Evidence map›Paper›PMID 26314692›Full record

ArticleBrain pathology (Zurich, Switzerland)2016

Tumor-Associated Macrophages Associate with Cerebrospinal Fluid Interleukin-10 and Survival in Primary Central Nervous System Lymphoma (PCNSL).

Takashi Sasayama, Kazuhiro Tanaka, Takashi Mizowaki, Hiroaki Nagashima, Satoshi Nakamizo, Hirotomo Tanaka, Masamitsu Nishihara, Katsu Mizukawa, Takanori Hirose, Tomoo Itoh and 1 more

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Takashi SasayamaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Kazuhiro TanakaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Takashi MizowakiDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Hiroaki NagashimaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Satoshi NakamizoDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Hirotomo TanakaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Masamitsu NishiharaDepartment of Neurosurgery, Nishi-Kobe Medical Center, Kobe, Japan.
Katsu MizukawaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Takanori HiroseDepartment of Pathology for Regional Communication, Kobe University Hospital, Kobe, Japan.
Tomoo ItohDiagnostic Pathology, Kobe University Hospital, Kobe, Japan.
Eiji KohmuraDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Kobe University · JPKobe University Hospital · JPKobe Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased tumor-associated macrophages (TAMs) have been reported to be associated with poor prognosis in various tumors; however, the importance of TAMs in primary central nervous system lymphoma (PCNSL) has not been clarified. In 47 patients with PCNSL who were treated with high-dose methotrexate (MTX) and radiotherapy, the relationships between the infiltration levels of TAMs and the clinicopathological parameters were analyzed. Univariate analysis of the Cox proportional hazards model using continuous scales revealed that increased CD68 positive (+) TAMs was significantly associated with inferior progression-free survival (PFS) (P = 0.04), and trends were observed for the increased CD163(+)  TAMs and having shorter PFS (P = 0.05). However, increased TAMs were not associated with overall survival. Because TAMs are known to produce various cytokines, we examined the relationships between cerebrospinal fluid (CSF) cytokines and TAMs. CSF interleukin-6 (IL-6) and soluble IL-2 receptor were not correlated with the infiltration rate of TAMs; however, CSF IL-10 level was correlated with infiltration levels of CD68 and CD163(+)  TAMs. We also confirmed the expression of IL-10 in CD68(+)  and CD163(+)  TAMs by double immunostaining analysis. Our results indicate that a high level of IL-10 in CSF may be positively associated with the infiltration level of TAMs in PCNSLs.

Indexed as

AdultAgedCentral Nervous System NeoplasmsDisease-Free SurvivalFemaleHumansInterleukin-10LymphomaMacrophagesMaleMiddle AgedPrognosisProportional Hazards ModelsIL10 protein, humanInterleukin-10cerebrospinal fluidIL-10primary central nervous system lymphomaprognosistumor-associated macrophage

Identifiers

PMID26314692
PMCPMC8029390
OpenAlexW1949207081

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.