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Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification

In the REAL classification the diffuse large B-cell non-Hodgkin lymphomas (NHL) are grouped together, because subclassifications are considered to lack both reproducibility and clinical significance. Others, however, claim that patients with an immunoblastic NHL have a worse prognosis than patients...

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Autores principales: Baars, J W, Jong, D de, Willemse, E M, Gras, L, Dalesio, O, Heerde, P v, Huygens, P C, Lelie, H v d, Borne, A E G Kr v.d.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362805/
https://www.ncbi.nlm.nih.gov/pubmed/10206291
http://dx.doi.org/10.1038/sj.bjc.6690282
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author Baars, J W
Jong, D de
Willemse, E M
Gras, L
Dalesio, O
Heerde, P v
Huygens, P C
Lelie, H v d
Borne, A E G Kr v.d.
author_facet Baars, J W
Jong, D de
Willemse, E M
Gras, L
Dalesio, O
Heerde, P v
Huygens, P C
Lelie, H v d
Borne, A E G Kr v.d.
author_sort Baars, J W
collection PubMed
description In the REAL classification the diffuse large B-cell non-Hodgkin lymphomas (NHL) are grouped together, because subclassifications are considered to lack both reproducibility and clinical significance. Others, however, claim that patients with an immunoblastic NHL have a worse prognosis than patients with other types of diffuse large B-cell NHL. Therefore, we investigated the prognostic and clinical significance of histological subclassification of diffuse large B-cell NHL in a uniformly treated series of patients. For this retrospective study, all patients diagnosed as having an immunoblastic (IB) B-cell NHL by the Lymphoma Review Panel of the Comprehensive Cancer Center Amsterdam (CCCA) between 1984 and 1994, and treated according to the guidelines of the CCCA, were analysed. Patients with a centroblastic polymorphic subtype (CB-Poly) or centroblastic (CB) NHL by the Lymphoma Review Panel who were treated in the Netherlands Cancer Institute during the same period according to CCCA guidelines were used as reference groups. All patients' records were reviewed. Clinical parameters at presentation, kind of therapy and clinical outcome were recorded. All available histological slides were separately reviewed by two haemato-pathologists. One hundred and seventy-seven patients were included in the study: 36 patients (20.3%) with an IB NHL, 69 patients (39%) with a CB-Poly NHL and 72 patients (40.7%) with a CB NHL. The patients with an IB NHL tended to be older and presented more often with stage I or II and one extranodal site than patients with a CB and CB-Poly NHL. None of the subtypes showed a clear preference for localization in a particular site. The patients with IB or CB-Poly NHL showed a significantly worse prognosis than patients with CB NHL, with a 5-year overall survival for patients with CB NHL of 56.3% and for patients with IB or CB-Poly NHL 39.1% and 41.6% respectively. The 5-year disease free survival was 53.2% for the patients with CB, 32% for the patients with CB-Poly and 26.9% for the patients with IB NHL. A multivariate analysis showed that histological subtyping was of prognostic significance independent of the International Prognostic Index. This finding merits further exploration in prospective studies in order to judge the value of subclassification of large B-cell NHL as a guideline in therapy choice. © 1999 Cancer Research Campaign
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spelling pubmed-23628052009-09-10 Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification Baars, J W Jong, D de Willemse, E M Gras, L Dalesio, O Heerde, P v Huygens, P C Lelie, H v d Borne, A E G Kr v.d. Br J Cancer Regular Article In the REAL classification the diffuse large B-cell non-Hodgkin lymphomas (NHL) are grouped together, because subclassifications are considered to lack both reproducibility and clinical significance. Others, however, claim that patients with an immunoblastic NHL have a worse prognosis than patients with other types of diffuse large B-cell NHL. Therefore, we investigated the prognostic and clinical significance of histological subclassification of diffuse large B-cell NHL in a uniformly treated series of patients. For this retrospective study, all patients diagnosed as having an immunoblastic (IB) B-cell NHL by the Lymphoma Review Panel of the Comprehensive Cancer Center Amsterdam (CCCA) between 1984 and 1994, and treated according to the guidelines of the CCCA, were analysed. Patients with a centroblastic polymorphic subtype (CB-Poly) or centroblastic (CB) NHL by the Lymphoma Review Panel who were treated in the Netherlands Cancer Institute during the same period according to CCCA guidelines were used as reference groups. All patients' records were reviewed. Clinical parameters at presentation, kind of therapy and clinical outcome were recorded. All available histological slides were separately reviewed by two haemato-pathologists. One hundred and seventy-seven patients were included in the study: 36 patients (20.3%) with an IB NHL, 69 patients (39%) with a CB-Poly NHL and 72 patients (40.7%) with a CB NHL. The patients with an IB NHL tended to be older and presented more often with stage I or II and one extranodal site than patients with a CB and CB-Poly NHL. None of the subtypes showed a clear preference for localization in a particular site. The patients with IB or CB-Poly NHL showed a significantly worse prognosis than patients with CB NHL, with a 5-year overall survival for patients with CB NHL of 56.3% and for patients with IB or CB-Poly NHL 39.1% and 41.6% respectively. The 5-year disease free survival was 53.2% for the patients with CB, 32% for the patients with CB-Poly and 26.9% for the patients with IB NHL. A multivariate analysis showed that histological subtyping was of prognostic significance independent of the International Prognostic Index. This finding merits further exploration in prospective studies in order to judge the value of subclassification of large B-cell NHL as a guideline in therapy choice. © 1999 Cancer Research Campaign Nature Publishing Group 1999-04 /pmc/articles/PMC2362805/ /pubmed/10206291 http://dx.doi.org/10.1038/sj.bjc.6690282 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Baars, J W
Jong, D de
Willemse, E M
Gras, L
Dalesio, O
Heerde, P v
Huygens, P C
Lelie, H v d
Borne, A E G Kr v.d.
Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification
title Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification
title_full Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification
title_fullStr Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification
title_full_unstemmed Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification
title_short Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification
title_sort diffuse large b-cell non-hodgkin lymphomas: the clinical relevance of histological subclassification
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362805/
https://www.ncbi.nlm.nih.gov/pubmed/10206291
http://dx.doi.org/10.1038/sj.bjc.6690282
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