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WHOLE-BODY-LOW-DOSE MDCT

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WHOLE-BODY-LOW-DOSE MDCT IN THE INVESTIGATION OF MULTIPLE MYELOMA (MM) A NEW APPROCH AND OUR EXPERIENCE Kamenetsky Natalya (1), Rachmilewitz Eliezer (2), – PowerPoint PPT presentation

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Title: WHOLE-BODY-LOW-DOSE MDCT


1
  • WHOLE-BODY-LOW-DOSE MDCT
  • IN THE INVESTIGATION OF
  • MULTIPLE MYELOMA (MM)
  • A NEW APPROCH AND OUR EXPERIENCE
  • Kamenetsky Natalya (1), Rachmilewitz Eliezer (2),
  • Katz Rama (1),
  • (1)Department of Diagnostic Imaging
  • (2) Department of Heamatology
  • E. Wolfson Medical Center, Holon, Israel.

2
  • The idea of our study came from lately published
    literature, especially the article
  • Whole-body low dose multidetector row-CT
  • in the diagnosis of MM
  • an alternative to conventional radiography
  • EJR,2005.

3
MM Definition and diagnosis
  • Uncontrolled proliferation of neoplasticplasma
    cell clone in the bone marrow.
  • Diagnosis based on laboratory and radiographic
    findings
  • Bone marrow containing more then 15 plasma cells
    (normally no more then 4).
  • Blood serum or urine containing an abnormal
    protein (M protein, Bence-Jones protein).
  • Bone lesions found on skeletal survey as
    generalized osteopenia or lytic bone deposits.

4
MM Demographics
  • Most common primary bone tumor in adult.
  • Multifocal lesions more common
  • Solitary (Plasmacytoma) less common
  • may be Intra/Extraosseous.
  • Age 40 years or older.
  • MF 21
  • More common in Afro-Americans then in Caucasians.
    Less common in Asians.
  • Median survival 3-4 years.

5
MM Skeletal involvement
  • Osteolytic lesion (80) - found
  • particularly with nodular marrow infiltration.
  • small discrete lytic areas of bone destruction
  • with no reactive bone formation.
  • Arises within the medulla, may progress to
  • infiltrate the cortex and periosteum and be
  • accompanied with extraosseous soft tissue masses.

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MM-Skeletal involvment
  • Diffuse osteopenia (85) is associated with a
    packed pattern of marrow infiltration thinning
    of all trabeculae, vertebral body collapse.
  • Osteosclerosis rare (1-3), may be focal or
    diffuse.
  • Normal survey (10).

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Skeletal involvement in MM
  • Frequency in different bones correlates with
    normal sites of red marrow distribution
  • Vertebra (66).
  • Ribs (45).
  • Skull (40).
  • Shoulder (40).
  • Pelvis (30).
  • Long bones (25).

10
CT versus plain film
  • Bone lesions of the axial skeleton, are
    significantly better recognized by CT by reducing
    the effects of overlying soft tissue and bony
    structures.
  • Bone lesions of the appendicular skeleton are
    mostly well recognized in both modalities.

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Roll of imaging in MM patients
  • Diagnosis and staging.
  • Diagnosis of extramedullary or solitary
    plasmacytoma and directing a biopsy if needed.
  • Monitoring treatment response.
  • Detection of relapse.
  • Assessing fracture risk and directing
    prophylactic treatment.

14
Staging by Durie and Saimon
  • Stage 1 Stage
    3
  • (All) (1
    or more)
  • Hemoglobin gt10g/100ml
    lt8.5 g/100ml
  • Serum calcium lt12mg/100ml
    gt12mg/100ml
  • M component IgG lt5g/100ml
    gt7g/100ml
  • IgA lt3g/100ml
    gt5g/100ml
  • Urine light chain lt4 g/24hr
    gt12g/24hr
  • Bone Lesion none /solitary multiple
  • Stage 2 Between Stage 1 and 3.

15
MM Staging
  • Patients with more then two unequivocal lytic
    lesions are classified as stage 3, indicating
    immediate treatment.

16
Different imaging modalities
in MM
  • X-ray Conventional plain film survey, CT.
  • MRI
  • Radionuclid imaging Tc(99m)- MIBI,
  • F-18 FDG-PET.

