Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.

Cytogenetic, clinical and laboratory features at diagnosis were examined in a group of 80 children with acute lymphoblastic leukaemia (ALL) who had been followed up for a minimum of 5 1/2 years. The 17 (21%) with high hyperdiploidy tended to have low leucocyte counts and common ALL, but their favour...

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Main Authors: Secker-Walker, L, Chessells, J, Stewart, E, Swansbury, G, Richards, S, Lawler, S
Format: Journal article
Language:English
Published: 1989
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author Secker-Walker, L
Chessells, J
Stewart, E
Swansbury, G
Richards, S
Lawler, S
author_facet Secker-Walker, L
Chessells, J
Stewart, E
Swansbury, G
Richards, S
Lawler, S
author_sort Secker-Walker, L
collection OXFORD
description Cytogenetic, clinical and laboratory features at diagnosis were examined in a group of 80 children with acute lymphoblastic leukaemia (ALL) who had been followed up for a minimum of 5 1/2 years. The 17 (21%) with high hyperdiploidy tended to have low leucocyte counts and common ALL, but their favourable outcome (75% event-free survival) was independent of these factors. No patient with hypodiploidy survives while the pseudodiploid and normal groups have an intermediate prognosis. Cytogenetic analysis showed examples of patients with the well-recognized translocations and a number with apparently unique ones. Among the latter were some long-term survivors. We conclude that cytogenetic analysis identifies a good risk group of patients who remain well on long-term follow-up, but that the presence of a translocation does not necessarily imply a poor outcome.
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spelling oxford-uuid:3a7fe6a8-636d-4aea-8b18-9047e9b2406b2022-03-26T14:01:59ZChromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3a7fe6a8-636d-4aea-8b18-9047e9b2406bEnglishSymplectic Elements at Oxford1989Secker-Walker, LChessells, JStewart, ESwansbury, GRichards, SLawler, SCytogenetic, clinical and laboratory features at diagnosis were examined in a group of 80 children with acute lymphoblastic leukaemia (ALL) who had been followed up for a minimum of 5 1/2 years. The 17 (21%) with high hyperdiploidy tended to have low leucocyte counts and common ALL, but their favourable outcome (75% event-free survival) was independent of these factors. No patient with hypodiploidy survives while the pseudodiploid and normal groups have an intermediate prognosis. Cytogenetic analysis showed examples of patients with the well-recognized translocations and a number with apparently unique ones. Among the latter were some long-term survivors. We conclude that cytogenetic analysis identifies a good risk group of patients who remain well on long-term follow-up, but that the presence of a translocation does not necessarily imply a poor outcome.
spellingShingle Secker-Walker, L
Chessells, J
Stewart, E
Swansbury, G
Richards, S
Lawler, S
Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.
title Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.
title_full Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.
title_fullStr Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.
title_full_unstemmed Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.
title_short Chromosomes and other prognostic factors in acute lymphoblastic leukaemia: a long-term follow-up.
title_sort chromosomes and other prognostic factors in acute lymphoblastic leukaemia a long term follow up
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