Evidence map›Paper›PMID 32215786›Full record

ArticleJournal of neuro-oncology2020

Repolarized macrophages, induced by intermediate stereotactic dose radiotherapy and immune checkpoint blockade, contribute to long-term survival in glioma-bearing mice.

Alexander M Stessin, Mariano Guardia Clausi, Zirun Zhao, Hong Lin, Wei Hou, Zhao Jiang, Timothy Q Duong, Stella E Tsirka, Samuel Ryu

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In one paragraph

Article in Journal of neuro-oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Modulation of tumor-associated macrophage activity with radiation therapy: a systematic review.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2023
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  14. Immune Checkpoint Inhibitors in Cancer Therapy.Current oncology (Toronto, Ont.) · 2022
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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

9 authors at 2 institutions in 1 country.

Alexander M StessinDepartment of Radiation Oncology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Mariano Guardia ClausiDepartment of Radiation Oncology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Zirun ZhaoDepartment of Radiation Oncology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Hong LinDepartment of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Wei HouDepartment of Family, Population, and Preventive Medicine, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Zhao JiangDepartment of Radiology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Timothy Q DuongDepartment of Radiology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Stella E TsirkaDepartment of Pharmacology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA.
Samuel RyuDepartment of Radiation Oncology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, 11794, USA. Samuel.Ryu@stonybrookmedicine.edu.
Stony Brook University · USStony Brook School · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGlioblastoma multiforme (GBM) is a deadly brain tumor with a short expected median survival, despite current standard-of-care treatment. We explored the combination of intermediate stereotactic dose radiation therapy and immune checkpoint inhibitor therapy as a novel treatment strategy for GBM.

methodsGlioma xenograft-bearing mice were exposed to high dose brain-directed radiation (10 Gy single exposure) as well as mouse anti-PD-1 antibody. The tumor-bearing animals were randomized to four groups: no treatment, radiation alone, anti-PD-1 alone, and radiation + anti-PD-1. Survival was followed, and tumor growth was monitored using MRI. Immunohistochemistry, gene expression arrays, and flow cytometry were used to characterize the treatment-induced effects. Pharmacologic inhibitors of T-lymphocytes, bone marrow derived macrophages, and microglia were used to assess the respective roles of different immune populations in observed treatment effects.

resultsWe found the combined treatment with high dose radiation and immunotherapy to be highly effective with a 75% complete pathologic response and dramatically improved survival outcomes. We found both CD8+ T-cells and macrophages to be necessary for the full effect of combined therapy, with T lymphocytes appearing to play a role early on and macrophages mediating a later phase of the combined treatment effect. Radiation treatment appeared to trigger macrophage repolarization, increasing M1/M2 ratio.

conclusionsThese findings point to a novel immunologic mechanism underlying the interaction between radiotherapy and immunotherapy. They also provide the basis for clinical investigation of immunogenic dose radiation in combination with immune checkpoint blockade as a potential treatment approach for newly diagnosed high grade gliomas.

Indexed as

AnimalsBrain NeoplasmsCell Line, TumorCombined Modality TherapyGene ExpressionGliomaImmune Checkpoint InhibitorsMacrophagesMice, Inbred C57BLRadiation DosageRadiosurgerySurvival AnalysisImmune Checkpoint InhibitorsGlioblastomaImmunotherapyMacrophagesMouse modelRadiosurgeryT-lymphocytes

Identifiers

PMID32215786
OpenAlexW3013766663

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.