Evidence map›Paper›PMID 30346600›Full record

ReviewNeuro-oncology2019

Viral and other therapies for recurrent glioblastoma: is a 24-month durable response unusual?

E Antonio Chiocca, Farshad Nassiri, Justin Wang, Pierpaolo Peruzzi, Gelareh Zadeh

Open access · bronzeAbstract readReview
In one paragraph

Review in Neuro-oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

58 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. Once, Twice, Three Times a Finding: Reproducibility of Dendritic Cell Vaccine Trials Targeting Cytomegalovirus in Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Trial
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  4. Article
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  7. Article
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  12. Article
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  15. Article
  16. Article
  17. Glioblastoma Therapy: Past, Present and Future.International journal of molecular sciences · 2024
    Review
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  19. Review
  20. Review
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

5 authors at 2 institutions in 2 countries.

E Antonio ChioccaDepartment of Neurosurgery, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Farshad NassiriDivision of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.
Justin WangDivision of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.
Pierpaolo PeruzziDepartment of Neurosurgery, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Gelareh ZadehDivision of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.
University of Toronto · CABrigham and Women's Hospital · US

Funding

Targeting the Vasular SystemP50CA165962 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Benjamin Harris Kann · 2013 to 2026
$33.5M
The Tumor Microenvironmental Barrier to Effective Viral OncolysisP01CA163205 · NCI · OHIO STATE UNIVERSITY · PI E. Antonio Chiocca · 2013 to 2026
$26.0M
Characterization of a microRNA network regulating glioblastoma epigenetics, cell reprogramming and DNA repairK08NS101091 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI PERUZZI, PIER PAOLO · 2017 to 2021
$992k
NCI NIH HHS P01 CA163205NCI NIH HHS P50 CA165962NINDS NIH HHS K08 NS101091
6 · The paper itself

Abstract

A phase I trial of an engineered poliovirus for the treatment of recurrent glioblastoma (GBM) has attracted attention due to 8 survivors reaching the 24-month and 5 reaching the 36-month survival landmarks.1 Genetically engineered viruses (oncolytic viruses) have been in trials for GBM for almost two decades.2 These replication-competent (tumor-selective, oncolytic, replication-conditional) viruses or replication-defective viral vectors (gene therapy) deliver cytotoxic payloads to tumors, leading to immunogenic death and intratumoral inflammatory responses. This transforms the tumor microenvironment from immunologically naïve ("cold") to inflamed ("hot"), increasing immune cell recognition of tumor antigens and the durable responses observed in virotherapy.3,4 Several current and past virotherapy trials have reported a "tail" of apparent responders at the 24-month landmark. Other modalities have also reported a "tail" of seemingly long-term survivors. These trials seem to show that these responder "tails" characterize a defined subset of GBM patients.

Indexed as

AnimalsBrain NeoplasmsGenetic TherapyGlioblastomaHumansOncolytic VirotherapyPrognosis

Identifiers

PMID30346600
PMCPMC6303472
OpenAlexW2897975460

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.