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MIBG scans in patients with stage 4 neuroblastoma reveal two metastatic patterns, one is associated with MYCN amplification and in MYCN-amplified tumours correlates with a better prognosis.

AbstractPURPOSE:
The aim of this study was to find clinically relevant MIBG-avid metastatic patterns in patients with newly diagnosed stage 4 neuroblastoma.
METHODS:
Diagnostic (123)I-MIBG scans from 249 patients (123 from a European and 126 from the COG cohort) were assessed for metastatic spread in 14 body segments and the form of the lesions: "focal" (clear margins distinguishable from adjacent background) or "diffuse" (indistinct margins, dispersed throughout the body segment). The total numbers of diffuse and focal lesions were recorded. Patients were then categorized as having lesions exclusively focal, lesions more focal than diffuse, lesions more diffuse than focal, or lesions exclusively diffuse.
RESULTS:
Diffuse lesions affected a median of seven body segments and focal lesions a median of two body segments (P < 0.001, both cohorts). Patients with a focal pattern had a median of 2 affected body segments and those with a diffuse pattern a median of 11 affected body segments (P < 0.001, both cohorts). Thus, two MIBG-avid metastatic patterns emerged: "limited-focal" and "extensive-diffuse". The median numbers of affected body segments in MYCN-amplified (MNA) tumours were 5 (European cohort) and 4 (COG cohort) compared to 9 and 11, respectively, in single-copy MYCN (MYCNsc) tumours (P < 0.001). Patients with exclusively focal metastases were more likely to have a MNA tumour (60% and 70%, respectively) than patients with the other types of metastases (23% and 28%, respectively; P < 0.001). In a multivariate Cox regression analysis, focal metastases were associated with a better event-free and overall survival than the other types of metastases in patients with MNA tumours in the COG cohort (P < 0.01).
CONCLUSION:
Two metastatic patterns were found: a "limited and focal" pattern found mainly in patients with MNA neuroblastoma that correlated with prognosis, and an "extensive and diffuse" pattern found mainly in patients with MYCNsc neuroblastoma.
AuthorsGitta Bleeker, Berthe L van Eck-Smit, Koos H Zwinderman, Rogier Versteeg, Max M van Noesel, Boen L Kam, Gertjan J Kaspers, Annelies van Schie, Susan G Kreissman, Gregory Yanik, Barbara Hero, Matthias Schmidt, Geneviève Laureys, Bieke Lambert, Ingrid Øra, Johannes H Schulte, Huib N Caron, Godelieve A Tytgat
JournalEuropean journal of nuclear medicine and molecular imaging (Eur J Nucl Med Mol Imaging) Vol. 42 Issue 2 Pg. 222-30 (Feb 2015) ISSN: 1619-7089 [Electronic] Germany
PMID25267348 (Publication Type: Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • MYCN protein, human
  • N-Myc Proto-Oncogene Protein
  • Nuclear Proteins
  • Oncogene Proteins
  • Radiopharmaceuticals
  • 3-Iodobenzylguanidine
Topics
  • 3-Iodobenzylguanidine
  • Adolescent
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Male
  • Multimodal Imaging
  • N-Myc Proto-Oncogene Protein
  • Neoplasm Metastasis (diagnostic imaging, genetics, pathology)
  • Neuroblastoma (diagnostic imaging, genetics, pathology)
  • Nuclear Proteins (genetics)
  • Oncogene Proteins (genetics)
  • Positron-Emission Tomography
  • Predictive Value of Tests
  • Prognosis
  • Radiopharmaceuticals
  • Tomography, X-Ray Computed

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