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Update on the development of the international neuroblastoma risk group (INRG) classification schema.

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Sub-category:
Pediatric Solid Tumors

Category:
Pediatric Oncology

Meeting:
2007 ASCO Annual Meeting

Abstract No:
9503

Citation:
Journal of Clinical Oncology, 2007 ASCO Annual Meeting Proceedings Part I. Vol 25, No. 18S (June 20 Supplement), 2007: 9503

Author(s):
S. L. Cohn, W. B. London, T. Monclair, K. K. Matthay, P. F. Ambros, A. D. Pearson, for the INRG Working Group

Abstract:

Background: Modern treatment strategies for neuroblastoma (NB) are tailored according to patient risk. However, it is not currently possible to compare the results of clinical studies conducted around the globe because the criteria used to define risk are not uniform. A committee of international investigators with expertise in NB have worked during the past 2 years to develop a uniform International NB Risk Group (INRG) Classification System for pre-treatment stratification. Methods: Investigators from North America and Australia (COG); Europe (SIOPEN and Germany), and Japan collated data on 8,800 children with NB diagnosed between 1990 and 2002. Survival tree regression analyses tested 13 potential prognostic factors. Tumor differentiation, MKI, and diagnostic category were evaluated individually in lieu of the International NB Pathology Classification (INPC) system to determine if these histologic features had prognostic value independent from age. To stage patients at the time of diagnosis prior to surgery, a new staging system was developed (INRGSS) based on the presence or absence of image-defined risk factors (IDRFs) and metastases. Results: Since statistical analyses demonstrated support for an optimal age cut- off between 14-19 months, 18 months was selected. In addition to age, stage, MYCN amplification, tumor differentiation, ploidy, and genetic aberrations of 11q were found to be the most highly prognostically significant factors. These clinical and biological factors were combined to define 15 INRG pre-treatment groups. Patients with low- (3 groups), intermediate- (4 groups), high- (4 groups), or ultra-high-risk NB (4 groups) had EFS of >85%, >70-85%, >50-70%, or <50%, respectively. Conclusion: International collaborative studies in NB will be greatly facilitated by the INRG classification system which will allow comparisons of different risk-based therapeutic approaches in homogeneous patient cohorts.


Abstract Disclosures

Abstracts that were granted an exception in accordance with ASCO's Conflict of Interest Policy and are designated with a caret symbol (^) here and in the print version.


  Associated Presentation(s):

    

1. Update on the development of the international neuroblastoma risk group (INRG) classification schema.

Meeting: 2007 ASCO Annual Meeting
Presenter: Susan L Cohn, MD
Session: Pediatric Cancer I (Oral Presentation)


  Other Abstracts in this Sub-Category:

    

1. Identification of genomic DNA signatures predicting relapse in low- and intermediate-risk neuroblastoma using a case control design and high-density SNP genotyping: A Children's Oncology Group (COG) study.

Meeting: 2007 ASCO Annual Meeting   Abstract No: 9500   First Author: E. F. Attiyeh
Category: Pediatric Oncology - Pediatric Solid Tumors

    

2. Specific gene expression profiles and unique chromosomal abnormalities are associated with regressing tumors among infants with disseminated neuroblastoma.

Meeting: 2007 ASCO Annual Meeting   Abstract No: 9501   First Author: C. Lavarino
Category: Pediatric Oncology - Pediatric Solid Tumors

    

3. Anti-GD2 monoclonal antibody 3F8 plus granulocyte-macrophage colony-stimulating factor (GM-CSF) for primary refractory neuroblastoma (NB) in bone marrow (BM).

Meeting: 2007 ASCO Annual Meeting   Abstract No: 9502   First Author: B. H. Kushner
Category: Pediatric Oncology - Pediatric Solid Tumors

    

More...


  Abstracts by S. L. Cohn:

    

1. A phase III randomized trial of the chimeric anti-GD2 antibody ch14.18 with GM-CSF and IL2 as immunotherapy following dose intensive chemotherapy for high-risk neuroblastoma: Children’s Oncology Group (COG) study ANBL0032

Meeting: 2009 ASCO Annual Meeting   Abstract No: 10067z   First Author: A. L. Yu
Category: Pediatric Cancer - Pediatric Solid Tumors

    

2. Irinotecan plus temozolomide in children with recurrent or refractory neuroblastoma: A phase II Children's Oncology Group study.

Meeting: 2009 ASCO Annual Meeting   Abstract No: 10011   First Author: R. Bagatell
Category: Pediatric Cancer - Pediatric Solid Tumors

    

3. Significance of tumor biology compared to metastatic pattern (INSS 4 versus 4s) and age for prognosis of neuroblastoma less than 18 months of age.

Meeting: 2009 ASCO Annual Meeting   Abstract No: 10010   First Author: D. R. Taggart
Category: Pediatric Cancer - Pediatric Solid Tumors

    

More...


  Presentations by S. L. Cohn:

    

1. Pediatric Cancer

Meeting: 2007 ASCO Annual Meeting
Chair: Susan L Cohn, MD
Session: Pediatric Cancer (Poster Discussion)

    

2. Update on the development of the international neuroblastoma risk group (INRG) classification schema.

Meeting: 2007 ASCO Annual Meeting
Presenter: Susan L Cohn, MD
Session: Pediatric Cancer I (Oral Presentation)

    

3. Discussion

Meeting: 2006 ASCO Annual Meeting
Discussant: Susan Lerner Cohn, MD
Session: Pediatric Cancer II (Oral Presentation)

    

More...


  Educational Book Manuscripts by S. L. Cohn:

    

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