Evidence map›Paper›PMID 30150597›Full record

ReviewInternational journal of molecular sciences2018

Therapeutic Immunization against Glioblastoma.

Virgil E J C Schijns, Chrystel Pretto, Anna M Strik, Rianne Gloudemans-Rijkers, Laurent Deviller, Denis Pierre, Jinah Chung, Manisha Dandekar, Jose A Carrillo, Xiao-Tang Kong and 7 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Advances in Immunotherapies for Gliomas.Current neurology and neuroscience reports · 2022
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2019
    Article
  12. Article
  13. Review
  14. 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

17 authors at 5 institutions in 4 countries.

Virgil E J C SchijnsEpitopoietic Research Corporation ERC-The Netherlands Nistelrooisebaan 3, 5374 RE Schaijk, The Netherlands. schijns.virgil@gmail.com.
Chrystel PrettoERC-Belgium Gembloux Isnes, Rue Jean Sonet 10, 5031 Isnes Belgium, Belgium. pretto@ercbelgium.eu.
Anna M StrikEpitopoietic Research Corporation ERC-The Netherlands Nistelrooisebaan 3, 5374 RE Schaijk, The Netherlands. a.strik@ercnetherlands.nl.
Rianne Gloudemans-RijkersEpitopoietic Research Corporation ERC-The Netherlands Nistelrooisebaan 3, 5374 RE Schaijk, The Netherlands. r.gloudemans@ercnetherlands.nl.
Laurent DevillerERC-Belgium Gembloux Isnes, Rue Jean Sonet 10, 5031 Isnes Belgium, Belgium. devillers@ercbelgium.eu.
Denis PierreERC-Belgium Gembloux Isnes, Rue Jean Sonet 10, 5031 Isnes Belgium, Belgium. dpierre@ercbelgium.eu.
Jinah ChungChao Family Comprehensive Cancer Center, 101 The City Drive Bldg. 23, Route 81, Orange, CA 92868, USA. jinahec@uci.edu.
Manisha DandekarChao Family Comprehensive Cancer Center, 101 The City Drive Bldg. 23, Route 81, Orange, CA 92868, USA. mdandeka@uci.edu.
Jose A CarrilloDepartment of Neurological Surgery; University of California Irvine, Irvine, CA 92697, USA. Carrilj2@uci.edu.
Xiao-Tang KongChao Family Comprehensive Cancer Center, 101 The City Drive Bldg. 23, Route 81, Orange, CA 92868, USA. xkong@uci.edu.
Beverly D FuChao Family Comprehensive Cancer Center, 101 The City Drive Bldg. 23, Route 81, Orange, CA 92868, USA. dfu@uci.edu.
Frank P K HsuChao Family Comprehensive Cancer Center, 101 The City Drive Bldg. 23, Route 81, Orange, CA 92868, USA. fpkhsu@uci.edu.
Florence M HofmanDepartment of Pathology, University of California Irvine, Irvine, CA 92697, USA. hofman@usc.edu.
Thomas C ChenDepartment of Neurosurgery, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA. tchen68670@gmail.com.
Raphael ZidovetzkiCell Biology and Neuroscience, University of California, Riverside, CA 92521, USA. zidovet@ucr.edu.
Daniela A BotaChao Family Comprehensive Cancer Center, 101 The City Drive Bldg. 23, Route 81, Orange, CA 92868, USA. dbota@uci.edu.
Apostolos StathopoulosEpitopoietic Research Corporation ERC-The Netherlands Nistelrooisebaan 3, 5374 RE Schaijk, The Netherlands. tstath@hotmail.com.ORCID 0000-0002-0406-6766
University of California, Irvine · USGembloux Agro-Bio Tech · BEUniversity of Southern California · USCommunity Cancer Center · USUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most common form of brain cancer in adults that produces severe damage to the brain leading to a very poor survival prognosis. The standard of care for glioblastoma is usually surgery, as well as radiotherapy followed by systemic temozolomide chemotherapy, resulting in a median survival time of about 12 to 15 months. Despite these therapeutic efforts, the tumor returns in the vast majority of patients. When relapsing, statistics suggest an imminent death dependent on the size of the tumor, the Karnofsky Performance Status, and the tumor localization. Following the standard of care, the administration of Bevacizumab, inhibiting the growth of the tumor vasculature, is an approved medicinal treatment option approved in the United States, but not in the European Union, as well as the recently approved alternating electric fields (AEFs) generator NovoTTF/Optune. However, it is clear that regardless of the current treatment regimens, glioma patients continue to have dismal prognosis and novel treatments are urgently needed. Here, we describe different approaches of recently developed therapeutic glioma brain cancer vaccines, which stimulate the patient's immune system to recognize tumor-associated antigens (TAA) on cancer cells, aiming to instruct the immune system to eventually attack and destroy the brain tumor cells, with minimal bystander damage to normal brain cells. These distinct immunotherapies may target particular glioma TAAs which are molecularly defined, but they may also target broad patient-derived tumor antigen preparations intentionally evoking a very broad polyclonal antitumor immune stimulation.

Indexed as

BrainBrain NeoplasmsCancer VaccinesGlioblastomaHumansImmune SystemImmunizationSurvival AnalysisCancer Vaccinesallogenicautologousbrain tumorglioma tumorimmunotherapytherapeutic vaccine

Identifiers

PMID30150597
PMCPMC6163986
OpenAlexW2889447981

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.