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  1. Article

    Open Access

    Salvage peptide receptor radionuclide therapy with [177Lu-DOTA,Tyr3]octreotate in patients with bronchial and gastroenteropancreatic neuroendocrine tumours

    Therapy with [177Lu-DOTA,Tyr3]octreotate is effective in patients with grade I/II metastasized and/or inoperable bronchial neuroendocrine tumour (NET) or gastroenteropancreatic NET (GEP-NET). In this study, we in...

    W. A. van der Zwan, T. Brabander in European Journal of Nuclear Medicine and M… (2019)

  2. No Access

    Article

    Measurement of circulating transcripts and gene cluster analysis predicts and defines therapeutic efficacy of peptide receptor radionuclide therapy (PRRT) in neuroendocrine tumors

    Peptide receptor radionuclide therapy (PRRT) is an effective method for treating neuroendocrine tumors (NETs). It is limited, however, in the prediction of individual tumor response and the precise and early i...

    L. Bodei, M. Kidd, I. M. Modlin, S. Severi in European Journal of Nuclear Medicine and M… (2016)

  3. No Access

    Article

    Gene transcript analysis blood values correlate with 68Ga-DOTA-somatostatin analog (SSA) PET/CT imaging in neuroendocrine tumors and can define disease status

    Precise determination of neuroendocrine tumor (NET) disease status and response to therapy remains a rate-limiting concern for disease management. This reflects limitations in biomarker specificity and resolut...

    L. Bodei, M. Kidd, I. M. Modlin, V. Prasad in European Journal of Nuclear Medicine and M… (2015)

  4. Article

    Open Access

    Lutetium-labelled peptides for therapy of neuroendocrine tumours

    Treatment with radiolabelled somatostatin analogues is a promising new tool in the management of patients with inoperable or metastasized neuroendocrine tumours. Symptomatic improvement may occur with 177Lu-label...

    B. L. R. Kam, J. J. M. Teunissen in European Journal of Nuclear Medicine and M… (2012)

  5. Article

    Open Access

    Gastrin-releasing peptide receptor-based targeting using bombesin analogues is superior to metabolism-based targeting using choline for in vivo imaging of human prostate cancer xenografts

    Prostate cancer (PC) is a major health problem. Overexpression of the gastrin-releasing peptide receptor (GRPR) in PC, but not in the hyperplastic prostate, provides a promising target for staging and monitori...

    Rogier P. J. Schroeder, W. M. van Weerden in European Journal of Nuclear Medicine and M… (2011)

  6. No Access

    Article

    Novel 111In-labelled bombesin analogues for molecular imaging of prostate tumours

    It has been shown that some primary human tumours and their metastases, including prostate and breast tumours, overexpress gastrin-releasing peptide (GRP) receptors. Bombesin (BN) is a neuropeptide with a high...

    M. de Visser, H. F. Bernard, J. L. Erion in European Journal of Nuclear Medicine and M… (2007)

  7. Article

    Open Access

    Reply

    F. Forrer, E. Rolleman, N. Schramm in European Journal of Nuclear Medicine and M… (2007)

  8. No Access

    Article

    Comparison of [177Lu-DOTA0,Tyr3]octreotate and [177Lu-DOTA0,Tyr3]octreotide: which peptide is preferable for PRRT?

    Patients with somatostatin receptor subtype 2-positive metastasised neuroendocrine tumours can be treated with [177Lu-DOTA0,Tyr3]octreotate. Some use octreotide as the peptide for peptide receptor radionuclide th...

    J. P. Esser, E. P. Krenning in European Journal of Nuclear Medicine and M… (2006)

  9. No Access

    Article

    In vivo radionuclide uptake quantification using a multi-pinhole SPECT system to predict renal function in small animals

    In vivo quantification of radiopharmaceuticals has great potential as a tool in develo** new drugs. We investigated the accuracy of in vivo quantification with multi-pinhole single-photon emission computed t...

    F. Forrer, R. Valkema, B. Bernard in European Journal of Nuclear Medicine and M… (2006)

  10. No Access

    Article

    Stabilised 111In-labelled DTPA- and DOTA-conjugated neurotensin analogues for imaging and therapy of exocrine pancreatic cancer

    Neurotensin (NT) receptors are overexpressed in exocrine pancreatic cancer and Ewing's sarcoma. The potential utility of native NT in cancer diagnosis and therapy is, however, limited by its rapid degradation ...

