TY - JOUR
T1 - Neuroblastoma messenger RNA is frequently detected in bone marrow at diagnosis of localised neuroblastoma patients
AU - van Wezel, Esther M
AU - Decarolis, Boris
AU - Stutterheim, Janine
AU - Zappeij-Kannegieter, Lily
AU - Berthold, Frank
AU - Schumacher-Kuckelkorn, Roswitha
AU - Simon, Thorsten
AU - Fiocco, Marta
AU - van Noesel, Max M
AU - Caron, Huib N
AU - van der Schoot, C Ellen
AU - Hero, Barbara
AU - Tytgat, Godelieve A M
N1 - Copyright © 2015 Elsevier Ltd. All rights reserved.
PY - 2016/2
Y1 - 2016/2
N2 - INTRODUCTION: The clinical importance of the detection of neuroblastoma messenger RNA (mRNA) in bone marrow (BM) of localised neuroblastoma patients at diagnosis remains unclear. In this prospective multicentre study, BM samples of a large cohort, were studied using real-time quantitative polymerase chain reaction (qPCR).METHODS: BM samples at diagnosis from 160 patients with localised neuroblastoma were prospectively collected at Dutch and German centres between 2009 and 2013. qPCR was performed using five neuroblastoma specific markers. The association with other biological factors and the prognostic impact of BM positivity and clinical response was assessed.RESULTS: In 58 out of 160 patients neuroblastoma mRNA was detected in BM. In 47 of the 58 positive samples only one marker was found positive. BM positivity was significantly associated with MYCN amplification (p = 0.02) and deletion of chromosome 1p (p = 0.04). In total 31 patients had an event, of which only five patients had progression to stage IV. BM positivity was not associated with an unfavourable outcome. However, the detection of more than one marker was associated with an unfavourable outcome (systemic or local relapse) (event free survival 48% versus 85%; p = 0.03) in the whole cohort and in the observation group.CONCLUSIONS: BM positivity was associated with unfavourable biological factors and might represent more aggressive tumours. Patients with qPCR positive BM should not be upstaged, because of very few systemic events in the cohort. However, for patients with more than one marker positive a more careful follow-up is advisable. These results need to be verified in a very large cohort of localised patients.
AB - INTRODUCTION: The clinical importance of the detection of neuroblastoma messenger RNA (mRNA) in bone marrow (BM) of localised neuroblastoma patients at diagnosis remains unclear. In this prospective multicentre study, BM samples of a large cohort, were studied using real-time quantitative polymerase chain reaction (qPCR).METHODS: BM samples at diagnosis from 160 patients with localised neuroblastoma were prospectively collected at Dutch and German centres between 2009 and 2013. qPCR was performed using five neuroblastoma specific markers. The association with other biological factors and the prognostic impact of BM positivity and clinical response was assessed.RESULTS: In 58 out of 160 patients neuroblastoma mRNA was detected in BM. In 47 of the 58 positive samples only one marker was found positive. BM positivity was significantly associated with MYCN amplification (p = 0.02) and deletion of chromosome 1p (p = 0.04). In total 31 patients had an event, of which only five patients had progression to stage IV. BM positivity was not associated with an unfavourable outcome. However, the detection of more than one marker was associated with an unfavourable outcome (systemic or local relapse) (event free survival 48% versus 85%; p = 0.03) in the whole cohort and in the observation group.CONCLUSIONS: BM positivity was associated with unfavourable biological factors and might represent more aggressive tumours. Patients with qPCR positive BM should not be upstaged, because of very few systemic events in the cohort. However, for patients with more than one marker positive a more careful follow-up is advisable. These results need to be verified in a very large cohort of localised patients.
KW - Adolescent
KW - Biomarkers, Tumor/genetics
KW - Bone Marrow/chemistry
KW - Bone Marrow Examination
KW - Child
KW - Child, Preschool
KW - Chromosome Deletion
KW - Chromosomes, Human, Pair 1
KW - Disease Progression
KW - Disease-Free Survival
KW - Female
KW - Gene Amplification
KW - Genetic Predisposition to Disease
KW - Germany
KW - Humans
KW - Infant
KW - Infant, Newborn
KW - Kaplan-Meier Estimate
KW - Male
KW - N-Myc Proto-Oncogene Protein
KW - Neoplasm Recurrence, Local
KW - Neoplasm Staging
KW - Netherlands
KW - Neuroblastoma/genetics
KW - Nuclear Proteins/genetics
KW - Oncogene Proteins/genetics
KW - Phenotype
KW - Predictive Value of Tests
KW - Prospective Studies
KW - RNA, Messenger/genetics
KW - RNA, Neoplasm/genetics
KW - Real-Time Polymerase Chain Reaction
KW - Risk Factors
KW - Time Factors
KW - Treatment Outcome
KW - Young Adult
UR - http://www.scopus.com/inward/record.url?scp=84954175650&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2015.11.007
DO - 10.1016/j.ejca.2015.11.007
M3 - Article
C2 - 26796600
SN - 1879-0852
VL - 54
SP - 149
EP - 158
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -