PET (C)
shows pathologically increased focal tracer uptake.
On fused images focal tracer uptake can be accurately
attributed to the lesion in question.
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SOMATOM SESSIONS 11
A
B
C
A
B
C
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COMMENTS
Dual-modality PET/CT is a useful tool for tumor staging.
The application of a whole-body protocol (head to upper
thigh) is required to ensure visualization of distant meta-
stases. In this case, the bone metastasis would have beenmissed if scanning had been limited to the thorax. The ben-
efit of the combined approach over CT alone is demon-
strated by the visualization of the bone metastasis which is
characterized by only mild sclerosis on conventional CT
imaging. The acquisition of a fully diagnostic CT compo-
nent is, however, of importance, as there are tumors that
do not show increased glucose metabolism, or metastases
from a tumor may express FDG-uptake characteristics dif-
ferent from the primary lesion. A fully diagnostic, contrast-
enhanced CT can be of great value in these cases.
[ 5 ] biograph system
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CASE 2: Diagnosis of Non-Small Cell Lung Cancer with Multiple Metastases
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SOMATOM SESSIONS 11
PATIENT HISTORY
66-year-old male patient with recurrent hepatic metastasis
from colorectal carcinoma in segment 4 of the liver.
The patient had undergone resection of the rectum and
resection of a solitary hepatic metastasis in segment
4 one year prior. Radiofrequency ablation was carried out
for treatment of metastatic recurrence. A combined
PET/CT examination was scheduled before and after
radiofrequency ablation to determine the therapeutic
effectiveness.
DIAGNOSIS AND FOLLOW-UP
Dual-modality PET/CT imaging revealed an ill-defined
hypodense lesion in the area of prior resection in segment
4 of the liver [Fig. 1A]. Fused images demonstrated patho-
logically increased tracer uptake of the lesion as a sign of
metastatic recurrence [Fig. 1B and C]. Radiofrequency
ablation was carried out featuring an ablative device with
3 cm distal tip exposure (Cool-Tip, Radionics, Burlington,MA, USA) over a time period of 20 minutes. No compli-
cations occurred. In the 4 weeks following radiofrequency
treatment the patient had another PET/ CT scan to deter-
mine the effectiveness of the RF-ablation procedure. Figure
2A demonstrates the thermo-induced hepatic necrosis on
plain CT imaging. Fused images showed a small area of
decreased glucose metabolism in the necrotic region
[Fig. 2B and C]. There is no increased FDG uptake visible in
the periphery of the necrotic lesion. Complete necrosis of
the metastasis was demonstrated by PET/ CT.
COMMENTS
Follow-up examinations to evaluate the effectiveness of
tumor therapy are frequently compromised by the inability
to differentiate viable tumor areas from therapy-induced
necrosis on CT imaging. As demonstrated in this case, com-
bined PET/ CT can accurately evaluate metabolism in liver
tissue adjacent to the necrotic area to exclude residual or
recurrent viable tumor.
Case 3: Therapy Monitoring in the Treatmentof Hepatic Metastasis with Radiofrequency Ablation
EXAMINATION PROTOCOLS
CT examination
Scanned body regions Liver
Arm positioning Raised above head
mAs 140
kV 120
Slice width 5 mm
Table feed/rotation 8 mm
Pitch 1.6
Rotation time 800 msIncrement 2.5 mm
Scanning direction Craniocaudal
Oral contrast material none
i.v. contrast material 100 ml at 3 ml/ sDelay 70 seconds
PET examination
Tracer 350 MBq FDG
Scanned body regions Liver
Arm positioning Raised above head
Number of bed positions 2
Scan time/bed position 5 minutes
Reconstruction algorithms Iterative (FORE and
AWOSEM); 2 iterations and
8 subsets; Data filtered
(FWHM 3.2 mm)Data scatter corrected
Reconstructed slice width 5 mm
Scanning direction Caudocranial
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[ 1 ] CT (A), fused PET/CT (B), and PET (C) images of
recurrent hepatic metastasis from colorectal carcinoma
one year after resection. Images prior to radiofrequency
ablation.
[ 2 ] Successful treatment of recurrent hepatic metastasis
by radiofrequency ablation.
