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


Journal

Cancer research
ISSN: 1538-7445
Titre abrégé: Cancer Res
Pays: United States
ID NLM: 2984705R

Informations de publication

Date de publication:
15 06 2023
Historique:
received: 14 09 2022
revised: 29 12 2022
accepted: 08 03 2023
medline: 16 6 2023
pubmed: 20 3 2023
entrez: 19 3 2023
Statut: ppublish

Résumé

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. 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.

Identifiants

pubmed: 36934744
pii: 718789
doi: 10.1158/0008-5472.CAN-22-2918
pmc: PMC10267675
doi:

Substances chimiques

Antineoplastic Agents 0
Coloring Agents 0
Fluorescent Dyes 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2077-2089

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T005491/1
Pays : United Kingdom

Informations de copyright

©2023 The Authors; Published by the American Association for Cancer Research.

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Auteurs

Laura Privitera (L)

University College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.
Cancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.

Dale J Waterhouse (DJ)

University College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.

Alessandra Preziosi (A)

Cancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Department of Paediatric Surgery, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milano, Italy.

Irene Paraboschi (I)

Department of Paediatric Urology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milano, Italy.

Olumide Ogunlade (O)

University College London, Department of Medical Physics and Biomedical Engineering, London, United Kingdom.

Chiara Da Pieve (C)

Preclinical Molecular Imaging, Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, United Kingdom.

Marta Barisa (M)

Cancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.

Olumide Ogunbiyi (O)

Department of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

Gregory Weitsman (G)

Richard Dimbleby Department of Cancer Research, School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Campus, London, United Kingdom.

J Ciaran Hutchinson (JC)

Department of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

Kate Cross (K)

Department of Specialist Neonatal and Paediatric Surgery, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

Lorenzo Biassoni (L)

Department of Radiology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

Danail Stoyanov (D)

University College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.

Neil Sebire (N)

Department of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

Paul Beard (P)

University College London, Department of Medical Physics and Biomedical Engineering, London, United Kingdom.

Paolo De Coppi (P)

Department of Specialist Neonatal and Paediatric Surgery, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

Gabriela Kramer-Marek (G)

Preclinical Molecular Imaging, Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, United Kingdom.

John Anderson (J)

Cancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.

Stefano Giuliani (S)

University College London, Wellcome/EPSRC Centre for Interventional and Surgical Sciences, London, United Kingdom.
Cancer Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Department of Specialist Neonatal and Paediatric Surgery, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

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