Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.

The outcomes of Central Nervous System (CNS) relapses in children with acute lymphoblastic leukaemia (ALL) treated in the ALL R3 trial, between January 2003 and March 2011 were analysed. Patients were risk stratified, to receive a matched donor allogeneic transplant or fractionated cranial irradiati...

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Main Authors: Ashish Narayan Masurekar, Catriona A Parker, Milensu Shanyinde, Anthony V Moorman, Jeremy P Hancock, Rosemary Sutton, Philip J Ancliff, Mary Morgan, Nicholas J Goulden, Chris Fraser, Peter M Hoogerbrugge, Tamas Revesz, Philip J Darbyshire, Shekhar Krishnan, Sharon B Love, Vaskar Saha
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4184796?pdf=render
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author Ashish Narayan Masurekar
Catriona A Parker
Milensu Shanyinde
Anthony V Moorman
Jeremy P Hancock
Rosemary Sutton
Philip J Ancliff
Mary Morgan
Nicholas J Goulden
Chris Fraser
Peter M Hoogerbrugge
Tamas Revesz
Philip J Darbyshire
Shekhar Krishnan
Sharon B Love
Vaskar Saha
author_facet Ashish Narayan Masurekar
Catriona A Parker
Milensu Shanyinde
Anthony V Moorman
Jeremy P Hancock
Rosemary Sutton
Philip J Ancliff
Mary Morgan
Nicholas J Goulden
Chris Fraser
Peter M Hoogerbrugge
Tamas Revesz
Philip J Darbyshire
Shekhar Krishnan
Sharon B Love
Vaskar Saha
author_sort Ashish Narayan Masurekar
collection DOAJ
description The outcomes of Central Nervous System (CNS) relapses in children with acute lymphoblastic leukaemia (ALL) treated in the ALL R3 trial, between January 2003 and March 2011 were analysed. Patients were risk stratified, to receive a matched donor allogeneic transplant or fractionated cranial irradiation with continued treatment for two years. A randomisation of Idarubicin with Mitoxantrone closed in December 2007 in favour of Mitoxantrone. The estimated 3-year progression free survival for combined and isolated CNS disease were 40.6% (25·1, 55·6) and 38.0% (26.2, 49.7) respectively. Univariate analysis showed a significantly better survival for age <10 years, progenitor-B cell disease, good-risk cytogenetics and those receiving Mitoxantrone. Adjusting for these variables (age, time to relapse, cytogenetics, treatment drug and gender) a multivariate analysis, showed a poorer outcome for those with combined CNS relapse (HR 2·64, 95% CI 1·32, 5·31, p = 0·006 for OS). ALL R3 showed an improvement in outcome for CNS relapses treated with Mitoxantrone compared to Idarubicin; a potential benefit for matched donor transplant for those with very early and early isolated-CNS relapses.Controlled-Trials.com ISRCTN45724312.
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spelling doaj.art-a33a747b941a4d608fce9341901310892022-12-22T00:48:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01910e10810710.1371/journal.pone.0108107Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.Ashish Narayan MasurekarCatriona A ParkerMilensu ShanyindeAnthony V MoormanJeremy P HancockRosemary SuttonPhilip J AncliffMary MorganNicholas J GouldenChris FraserPeter M HoogerbruggeTamas ReveszPhilip J DarbyshireShekhar KrishnanSharon B LoveVaskar SahaThe outcomes of Central Nervous System (CNS) relapses in children with acute lymphoblastic leukaemia (ALL) treated in the ALL R3 trial, between January 2003 and March 2011 were analysed. Patients were risk stratified, to receive a matched donor allogeneic transplant or fractionated cranial irradiation with continued treatment for two years. A randomisation of Idarubicin with Mitoxantrone closed in December 2007 in favour of Mitoxantrone. The estimated 3-year progression free survival for combined and isolated CNS disease were 40.6% (25·1, 55·6) and 38.0% (26.2, 49.7) respectively. Univariate analysis showed a significantly better survival for age <10 years, progenitor-B cell disease, good-risk cytogenetics and those receiving Mitoxantrone. Adjusting for these variables (age, time to relapse, cytogenetics, treatment drug and gender) a multivariate analysis, showed a poorer outcome for those with combined CNS relapse (HR 2·64, 95% CI 1·32, 5·31, p = 0·006 for OS). ALL R3 showed an improvement in outcome for CNS relapses treated with Mitoxantrone compared to Idarubicin; a potential benefit for matched donor transplant for those with very early and early isolated-CNS relapses.Controlled-Trials.com ISRCTN45724312.http://europepmc.org/articles/PMC4184796?pdf=render
spellingShingle Ashish Narayan Masurekar
Catriona A Parker
Milensu Shanyinde
Anthony V Moorman
Jeremy P Hancock
Rosemary Sutton
Philip J Ancliff
Mary Morgan
Nicholas J Goulden
Chris Fraser
Peter M Hoogerbrugge
Tamas Revesz
Philip J Darbyshire
Shekhar Krishnan
Sharon B Love
Vaskar Saha
Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.
PLoS ONE
title Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.
title_full Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.
title_fullStr Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.
title_full_unstemmed Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.
title_short Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.
title_sort outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia prospective open cohort analyses of the allr3 trial
url http://europepmc.org/articles/PMC4184796?pdf=render
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