Evidence map›Paper›PMID 38024830›Full record

ArticleJournal of medicine and life2023

Tumor microenvironment in Hodgkin lymphoma: novel prognostic factors for assessing disease evolution.

Andrei Turbatu, Camelia Dobrea, Marilena Stoian, Cristian Tudor Barta, Georgian Halcu, Adelina Birceanu, Ana-Maria Bordea, Cecilia Gabriela Ghimici, Mădălina Marilena Oprea, Livia Doria Neacșu and 2 more

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Article in Journal of medicine and life, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 63% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Andrei TurbatuDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Camelia DobreaDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Marilena StoianClinic of Internal Medicine, Dr. I. Cantacuzino Clinical Hospital, Bucharest, Romania.
Cristian Tudor BartaDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Georgian HalcuClinic of Pathology, Colțea Clinical Hospital, Bucharest, Romania.
Adelina BirceanuPathoTeam Diagnostic Laboratory, Bucharest, Romania.
Ana-Maria BordeaClinic of Hematology, Colțea Clinical Hospital, Bucharest, Romania.
Cecilia Gabriela GhimiciClinic of Hematology, Colțea Clinical Hospital, Bucharest, Romania.
Mădălina Marilena OpreaClinic of Hematology, Colțea Clinical Hospital, Bucharest, Romania.
Livia Doria NeacșuDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Anca-Roxana LupuDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Andrei ColițăDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Carol Davila University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hodgkin lymphoma (HL) has become one of the most curable hematological neoplasia. Clinical and biological factors remain the main pillars guiding therapeutic strategies in HL. Recent studies have improved our understanding of the phenotype, the characteristics of histogenesis, and other possible mechanisms of lymphomagenesis, including the role of Epstein-Barr virus (EBV) infection. Tumor cells manipulate the microenvironment, allowing them to develop their malignant phenotype and evade the attack of the host's immune response so that the interaction between tumor cells and the reactive microenvironment determines not only the histological features but also the clinical-pathological characteristics and prognosis of these patients - essential for the development of future therapies targeting various other cellular components of the tumor microenvironment. This article aimed to evaluate the characteristics of the tumor microenvironment and malignant cells using histopathology and immunohistochemistry (IHC) techniques to highlight the association of EBV and to study the expression of characteristic antigens in malignant and non-malignant cells within the tumor mass (overexpression of BCL2 (B-cell lymphoma 2) in malignant cells, presence of PD1 (Programmed cell death Protein 1) on T lymphocytes, CD68+ macrophages in the tumor microenvironment, and presence of EGFR (epidermal growth factor receptor). The analysis of the data collected in this paper highlights several key parameters with prognostic value and statistical significance: the EBV infection at diagnosis, its association with low-intensity BCL2(+), the presence of CD68 with rosette formation, and the identification of specific vascularization patterns. The development of prognostic systems that take into account the integration of biological prognostic markers seems essential for a better risk stratification.

Indexed as

Epstein-Barr Virus InfectionsHodgkin DiseaseHerpesvirus 4, HumanHumansPrognosisProto-Oncogene Proteins c-bcl-2Tumor MicroenvironmentProto-Oncogene Proteins c-bcl-2Epstein-Barr virus (EBV)Hodgkin lymphomaimmunohistochemistry (IHC)microenvironmentprognostic factors

Identifiers

PMID38024830
PMCPMC10652678
OpenAlexW4389178765

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.