Evidence map›Paper›PMID 35019636›Full record

ArticleACS applied bio materials2020

Off-Peak Near-Infrared-II (NIR-II) Bioimaging of an Immunoconjugate Having Peak Fluorescence Emission in the NIR-I Spectral Region for Improving Tumor Margin Delineation.

Kenneth S Hettie, Nutte Tarn Teraphongphom, Robert Ertsey, Frederick T Chin

Open access · greenAbstract read
In one paragraph

Article in ACS applied bio materials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
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

4 authors at 1 institution in 1 country.

Kenneth S HettieDepartment of Radiology, Stanford University School of Medicine, Stanford, California, 94305, United States.ORCID http://orcid.org/0000-0002-0607-7944
Nutte Tarn TeraphongphomDepartment of Otolaryngology - Head & Neck Surgery, Stanford University, Stanford, California 94305, United States.
Robert ErtseyDepartment of Otolaryngology - Head & Neck Surgery, Stanford University, Stanford, California 94305, United States.
Frederick T ChinDepartment of Radiology, Stanford University School of Medicine, Stanford, California, 94305, United States.
Stanford University · US

Funding

A new class of CSF-1R radioligands for monitoring glioblastoma progression and therapyR21CA205564 · NCI · STANFORD UNIVERSITY · PI CHIN, FREDERICK T · 2017 to 2018
$376k
An 18F PET/NIRF Smart Probe for Identifying, Grading, and Visualizing Astrocytic GliomasF32CA213620 · NCI · STANFORD UNIVERSITY · PI HETTIE, KENNETH SCOTT · 2017 to 2020
$234k
NCI NIH HHS F32 CA213620NCI NIH HHS R21 CA205564
6 · The paper itself

Abstract

The primary treatment for malignant tumors remains to be resection. The strongest predictor of recurrence and postoperative prognosis is whether diseased tissue/cells remain(s) at the surgical margin. Cancer surgery entails surgeons having the capability to visually distinguish between subtle shades of color in attempts of differentiating between diseased tissue and healthy tissue under standard white-light illumination, as such tissue states appear identical at the meso-/macroscopic level. Accordingly, enhancing the capability of surgeons to do so such that they can accurately delineate the tumor margin is of paramount importance. Fluorescence-guided surgery facilitates in enhancing such capability by color-coding the surgical field with overlaid contrasting pseudo-colors from real-time intraoperative fluorescence emission via utilizing fluorescent constructs in tandem. Constructs undergoing clinical trials or that are FDA-approved provide peak fluorescence emission in the visible (405 - 700 nm) or near-infrared-I (NIR-I) spectral region (700-900 nm), whereby differentiation between tissue states progressively improves in sync with using constructs that emit longer wavelengths of light. Here, we repurpose the usage of such fluorescent constructs by establishing feasibility of a tumor-targeting immunoconjugate (cetuximab-IRDye800) having peak fluorescence emission at the NIR-I spectral region to provide improved tumor margin delineation by affording higher tumor-to-background ratios (TBRs) when measuring its off-peak fluorescence emission at the near-infrared-II (NIR-II) spectral region (1000-1700 nm) in

Indexed as

bioimagingfluorescence-guided surgeryimmunoconjguatenear-infrared-IItumor margin delineation

Identifiers

PMID35019636
PMCPMC9826717
OpenAlexW3093687383

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.