Cargando…

Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.

beta-2 microglobulin levels were measured in stored serum taken at presentation from 262 patients treated with combination chemotherapy for Kiel classification high-grade lymphoma at a single centre over a 15 year period. A significant association was found between elevated levels and advanced (Ann...

Descripción completa

Detalles Bibliográficos
Autores principales: Johnson, P. W., Whelan, J., Longhurst, S., Stepniewska, K., Matthews, J., Amess, J., Norton, A., Rohatiner, A. Z., Lister, T. A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968369/
https://www.ncbi.nlm.nih.gov/pubmed/8471438
_version_ 1782134725691834368
author Johnson, P. W.
Whelan, J.
Longhurst, S.
Stepniewska, K.
Matthews, J.
Amess, J.
Norton, A.
Rohatiner, A. Z.
Lister, T. A.
author_facet Johnson, P. W.
Whelan, J.
Longhurst, S.
Stepniewska, K.
Matthews, J.
Amess, J.
Norton, A.
Rohatiner, A. Z.
Lister, T. A.
author_sort Johnson, P. W.
collection PubMed
description beta-2 microglobulin levels were measured in stored serum taken at presentation from 262 patients treated with combination chemotherapy for Kiel classification high-grade lymphoma at a single centre over a 15 year period. A significant association was found between elevated levels and advanced (Ann Arbor stage III or IV) disease or hepatic infiltration, but not with other sites of extranodal involvement or bulky disease. Patients with normal levels at presentation had a 70% remission rate with treatment compared to 37% of those with elevated levels (P < 0.001). With median follow up of 6 years duration of remission was significantly greater in patients with normal beta-2 microglobulin at presentation (plateau at 70%, compared to median remission of 19 months in those with raised levels, P < 0.001). Survival overall was also better in the group with normal levels (actuarial median 9 years compared to 1 year, P < 0.001). Multivariate analyses including treatment type, age, sex, B symptoms, stage, bulk, albumin, sodium, alkaline phosphatase, aspartate aminotransferase, lactate dehydrogenase and beta-2 microglobulin, placed beta-2 microglobulin among the three most influential independent variables for prediction of response rate, duration of remission and overall survival.
format Text
id pubmed-1968369
institution National Center for Biotechnology Information
language English
publishDate 1993
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-19683692009-09-10 Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas. Johnson, P. W. Whelan, J. Longhurst, S. Stepniewska, K. Matthews, J. Amess, J. Norton, A. Rohatiner, A. Z. Lister, T. A. Br J Cancer Research Article beta-2 microglobulin levels were measured in stored serum taken at presentation from 262 patients treated with combination chemotherapy for Kiel classification high-grade lymphoma at a single centre over a 15 year period. A significant association was found between elevated levels and advanced (Ann Arbor stage III or IV) disease or hepatic infiltration, but not with other sites of extranodal involvement or bulky disease. Patients with normal levels at presentation had a 70% remission rate with treatment compared to 37% of those with elevated levels (P < 0.001). With median follow up of 6 years duration of remission was significantly greater in patients with normal beta-2 microglobulin at presentation (plateau at 70%, compared to median remission of 19 months in those with raised levels, P < 0.001). Survival overall was also better in the group with normal levels (actuarial median 9 years compared to 1 year, P < 0.001). Multivariate analyses including treatment type, age, sex, B symptoms, stage, bulk, albumin, sodium, alkaline phosphatase, aspartate aminotransferase, lactate dehydrogenase and beta-2 microglobulin, placed beta-2 microglobulin among the three most influential independent variables for prediction of response rate, duration of remission and overall survival. Nature Publishing Group 1993-04 /pmc/articles/PMC1968369/ /pubmed/8471438 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
Johnson, P. W.
Whelan, J.
Longhurst, S.
Stepniewska, K.
Matthews, J.
Amess, J.
Norton, A.
Rohatiner, A. Z.
Lister, T. A.
Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.
title Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.
title_full Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.
title_fullStr Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.
title_full_unstemmed Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.
title_short Beta-2 microglobulin: a prognostic factor in diffuse aggressive non-Hodgkin's lymphomas.
title_sort beta-2 microglobulin: a prognostic factor in diffuse aggressive non-hodgkin's lymphomas.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968369/
https://www.ncbi.nlm.nih.gov/pubmed/8471438
work_keys_str_mv AT johnsonpw beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT whelanj beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT longhursts beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT stepniewskak beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT matthewsj beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT amessj beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT nortona beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT rohatineraz beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas
AT listerta beta2microglobulinaprognosticfactorindiffuseaggressivenonhodgkinslymphomas