PET/ CT demonstrated tumor-free margins of the
ablated area 4 weeks post-intervention.
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A
B
C
A
B
C
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PATIENT HISTORY
51-year-old male patient who had undergone multiple
cycles of chemotherapy for non-Hodgkins lymphoma with
mediastinal, pulmonary, and cerebral involvement. A PET /
CT staging examination was carried out 6 months after ter-
mination of therapy. The patient had been disease-free
over the past 6 months.
DIAGNOSIS
Combined PET/ CT imaging revealed focal FDG (SUV 4.3)
uptake in the left axilla [Fig. 1 and 2] which could be accu-
rately co-registered with a lymph node. The lymph node
was determined to be 1.3 cm in size on CT imaging. From
PET/ CT findings recurrence of non-Hodgkins lymphoma
was diagnosed and diagnosis was verified histologically
after lymph node excision.
COMMENTSBy demonstrating focal tracer uptake within a lymph node,
combined PET/ CT improves differential diagnosis of benign
and malignant diseases. FDG-PET/ CT will play an important
role in tumor follow-up with emphasis on early diagnosis of
tumor recurrence.
Case 4: Diagnosis of RecurrentNon-Hodgkins Lymphoma
EXAMINATION PROTOCOLS
CT examination
Scanned body regions Head, neck, thorax, abdomen,
pelvis
Arm positioning Beside trunk
mAs 140
kV 120
Slice width 5 mm
Table feed/rotation 8 mm
Pitch 1.6Rotation time 800 ms
Increment 2.5 mm
Scanning direction Craniocaudal
Oral contrast material none
i.v. contrast material 1.80 ml at 3 ml/s
2.60 ml at 2 ml/ s
PET examination
Tracer 350 MBq FDG
Scanned body regions Head, neck, thorax,
abdomen, pelvis
Arm positioning Beside trunk
Number of bed positions 7
Scan time/bed position 5 minutes
Reconstruction algorithms Iterative (FORE and
AWOSEM); 2 iterations and
8 subsets; Data filtered(FWHM 3.2 mm)
Data scatter corrected
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[ 1 ] Coronal CT (A), fused PET/ CT (B), and PET (C) images of a patient with recurrence of
non-Hodgkins lymphoma in the left axilla.
[ 2 ] Accurate co-registration of CT and PET images (B)
demonstrates FDG uptake in a lymph node suspected for
recurrence of non-Hodgkins lymphoma.
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A B
C
A B C
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[ 1 ] Angiography performed through the common
hepatic artery.
[ 2 ] Angiography performed superselectively through the
right hepatic artery.
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SOMATOM SESSIONS 11
PATIENT HISTORY
A 65-year-old male patient had a history of chronic hepati-
tis C. Hypoechoic lesion was visualized in the right lobe of
the liver by ultrasonography. Serum PIVKA-II level was
elevated, which is well known as a tumor marker of hepa-
tocellular carcinoma (HCC). Dynamic arterial phase CT
scan showed high attenuation area in the liver (segment
eight/ tumor size: 3.5 x 3 cm).
DIAGNOSIS
Angiography was performed for preoperative examination
[Fig. 1 and 2]. In addition to hepatic angiography, the pa-
tient underwent CT during arterioportography (CTAP) and
CT during hepatic arteriography (CTA) using the Angio-CT
system MIYABI [Fig. 3]. The tumor was manifested as a
solitary perfusion defect of portal venous flow on CTAP and
no other portal perfusion defect was seen in the liver. On
CTA,the tumor was depicted as a hypervascular lesion. Par-
tial hepatic lobectomy was performed and histologicalexamination of the tumor showed moderately differenti-
ated HCC.
COMMENTS
CT during arteriography with the Angio-CT system
MIYABI provides useful information about tumor visuali-
zation and drug distribution. In this case, such information
helps to determine surgery plan. Patients with severe liver
dysfunction may not tolerate an operation or transcatheter
arterial chemoembolization (TACE) covering a wide area.To reduce damage of normal liver tissue, superselective
TACE is necessary. MIYABI enables us to identify whether
drug infusion area contains whole area of the tumor with
minimal surrounding liver tissue.
