Evidence map›Paper›PMID 32923089›Full record

ArticleAmerican journal of blood research2020

Prognostic impact of tumor-associated macrophages, lymphocyte-to-monocyte and neutrophil-to-lymphocyte ratio in diffuse large B-cell lymphoma.

Emanuele Cencini, Alberto Fabbri, Luana Schiattone, Anna Sicuranza, Bianca Mecacci, Massimo Granai, Virginia Mancini, Stefano Lazzi, Monica Bocchia, Lorenzo Leoncini

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in American journal of blood research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07638982 (An Open-label, Phase I Trial, With an Expansion Cohort), which is not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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.

NCT07638982 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

An Open-label, Phase I Trial, With an Expansion Cohort: Macrophage Conditioning to Synergize With CAR-T in High-risk Lymphoma (MAC-SHIFT)

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2026 to 2029Enrolled29ConditionsDiffuse Large B Cell Lymphoma (DLBCL), Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma, High-grade B-cell Lymphoma (HGBCL), High-Grade B-Cell Lymphoma, NosArmsAxatilimab
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 2 institutions in 1 country.

Emanuele CenciniUnit of Hematology, Azienda Ospedaliera Universitaria Senese & University of Siena Siena, Italy.
Alberto FabbriUnit of Hematology, Azienda Ospedaliera Universitaria Senese & University of Siena Siena, Italy.
Luana SchiattoneUnit of Hematology, Azienda Ospedaliera Universitaria Senese & University of Siena Siena, Italy.
Anna SicuranzaUnit of Hematology, Azienda Ospedaliera Universitaria Senese & University of Siena Siena, Italy.
Bianca MecacciUnit of Hematology, Azienda Ospedaliera Universitaria Senese & University of Siena Siena, Italy.
Massimo GranaiUnit of Pathology, Department of Medical Biotechnologies, University of Siena Siena, Italy.
Virginia ManciniUnit of Pathology, Department of Medical Biotechnologies, University of Siena Siena, Italy.
Stefano LazziUnit of Pathology, Department of Medical Biotechnologies, University of Siena Siena, Italy.
Monica BocchiaUnit of Hematology, Azienda Ospedaliera Universitaria Senese & University of Siena Siena, Italy.
Lorenzo LeonciniUnit of Pathology, Department of Medical Biotechnologies, University of Siena Siena, Italy.
Azienda Ospedaliera Universitaria Senese · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMicroenvironment has a prognostic influence in diffuse large B-cell lymphoma (DLBCL); among its components, tumor-associated macrophages (TAM) play a leading role. TAM can be classified into M1 (anti-tumor) and M2 (pro-tumor). Another prognostic factor could be represented by lymphocyte-to-monocyte and neutrophil-to-lymphocyte ratio (LMR and NLR).

objectiveThe aim of the study is to evaluate the prognostic impact of M1 and M2 TAM subtypes, LMR and NLR in DLBCL.

methodsWe analyzed 37 consecutive patients between 2009 and 2013. Out of 37 patients, 28/37 (75.6%) received R-CHOP/CHOP-like regimens, 9/37 (24.4%) less intensive therapies. Immunohistochemistry was performed with antibodies against CD68 and CD163. We divided our cohort into 2 categories according to the Steidl score. TAM who coexpressed CD68 and CD163 were considered as M2. For LMR and NLR we used previously published cut-offs of 2.71 and 2.81.

resultsCR rate was 70.3%; we did not record a significant correlation between CD68+ TAM, CD163+ TAM, CD68+/CD163+ TAM, LMR, NLR and CR. We observed a reduced PFS in patients with IPI ≥ 2 and high M2 TAM expression and a trend between higher expression of CD68+ TAM and improved PFS.

conclusionM2 TAM could have a prognostic role for IPI ≥ 2 DLBCL patients receiving R-CHOP, which thus warrants further investigation.

Indexed as

Diffuse large B-cell lymphomaprognosisTAM

Identifiers

PMID32923089
PMCPMC7486489
OpenAlexW3085045134

What OpenQuestion holds

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Registered trials

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.