Evidence map›Paper›PMID 32885452›Full record

ArticleJournal of surgical oncology2020

Dual-agent fluorescent labeling of soft-tissue sarcomas improves the contrast based upon targeting both interstitial and cellular components of the tumor milieu.

Hira S Sardar, Qais Zai, Xiaochun Xu, Jason R Gunn, Brian W Pogue, Keith D Paulsen, Eric R Henderson, Kimberley S Samkoe

Open access · greenAbstract read
In one paragraph

Article in Journal of surgical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  4. Dynamic Tracking ofMolecular pharmaceutics · 2025
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  11. Synthesis andBioconjugate chemistry · 2022
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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 1 country.

Hira S SardarThayer School of Engineering, Dartmouth College, Hanover, New Hampshire.ORCID http://orcid.org/0000-0001-7127-6643
Qais ZaiGeisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
Xiaochun XuDepartment of Surgery, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Jason R GunnThayer School of Engineering, Dartmouth College, Hanover, New Hampshire.
Brian W PogueThayer School of Engineering, Dartmouth College, Hanover, New Hampshire.
Keith D PaulsenThayer School of Engineering, Dartmouth College, Hanover, New Hampshire.
Eric R HendersonThayer School of Engineering, Dartmouth College, Hanover, New Hampshire.
Kimberley S SamkoeThayer School of Engineering, Dartmouth College, Hanover, New Hampshire.ORCID http://orcid.org/0000-0002-8234-2308
Dartmouth College · USDartmouth–Hitchcock Medical Center · US

Funding

Molecular Fluorescence-Guided Surgery PlatformR01CA167413 · NCI · DARTMOUTH COLLEGE · PI PAULSEN, KEITH D., SAMKOE, KIMBERLEY · 2013 to 2025
$5.7M
Paired-agent imaging for resection during surgery (PAIRS) for head & neck cancersR37CA212187 · NCI · DARTMOUTH-HITCHCOCK CLINIC · PI SAMKOE, KIMBERLEY · 2018 to 2024
$2.7M
Multimodal Fluorescence- and Imaging-Guided Surgical Navigation: Developing Methods for Subsurface, Indirect Visualization of Cancers Requiring Wide Local ExcisionK23EB026507 · NIBIB · DARTMOUTH-HITCHCOCK CLINIC · PI HENDERSON, ERIC R · 2018 to 2021
$679k
Development of Near-Infrared Molecular Surgical Imaging for Sarcoma Margin DefinitionR03CA219445 · NCI · DARTMOUTH-HITCHCOCK CLINIC · PI HENDERSON, ERIC R · 2017 to 2018
$162k
NCI NIH HHS R01 CA167413NCI NIH HHS R03 CA219445NCI NIH HHS R37 CA212187NIBIB NIH HHS K23 EB026507
6 · The paper itself

Abstract

backgroundCurrent practices for fluorescence-guided cancer surgery utilize a single fluorescent agent, but homogeneous distribution throughout the tumor is difficult to achieve. We hypothesize that administering a perfusion and a molecular-targeted agent at their optimal administration-to-imaging time will improve whole-tumor contrast. EXPERIMENTAL

designMice bearing subcutaneous xenograft human synovial sarcomas were administered indocyanine green (ICG) (3 mg/kg) or ABY-029 (48.7 μg/kg)-an epidermal growth factor receptor-targeted Affibody molecule-alone or in combination. Fluorescence contrast and signal distribution were compared between treatment groups. Two commercial fluorescence imaging systems were tested for simultaneous imaging of ICG and ABY-029.

resultsABY-029 has a moderate positive correlation with viable tumor (ρ = 0.2 ± 0.4), while ICG demonstrated a strong negative correlation (ρ = -0.6 ± 0.1). The contrast-to-variance ratio was highest in the ABY-029 +ICG (2.5 ± 0.8), compared to animals that received ABY-029 (2.3 ± 0.8) or ICG (2.0 ± 0.5) alone. Moreover, the combination of ABY-029 + ICG minimizes the correlation between viable tumor and fluorescence intensity (ρ = -0.1 ± 0.2) indicating the fluorescence signal distribution is more homogeneous throughout the tumor milieu.

conclusionDual-agent imaging utilizing a single channel in a commercial fluorescence-guided imaging system tailored for IRDye 800CW is a promising method to increase tumor contrast in a clinical setting.

Indexed as

FluorescenceAnimalsCell ProliferationFluorescent DyesHumansIndocyanine GreenMiceMolecular ImagingOptical ImagingRecombinant Fusion ProteinsSarcomaTumor Cells, CulturedXenograft Model Antitumor AssaysABY-029Fluorescent DyesIndocyanine GreenRecombinant Fusion Proteinsaffibodyfluorescence guidanceICG

Identifiers

PMID32885452
PMCPMC8287542
OpenAlexW3083568998

What OpenQuestion holds

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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.