Evidence map›Paper›PMID 27379987›Full record

ArticleMolecular imaging and biology2017

Fluorescent Affibody Molecule Administered In Vivo at a Microdose Level Labels EGFR Expressing Glioma Tumor Regions.

Ana Luiza Ribeiro de Souza, Kayla Marra, Jason Gunn, Kimberley S Samkoe, P Jack Hoopes, Joachim Feldwisch, Keith D Paulsen, Brian W Pogue

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 41 citations in OpenAlex.

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  19. Targeting MMP-14 for dual PET and fluorescence imaging of glioma in preclinical models.European journal of nuclear medicine and molecular imaging · 2020
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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

8 authors at 2 institutions in 3 countries.

Ana Luiza Ribeiro de SouzaThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA.
Kayla MarraThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA.
Jason GunnThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA.
Kimberley S SamkoeThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA.
P Jack HoopesThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA.
Joachim FeldwischAffibody AB, SE-171 69, Solna, Sweden.
Keith D PaulsenThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA.
Brian W PogueThayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover, NH, 03755, USA. brian.w.pogue@dartmouth.edu.
Dartmouth College · USAffibody (Sweden) · SE

Funding

Molecular Fluorescence-Guided Surgery PlatformR01CA167413 · NCI · DARTMOUTH COLLEGE · PI PAULSEN, KEITH D., SAMKOE, KIMBERLEY · 2013 to 2025
$5.7M
NCI NIH HHS R01 CA167413
6 · The paper itself

Abstract

purposeFluorescence guidance in surgical oncology provides the potential to realize enhanced molecular tumor contrast with dedicated targeted tracers, potentially with a microdose injection level. For most glioma tumors, the blood brain barrier is compromised allowing some exogenous drug/molecule delivery and accumulation for imaging. The aberrant overexpression and/or activation of epidermal growth factor receptor (EGFR) is associated with many types of cancers, including glioblastoma, and so the use of a near-infrared (NIR) fluorescent molecule targeted to the EGFR receptor provides the potential for improving tumor contrast during surgery. Fluorescently labeled affibody molecule (ABY-029) has high EGFR affinity and high potential specificity with reasonably fast plasma clearance. In this study, ABY-29 was evaluated in glioma versus normal brain uptake from intravenous injection at a range of doses, down to a microdose injection level. PROCEDURE: Nude rats were inoculated with the U251 human glioma cell line in the brain. Tumors were allowed to grow for 3-4 weeks. ABY-029 fluorescence ex vivo imaging of brain slices was acquired at different time points (1-48 h) and varying injection doses from 25 to 122 μg/kg (from human protein microdose equivalent to five times microdose levels).

resultsThe tumor was most clearly visualized at 1-h post-injection with 8- to 16-fold average contrast relative to normal brain. However, the tumor still could be identified after 48 h. In all cases, the ABY-029 fluorescence appeared to localize preferentially in EGFR-positive regions. Increasing the injected dose from a microdose level to five times, a microdose level increased the signal by 10-fold, and the contrast was from 8 to 16, showing that there was value in doses slightly higher than the microdose restriction. Normal tissue uptake was found to be affected by the tumor size, indicating that edema was a likely factor affecting the expected tumor to normal tissue contrast.

conclusionThese results suggest that the NIR-labeled affibody molecules provide an excellent potential to increase surgical visualization of EGFR-positive tumor regions.

Indexed as

Staining and LabelingAnimalsBrain NeoplasmsCell Line, TumorErbB ReceptorsFemaleFluorescenceGliomaHumansImage Processing, Computer-AssistedRats, NudeRecombinant Fusion ProteinsSignal Processing, Computer-AssistedErbB ReceptorsRecombinant Fusion ProteinsAnti-EGFR affibody moleculefluorescence-guided surgeryGliomaPre-GMP ABY-029

Identifiers

PMID27379987
PMCPMC5209393
OpenAlexW2470859535

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.