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Research ArticleCLINICAL INVESTIGATIONS

In Vivo Characterization of Proliferation for Discriminating Cancer from Pancreatic Pseudotumors

Ken Herrmann, Florian Eckel, Stefan Schmidt, Klemens Scheidhauer, Bernd Joachim Krause, Joerg Kleeff, Tibor Schuster, Hans-Juergen Wester, Helmut Friess, Roland M. Schmid, Markus Schwaiger and Andreas K. Buck
Journal of Nuclear Medicine September 2008, 49 (9) 1437-1444; DOI: https://doi.org/10.2967/jnumed.108.052027
Ken Herrmann
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Florian Eckel
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Stefan Schmidt
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Klemens Scheidhauer
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Bernd Joachim Krause
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Joerg Kleeff
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Tibor Schuster
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Hans-Juergen Wester
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Helmut Friess
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Roland M. Schmid
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Markus Schwaiger
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Andreas K. Buck
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  • FIGURE 1. 
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    FIGURE 1. 

    Scatter plot of mean 18F-FLT SUV in pancreatic cancer with focal 18F-FLT uptake (PET-positive), in pancreatic cancer negative on visual interpretation (PET-negative), and in benign pancreatic lesions (PET-negative). MFP = mass-forming pancreatitis; PC = pancreatic cancer.

  • FIGURE 2. 
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    FIGURE 2. 

    Spiral CT and 18F-FLT PET of patient 21, with CP, and patient 23, with pancreatic cancer. Physiologically increased 18F-FLT uptake is seen in bone marrow and liver, but only background activity of 18F-FLT is seen in area of inflammatory pancreatic mass (true-negative). Focal 18F-FLT uptake is seen in pancreatic carcinoma (true-positive).

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    FIGURE 3. 

    Spiral CT and 18F-FLT PET of patient 18, with pancreatic cancer, and false-negative findings on 18F-FLT PET. Physiologic 18F-FLT uptake is seen in bone marrow and liver. Histology indicated T1 adenocarcinoma.

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    FIGURE 4. 

    Receiver-operating-characteristic analysis of 18F-FLT PET for discriminating cancer from benign pancreatic lesions. Area under curve is 0.93 using cutoff of 1.8 for mean SUV or 0.92 using cutoff of 2.1 for maximal SUV.

Tables

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    TABLE 1

    Tumor Characteristics, Lesion Location, 18F-FLT PET Findings, Reference Method, and Clinical Consensus

    Patient no.Lesion location18F-FLT mean SUV18F-FLT maximal SUV18F-FLT PET visual scoreReference methodClinical consensus
    1Head3.64.21Met, CFU1
    2Head1.21.50Benign pancreatic tissue (C), CFU0
    3Tail3.23.51Adenocarcinoma (H)1
    4Head1.61.80Benign pancreatic tissue (C), CFU0
    5Head3.74.41Adenocarcinoma (H)1
    6Tail2.83.51Adenocarcinoma (H)1
    7Head1.72.00Benign pancreatic tissue (H)0
    8Head/corpus1.41.70Benign pancreatic tissue (H)0
    9Head1.41.60Benign pancreatic tissue (C), CFU0
    10Head6.57.31Squamous cell carcinoma (H)1
    11Head2.63.11Adenocarcinoma (H)1
    12Head8.59.81Undifferentiated adenocarcinoma (H)1
    13Head1.31.60Benign pancreatic tissue (H)0
    14Head2.42.61Neuroendocrine carcinoma (H)1
    15Head2.83.81Adenocarcinoma (H)1
    16Corpus1.72.00Adenocarcinoma (H)1
    17Head2.02.20Cystadenocarcinoma (H)1
    18Head1.31.50Adenocarcinoma (H)1
    19Head3.43.91Adenocarcinoma (H)1
    20Corpus1.92.30Adenocarcinoma (H)1
    21Corpus1.31.50CFU0
    22Head1.41.60Benign pancreatic tissue (H)0
    23Head4.95.11Adenocarcinoma (H)1
    24Head1.71.90Benign pancreatic tissue (C), CFU0
    25Head1.41.60Benign pancreatic tissue (C), CFU0
    26Corpus2.63.01Adenocarcinoma (H)1
    27Head3.03.41Adenocarcinoma (H)1
    28Head2.14.11Adenocarcinoma (H)1
    29Head1.71.90Adenocarcinoma (H)1
    30Corpus1.41.60Met, CFU1
    31Head3.64.21Adenocarcinoma (H)1
    • 0 = benign; 1 = malignant; met = liver mets at MRI/CT; CFU = clinical follow-up; C = cytology; H = histology.

    • Nineteen of 21 malignant and 4 of 10 benign lesions were verified histologically. Cytology or clinical follow-up served as reference in remaining patients.

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    TABLE 2

    18F-FLT PET Findings, Using Visual Interpretation, Compared with Clinical Consensus

    Clinical consensus
    18F-FLT PET findingPancreatic cancerBenign pancreatic lesionTotal
    Negative61016
    Positive15015
    Total211031
    • Clinical consensus is based on histologic verification in 23 patients, clinical follow-up/cytologic analysis in 7 patients, and evidence of metastatic disease on CT and MRI in 1 patient. Sensitivity of 18F-FLT PET is 71%; specificity, 100%.

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    TABLE 3

    18F-FLT PET Findings, Using Cutoff of 1.8 for Mean SUV or 2.1 for Maximal SUV, Compared with Clinical Consensus

    Clinical consensus
    18F-FLT PET findingPancreatic cancerBenign pancreatic lesionTotal
    Negative41014
    Positive17017
    Total211031
    • Clinical consensus is based on histologic verification in 23 patients, clinical follow-up/cytologic analysis in 7 patients, and evidence of metastatic disease on CT and MRI in 1 patient. Sensitivity of 18F-FLT PET is 81%; specificity, 100%.

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Journal of Nuclear Medicine: 49 (9)
Journal of Nuclear Medicine
Vol. 49, Issue 9
September 2008
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In Vivo Characterization of Proliferation for Discriminating Cancer from Pancreatic Pseudotumors
Ken Herrmann, Florian Eckel, Stefan Schmidt, Klemens Scheidhauer, Bernd Joachim Krause, Joerg Kleeff, Tibor Schuster, Hans-Juergen Wester, Helmut Friess, Roland M. Schmid, Markus Schwaiger, Andreas K. Buck
Journal of Nuclear Medicine Sep 2008, 49 (9) 1437-1444; DOI: 10.2967/jnumed.108.052027

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In Vivo Characterization of Proliferation for Discriminating Cancer from Pancreatic Pseudotumors
Ken Herrmann, Florian Eckel, Stefan Schmidt, Klemens Scheidhauer, Bernd Joachim Krause, Joerg Kleeff, Tibor Schuster, Hans-Juergen Wester, Helmut Friess, Roland M. Schmid, Markus Schwaiger, Andreas K. Buck
Journal of Nuclear Medicine Sep 2008, 49 (9) 1437-1444; DOI: 10.2967/jnumed.108.052027
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