Neuroblastoma mRNAs predict outcome in children with stage 4 neuroblastoma: a European HR-NBL1/SIOPEN study
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
18226
Cancer Research UK - United Kingdom
MR/L01629X/1
Medical Research Council - United Kingdom
C5651/A9663
Cancer Research UK - United Kingdom
PubMed
24590653
DOI
10.1200/jco.2013.53.3604
PII: JCO.2013.53.3604
Knihovny.cz E-resources
- MeSH
- Cisplatin administration & dosage MeSH
- Cyclophosphamide administration & dosage MeSH
- Child MeSH
- Doublecortin Domain Proteins MeSH
- Etoposide administration & dosage MeSH
- Homeodomain Proteins genetics MeSH
- Induction Chemotherapy MeSH
- Kaplan-Meier Estimate MeSH
- Carboplatin administration & dosage MeSH
- Infant MeSH
- Bone Marrow metabolism MeSH
- Humans MeSH
- RNA, Messenger blood MeSH
- Survival Rate MeSH
- Adolescent MeSH
- Biomarkers, Tumor blood metabolism MeSH
- Neuroblastoma drug therapy genetics metabolism MeSH
- Neuropeptides genetics MeSH
- Computer Simulation MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Predictive Value of Tests MeSH
- Child, Preschool MeSH
- Disease-Free Survival MeSH
- Proportional Hazards Models MeSH
- Doublecortin Protein MeSH
- Microtubule-Associated Proteins genetics MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Transcription Factors genetics MeSH
- Tyrosine 3-Monooxygenase genetics MeSH
- Vincristine administration & dosage MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Child, Preschool MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cisplatin MeSH
- Cyclophosphamide MeSH
- DCX protein, human MeSH Browser
- Doublecortin Domain Proteins MeSH
- Etoposide MeSH
- Homeodomain Proteins MeSH
- Carboplatin MeSH
- RNA, Messenger MeSH
- Biomarkers, Tumor MeSH
- NBPhox protein MeSH Browser
- Neuropeptides MeSH
- Doublecortin Protein MeSH
- Microtubule-Associated Proteins MeSH
- Transcription Factors MeSH
- Tyrosine 3-Monooxygenase MeSH
- Vincristine MeSH
PURPOSE: To evaluate the hypothesis that detection of neuroblastoma mRNAs by reverse transcriptase quantitative polymerase chain reaction (RTqPCR) in peripheral blood (PB) and bone marrow aspirates (BM) from children with stage 4 neuroblastoma are clinically useful biomarkers of risk. METHODS: RTqPCR for paired-like homeobox 2b (PHOX2B), tyrosine hydroxylase (TH), and doublecortin (DCX) mRNA in PB and BM of children enrolled onto the High-Risk Neuroblastoma Trial-1 of the European Society of Pediatric Oncology Neuroblastoma Group (HR-NBL1/SIOPEN) was performed at diagnosis and after induction therapy. RESULTS: High levels of TH, PHOX2B, or DCX mRNA in PB or BM at diagnosis strongly predicted for worse event-free survival (EFS) and overall survival (OS) in a cohort of 290 children. After induction therapy, high levels of these mRNAs predicted worse EFS and OS in BM but not in PB. Combinations of mRNAs in BM did not add to the predictive power of any single mRNA. However, in the original (n = 182) and validation (n = 137) PB cohorts, high TH (log10TH > 0.8) or high PHOX2B (log10PHOX2B > 0.28) identify 19% of children as ultrahigh risk, with 5-year EFS and OS rates of 0%; OS rate was 25% (95% CI, 16% to 36%) and EFS rate was 38% (95% CI, 28% to 49%) in the remaining children. The magnitude of reduction in mRNA level between diagnosis and postinduction therapy in BM or PB was not of additional predictive value. CONCLUSION: High levels of TH and PHOX2B mRNA in PB at diagnosis objectively identify children with ultrahigh-risk disease who may benefit from novel treatment approaches. The level of TH, PHOX2B, and DCX mRNA in BM and/or PB at diagnosis might contribute to an algorithm to improve stratification of children for treatment.
References provided by Crossref.org
ClinicalTrials.gov
NCT01704716