High tumour plasma cell infiltration reflects an important microenvironmental component in classic Hodgkin lymphoma linked to presence of B-symptoms.
Adolescent
Adult
Aged
Disease-Free Survival
Female
Follow-Up Studies
Hodgkin Disease
/ metabolism
Humans
Immunoglobulin G
/ metabolism
Kaplan-Meier Estimate
Lymphoma, B-Cell
/ metabolism
Male
Middle Aged
Neoplasm Proteins
/ metabolism
Plasma Cells
/ metabolism
Survival Rate
Syndecan-1
/ metabolism
Tumor Microenvironment
CD138 plasma cells
Hodgkin's lymphoma
IgG4-producing plasma cells
Syndecan-1
tumour microenvironment
Journal
British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
10
07
2018
accepted:
25
09
2018
pubmed:
7
12
2018
medline:
19
9
2019
entrez:
4
12
2018
Statut:
ppublish
Résumé
Plasma cells are important prognostic actors in different malignancies. The tumour microenvironmental composition in classic Hodgkin lymphoma (cHL) is a major prognostic key element; however, clinicopathological studies regarding plasma cells in cHL are lacking. The aim of this study was to investigate CD138+ (also termed SDC1+) plasma cell and IgG4 producing (IgG4+) plasma cells infiltration in the microenvironment of cHL. Immunohistochemistry with anti-CD138 and IgG4 antibodies was performed on diagnostic tumour biopsies from 124 patients with cHL, on tissue micro array (TMA). In 120 cases, CD138+ plasma cell-infiltration was associated with the presence of B-symptoms (P = 0·028) and advanced stage, IIB-IVB (P = 0·009). In multivariate analysis, CD138+ plasma cells correlated with eosinophil infiltration (P = 0·013). The subgroup of IgG4+ plasma cells was analysed in 122 cases and only correlated to CD138+ plasma cells (P = 0·004). Patients with high proportion of tumour infiltrating CD138+ plasma cells (defined as ≥10%), had a more inferior event-free survival (P = 0·007) and overall survival (P = 0·004) than patients with a low proportion of infiltrating CD138+ plasma cells (<10%), although significance was not maintained in multivariate analysis. In summary, a high proportion of tumour-associated plasma cells in cHL reflect an important component in the microenvironment of cHL.
Substances chimiques
Immunoglobulin G
0
Neoplasm Proteins
0
SDC1 protein, human
0
Syndecan-1
0
Types de publication
Clinical Trial
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
192-201Informations de copyright
© 2018 British Society for Haematology and John Wiley & Sons Ltd.