Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial (Q58481820)

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scientific article published on 19 April 2010

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English	Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial	scientific article published on 19 April 2010

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31 January 2020

Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial (English)

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31 January 2020

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Anthony V. Moorman

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31 January 2020

Christine J Harrison

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31 January 2020

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Hannah M Ensor

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31 January 2020

Sue M Richards

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31 January 2020

Claire Schwab

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31 January 2020

Sally E Kinsey

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31 January 2020

Ajay Vora

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31 January 2020

Chris D Mitchell

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31 January 2020

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19 April 2010

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31 January 2020

Lancet Oncology Commission

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31 January 2020

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31 January 2020

429-438

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31 January 2020

randomized experiment

0 references

Treatment of acute lymphoblastic leukemia

1 reference

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Bone-marrow relapse in paediatric acute lymphoblastic leukaemia

1 reference

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Benefit of dexamethasone compared with prednisolone for childhood acute lymphoblastic leukaemia: results of the UK Medical Research Council ALL97 randomized trial

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The impact of risk stratification by early bone-marrow response in childhood lymphoblastic leukaemia: results from the United Kingdom Medical Research Council trial ALL97 and ALL97/99.

1 reference

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Toxicity and efficacy of 6-thioguanine versus 6-mercaptopurine in childhood lymphoblastic leukaemia: a randomised trial

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The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation

1 reference

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Interphase molecular cytogenetic screening for chromosomal abnormalities of prognostic significance in childhood acute lymphoblastic leukaemia: a UK Cancer Cytogenetics Group Study.

1 reference

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High concordance from independent studies by the Children's Cancer Group (CCG) and Pediatric Oncology Group (POG) associating favorable prognosis with combined trisomies 4, 10 and 17 in children with NCI Standard-Risk B-precursor Acute Lymphoblastic

1 reference

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Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia

1 reference

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Outcome after first relapse in childhood acute lymphoblastic leukaemia - lessons from the United Kingdom R2 trial

1 reference

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Prospective analysis of TEL gene rearrangements in childhood acute lymphoblastic leukemia: a Children's Oncology Group study

1 reference

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Treating childhood acute lymphoblastic leukemia without cranial irradiation

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Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival

1 reference

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TEL/AML1 rearrangement and the prognostic significance in childhood acute lymphoblastic leukemia in Hong Kong

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Determinants of outcome after intensified therapy of childhood lymphoblastic leukaemia: results from Medical Research Council United Kingdom acute lymphoblastic leukaemia XI protocol

1 reference

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Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements

1 reference

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7 January 2021

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Outcome of treatment in childhood acute lymphoblastic leukaemia with rearrangements of the 11q23 chromosomal region

1 reference

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7 January 2021

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A treatment protocol for infants younger than 1 year with acute lymphoblastic leukaemia (Interfant-99): an observational study and a multicentre randomised trial.

1 reference

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Gene expression profiling-based dissection of MLL translocated and MLL germline acute lymphoblastic leukemia in infants

1 reference

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T-cell acute lymphoblastic leukemia in adults: clinical features, immunophenotype, cytogenetics, and outcome from the large randomized prospective trial (UKALL XII/ECOG 2993)

1 reference

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7 January 2021

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Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

1 reference

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7 January 2021

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Acute myeloid leukemia with a complex aberrant karyotype is a distinct biological entity characterized by genomic imbalances and a specific gene expression profile

1 reference

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7 January 2021

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Abnormalities of chromosome bands 13q12 to 13q14 in childhood acute lymphoblastic leukemia

1 reference

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Increased risk for CNS relapse in pre-B cell leukemia with the t(1;19)/TCF3-PBX1

1 reference

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A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study

1 reference

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Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature

1 reference

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Heterogeneous breakpoints in patients with acute lymphoblastic leukemia and the dic(9;20)(p11-13;q11) show recurrent involvement of genes at 20q11.21.

1 reference

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7 January 2021

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inferred from DOI database lookup

Hemizygous p16(INK4A) deletion in pediatric acute lymphoblastic leukemia predicts independent risk of relapse

1 reference

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7 January 2021

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inferred from DOI database lookup

p16(INK4a) immunocytochemical analysis is an independent prognostic factor in childhood acute lymphoblastic leukemia

1 reference

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CDKN2 deletions have no prognostic value in childhood precursor-B acute lymphoblastic leukaemia

1 reference

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7 January 2021

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Deletion analysis of p16(INKa) and p15(INKb) in relapsed childhood acute lymphoblastic leukemia.

1 reference

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7 January 2021

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inferred from DOI database lookup

Shortened survival after relapse in T-cell acute lymphoblastic leukemia patients with p16/p15 deletions

1 reference

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A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.

1 reference

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1 reference

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10.1016/S1470-2045(10)70066-8

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31 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20409752%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

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