The Angio-CT system MIYABI is useful not only for diag-
nosing tumor but also for performing safe and effective
interventional treatments.
According to our experience, syngo viewer is very useful
for the comparison of images between different phases
[Fig. 3]. It is very easy to identify even very small lesions.
The stack mode is ideal for ICT image viewing.
Case 5: Diagnosis of Hepatocellular Carcinoma
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[ 4 ] Image comparison between different phases with
syngo viewer in Stack mode simultaneous image
scrolling within different segments an easy, useful andideal way of ICT image viewing.
LU: plain CT
RU: CTAP (portal venous phase, through superior
mesenteric artery)
LL: CTA (early arterial phase, through hepatic artery)
RL: CTA (later arterial phase, through hepatic artery)
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[ 4 ] Axial CT image revealed a tumor arising in the
bladder wall.
[ 1 ] Angio-CT system, MIYABI
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SOMATOM SESSIONS 11
PATIENT HISTORY
An 83-year-old male patient presented with hematuria.
Computed Tomography (CT) revealed a tumor arising in
the bladder wall [Fig. 4]. Left hydroureter was seen due to
tumor invasion. Transurethral partial resection of the blad-
der tumor was performed and the histopathological diag-
nosis was transitional cell carcinoma.
INTERVENTIONAL TREATMENTTranscatheter arterial chemoembolization was performed.
The contralateral internal iliac artery was catheterized with
a 4-F cobra type catheter [Fig. 2]. Using a coaxial tech-
nique, a microcatheter was introduced into bladder artery
superselectively [Fig. 3]. Then, CT images during super-
selective bladder arteriography were acquired with the
Angio-CT system MIYABI, and the tumor included in
the enhanced areas was confirmed [Fig. 5]. CDDP (50 mg/
body) was infused through this feeding artery, which was
subsequently embolized with gelatine sponge.
COMMENTS
The advantages of this treatment are its abilities to expose
tumor to a highly concentrated anticancer agent and to
avoid unexpected normal tissue damages. Because
patients with bladder cancer are generally elderly and
usually have severe arteriosclerosis, and because many
arterial variants exist around the bladder, superselective
bladder arteriography is technically difficult. In such cases,
the Angio-CT system MIYABI helps us to determine
the final position of the catheter tip for safe and effective
treatment.
Case 6: Diagnosis and Interventionsof Bladder Cancer
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[ 2 ] Contralateral internal iliac artery was catheterized
with a 4-F cobra type catheter. Image shows the feeding
artery of the tumor (arrow).
[ 3 ] Using a coaxial technique, a microcatheter was
introduced into bladder artery superselectively.
Image shows the feeding artery of the tumor (arrow).
[ 5 ] CT images acquired during superselective bladder arteriography confirmed the tumor was
included in the enhanced areas.
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[ 1 ] The PRIMATOM installation at Morristown Memorial
Hospital, Morristown, New Jersey, USA.
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SOMATOM SESSIONS 11
The PRIMATOM system is a unique combination of a
Siemens PRIMUS linear accelerator and Siemens
SOMATOM CT* technologies. Using the PRIMATOM,
daily CT localization can be performed prior to each
radiation treatment, thus reducing significantly the
extrinsic and intrinsic uncertainties that are associated
with patient set up and organ motion, respectively. We
illustrate this principle in the radiation treatment of a
very common cancer in men, prostate cancer.
PATIENT HISTORY
A 73-year-old white male with prostate cancer was
referred to radiation therapy. The patient consented to the
use of the PRIMATOM because of the extreme precision of
the radiation beams. The imaging property of the
PRIMATOM directs the radiation beams to the target
(prostate) while sparing radiation dose to the adjacentnormal tissues.
