Evidence map›Paper›PMID 32862726›Full record

SynthesisExpert review of clinical pharmacology2020

Checkpoint inhibitor immunotherapy for glioblastoma: current progress, challenges and future outlook.

Patrick C Gedeon, Cosette D Champion, Kristen E Rhodin, Karolina Woroniecka, Hanna R Kemeny, Alexa N Bramall, Joshua D Bernstock, Bryan D Choi, John H Sampson

Open access · hybridAbstract readSystematic Review
In one paragraph

Synthesis in Expert review of clinical pharmacology, 2020. 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
1.0field-weighted citation impact, top 23% 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.

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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 4 institutions in 1 country.

Patrick C GedeonDepartment of Surgery, Brigham and Women's Hospital and Harvard Medical School , Boston, MA, USA.ORCID https://orcid.org/0000-0002-5387-1833
Cosette D ChampionDepartment of Neurosurgery, Duke University Medical Center , Durham, NC, USA.
Kristen E RhodinDepartment of Surgery, Duke University Medical Center , Durham, NC, USA.
Karolina WoronieckaDepartment of Neurosurgery, Duke University Medical Center , Durham, NC, USA.
Hanna R KemenyDepartment of Neurological Surgery, Northwestern University Feinberg School of Medicine , Chicago, IL, USA.
Alexa N BramallDepartment of Neurosurgery, Duke University Medical Center , Durham, NC, USA.
Joshua D BernstockDepartment of Neurosurgery, Brigham and Women's Hospital and Harvard Medical School , Boston, MA, USA.
Bryan D ChoiDepartment of Neurosurgery, Massachusetts General Hospital and Harvard Medical School , Boston, MA, USA.
John H SampsonDepartment of Neurosurgery, Duke University Medical Center , Durham, NC, USA.
Duke Medical Center · USBrigham and Women's Hospital · USHarvard University · USNorthwestern University · US

Funding

Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
Human EGFRvIII-specific BiTE for the treatment of GlioblastomaU01NS090284 · NINDS · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2015 to 2019
$5.2M
Brain tumors with regulatory T-cells treated with EGFRvIII-specific T-cellsR01CA177476 · NCI · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2013 to 2017
$2.3M
EGFRvIII-targeted Bispecific T cell Engagers for brain tumorsR01NS085412 · NINDS · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2013 to 2017
$2.0M
CCL3 as a Developmental Therapeutic to Enhance Brain Tumor TherapyR01NS099463 · NINDS · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2017 to 2021
$1.7M
Brain Tumor Targeting Using Tumor-Specific NeuroimmunologyR01NS086943 · NINDS · DUKE UNIVERSITY · PI SAMPSON, JOHN H., YAN, HAI · 2014 to 2017
$1.4M
Systemic EGFRvIII-targeted bispecific antibody as immunotherapy for glioblastomaF30CA196199 · NCI · DUKE UNIVERSITY · PI GEDEON, PATRICK C · 2015 to 2018
$165k
NCI NIH HHS F30 CA196199NCI NIH HHS R01 CA177476NIGMS NIH HHS T32 GM145449NINDS NIH HHS R01 NS085412NINDS NIH HHS R01 NS086943NINDS NIH HHS R01 NS099463NINDS NIH HHS U01 NS090284
6 · The paper itself

Abstract

introductionDespite maximal surgical resection and chemoradiation, glioblastoma (GBM) continues to be associated with significant morbidity and mortality. Novel therapeutic strategies are urgently needed. Given success in treating multiple other forms of cancer, checkpoint inhibitor immunotherapy remains foremost amongst novel therapeutic strategies that are currently under investigation. AREAS COVERED: Through a systematic review of both published literature and the latest preliminary data available from ongoing clinical studies, we provide an up-to-date discussion on the immune system in the CNS, a detailed mechanistic evaluation of checkpoint biology in the CNS along with evidence for disruption of these pathways in GBM, and a summary of available preclinical and clinical data for checkpoint blockade in GBM. We also include a discussion of novel, emerging targets for checkpoint blockade which may play an important role in GBM immunotherapy. EXPERT OPINION: Evidence indicates that while clinical success of checkpoint blockade for the treatment of GBM has been limited to date, through improved preclinical models, optimization in the context of standard of care therapies, assay standardization and harmonization, and combinatorial approaches which may include novel targets for checkpoint blockade, checkpoint inhibitor immunotherapy may yield a safe and effective therapeutic option for the treatment of GBM.

Indexed as

AnimalsBrain NeoplasmsGlioblastomaHumansImmune Checkpoint InhibitorsImmunotherapyMolecular Targeted TherapyImmune Checkpoint InhibitorsantibodiesCancercheckpoint inhibitorsclinical trialsgliomaimmunotherapy

Identifiers

PMID32862726
PMCPMC7658017
OpenAlexW3081569001

What OpenQuestion holds

Textmetadata
LicenceTDM
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.