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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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    2

    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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    4

    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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    5

    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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    6

    SOMATOM SESSIONS 11

    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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    SOMATOM SESSIONS 11

    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.

    11

    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.

    12

    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

    13

    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.

    15

    A

    B

    C

    A

    B

    C

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    SOMATOM SESSIONS 11

    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.

    17

    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.

    18

    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)

    19

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    [ 4 ] Axial CT image revealed a tumor arising in the

    bladder wall.

    [ 1 ] Angio-CT system, MIYABI

    20

    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.

    21

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    [ 1 ] The PRIMATOM installation at Morristown Memorial

    Hospital, Morristown, New Jersey, USA.

    22

    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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    24

    SOMATOM SESSIONS 11

    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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    27

    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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    28

    [ 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