Evidence map›Paper›PMID 25344739›Full record

ArticleNature medicine2014

Microscopic lymph node tumor burden quantified by macroscopic dual-tracer molecular imaging.

Kenneth M Tichauer, Kimberley S Samkoe, Jason R Gunn, Stephen C Kanick, P Jack Hoopes, Richard J Barth, Peter A Kaufman, Tayyaba Hasan, Brian W Pogue

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 120 citations in OpenAlex.

  1. Trial
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8 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Kenneth M TichauerDepartment of Biomedical Engineering, Illinois Institute of Technology, Chicago, Illinois, USA.
Kimberley S SamkoeDepartment of Surgery, Geisel School of Medicine, Hanover, New Hampshire, USA.
Jason R GunnThayer School of Engineering, Dartmouth College, Hanover, New Hampshire, USA.
Stephen C KanickThayer School of Engineering, Dartmouth College, Hanover, New Hampshire, USA.ORCID 0000000220468298
P Jack Hoopes1] Department of Surgery, Geisel School of Medicine, Hanover, New Hampshire, USA. [2] Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire, USA.
Richard J BarthDepartment of Surgery, Geisel School of Medicine, Hanover, New Hampshire, USA.
Peter A KaufmanDepartment of Medicine, Geisel School of Medicine, Lebanon, New Hampshire, USA.
Tayyaba HasanWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Brian W Pogue1] Department of Surgery, Geisel School of Medicine, Hanover, New Hampshire, USA. [2] Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire, USA. [3] Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Dartmouth College · USIllinois Institute of Technology · USMassachusetts General Hospital · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
Toxicology, Pathology and Biodistribution Core (TPB Core)U54CA151662 · NCI · DARTMOUTH COLLEGE · PI BAKER, IAN · 2010 to 2014
$11.6M
Fluorescence Imaging to Optimize Cancer TherapyR01CA109558 · NCI · DARTMOUTH COLLEGE · PI POGUE, BRIAN WILLIAM · 2005 to 2015
$2.8M
Targeted Photoactivable Nanocells: Image-based Drug Delivery and Dosimetry in GBMR01CA156177 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA, POGUE, BRIAN WILLIAM · 2011 to 2015
$2.5M
Canadian Institutes of Health ResearchNCI NIH HHS P30 CA023108NCI NIH HHS R01 CA109558NCI NIH HHS R01 CA156177NCI NIH HHS U54 CA151662
6 · The paper itself

Abstract

Lymph node biopsy is employed in many cancer surgeries to identify metastatic disease and to determine cancer stage, yet morbidity and diagnostic delays associated with lymph node biopsy could be avoided if noninvasive imaging of nodal involvement were reliable. Molecular imaging has potential in this regard; however, variable delivery and nonspecific uptake of imaging tracers have made conventional approaches ineffective clinically. Here we present a method of correcting for nonspecific uptake with injection of a second untargeted tracer that allows for quantification of tumor burden in lymph nodes. We confirmed the approach in an athymic mouse model of metastatic human breast cancer by targeting epidermal growth factor receptor, a cell surface receptor overexpressed by many cancers. We observed a significant correlation between in vivo (dual-tracer) and ex vivo measures of tumor burden (r = 0.97, P < 0.01), with an ultimate sensitivity of approximately 200 cells (potentially more sensitive than conventional lymph node biopsy).

Indexed as

Tumor BurdenAlgorithmsAnimalsCell Line, TumorFluorescent DyesHumansKineticsLymphatic MetastasisLymph NodesMiceMolecular ImagingSentinel Lymph Node BiopsyStaining and LabelingFluorescent Dyes

Identifiers

PMID25344739
PMCPMC4224611
OpenAlexW2027008808

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.