Evidence map›Paper›PMID 33737338›Full record

ArticleJournal for immunotherapy of cancer2021

Combination immunotherapy using G-CSF and oncolytic virotherapy reduces tumor growth in osteosarcoma.

Alvaro Morales-Molina, Stefano Gambera, Angela Leo, Javier García-Castro

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  3. Natural and Engineered Cytokines as Cancer Therapeutics.Annual review of cancer biology · 2026
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  4. Article
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  6. From conventional to cutting edge: an exploration of osteosarcoma treatments.Medical oncology (Northwood, London, England) · 2025
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  16. Telomeres and telomerase in Sarcoma disease and therapy.International journal of medical sciences · 2024
    Review
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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

4 authors at 2 institutions in 2 countries.

Alvaro Morales-MolinaCellular Biotechnology Unit, Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0003-4532-7667
Stefano GamberaCellular Biotechnology Unit, Instituto de Salud Carlos III, Madrid, Spain.
Angela LeoDepartment of Biomedical, Experimental and Clinical Sciences, University of Florence, Firenze, Italy.
Javier García-CastroCellular Biotechnology Unit, Instituto de Salud Carlos III, Madrid, Spain jgcastro@isciii.es.ORCID 0000-0001-7604-1640
Instituto de Salud Carlos III · ESUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma is the most common malignant solid tumor that affects bones, however, survival rates of patients with relapsed osteosarcoma have not improved in the last 30 years. Oncolytic virotherapy, which uses viruses designed to selectively replicate in cancer cells, has emerged as a promising treatment for solid tumors. Our group uses mesenchymal stem cells (MSCs) to transport oncolytic adenoviruses (OAds) to the tumor site, a therapeutic strategy called Celyvir. This treatment has been already applied in human patients, canine patients and different mouse models. In parallel, previous results have probed that administration of granulocyte-colony stimulating factor (G-CSF) increased immune infiltration in tumors. We then hypothesized that the mobilization of immune cells by G-CSF may increase the antitumor efficacy of Celyvir treatment by increasing the immune infiltration into the tumors.

methodsIn this study, we use a murine version of Celyvir consisting in murine MSCs carrying the murine OAd dlE102-here called OAd-MSCs-in an immunocompetent model of osteosarcoma. We tested the antitumoral efficacy of the combination of OAd-MSCs plus G-CSF.

resultsOur results show that treatment with OAd-MSCs or the union of OAd-MSCs with G-CSF (Combination) significantly reduced tumor growth of osteosarcoma in vivo. Moreover, treated tumors presented higher tumor infiltration of immune cells-especially tumor-infiltrating lymphocytes-and reduced T cell exhaustion, which seems to be enhanced in tumors treated with the Combination. The comparison of our results to those obtained from a cohort of pediatric osteosarcoma patients showed that the virotherapy induces immunological changes similar to those observed in patients with good prognosis.

conclusionsThe results open the possibility of using cellular virotherapy for the treatment of bone cancers. Indeed, its combination with G-CSF may be considered for the improvement of the therapy.

Indexed as

Oncolytic VirotherapyAdenoviridaeAnimalsBone NeoplasmsCell Line, TumorCombined Modality TherapyCytopathogenic Effect, ViralDatabases, GeneticGranulocyte Colony-Stimulating FactorHumansImmunomodulating AgentsLymphocytes, Tumor-InfiltratingMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMiceMice, Inbred BALB CGranulocyte Colony-Stimulating FactorImmunomodulating Agentsimmunotherapylymphocytesoncolytic virotherapyprogrammed cell death 1 receptort-lymphocytestumor-infiltrating

Identifiers

PMID33737338
PMCPMC7978281
OpenAlexW3139325271

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.