Browse by author
Lookup NU author(s): Dr Simon BomkenORCiD, Dr Barry Davies, Mike Cole, Dr Katrina Wood, Maritsa McDermott, Professor Deborah Tweddle
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The percentage of chemotherapy-induced necrosis in primary tumors corresponds with outcome in several childhood malignancies, including high-risk metastatic diseases. In this retrospective pilot study, the authors assessed the importance of postchemotherapy necrosis in high-risk neuroblastoma with a histological and case notes review of surgically resected specimens. The authors reviewed all available histology of 31 high-risk neuroblastoma cases treated with COJEC (dose intensive etoposide and vincristine with either cyclophosphamide, cisplatin or carboplatin) or OPEC/OJEC (etoposide, vincristine and cyclosphosphamide with alternating cisplatin [OPEC] or carboplatin [OJEC]) induction chemotherapy in 2 Children's Cancer & Leukaemia Group (CCLG) pediatric oncology centers. The percentage of postchemotherapy necrosis was assessed and compared with MYCN amplification status and overall survival. The median percentage of postchemotherapy tumor necrosis was 60%. MYCN status was available for 28 cases, of which 12 were amplified (43%). Survival in cases with ≥60% necrosis or ≥90% necrosis was not better than those with less necrosis, nor was percentage necrosis associated with survival using Cox regression. However, MYCN-amplified tumors showed a higher percentage of necrosis than non–MYCN-amplified tumors, 71.3% versus 37.2% (P = .006). This effect was not related to prechemotherapy necrosis and did not confer improved overall survival. Postchemotherapy tumor necrosis is higher in patients with MYCN amplification. In this study, postchemotherapy necrosis did not correlate with overall survival and should not lead to modification of postoperative treatment. However, these findings need to be confirmed in a larger prospective study of children with high-risk neuroblastoma.
Author(s): Bomken S, Davies B, Chong L, Cole M, Wood KM, McDermott M, Tweddle DA
Publication type: Article
Publication status: Published
Journal: Pediatric Hematology & Oncology
Year: 2011
Volume: 28
Issue: 2
Pages: 106-114
Print publication date: 08/01/2011
ISSN (print): 0888-0018
ISSN (electronic): 1521-0669
Publisher: Informa Healthcare
URL: http://dx.doi.org/10.3109/08880018.2010.526684
DOI: 10.3109/08880018.2010.526684
Altmetrics provided by Altmetric