110mIn-DTPA-D-Phe1-octreotide for imaging of neuroendocrine tumors with PET

Mark Lubberink, Vladimir Tolmachev, Charles Widström, Alexander Bruskin, Hans Lundqvist, Jan Erik Westlin

Результат исследований: Материалы для журналаСтатьярецензирование

49 Цитирования (Scopus)


The somatostatin analog diethylenetriaminepentaacetic acid (DTPA)-D-Phe1-octreotide labeled with 111In has been applied extensively for diagnosis of neuroendocrine tumors using SPECT or planar scintigraphy. However, the spatial resolution of planar scintigraphy and SPECT prohibits imaging of small tumors, and the quantification accuracy of both methods is limited. Methods: We developed a method to prepare the positron-emitting radiopharmaceutical 11OmIn-DTPA-D-Phe1-octreotide based on a commercially available kit. Phantom studies were done to investigate and compare the performance of 110mIn PET and 111In SPECT. A clinical imaging study using 110mIn-DTPA-D-Phe1-octreotide and PET was done to investigate the application of this radiopharmaceutical. Results: An almost 3-fold better resolution and much better quantitative capabilities were found for 110mIn PET than for 111In SPECT. The clinical imaging study demonstrated the potential use of 110mIn-octreotide in PET to image tumors and quantify radioactivity uptake in humans using 110mIn-DTPA-D-Phe1-octreotide. Conclusion: PET with 110mIn-DTPA-D-Phe1-octreotide greatly improved detection of small tumors and offers a possibility of more accurate quantification of tumor uptake than can be obtained with 111In-DTPA-D-Phe1-octreotide and SPECT.

Язык оригиналаАнглийский
Страницы (с-по)1391-1397
Число страниц7
ЖурналJournal of Nuclear Medicine
Номер выпуска10
СостояниеОпубликовано - 1 окт 2002
Опубликовано для внешнего пользованияДа

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

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