Evidence map›Paper›PMID 23296073›Full record

ArticleOncotarget2013

Enhancing the efficacy of drug-loaded nanocarriers against brain tumors by targeted radiation therapy.

Brian C Baumann, Gary D Kao, Abdullah Mahmud, Takamasa Harada, Joe Swift, Christina Chapman, Xiangsheng Xu, Dennis E Discher, Jay F Dorsey

Abstract read
In one paragraph

Article in Oncotarget, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Review
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  15. Article
  16. Radiation-enhanced delivery of systemically administered amphiphilic-CpG oligodeoxynucleotide.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  17. Review
  18. Article
  19. Article
  20. It's Getting Hot in Here: Targeting Cancer Stem-like Cells with Hyperthermia.Journal of stem cell and transplantation biology · 2017
    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

9 authors.

Brian C BaumannDepartment of Radiation Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Gary D Kao
Abdullah Mahmud
Takamasa Harada
Joe Swift
Christina Chapman
Xiangsheng Xu
Dennis E Discher
Jay F Dorsey

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
RADIATION BIOLOGY TRAINING GRANTT32CA009677 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KENNEDY, ANN R · 1992 to 2011
$5.0M
Targeted Modulation of the Death Receptor as a Therapeutic Strategy for GliomaK08NS076548 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI DORSEY, JAY FITZGERALD · 2011 to 2015
$932k
NCI NIH HHS L30 CA142178NCI NIH HHS P30 CA016520NCI NIH HHS T32 CA009677NINDS NIH HHS K08 NS076548
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is a common, usually lethal disease with a median survival of only ~15 months. It has proven resistant in clinical trials to chemotherapeutic agents such as paclitaxel that are highly effective in vitro, presumably because of impaired drug delivery across the tumor's blood-brain barrier (BBB). In an effort to increase paclitaxel delivery across the tumor BBB, we linked the drug to a novel filomicelle nanocarrier made with biodegradable poly(ethylene-glycol)-block-poly(ε-caprolactone-r-D,L-lactide) and used precisely collimated radiation therapy (RT) to disrupt the tumor BBB's permeability in an orthotopic mouse model of GBM. Using a non-invasive bioluminescent imaging technique to assess tumor burden and response to therapy in our model, we demonstrated that the drug-loaded nanocarrier (DLN) alone was ineffective against stereotactically implanted intracranial tumors yet was highly effective against GBM cells in culture and in tumors implanted into the flanks of mice. When targeted cranial RT was used to modulate the tumor BBB, the paclitaxel-loaded nanocarriers became effective against the intracranial tumors. Focused cranial RT improved DLN delivery into the intracranial tumors, significantly improving therapeutic outcomes. Tumor growth was delayed or halted, and survival was extended by >50% (p less than 0.05) compared to the results obtained with either RT or the DLN alone. Combinations of RT and chemotherapeutic agents linked to nanocarriers would appear to be an area for future investigations that could enhance outcomes in the treatment of human GBM.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicBlood-Brain BarrierBrain NeoplasmsCell Line, TumorChemoradiotherapyDrug CarriersDrug Delivery SystemsGlioblastomaGreen Fluorescent ProteinsHumansLuciferasesMiceMicellesMice, NudeMicroscopy, FluorescenceAntineoplastic Agents, PhytogenicDrug CarriersGreen Fluorescent ProteinsLuciferasesMicellesPaclitaxelPolymers

Identifiers

PMID23296073
PMCPMC3702208

What OpenQuestion holds

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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.