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T lymphoblastic leukaemia and the central nervous system.

Of 100 children and adolescents with lymphoblastic leukaemia (ALL) seen over a 6-year period, 25 developed clinically evident infiltration of the central nervous system (CNS), despite early treatment with cranial radiotherapy and intrathecal methotrexate. Nine of these 25 had the features of T ALL,...

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Autores principales: Lilleyman, J. S., Sugden, P. J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010617/
https://www.ncbi.nlm.nih.gov/pubmed/6971649
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author Lilleyman, J. S.
Sugden, P. J.
author_facet Lilleyman, J. S.
Sugden, P. J.
author_sort Lilleyman, J. S.
collection PubMed
description Of 100 children and adolescents with lymphoblastic leukaemia (ALL) seen over a 6-year period, 25 developed clinically evident infiltration of the central nervous system (CNS), despite early treatment with cranial radiotherapy and intrathecal methotrexate. Nine of these 25 had the features of T ALL, though there were only 17 such patients overall. Not only did those with T ALL get CNS disease more frequently, but they did so much sooner after diagnosis (P less than 0.001) and more commonly had associated facial palsies (P less than 0.05). The tendency to develop CNS infiltration appeared to be significantly related to the possession of T-cell markers (P less than 0.02), but not to the diagnostic white cell count (P = 0.37). These findings suggest that current CNS prophylactic therapy is ineffective in most patients with T ALL.
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spelling pubmed-20106172009-09-10 T lymphoblastic leukaemia and the central nervous system. Lilleyman, J. S. Sugden, P. J. Br J Cancer Research Article Of 100 children and adolescents with lymphoblastic leukaemia (ALL) seen over a 6-year period, 25 developed clinically evident infiltration of the central nervous system (CNS), despite early treatment with cranial radiotherapy and intrathecal methotrexate. Nine of these 25 had the features of T ALL, though there were only 17 such patients overall. Not only did those with T ALL get CNS disease more frequently, but they did so much sooner after diagnosis (P less than 0.001) and more commonly had associated facial palsies (P less than 0.05). The tendency to develop CNS infiltration appeared to be significantly related to the possession of T-cell markers (P less than 0.02), but not to the diagnostic white cell count (P = 0.37). These findings suggest that current CNS prophylactic therapy is ineffective in most patients with T ALL. Nature Publishing Group 1981-03 /pmc/articles/PMC2010617/ /pubmed/6971649 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Lilleyman, J. S.
Sugden, P. J.
T lymphoblastic leukaemia and the central nervous system.
title T lymphoblastic leukaemia and the central nervous system.
title_full T lymphoblastic leukaemia and the central nervous system.
title_fullStr T lymphoblastic leukaemia and the central nervous system.
title_full_unstemmed T lymphoblastic leukaemia and the central nervous system.
title_short T lymphoblastic leukaemia and the central nervous system.
title_sort t lymphoblastic leukaemia and the central nervous system.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010617/
https://www.ncbi.nlm.nih.gov/pubmed/6971649
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