|
|
||||||||
University Clinics of Nuclear Medicine and Internal Medicine, Vienna
Chemical Institute, Austrian Research Center, Seibersdorf
Center for Pulmonary Diseases, Vienna
Second University Clinic of Surgery, Vienna, Austria
Correspondence: For correspondence and reprints contact: Thomas Leitha, MD, University Clinic of Nuclear Medicine, University Vienna, Waehringer Guertel 18-20; 1090 Vienna, Austria
ABSTRACT
The purpose of this study is to investigate the role of 123I-Tyr-3-octreotide scintigraphy in staging small-cell lung cancer (SCLC), its efficacy for the discrimination of limited and extensive disease stages and its regional sensitivity for different metastatic locations. Twenty patients with histologically confirmed SCLC and 50 radiologically staged tumor sites were investigated by an imaging protocol including dynamic (030 min p.i.), static (30 min, 90 min, 4 hr, 24 hr p.i.) and SPECT (90 min p.i.) studies. The primary tumor site was visualized in 84%, whereas the best delineation was noted in early planar (1530 min p.i.) and SPECT studies, due to a rapidly decreasing tumor-to-background ratio. Lymph node metastases were seen in 73%, but SPECT was needed anatomical localization. All three adrenal metastases could be identified in sequential planar images. One clinically unsuspected brain metastasis was seen, whereas a second clinically overt metastasis was not visualized. The global and regional sensitivity for liver and bone metastases was unsatisfactory. In summary, 78% (7/9) of the patients with extensive disease were correctly identified by scintigraphy alone. We conclude that 123I-Tyr-3-octreotide scintigraphy is a substantial tool in the staging work-up of SCLC if it is performed initially to allow fast identification of patients with extensive disease stages and save additional radiological or invasive examinations. Yet, 123I-Tyr-3-octreotide scintigraphy cannot substitute liver sonography or conventional bone scanning in patients who have no scintigraphic evidence of distant tumor spread.
This article has been cited by other articles:
![]() |
J. P. Norenberg, B. J. Krenning, I. R.H.M. Konings, D. F. Kusewitt, T. K. Nayak, T. L. Anderson, M. de Jong, K. Garmestani, M. W. Brechbiel, and L. K. Kvols 213Bi-[DOTA0, Tyr3]Octreotide Peptide Receptor Radionuclide Therapy of Pancreatic Tumors in a Preclinical Animal Model Clin. Cancer Res., February 1, 2006; 12(3): 897 - 903. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY | THE JOURNAL OF NUCLEAR MEDICINE |