New cellular markers at diagnosis are associated with isolated central nervous system relapse in paediatric B‐cell precursor acute lymphoblastic leukaemia. (21st December 2015)
- Record Type:
- Journal Article
- Title:
- New cellular markers at diagnosis are associated with isolated central nervous system relapse in paediatric B‐cell precursor acute lymphoblastic leukaemia. (21st December 2015)
- Main Title:
- New cellular markers at diagnosis are associated with isolated central nervous system relapse in paediatric B‐cell precursor acute lymphoblastic leukaemia
- Authors:
- van der Velden, Vincent H. J.
de Launaij, Daphne
de Vries, Jeltje F.
de Haas, Valerie
Sonneveld, Edwin
Voerman, Jane S. A.
de Bie, Maaike
Revesz, Tamas
Avigad, Smadar
Yeoh, Allen E. J.
Swagemakers, Sigrid M. A.
Eckert, Cornelia
Pieters, Rob
van Dongen, Jacques J. M. - Abstract:
- Summary: In childhood acute lymphoblastic leukaemia (ALL), central nervous system (CNS) involvement is rare at diagnosis (1–4%), but more frequent at relapse (~30%). Because of the significant late sequelae of CNS treatment, early identification of patients at risk of CNS relapse is crucial. Using microarray‐analysis, we discovered multiple differentially expressed genes between B‐cell precursor (BCP) ALL cells in bone marrow (BM) and BCP‐ALL cells in cerebrospinal fluid (CSF) at the time of isolated CNS relapse. After confirmation by real‐time quantitative polymerase chain reaction, selected genes (including SCD and SPP1 ) were validated at the protein level by flowcytometric analysis of BCP‐ALL cells in CSF. Further flowcytometric validation showed that a subpopulation of BCP‐ALL cells (>1%) with a 'CNS protein profile' (SCD positivity and increased SPP1 expression) was present in the BM at diagnosis in patients who later developed an isolated CNS relapse, whereas this subpopulation was <1% or absent in all other patients. These data indicate that the presence of a (small) subpopulation of BCP‐ALL cells with a 'CNS protein profile' at diagnosis (particularly SCD‐positivity) is associated with isolated CNS relapse. Such information can be used to design new diagnostic and treatment strategies that aim at prevention of CNS relapse with reduced toxicity.
- Is Part Of:
- British journal of haematology. Volume 172:Number 5(2016)
- Journal:
- British journal of haematology
- Issue:
- Volume 172:Number 5(2016)
- Issue Display:
- Volume 172, Issue 5 (2016)
- Year:
- 2016
- Volume:
- 172
- Issue:
- 5
- Issue Sort Value:
- 2016-0172-0005-0000
- Page Start:
- 769
- Page End:
- 781
- Publication Date:
- 2015-12-21
- Subjects:
- acute lymphoblastic leukaemia -- central nervous system -- prediction of CNS relapse -- SCD -- SPP1
Hematology -- Periodicals
Blood -- Diseases -- Periodicals
616.15 - Journal URLs:
- http://www.blacksci.co.uk/%7Ecgilib/jnlpage.bin?Journal=bjh&File=bjh&Page=aims ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2141 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjh.13887 ↗
- Languages:
- English
- ISSNs:
- 0007-1048
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2309.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 610.xml