    M. de Visser, P. J. J. M. Janssen in European Journal of Nuclear Medicine and M… (2003)

  11. No Access

    Article

    Treatment of patients with gastro-entero-pancreatic (GEP) tumours with the novel radiolabelled somatostatin analogue [177Lu-DOTA0,Tyr3]octreotate

    Medical treatment and chemotherapy are seldom successful in achieving objective tumour reduction in patients with metastatic neuroendocrine tumours. Treatment with the radiolabelled somatostatin analogue [90Y-DOT...

    D. J. Kwekkeboom, W. H. Bakker, B. L. Kam in European Journal of Nuclear Medicine and M… (2003)

  12. No Access

    Article

    Comparison of iodine-123 epidepride and iodine-123 IBZM for dopamine D2 receptor imaging in clinically non-functioning pituitary macroadenomas and macroprolactinomas

    We compared pituitary iodine-123 epide- pride single-photon emission tomography (SPET) and 123I-IBZM SPET for the in vivo imaging of dopamine D2 receptors in 15 patients with clinically non-functioning pituitary...

    W. W. de Herder, A. E. M. Reijs, J. de Swart in European Journal of Nuclear Medicine (1999)

  13. No Access

    Chapter

    Somatostatin Receptor Imaging in Oncology

    In diagnosing or staging cancer, conventional imaging techniques such as X-ray computed tomography (CT) or nuclear magnetic resonance imaging (MRI) often seem adequate in detecting tumors commonly encountered ...

    D. J. Kwekkeboom, E. P. Krenning in Nuclear Oncology (1999)

  14. No Access

    Article

    Visualization of the thymus by substance P receptor scintigraphy in man

    Substance P, an 11-amino acid neuropeptide, has an important role in modulating pain transmission through neurokinin 1 and 2 receptors. Substance P and other tachykinins may also play a role in the pathogenesi...

    P. M. van Hagen, W. A. P. Breeman, J. C. Reubi in European Journal of Nuclear Medicine (1996)

  15. No Access

    Article

    Somatostatin-receptor scintigraphy in Graves' orbitopathy

    P. T. E. Postema, D. J. Kwekkeboom, P. M. van Hagen in European Journal of Nuclear Medicine (1996)

  16. No Access

    Article

    Vascular risk factors, atherosclerosis, cerebral white matter lesions and cerebral perfusion in a population-based study

    We studied risk factors for cerebral vascular disease (blood pressure and hypertension, factor VIIc, factor VIIIc, fibrinogen), indicators of atherosclerosis (intima-media thickness and plaques in the carotid ...

    J. J. Claus, M. M. B. Breteler, D. Hasan in European Journal of Nuclear Medicine (1996)

  17. No Access

    Article

    Assessment of cerebral perfusion with single-photon emission tomography in normal subjects and in patients with Alzheimer's disease: effects of region of interest selection

    The shape, size and location of regions of interest (ROls) show considerable variability between single-photon emission tomography (SPET) studies in aging and Alzheimer's disease, but the possible influence on...

    J. J. Claus, F. van Harskamp, M. M. B. Breteler in European Journal of Nuclear Medicine (1994)

  18. No Access

    Article

    Somatostatin analogue scintigraphy in granulomatous diseases

    Normal as well as activated lymphocytes and macrophages have previously been shown by radioreceptor analysis to express somatostatin receptors (SS-R). The somatostatin (SS) analogue [111In-DTPA-d-Phe1]octreotide ...

    P. M. Vanhagen, E. P. Krenning, J. C. Reubi in European Journal of Nuclear Medicine (1994)

  19. No Access

    Article

    A new radiolabelled somatostatin analogue [111In-DTPA-D-Phe1]RC-160: preparation, biological activity, receptor scintigraphy in rats and comparison with [111In-DTPA-D-Phe1]octreotide

    We have evaluated the potential usefulness of indium-111 labelled [DTPA-D-Phe1]RC-160, derived from the octapeptide somatostatin analogue RC-160, as a radiopharmaceutical for the in vivo detection of somatostatin...

    W. A. P. Breeman, L. J. Hofland, M. van der Pluijm in European Journal of Nuclear Medicine (1994)

  20. No Access

    Article

    A new radiolabelled somatostatin analogue [111In-DTPA-D-Phe1]RC-160: preparation, biological activity, receptor scintigraphy in rats and comparison with [111In-DTPA-D-Phe1]octreotide

    We have evaluated the potential usefulness of indium-111 labelled [DTPA-D-Phe1]RC-160, derived from the octapeptide somatostatin analogue RC-160, as a radiopharmaceutical for the in vivo detection of somatostatin...

    W. A. P. Breeman, L. J. Hofland, M. van der Pluijm in European Journal of Nuclear Medicine (1994)

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