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Research ArticleClinical Investigations

68Ga-PSMA-HBED-CC PET for Differential Diagnosis of Suggestive Lung Lesions in Patients with Prostate Cancer

Thomas Pyka, Gregor Weirich, Ingo Einspieler, Tobias Maurer, Jörg Theisen, Georgios Hatzichristodoulou, Kristina Schwamborn, Markus Schwaiger and Matthias Eiber
Journal of Nuclear Medicine March 2016, 57 (3) 367-371; DOI: https://doi.org/10.2967/jnumed.115.164442
Thomas Pyka
1Department of Nuclear Medicine, Klinikum Rechts der Isar der TU München, Munich, Germany
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Gregor Weirich
2Institute of Pathology, Klinikum Rechts der Isar der TU München, Munich, Germany
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Ingo Einspieler
1Department of Nuclear Medicine, Klinikum Rechts der Isar der TU München, Munich, Germany
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Tobias Maurer
3Department of Urology, Klinikum Rechts der Isar der TU München, Munich, Germany; and
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Jörg Theisen
4Department of Surgery, Klinikum Rechts der Isar der TU München, Munich, Germany
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Georgios Hatzichristodoulou
3Department of Urology, Klinikum Rechts der Isar der TU München, Munich, Germany; and
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Kristina Schwamborn
2Institute of Pathology, Klinikum Rechts der Isar der TU München, Munich, Germany
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Markus Schwaiger
1Department of Nuclear Medicine, Klinikum Rechts der Isar der TU München, Munich, Germany
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Matthias Eiber
1Department of Nuclear Medicine, Klinikum Rechts der Isar der TU München, Munich, Germany
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Figures

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  • FIGURE 1.
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    FIGURE 1.

    Example PSMA PET/CT scan of patient with pulmonary PC metastasis. (A) CT shows irregularly shaped lesion in left upper lobe in PC patient after radical prostatectomy, no known metastases, and PSA of 1.58 ng/mL. Lesion was subsequently biopsied and diagnosed as pulmonary PC metastasis. (B) PSMA PET is positive, with SUVmax of 7.1. (C) PET/CT fusion image.

  • FIGURE 2.
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    FIGURE 2.

    Example PET/CT scans of patient with primary lung cancer (adenocarcinoma). (A) CT shows spiculated lesion in right upper lobe in PC patient after prostatectomy and suspected local recurrence; PSA was 4.09 ng/mL. (B) PSMA PET exhibits focal tracer enhancement in pulmonary lesion (SUVmax, 5.3) and in 2 mediastinal lymph nodes, which were histologically confirmed as primary lung cancer and associated lymph node metastases. This was the only case for which lymph node uptake was evaluated. (C) 18F-FDG PET as established imaging method of choice for lung cancer shows similar enhancement in primary tumor and 2 mediastinal lymph node metastases.

  • FIGURE 3.
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    FIGURE 3.

    Distribution of SUVmax for different lesion classes. No significant difference was shown when comparing SUVmax distributions between groups: PC all (n = 76) consisting of PC-proven and PC highly probable vs. lung cancer–proven (n = 7) (P = 0.408) and PC-proven (n = 39) only vs. lung cancer–proven (P = 0.780).

  • FIGURE 4.
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    FIGURE 4.

    Intraindividual variability of PSMA uptake in pulmonary PC metastases. Shown is distribution of SUVmax for proven or probable pulmonary PC metastases in patients exhibiting 3 or more lesions.

  • FIGURE 5.
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    FIGURE 5.

    Autoradiography and PSMA immunohistochemistry of exemplary case of primary lung cancer and PSMA immunohistology of tuberculous lesion. (A) PSMA autoradiography of primary lung carcinoma from imaged cohort, which exhibited strong signal in PSMA PET (SUVmax, 5.2). (B) Hematoxylin and eosin stain showing tumor contours. (C) PSMA immunohistochemistry of same tumor, showing detail of tumor region with high cell density and high signal in autoradiography (red arrowhead in A), exhibiting no tumor cells with clear PSMA expression but PSMA in neovasculature (black arrowheads). (D) PSMA immunohistochemistry of case of active tuberculosis from our histologic database, showing PSMA-positive blood vessels (black arrowheads).

  • FIGURE 6.
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    FIGURE 6.

    68Ga-PSMA autoradiography and PSMA immunohistochemistry of prostate carcinoma PC samples were used to establish autoradiography and immunohistology protocols. (A) PSMA autoradiography. (B) Hematoxylin and eosin stain. (C) Immunohistochemistry with anti-PSMA antibody 7E11 (aliquot kindly provided by Dr. Jan Grimm, Memorial Sloan Kettering Cancer Center).

Tables

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    TABLE 1

    Patients (n = 45)

    Characteristicn
    Age (y)68.8 (50–83)
    PSA (ng/mL)5.67 (0.2–18,000)
    Injected dose (MBq)151 (97–236)
    Classification
     PC-proven18
      By histology7
      By therapy response11
     Other entity–proven8
      Non–small cell lung cancer7
      Tuberculosis1
     PC highly probable15
     Unclear4
    • Data in parentheses are ranges.

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    TABLE 2

    Lesion Characteristics

    CharacteristicAllPC allPC-provenLung cancer–provenOther/unclear
    No. of lesions89763976
    Localization
     Right upper lobe22161051
     Right lower lobe1917911
     Middle lobe44100
     Left upper lobe25221412
     Left lower lobe1917502
    Configuration
     Smooth41391402
     Lobulated1110501
     Irregular30261913
     Speculated71160
    Mean CT diameter ± SD (mm)12.5 ± 6.311.8 ± 5.613.2 ± 6.921.0 ± 9.211.7 ± 1.8
    Mean SUVmax ± SD4.3 ± 3.74.4 ± 3.95.0 ± 4.45.5 ± 1.92.7 ± 2.5
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Journal of Nuclear Medicine: 57 (3)
Journal of Nuclear Medicine
Vol. 57, Issue 3
March 1, 2016
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68Ga-PSMA-HBED-CC PET for Differential Diagnosis of Suggestive Lung Lesions in Patients with Prostate Cancer
Thomas Pyka, Gregor Weirich, Ingo Einspieler, Tobias Maurer, Jörg Theisen, Georgios Hatzichristodoulou, Kristina Schwamborn, Markus Schwaiger, Matthias Eiber
Journal of Nuclear Medicine Mar 2016, 57 (3) 367-371; DOI: 10.2967/jnumed.115.164442

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68Ga-PSMA-HBED-CC PET for Differential Diagnosis of Suggestive Lung Lesions in Patients with Prostate Cancer
Thomas Pyka, Gregor Weirich, Ingo Einspieler, Tobias Maurer, Jörg Theisen, Georgios Hatzichristodoulou, Kristina Schwamborn, Markus Schwaiger, Matthias Eiber
Journal of Nuclear Medicine Mar 2016, 57 (3) 367-371; DOI: 10.2967/jnumed.115.164442
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Keywords

  • 68Ga-PSMA
  • prostate cancer
  • pulmonary metastasis
  • lung cancer
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