EXAMINATION PROTOCOLS
For PRIMATOM treatment of the prostate, the patient is set
up on the treatment couch, with radio-opaque markers
placed over skin marks that delineate the central axis
planes. The treatment couch is rotated 180 degrees for PRI-
MATOM CT scanning. The patient is scanned by way of a
SOMATOM Plus 4 with Sliding Gantry, a movable CT scan-
ner on a pair of horizontal rails. The exact position of theprostate and rectum are identified and localized. These
positions are then compared to the original simulated posi-
tions. Daily variations of the prostate gland and rectum
outlines from the original contour determine the daily
movement of the prostate gland in the anterior-posterior,
left-right, and cephalic-caudal directions. Similar variations
of the rectum determine the daily anterior-posterior move-
ment of the rectum. Deriving a new isocenter and then
shifting the treatment isocenter to this new position
enable corrections of these daily movements of the
prostate and rectum. The treatment table is then rotated
180 degrees back to the treatment position. Treatment on
the PRIMUS follows this position verification.
DIAGNOSIS AND COMMENTThe PRIMATOM provides a platform for extreme precision
in the radiation treatment of cancer. Here, the prostate
is used as an example of such treatment, but the principle
applies to cancers in any parts of the body. Image Guided
Radiation Therapy using the PRIMATOM allows no misses
and thus, can lead to delivery of higher doses to the tumor
while minimizing unwanted radiation to the adjacent nor-
mal tissues. With ever better imaging technologies such as
PET/ CT or other radiological advances, the PRIMATOM
could provide a platform for even more precise radiation
treatments.
Case 7: Image Guided Radiation Therapy ofProstate Cancer Using a Novel Combination of CT andLinear Accelerator, the PRIMATOM
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[ 3 ] Variation of radiation dose to the target with respect
to set up and organ movements. In a hypothetical case,if the allowed margin of set up and organ movement is
5 mm, then a 10 mm movement of the prostate gland
would lead to insufficient dose to the prostate target (red
line). The green line assumes that there is no movement.
[ 2 ] Daily movement of the prostate over 5 consecutive
treatment days. The prostate is outlined in red, while the
rectum is outlined in green. As can be seen in the figures,
the prostate and rectum are dynamic structures that take
on different positions with respect to the bony landmarks.
Treatment Planning Day 1
Day 2 Day 3
Day 4 Day 5
* The PRIMATOM solution is available with the following models of
SOMATOM CT scanners (with Sliding Gantry option): SOMATOM Balance,
SOMATOM Emotion, SOMATOM Emotion Duo, SOMATOM Sensation 4
and refurbished SOMATOM Plus 4.
An existing PRIMUS, PRIMART or MEVATRON linear accelerator room
can be upgraded with a SOMATOM CT Sliding Gantry for the
PRIMATOM solution. Contact your Siemens therapy representative
for more information.
23
120
100
80
60
40
20
040 50 60 70 80 90 100 110
% Dose Level
% Volume
0 mm
10 mm
CTV Dose coverage for 5 mm margin of PTV with prostate
movement 10 mm relative to original field
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PATIENT HISTORY
A 22-year-old male patient with cystic fibrosis had under-
gone bilateral lung transplantation. Although receiving
anti-rejection drug therapy, his lung function was deterio-
rating and he developed bronchiolitis obliterans
syndrome1. Chronic lung allograft rejection resulting in
sustained decline in lung function is the most common
cause of late death after lung transplantation. It was
decided to treat him with Total Nodal Irradiation (TNI) to try
to stabilise his condition2.
EXAMINATION PROTOCOLS
The patient is positioned supine and is scanned from
the level of the external auditory meatus to the level of the
greater trochanter. Landmarks are tattooed on the
patient to correlate with the scanned images. The images
from the CT scan are transferred to the planning station
(EXOMIO) and 3 separate fields are planned. These are
splenic/para aortic field, mantle field and pelvic/inguinal
field. Specific gaps are calculated between the fields to
avoid areas of overlap in underlying tissues.
Treatment consists of parallel opposed fields given
twice weekly with a mid plane dose of 0.8 Gy to a total
of 8 Gy. The blood count is monitored throughout the
treatment4.
According to our experience, the SOMATOM Emotion Duo
has the following advantages for radiotherapy planning:
3 Speed
Prior to the use of the Emotion Duo, patients for TNI
were planned on the Simulator and this imaging procedure
would take at least one hour. However, using the
SOMATOM Emotion Duo, the patient was on the CT couch
for less than 10 minutes.The scan was 862 mm in length and this was covered in
less than one minute, due to the sub-second rotation time.