17
Plain film skeletal survey
  • Multiple lytic lesions (80).
  • Solitary (Plasmacytoma) expansible lytic lesion.
  • Osteopenia (85).
  • Vertebral body collapse and pathological
    fractures.
  • Normal survey (10).
  • Shrinking or sclerosing deposits indicate a
    response.
  • Residual osteolysis may persist in inactive phase
    of disease.
  • No detection of extraosseous involvement.

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CT Imaging
  • Detect disease in bone, bone marrow and
    extramedullary sites.
  • Focal pattern sharp, lytic lesions with no
    sclerotic rim.
  • Diffuse faint osteolysis.
  • High (soft tissue) attenuation value of bone
    marrow.
  • Positive response to treatment Shrinking or
    sclerosing deposit, disappearance of soft tissue
    masses, reappearance of cortical contour and
    fatty marrow content.

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Our experience
  • On April - November 2006 we performed
  • 41 CT skeletal surveys
  • 30 patients with known diagnosis of MM.
  • 5 to exclude MM lesion in MGUS patients.
  • 6 in other patients.

25
CT survey study protocol
  • Patient laying supine, cranio-caudal position,
    arms on abdomen.
  • Scan length from top of the skull down to the end
    of the knees.
  • With suspended respiration when possible.
  • No oral or IV contrast material.

26
CT survey study protocol Low dose CT
parameters are based on the article from EJR
2005.
  • MDCT 16 slices.
  • Surview 1536 mm.
  • 120 KV, 70 mAs (300 mAs in spine CT)
  • Overall radiation dose of 5 mSv.
  • 160.75mm collimation with 0.5 sec rotation time.
  • Table speed 18mm/sec.
  • Slice thickness 3mm.
  • Mean acquisition time 38 sec.

27
CT survey study protocol
  • Reconstruction was done from raw data.
  • bone filter with B60f kernel.
  • F.O.V 500mm max.
  • multiplanar reformatted (MPR) whole body images
    were reconstructed in sagital and coronal planes.
  • Divided into 3 different body parts
  • Head and neck, including cervical spine
  • Chest and abdomen including the relevant spinal
    column and arms
  • pelvis and thighs.

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Plain film skeletal survey protocol
  • Skull AP and lateral.
  • Vertebral column AP and lateral for each level.
  • Ribs AP and oblique.
  • Pelvis AP.
  • Upper and lower extremities AP and lateral.
  • Overall - 20 different plain films per patient.
  • Radiation dose of 2.4 mSv.

32
Our experience results
  • The majority had IgG gammopathy and suffered from
    both osteopenia and lytic lesions.
  • 12 (29) patients had vertebral collapse.
  • 5 (12) patients had large vertebral lytic lesion
    at high risk for collapse.

33
Results
  • In 7 (17) patients we detected significant
    extramedullary finding
  • 2 (4) as part of the MM dieses itself.
  • 5 (12) not directly relevant to MM but demand
    forwarder investigation.

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CT versus plain film survey
  • 16 MM patients had a conventional plain film
    survey done no more than two weeks before the CT.
  • Comparing the two imaging modalities we found
  • In 5 (31) patients lytic lesion that where not
    found on the conventional survey.
  • In 2 (12.5) patients vertebral lytic lesion in
    risk of collapse that were not found on the plain
    film survey.

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CT versus plain film survey
  • Advantage
  • More sensitive and accurate in identifying and
    characterizing lytic lesions.
  • Especially important in the evaluation of
    vertebral collapse and their possible
    complications.
  • Most beneficial in the diagnosis of large lytic
    lesions in risk of phatological fracture.

45
CT versus plain film survey
  • Advantage
  • Identify extramedullary involvement of the
    dieses itself or incidental finding that may be
    important.
  • Guide biopsies.
  • Disadvantage
  • Higher radiation dose.

46
Radiation dose of X-ray Imaging
CT high dose 250 mAs CT low dose 70 mAs Plain film survey Exam type
25.5 mSv 5 mSv 2.4 mSv Radiation dose
47
Summary
  • Accurate detection of skeletal lesions is
    essential for the diagnosis, staging and
    treatment in MM.
  • The number, size and anatomic location of the
    lesions are important to evaluate the patients
    prognosis and quality of life.
  • Whole body low dose CT is much more sensitive and
    accurate than the classic plain film survey.

48
Summary
  • In low dose CT the radiation dose is about twice
    that of a plain film survey but much lower than
    conventional skeletal CT.
  • As in the literature, we propose this study as
    an efficient and relatively available in compare
    to other imaging modalities, for MM patients.

49
MERCI! THANK YOU!????!!
MERCI! THANK YOU!????!!
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