Evidence map›Paper›PMID 36934744›Full record

ArticleCancer research2023

Shortwave Infrared Imaging Enables High-Contrast Fluorescence-Guided Surgery in Neuroblastoma.

Laura Privitera, Dale J Waterhouse, Alessandra Preziosi, Irene Paraboschi, Olumide Ogunlade, Chiara Da Pieve, Marta Barisa, Olumide Ogunbiyi, Gregory Weitsman, J Ciaran Hutchinson and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. 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

19 authors at 6 institutions in 2 countries.

Laura Privitera *University College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.ORCID 0000-0002-6384-6367
Dale J Waterhouse *University College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.ORCID 0000-0001-5530-6857
Alessandra PreziosiCancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.ORCID 0000-0002-4649-6385
Irene ParaboschiDepartment of Paediatric Urology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milano, Italy.ORCID 0000-0003-3529-1437
Olumide OgunladeUniversity College London, Department of Medical Physics and Biomedical Engineering, London, United Kingdom.ORCID 0000-0003-0123-4397
Chiara Da PievePreclinical Molecular Imaging, Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-9038-9659
Marta BarisaCancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.ORCID 0000-0001-7846-6810
Olumide OgunbiyiDepartment of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.ORCID 0000-0001-5208-5526
Gregory WeitsmanRichard Dimbleby Department of Cancer Research, School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Campus, London, United Kingdom.ORCID 0000-0002-1313-6279
J Ciaran HutchinsonDepartment of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.ORCID 0000-0002-1708-2634
Kate CrossDepartment of Specialist Neonatal and Paediatric Surgery, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.ORCID 0000-0002-1070-7865
Lorenzo BiassoniDepartment of Radiology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.ORCID 0000-0002-5225-3996
Danail StoyanovUniversity College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.ORCID 0000-0002-0980-3227
Neil SebireDepartment of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.ORCID 0000-0001-5348-9063
Paul BeardUniversity College London, Department of Medical Physics and Biomedical Engineering, London, United Kingdom.ORCID 0000-0001-7710-2759
Paolo De CoppiDepartment of Specialist Neonatal and Paediatric Surgery, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.ORCID 0000-0002-1659-0207
Gabriela Kramer-MarekPreclinical Molecular Imaging, Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-8053-3880
John AndersonCancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.ORCID 0000-0001-7509-3203
Stefano GiulianiUniversity College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.ORCID 0000-0002-4555-3093
Great Ormond Street Hospital · GBInstitute of Cancer Research · GBUniversity College London · GBWellcome / EPSRC Centre for Interventional and Surgical Sciences · GBBreast Cancer Now · GBFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · IT

Funding

Medical Research Council MR/T005491/1Wellcome Trust
6 · The paper itself

Abstract

Fluorescence-guided surgery is set to play a pivotal role in the intraoperative management of pediatric tumors. Shortwave infrared imaging (SWIR) has advantages over conventional near-infrared I (NIR-I) imaging with reduced tissue scattering and autofluorescence. Here, two NIR-I dyes (IRDye800CW and IR12), with long tails emitting in the SWIR range, were conjugated with a clinical-grade anti-GD2 monoclonal antibody (dinutuximab-beta) to compare NIR-I and SWIR imaging for neuroblastoma surgery. A first-of-its-kind multispectral NIR-I/SWIR fluorescence imaging device was constructed to allow an objective comparison between the two imaging windows. Conjugates were first characterized in vitro. Tissue-mimicking phantoms, imaging specimens of known geometric and material composition, were used to assess the sensitivity and depth penetration of the NIR-I/SWIR device, showing a minimum detectable volume of ∼0.9 mm3 and depth penetration up to 3 mm. In vivo, fluorescence imaging using the NIR-I/SWIR device showed a high tumor-to-background ratio (TBR) for both dyes, with anti-GD2-IR800 being significantly brighter than anti-GD2-IR12. Crucially, the system enabled higher TBR at SWIR wavelengths than at NIR-I wavelengths, verifying SWIR imaging enables high-contrast delineation of tumor margins. This work demonstrates that by combining the high specificity of anti-GD2 antibodies with the availability and translatability of existing NIR-I dyes, along with the advantages of SWIR in terms of depth and tumor signal-to-background ratio, GD2-targeted NIR-I/SWIR-guided surgery could improve the treatment of patients with neuroblastoma, warranting investigation in future clinical trials. SIGNIFICANCE: Multispectral near-infrared I/shortwave infrared fluorescence imaging is a versatile system enabling high tumor-to-background signal for safer and more complete resection of pediatric tumors during surgery.

Indexed as

Antineoplastic AgentsNeuroblastomaChildColoring AgentsFluorescent DyesHumansOptical ImagingPhantoms, ImagingAntineoplastic AgentsColoring AgentsFluorescent Dyes

Identifiers

PMID36934744
PMCPMC10267675
OpenAlexW4327856911

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.