4.7 Article

Scintigraphic response by 123I-metaiodobenzylguanidine scan correlates with event-free survival in high-risk neuroblastoma

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 22, Issue 19, Pages 3909-3915

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2004.07.144

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Funding

  1. NCI NIH HHS [5P30CA60553C] Funding Source: Medline

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Purpose To investigate whether response to induction therapy, evaluated by metaiodobenzylguanadine (MIBG) and bone scintigraphy, correlates with event-free survival (EFS) in children with high-risk neuroblastoma (NB). Patients and Methods Twenty-nine high-risk NB patients were treated prospectively with an intensive induction regimen and consolidated with three cycles of high-dose therapy with peripheral blood stem-cell rescue. The scintigraphic response was evaluated by MIBG and bone scans using a semi-quantitative scoring system. The prognostic significance of the imaging scores at diagnosis and following induction therapy was evaluated. Results A trend associating worse 4-year EFS rates for patients with versus without osteomedullary uptake on MIBG scintigraphs at diagnosis was seen (35% +/- 11% v 80% +/- 18%, respectively; P = .13). Similarly, patients with positive bone scans at diagnosis had worse EFS than those with negative scans, although the difference did not receive statistical significance (34% +/- 10% v 83% +/- 15%, respectively; P = .06). However, significantly worse EFS was observed in patients with a postinduction MIBG score of greater than or equal to3 compared to those with scores of less than 3 (0% v 58% +/- 11%; P = .002). There was no correlation between bone scan scores and outcome following induction therapy. Conclusion MIBG scores greater than or equal to3 following induction therapy identifies a subset of NB patients who are likely to relapse following three cycles of high-dose therapy with peripheral blood stem-cell rescue, local radiotherapy, and 13-cis-retinoic acid. Alternative therapeutic strategies should be considered for patients with a poor response to induction therapy. (C) 2004 by American Society of Clinical Oncology.

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