This is a big advantage over single slice spiral scanning,
where such a scan would take between 2 3 minutes.
This short examination time also reduces the artefacts
produced from breathing and movement. The patient was
allowed to breathe gently throughout the scan in order to
reproduce the treatment conditions.
Multislice sub-second CT, as used in the SOMATOM
Emotion Duo, allows scanning of longer ranges without
compromise in slice thickness and therefore image
resolution. This is due to the SureView concept, wherebythe slice you select is the slice you get, independent of
pitch. This enables a longer range to be planned using an
increased feed per rotation with no compromise in the slice
thickness that is reconstructed.
Case 8: CT Imaging in Radiotherapy Planning
Scanner Emotion Duo
Scan area Head/Chest/Abdo/Pelvis
Scan length 862 mm
Scan time 58.4 s
Scan direction Craniocaudal
kV 130
Effective mAs 79 mAs (+CARE Dose)
Rotation time 0.8 s
Slice collimation 4 mm
Slice width 5 mm
Table feed/rotation 12 mm
Pitch 3
Reconstruction increment 5 mm
Kernel B 40 s
CTDIw 8.5 mGy
Comments
CTNI is used for transplant rejection in patients whodemonstrate severe or repetitive immunologic response
despite anti-rejection drug therapy. This could lead to fatal
loss of graft. The aim of TNI is to reduce the incidence of
recurrent rejection and decrease the amount of circling
lymphocytes3. The treatment fields include most of the
bodys lymphatic tissue. Supra diaphragmatically these are
the cervical, axillary, supraclavicular, mediastinal and pul-
monary hilar lymph node groups and the thymus gland.
Sub diaphragmatically these are the para aortic, iliac,
inguinal and femoral lymph node groups and the spleen.
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[ 2] (A) Axial head, top of the range (B) Axillary level
(C) Splenic level (D) Femoral level, bottom of range
[ 1 ] Coronal MPR
25
3 Accuracy
The use of the CT images for planning also enables the
spleen to be visualised with greater accuracy than onthe simulated radiographs, thus allowing more precise
planning of this treatment field. The ability of multislice CT
to acquire 5 mm slices throughout the volume produces
high quality digital radiographs on the planning system,
again allowing precise placement of the treatment fields.
3 Workflow
The syngo platform allows the user to automatically trans-
fer images to the planning station as they are recon-
structed, which saves valuable time in a busy department.
REFERENCES1 Tamm M. et al; Bronchiolitis Obliterans Syndrome following heart lung
transplantation Transplant International 1996; 9 Supplement 1: S. 299302.
2 Diamond D.A. et al Efficacy of total lymphoid irradiation for chronic
allograft rejection following bilateral lung tranplantation Int. Journal
Radiation Oncology-Biology-Physics 1998 July 1; 41(4): S. 795 800.
3 Wolden S. et al; Long term results of total lymphoid irradiation
in the treatment of cardiac allograft rejection Int. Journal Radiation
Oncology-Biology-Physics 1997; Vol 39 (5): S. 935 960.
4 Yang F. E. et al: Analysis of weekly complete blood counts in patients
receiving standard fractionated partial body radiation therapy Int. Journal
Radiation Oncology-Biology-Physics 1995, Oct 15; 33 (3): S. 617 620.
A C
B D
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[ 1 ] Marking of Isocenter-Coordinates for Laser System
26
SOMATOM SESSIONS 11
RADIATION TREATMENT PLANNING (RTP) has tradition-
ally been performed with the help of conventional X-ray
simulation systems, providing beam geometry thatmatches that of the linear accelerator. The radiographs
are then used by physicists or dosimetrists to establish the
margins of the area to be treated, and prescribe the radia-
tion dose.
Although this technique is still in widespread use today,
Virtual Simulation using CT or in some cases MR images
offers detail, software image manipulation and recon-
struction, and substantial increase in patient throughput
not known on conventional simulators. For example, CT
imaging offers virtual fluoroscopy and 3D Beam Design,
supporting more complex radiation treatments.
