Evidence map›Paper›PMID 22576886›Full record

Trial reportAJNR. American journal of neuroradiology2012

Metabolic response of glioblastoma to superselective intra-arterial cerebral infusion of bevacizumab: a proton MR spectroscopic imaging study.

J Y Jeon, I Kovanlikaya, J A Boockvar, X Mao, B Shin, J K Burkhardt, K Kesavabhotla, P Christos, H Riina, D C Shungu and 1 more

Open access · hybridAbstract readClinical Trial, Phase IClinical Trial, Phase III
In one paragraph

Trial report in AJNR. American journal of neuroradiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
1.5field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  14. Leakage decrease detected by dynamic susceptibility-weighted contrast-enhanced perfusion MRI predicts survival in recurrent glioblastoma treated with bevacizumab.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
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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

11 authors at 5 institutions in 1 country.

J Y JeonDepartments of Neuroradiology, New York Presbyterian Hospital, Weill Cornell Medical College, New York, NY 10065, USA.
I Kovanlikaya
J A Boockvar
X Mao
B Shin
J K Burkhardt
K Kesavabhotla
P Christos
H Riina
D C Shungu
A J Tsiouris
Imaging Center · USNewYork–Presbyterian Hospital · USPresbyterian Hospital · USColumbia University Irving Medical Center · USCornell University · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024996 · NCRR · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2007 to 2011
$49.6M
EGFR signaling and normal and tumor-derived neural stem cell behaviorK08CA130985 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BOOCKVAR, JOHN A · 2008 to 2012
$684k
NCI NIH HHS CA130985NCI NIH HHS K08 CA130985NCRR NIH HHS RR024996NCRR NIH HHS UL1 RR024996
6 · The paper itself

Abstract

background and purposeSIACI of bevacizumab has emerged as a promising novel therapy in the treatment of recurrent GB. This study assessed the potential of (1)H-MRS as an adjunctive technique in detecting metabolic changes reflective of antiproliferative effects of targeted infusion of bevacizumab in the treatment of GB. MATERIALS AND

methodsEighteen patients enrolled in a phase I/II study of SIACI of bevacizumab for treatment of recurrent GB were included. Concurrent MR imaging and (1)H-MRS scans were performed before and after treatment. Five distinct morphologic ROIs were evaluated for structural and metabolic changes on MR imaging and (1)H-MRS, which included enhancing, nonenhancing T2 hyperintense signal abnormality, and multiple control regions. Pre- and post-SIACI of bevacizumab peak areas for NAA, tCho, tCr, as well as tCho/tCr and tCho/NAA ratios, were derived for all 5 ROIs and compared using the Wilcoxon signed-rank test.

resultsA significant median decrease of 25.99% (range -55.76 to 123.94; P = .006) in tCho/NAA was found post-SIACI of bevacizumab relative to pretreatment values in regions of enhancing disease. A trend-level significant median decrease of 6.45% (range -23.71 to 37.67; P = .06) was noted in tCho/NAA posttreatment in regions of nonenhancing T2-hyperintense signal abnormality.

conclusionsThe results of this (1)H-MRS analysis suggest that GB treatment with SIACI of bevacizumab may be associated with a direct antiproliferative effect, as demonstrated by significant reductions of tCho/NAA after the intervention.

Indexed as

AgedAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedAspartic AcidBevacizumabBrainBrain NeoplasmsCerebral ArteriesCholineFemaleGlioblastomaHumansInfusions, Intra-ArterialMagnetic Resonance SpectroscopyMaleMiddle AgedAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedAspartic AcidBevacizumabCholineN-acetylaspartateProtons

Identifiers

PMID22576886
PMCPMC7965590
OpenAlexW2313439792

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.