Evidence map›Paper›PMID 23242736›Full record

ArticleJournal of neuro-oncology2013

Real-time multi-modality imaging of glioblastoma tumor resection and recurrence.

Shawn Hingtgen, Jose-Luiz Figueiredo, Christian Farrar, Matthias Duebgen, Jordi Martinez-Quintanilla, Deepak Bhere, Khalid Shah

Open access · greenAbstract read
In one paragraph

Article in Journal of neuro-oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

42 citing papers in PubMed, 69 citations in OpenAlex.

  1. Trial
  2. Article
  3. Biodegradable nanofibrous scaffolds enhance standard of care for glioblastoma via localized targeted therapy.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Collective invasion of glioma cells through OCT1 signalling and interaction with reactive astrocytes after surgery.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Shawn HingtgenMolecular Neurotherapy and Imaging Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Jose-Luiz Figueiredo
Christian Farrar
Matthias Duebgen
Jordi Martinez-Quintanilla
Deepak Bhere
Khalid Shah
Harvard University · USMassachusetts General Hospital · US

Funding

In vivo imaging of encapsulated stem cells in mouse models of tumor resectionR01CA173077 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SHAH, KHALID A · 2013 to 2017
$1.7M
Developing diagnostic and therapeutic stem cells for cancer therapyR01CA138922 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SHAH, KHALID A · 2010 to 2014
$1.7M
Stem cell mediated targeting of tumor cells and associated vasculature in gliomasR01NS071197 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI SHAH, KHALID A · 2011 to 2014
$1.5M
NCI NIH HHS R01 CA138922NCI NIH HHS R01 CA173077NINDS NIH HHS R01 NS071197PHS HHS R01-NSO71197
6 · The paper itself

Abstract

The lack of relevant pre-clinical animal models incorporating the clinical scenario of Glioblastoma multiforme (GBM) resection and recurrence has contributed significantly to the inability to successfully treat GBM. A multi-modality imaging approach that allows real-time assessment of tumor resection during surgery and non-invasive detection of post-operative tumor volumes is urgently needed. In this study, we report the development and implementation of an optical imaging and magnetic resonance imaging (MRI) approach to guide GBM resection during surgery and track tumor recurrence at multiple resolutions in mice. Intra-operative fluorescence-guided surgery allowed real-time monitoring of intracranial tumor removal and led to greater than 90 % removal of established intracranial human GBM. The fluorescent signal clearly delineated tumor margins, residual tumor, and correlated closely with the clinically utilized fluorescence surgical marker 5-aminolevulinic acid/porphyrin. Post-operative non-invasive optical imaging and MRI confirmed near-complete tumor removal, which was further validated by immunohistochemistry (IHC). Longitudinal non-invasive imaging and IHC showed rapid recurrence of multi-focal tumors that exhibited a faster growth rate and altered blood-vessel density compared to non-resected tumors. Surgical tumor resection significantly extended long-term survival, however mice ultimately succumbed to the recurrent GBM. This multi-modality imaging approach to GBM resection and recurrence in mice should provide an important platform for investigating multiple aspects of GBM and ultimately evaluating novel therapeutics.

Indexed as

Analysis of VarianceAnimalsBrain NeoplasmsCell Line, TumorDiffusion Magnetic Resonance ImagingDisease Models, AnimalGlioblastomaGreen Fluorescent ProteinsHumansKi-67 AntigenLuminescent MeasurementsMiceMice, NudeNeoplasm Recurrence, LocalPlatelet Endothelial Cell Adhesion Molecule-1Time FactorsGreen Fluorescent ProteinsKi-67 AntigenPlatelet Endothelial Cell Adhesion Molecule-1

Identifiers

PMID23242736
PMCPMC3548430
OpenAlexW2056921536

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.