The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://hdl.handle.net/11449/245485 |
Resumo: | Introduction: Classical Hodgkin lymphoma (CHL) has a unique cellular composition, containing a minority of neoplastic cells - Hodgkin and Reed-Sternberg (HRS) cells - in an inflammatory background. Investigations into this microenvironment have been given special importance in scientific hematopathology, playing an important role in elucidating its composition and its relationship to the prognosis of patients. Objective: To investigate microenvironment tumor markers in CHL, in order to analyze their interactions with clinical-morphological aspects of interest in onco-hematopathology. Methods: This retrospective study analyzed 184 patients with a pathologic diagnosis of CHL. Clinical data were reviewed from medical records. A morphological and immunophenotypic study with CD20, CD30, CD15, PAX-5, CD3, CD4, CD8, CD68, CD34, CD138 and PD-1 were performed. The data were tabulated and p value less than 0.05 was considered significant. Results: The time-to-cure was shorter in CD20+ patients, especially in those with more than 25% positivity (P=0.0183). The time-to-cure (P=0.0309) and the death (P=0.016) rates were shorter in PD-1 negative patients. Among patients with the presence of plasma cells in the microenvironment, those with lower numbers tend to be cured earlier (P=0.0374). Higher vascular density is associated with lower frequency of B symptoms (P=0.036) and presence of disease recurrence (P=0.004). Conclusions: The microenvironment is certainly the setting of increasingly robust studies and the findings of this work highlight non-neoplastic B lymphocytes, plasma cells, PD-1 lymphocytes, and vascular density, related to prognosis of CHL patients. |
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The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironmentHodgkin diseaseimmunohistochemistrytumor microenvironmentpatient outcome assessmentIntroduction: Classical Hodgkin lymphoma (CHL) has a unique cellular composition, containing a minority of neoplastic cells - Hodgkin and Reed-Sternberg (HRS) cells - in an inflammatory background. Investigations into this microenvironment have been given special importance in scientific hematopathology, playing an important role in elucidating its composition and its relationship to the prognosis of patients. Objective: To investigate microenvironment tumor markers in CHL, in order to analyze their interactions with clinical-morphological aspects of interest in onco-hematopathology. Methods: This retrospective study analyzed 184 patients with a pathologic diagnosis of CHL. Clinical data were reviewed from medical records. A morphological and immunophenotypic study with CD20, CD30, CD15, PAX-5, CD3, CD4, CD8, CD68, CD34, CD138 and PD-1 were performed. The data were tabulated and p value less than 0.05 was considered significant. Results: The time-to-cure was shorter in CD20+ patients, especially in those with more than 25% positivity (P=0.0183). The time-to-cure (P=0.0309) and the death (P=0.016) rates were shorter in PD-1 negative patients. Among patients with the presence of plasma cells in the microenvironment, those with lower numbers tend to be cured earlier (P=0.0374). Higher vascular density is associated with lower frequency of B symptoms (P=0.036) and presence of disease recurrence (P=0.004). Conclusions: The microenvironment is certainly the setting of increasingly robust studies and the findings of this work highlight non-neoplastic B lymphocytes, plasma cells, PD-1 lymphocytes, and vascular density, related to prognosis of CHL patients.Sao Paulo State Univ FMB UNESP, Botucatu Sch Med, Dept Pathol, Belo Horizonte, BrazilLuxemburgo Hosp, Dept Pathol, Belo Horizonte, BrazilAC Carmargo Canc Ctr, Dept Pathol, Sao Paulo, BrazilLuxemburgo Hosp, Dept Pathol, Rua Rio De Janeiro,1288-702, BR-30160041 Belo Horizonte, Minas Gerais, BrazilSao Paulo State Univ FMB UNESP, Botucatu Sch Med, Dept Pathol, Belo Horizonte, BrazilE-century Publishing CorpUniversidade Estadual Paulista (UNESP)Luxemburgo HospAC Carmargo Canc CtrLacet, Dominique Fonseca Rodrigues [UNESP]Oliveira, Cristiano Claudino [UNESP]2023-07-29T11:56:23Z2023-07-29T11:56:23Z2022-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article412-424International Journal of Clinical and Experimental Pathology. Madison: E-century Publishing Corp, v. 15, n. 10, p. 412-424, 2022.1936-2625http://hdl.handle.net/11449/245485WOS:000878579600003Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal Of Clinical And Experimental Pathologyinfo:eu-repo/semantics/openAccess2024-09-03T13:18:33Zoai:repositorio.unesp.br:11449/245485Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:18:33Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
