Evidence map›Paper›PMID 27576697›Full record

ArticleJournal of neuro-oncology2016

Safety, feasibility, and optimization of intra-arterial mitoxantrone delivery to gliomas.

Jason A Ellis, Johann Cooke, Rajinder P Singh-Moon, Mei Wang, Jeffrey N Bruce, Charles W Emala, Irving J Bigio, Shailendra Joshi

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
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

8 authors at 4 institutions in 1 country.

Jason A EllisDepartment of Neurological Surgery, Columbia University Medical Center, New York, NY, USA. jae2109@cumc.columbia.edu.
Johann CookeDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA.
Rajinder P Singh-MoonDepartment of Electrical Engineering, Columbia University, New York, NY, USA.
Mei WangDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA.
Jeffrey N BruceDepartment of Neurological Surgery, Columbia University Medical Center, New York, NY, USA.
Charles W EmalaDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA.
Irving J BigioDepartments of Electrical and Biomedical Engineering, Boston University, Boston, MA, USA.
Shailendra JoshiDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA.
Columbia University Irving Medical Center · USNeurological Surgery · USBoston University · USColumbia University · US

Funding

Optical Imaging of Chemotherapy for Brain TumorsR01CA138643 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JOSHI, SHAILENDRA · 2011 to 2015
$2.4M
NCI NIH HHS R01 CA138643
6 · The paper itself

Abstract

Mitoxantrone is a highly cytotoxic antineoplastic drug, however, its poor penetration of the blood-brain barrier has limited its role in the treatment of brain cancers. We hypothesize that intra-arterial (IA) delivery of mitoxantrone may enhance its capacity for regional brain deposition thus expanding its potential as a brain tumor therapy agent. In this study we assessed the dose-response characteristics as well as the feasibility and safety of mitoxantrone delivery to the brain and specifically to gliomas in a rodent model. We show that delivery optimization utilizing the technique of intra-arterial transient cerebral hypoperfusion (IA-TCH) facilitates achieving the highest peak- and end- brain drug concentrations as compared to intravenous and IA delivery without hypoperfusion. Additionally, we observed significant tumor-specific uptake of mitoxantrone when delivered by the IA-TCH method. No untoward effects of IA-TCH delivery of mitoxantrone were observed. The IA-TCH method is shown to be a safely tolerated and feasible strategy for delivering mitoxantrone to tumors in the glioma model tested. Additional investigation is warranted to determine if IA-TCH delivery of mitoxantrone produces clinically relevant benefit.

Indexed as

AnimalsAntineoplastic AgentsBrainBrain NeoplasmsCell Line, TumorDose-Response Relationship, DrugDrug Delivery SystemsFeasibility StudiesFemaleGliomaHumansInfusions, Intra-ArterialMaleMitoxantroneRatsXenograft Model Antitumor AssaysAntineoplastic AgentsMitoxantroneBrain tumorChemotherapyGlioblastomaTargeted therapy

Identifiers

PMID27576697
OpenAlexW2512365174

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.