Evidence map›Paper›PMID 34679325›Full record

ReviewBrain sciences2021

Oncolytic Virotherapy for Melanoma Brain Metastases, a Potential New Treatment Paradigm?

Sauson Soldozy, Kathleen M Mulligan, David X Zheng, Melissa A Levoska, Christopher R Cullison, Turki Elarjani, Daniel G Eichberg, Leonel E Ampie, Ashish H Shah, Kaan Yağmurlu and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Brain sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Overcoming Resistance Mechanisms to Melanoma Immunotherapy.American journal of clinical dermatology · 2025
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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

13 authors at 5 institutions in 1 country.

Sauson SoldozyDepartment of Neurological Surgery, University of Virginia Health System, Charlottesville, VA 22903, USA.
Kathleen M MulliganDepartment of Dermatology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.ORCID 0000-0002-4353-9255
David X ZhengDepartment of Dermatology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.ORCID 0000-0002-3351-023X
Melissa A LevoskaDepartment of Dermatology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Christopher R CullisonDepartment of Dermatology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.ORCID 0000-0002-9005-156X
Turki ElarjaniDepartment of Neurological Surgery, University of Miami, Miami, FL 33146, USA.
Daniel G EichbergDepartment of Neurological Surgery, University of Miami, Miami, FL 33146, USA.
Leonel E AmpieDepartment of Neurological Surgery, University of Virginia Health System, Charlottesville, VA 22903, USA.
Ashish H ShahDepartment of Neurological Surgery, University of Miami, Miami, FL 33146, USA.
Kaan YağmurluDepartment of Neurological Surgery, University of Virginia Health System, Charlottesville, VA 22903, USA.
Mark E ShaffreyDepartment of Neurological Surgery, University of Virginia Health System, Charlottesville, VA 22903, USA.
Jeffrey F ScottDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Ricardo J KomotarDepartment of Neurological Surgery, University of Miami, Miami, FL 33146, USA.
University of Miami · USUniversity School · USNational Institutes of Health · USUniversity of Virginia Health System · USJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMelanoma brain metastases remain a devastating disease process with poor prognosis. Recently, there has been a surge in studies demonstrating the efficacy of oncolytic virotherapy for brain tumor treatment. Given their specificity and amenability to genetic modification, the authors explore the possible role of oncolytic virotherapy as a potential treatment option for patients with melanoma brain metastases.

methodsA comprehensive literature review including both preclinical and clinical evidence of oncolytic virotherapy for the treatment of melanoma brain metastasis was performed.

resultsOncolytic virotherapy, specifically T-VEC (Imlygic™), was approved for the treatment of melanoma in 2015. Recent clinical trials demonstrate promising anti-tumor changes in patients who have received T-VEC; however, there is little evidence for its use in metastatic brain disease based on the existing literature. To date, only two single cases utilizing virotherapy in patients with metastatic brain melanoma have been reported, specifically in patients with treatment refractory disease. Currently, there is not sufficient data to support the use of T-VEC or other viruses for intracranial metastatic melanoma. In developing a virotherapy treatment paradigm for melanoma brain metastases, several factors must be considered, including route of administration, need to bypass the blood-brain barrier, viral tumor infectivity, and risk of adverse events.

conclusionsEvidence for oncolytic virotherapy treatment of melanoma is limited primarily to T-VEC, with a noticeable paucity of data in the literature with respect to brain tumor metastasis. Given the promising findings of virotherapy for other brain tumor types, oncolytic virotherapy has great potential to offer benefits to patients afflicted with melanoma brain metastases and warrants further investigation.

Indexed as

brain metastasesmelanomaneuroimmunologyneuro-oncologyoncolytic virotherapy

Identifiers

PMID34679325
PMCPMC8534242
OpenAlexW3199330223

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.