Evidence map›Paper›PMID 39406917›Full record

ArticleBritish journal of cancer2024

Improved ex vivo fluorescence imaging of human head and neck cancer using the peptide tracer TPP-IRDye800 targeting membrane-bound Hsp70 on tumor cells.

Katharina L K Holzmann, Johanna L Wolf, Stefan Stangl, Philipp Lennartz, Atsuko Kasajima, Carolin Mogler, Bernhard Haller, Eva-Vanessa Ebert, Daniel Jira, Maren L A Lauterbach and 7 more

Abstract read
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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

17 authors.

Katharina L K HolzmannDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany. katharina.holzmann@tum.de.ORCID http://orcid.org/0009-0008-3612-7237
Johanna L WolfDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Stefan StanglDepartment of Nuclear Medicine and Central Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Philipp LennartzDepartment of Radiation Oncology and Central Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Atsuko KasajimaInstitute of Pathology, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Carolin MoglerInstitute of Pathology, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Bernhard HallerInstitute of AI and Informatics in Medicine, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Eva-Vanessa EbertDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Daniel JiraDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Maren L A LauterbachDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Franziska von MeyerDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Leonhard StarkDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Leonie MauchDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Benedikt SchmidlDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Barbara WollenbergDepartment of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Gabriele Multhoff *Department of Radiation Oncology and Central Institute for Translational Cancer Research (TranslaTUM), Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.
Markus Wirth *Department of Otolaryngology - Head and Neck Surgery, Technical University of Munich (TUM), School of Medicine and Health, TUM University Hospital, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe primary goal of surgery in HNSCC is the complete resection of tumor cells with maximum preservation of normal tissue. The membrane Hsp70-targeting fluorescence labelled peptide TPP-IRDye800 represents a promising tool for real-time intraoperative tumor visualization, enabling the detection of true tumor margins, critical isles of high-grade dysplasia and LN metastases.

methodsMembrane Hsp70 (mHsp70) expression on HNSCC cell lines and primary HNSCC was determined by flow cytometry and fluorescence microscopy using FITC-conjugated mAb cmHsp70.1 and TPP. TPP-IRDye800 was sprayed on freshly resected tumor material of immunohistochemically confirmed HNSCC and LN metastases for tumor imaging. TBRs were compared using TPP-IRDye800 and Cetuximab-IRDye680, recognizing EGFR.

resultsmHsp70 expressing HNSCC cells specifically bind and internalize TPP in vitro. The TBR (2.56 ± 0.39) and AUC [0.98 CI, 0.95-1.00 vs. 0.91 CI, 0.85-0.97] of TPP-IRDye800 on primary HNSCC was significantly higher than Cetuximab-IRDye680 (1.61 ± 0.39) (p = 0.0068) and TPP-IRDye800 provided a superior tumor delineation. Fluorescence imaging showed higher AUC values than a visual inspection by surgeons [0.97 CI, 0.94-1.00 vs. 0.92 CI, 0.88-0.97] (p = 0.048). LN metastases could be visualized using TPP-IRDye800. Real-time tissue delineation was confirmed using the clinically applied KARL-STORZ imaging system.

conclusionTPP-IRDye800 is a promising fluorescence imaging probe for HNSCC.

Indexed as

Head and Neck NeoplasmsHSP70 Heat-Shock ProteinsIndolesCell Line, TumorCetuximabFemaleFluorescent DyesHumansMaleMicroscopy, FluorescenceMiddle AgedOptical ImagingPeptidesSquamous Cell Carcinoma of Head and NeckCetuximabFluorescent DyesHSP70 Heat-Shock ProteinsIndolesIRDye800Peptides

Identifiers

PMID39406917
PMCPMC11589746

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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.