title |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
spellingShingle |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment Lacet, Dominique Fonseca Rodrigues [UNESP] Hodgkin disease immunohistochemistry tumor microenvironment patient outcome assessment |
title_short |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
title_full |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
title_fullStr |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
title_full_unstemmed |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
title_sort |
The role of immunohistochemistry in the assessment of classical Hodgkin lymphoma microenvironment |
author |
Lacet, Dominique Fonseca Rodrigues [UNESP] |
author_facet |
Lacet, Dominique Fonseca Rodrigues [UNESP] Oliveira, Cristiano Claudino [UNESP] |
author_role |
author |
author2 |
Oliveira, Cristiano Claudino [UNESP] |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Luxemburgo Hosp AC Carmargo Canc Ctr |
dc.contributor.author.fl_str_mv |
Lacet, Dominique Fonseca Rodrigues [UNESP] Oliveira, Cristiano Claudino [UNESP] |
dc.subject.por.fl_str_mv |
Hodgkin disease immunohistochemistry tumor microenvironment patient outcome assessment |
topic |
Hodgkin disease immunohistochemistry tumor microenvironment patient outcome assessment |
description |
Introduction: Classical Hodgkin lymphoma (CHL) has a unique cellular composition, containing a minority of neoplastic cells - Hodgkin and Reed-Sternberg (HRS) cells - in an inflammatory background. Investigations into this microenvironment have been given special importance in scientific hematopathology, playing an important role in elucidating its composition and its relationship to the prognosis of patients. Objective: To investigate microenvironment tumor markers in CHL, in order to analyze their interactions with clinical-morphological aspects of interest in onco-hematopathology. Methods: This retrospective study analyzed 184 patients with a pathologic diagnosis of CHL. Clinical data were reviewed from medical records. A morphological and immunophenotypic study with CD20, CD30, CD15, PAX-5, CD3, CD4, CD8, CD68, CD34, CD138 and PD-1 were performed. The data were tabulated and p value less than 0.05 was considered significant. Results: The time-to-cure was shorter in CD20+ patients, especially in those with more than 25% positivity (P=0.0183). The time-to-cure (P=0.0309) and the death (P=0.016) rates were shorter in PD-1 negative patients. Among patients with the presence of plasma cells in the microenvironment, those with lower numbers tend to be cured earlier (P=0.0374). Higher vascular density is associated with lower frequency of B symptoms (P=0.036) and presence of disease recurrence (P=0.004). Conclusions: The microenvironment is certainly the setting of increasingly robust studies and the findings of this work highlight non-neoplastic B lymphocytes, plasma cells, PD-1 lymphocytes, and vascular density, related to prognosis of CHL patients. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-01-01 2023-07-29T11:56:23Z 2023-07-29T11:56:23Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
International Journal of Clinical and Experimental Pathology. Madison: E-century Publishing Corp, v. 15, n. 10, p. 412-424, 2022. 1936-2625 http://hdl.handle.net/11449/245485 WOS:000878579600003 |
identifier_str_mv |
International Journal of Clinical and Experimental Pathology. Madison: E-century Publishing Corp, v. 15, n. 10, p. 412-424, 2022. 1936-2625 WOS:000878579600003 |
url |
http://hdl.handle.net/11449/245485 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
International Journal Of Clinical And Experimental Pathology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
412-424 |
dc.publisher.none.fl_str_mv |
E-century Publishing Corp |
publisher.none.fl_str_mv |
E-century Publishing Corp |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1810021419410522112 |