Evidence map›Paper›PMID 35640060›Full record

ArticleMolecular pharmaceutics2022

Preclinical Evaluation of a Humanized, Near-Infrared Fluorescent Antibody for Fluorescence-Guided Surgery of MUC16-Expressing Pancreatic Cancer.

Madeline T Olson, Eric N Aguilar, Cory L Brooks, Carly C Isder, Kathryn M Muilenburg, Geoffrey A Talmon, Quan P Ly, Mark A Carlson, Michael A Hollingsworth, Aaron M Mohs

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
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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

10 authors at 3 institutions in 1 country.

Madeline T OlsonEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.ORCID 0000-0002-7373-2451
Eric N AguilarDepartment of Chemistry and Biochemistry, California State University Fresno, Fresno, California 93740, United States.
Cory L BrooksDepartment of Chemistry and Biochemistry, California State University Fresno, Fresno, California 93740, United States.
Carly C IsderFred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
Kathryn M MuilenburgFred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
Geoffrey A TalmonFred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
Quan P LyFred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
Mark A CarlsonFred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.ORCID 0000-0002-8113-9199
Michael A HollingsworthEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
Aaron M MohsFred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.ORCID 0000-0002-9353-5404
University of Nebraska Medical Center · USCalifornia State University, Fresno · USOmaha VA Medical Center · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Joann B. Sweasy · 1985 to 2026
$55.0M
Pancreatic Cancer Detection ConsortiumU01CA210240 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Michael A. Hollingsworth · 2017 to 2026
$12.9M
Project 3: MUC16-Mediated Metabolic Reprograming Induces PC MetastasisP01CA217798 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 2018 to 2022
$8.1M
CHEMICAL CARCINOGENESIS &CANCER BIOLOGYT32CA009476 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Jennifer D. Black · 1988 to 2026
$6.2M
Preclinical development of a novel antibody conjugate for intraoperative detection of pancreatic cancerR01CA259080 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Aaron M. Mohs · 2022 to 2026
$1.8M
Development and Application of a Porcine Model of Pancreatic CancerR01CA222907 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CARLSON, MARK A · 2018 to 2020
$1.7M
Role of Antigen Glycosylation in Mucin Binding by Monoclonal AntibodiesR15CA242349 · NCI · CALIFORNIA STATE UNIVERSITY FRESNO · PI BROOKS, CORY · 2020 to 2020
$415k
NCI NIH HHS P01 CA217798NCI NIH HHS P30 CA036727NCI NIH HHS R01 CA222907NCI NIH HHS R01 CA259080NCI NIH HHS R15 CA242349NCI NIH HHS T32 CA009476NCI NIH HHS U01 CA210240
6 · The paper itself

Abstract

Surgery remains the only potentially curative treatment option for pancreatic cancer, but resections are made more difficult by infiltrative disease, proximity of critical vasculature, peritumoral inflammation, and dense stroma. Surgeons are limited to tactile and visual cues to differentiate cancerous tissue from normal tissue. Furthermore, translating preoperative images to the intraoperative setting poses additional challenges for tumor detection, and can result in undetected and unresected lesions. Thus, pancreatic ductal adenocarcinoma (PDAC) has high rates of incomplete resections, and subsequently, disease recurrence. Fluorescence-guided surgery (FGS) has emerged as a method to improve intraoperative detection of cancer and ultimately improve surgical outcomes. Initial clinical trials have demonstrated feasibility of FGS for PDAC, but there are limited targeted probes under investigation for this disease, highlighting the need for development of additional novel biomarkers to reflect the PDAC heterogeneity. MUCIN16 (MUC16) is a glycoprotein that is overexpressed in 60-80% of PDAC. In our previous work, we developed a MUC16-targeted murine antibody near-infrared conjugate, termed AR9.6-IRDye800, that showed efficacy in detecting pancreatic cancer. To build on the translational potential of this imaging probe, a humanized variant of the AR9.6 fluorescent conjugate was developed and investigated herein. This conjugate, termed huAR9.6-IRDye800, showed equivalent binding properties to its murine counterpart. Using an optimized dye:protein ratio of 1:1,

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAnimalsCA-125 AntigenCell Line, TumorFluorescent DyesHumansMembrane ProteinsMiceNeoplasm Recurrence, LocalOptical ImagingTissue DistributionCA-125 AntigenFluorescent DyesMembrane ProteinsMUC16 protein, humanantibodyFluorescence-guided surgeryMUCIN16near-infrared fluorescencepancreatic cancer

Identifiers

PMID35640060
PMCPMC9864431
OpenAlexW4281851353

What OpenQuestion holds

Textmetadata
LicenceTDM
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.