Accurate virtual simulation begins with the acquisition of
thin-slice, high-resolution images. Choose from Siemens
SOMATOM family of CT scanners, covering the spectrum of
workflow needs and techniques. Through the DICOM inter-
face, Siemens CT image sets are compatible with the treat-
ment planning systems of RTP vendors such as ADAC,
NOMOS, CMS and MEDINTEC.
Siemens syngo-based Virtual Simulation* uses Siemens
imaging expertise, advanced data processing, and the
Virtual Simulation
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syngo software platform to provide a comprehensive
oncology workflow solution. The application is designed to
accurately model all structures, radiation beams and linear
accelerator parameters and to produce high-quality Digi-tal Reconstructed Radiographs (DRRs), Multiplanar Refor-
mats (MPRs), Maximum Intensity Projections (MIPs) and
Surface Shaded Displays (SSDs). A full suite of automatic/
manual contour and edit tools enables streamlined con-
touring of image data with real-time display while inter-
active 3D capabilities enable viewing of and navigation
through the generated structures. syngo brings fast pro-
cessing, image fusion, innovative filming tools, DICOM-RT
compliance, and any easy-to-use interface common to all
Siemens medical imaging modalities.
[ 2 ] PET/ CT tumor visualization
* The information about this product is being provided for planning
purposes. The product is pending 510(k) review, and is not yet commercially
available.
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[ 4 ] Tissue definition
[ 3] Planning target definition
[ 5 ] Beam placement, Rooms-Eye-View
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THIS ISSUES AUTHORS
Computed Tomography for
Oncology Care
Virtual Simulation
Roselle Anderson
Marketing Communications
Siemens Medical Solutions USA, Inc.
Oncology Care Systems
4040 Nelson Avenue
Concord, CA 94520
USA
Case 1 4
Gerald Antoch, M.D.
Joerg F. Debatin, M.D., MBA
Department of Diagnostic and
Interventional Radiology
University Hospital Essen
Hufelandstrasse 55
45122 Essen
Germany
Andreas Bockisch, M.D., PhDDepartment of Nuclear Medicine
University Hospital Essen
Hufelandstrasse 55
45122 Essen
Germany
Case 56
Nakajima Takahito, M.D.
Keigo Endo, M.D.
Jun Aoki, M.D.
Gunma University Hospital
Shouwa Town, 3-39-15
Maebashi City
Gunma Prefecture,
371-8511, Japan
Case 7
James R. Wong1, Lisa Grimm1,
Reva Oren1, Allan Scher1,
Chester Wilson1, Ian Altas1,
Albert Fung1, Peter Schiff3,
Michal Chow1 and Minoru Uematsu2
1 Department of Radiation Oncology,
Morristown Memorial Hospital/Atlantic Health
System, NJ, USA;2
National Defense Medical College, Namiki,Tokorozawa, Japan;
3 Department of Radiation Oncology,
The New York Presbyterian Hospital, NY, USA
Case 8
Susan Dixon, Damien Parr
CT Scanning Dept.
Northern Centre for Cancer Treatment
Newcastle General Hospital
Newcastle-upon-Tyne NE4 6BE
UK
Sue Taylor
CT Applications Specialist
Siemens Medical SolutionsUK
IMPRESSUM
Published by
CT Marketing
Siemens AG
Medical Solutions
Siemensstrasse 1
91301 Forchheim, Germany
International Distribution
Xiaoyan Chen, M.D., MBA
CT Concepts
Siemens AG, Medical Solutions
Siemensstrasse 1
91301 Forchheim, Germany
Phone +49-9191-18-9652
Fax +49-9191-18-9996
eMail [email protected]
Anil Gupta
CT Marketing
Siemens AG, Medical Solutions
Siemensstrasse 1
91301 Forchheim, Germany
Phone +49-9191-18-8121
Fax +49-9191-18-9998
eMail [email protected]
Stefan Schaller, Ph.D.
CT Concepts
Siemensstrasse 1
91301 Forchheim, Germany
Phone +49-9191-18-8160
Fax +49-9191-18-9996
eMail [email protected]
SOMATOM SESSIONS 11
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SOMATOM SESSIONS 11