Evidence map›Paper›PMID 23138852›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2013

Clinically-translated silica nanoparticles as dual-modality cancer-targeted probes for image-guided surgery and interventions.

Michelle S Bradbury, Evan Phillips, Pablo H Montero, Sarah M Cheal, Hilda Stambuk, Jeremy C Durack, Constantinos T Sofocleous, Richard J C Meester, Ulrich Wiesner, Snehal Patel

Abstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 176 citations in OpenAlex.

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  10. Medical Imaging Technology and Imaging Agents.Advances in experimental medicine and biology · 2023
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  15. Physiological and Pathological Factors Affecting Drug Delivery to the Brain by Nanoparticles.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
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12 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

10 authors at 3 institutions in 1 country.

Michelle S BradburyDepartment of Radiology, Sloan Kettering Institute for Cancer Research, 1275 York Ave., Z-2001, New York, NY 10065, USA. bradburm@mskcc.org
Evan Phillips
Pablo H Montero
Sarah M Cheal
Hilda Stambuk
Jeremy C Durack
Constantinos T Sofocleous
Richard J C Meester
Ulrich Wiesner
Snehal Patel
In-Q-Tel · USKettering University · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Renally Excreted Multimodal Core-Shell Silica Nanoparticles as Tumor-Selective RaR01CA161280 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BRADBURY, MICHELLE S, WIESNER, ULRICH · 2012 to 2016
$2.7M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA08748NCI NIH HHS R01 CA161280
6 · The paper itself

Abstract

Early diagnosis and treatment of melanoma are essential to minimizing morbidity and mortality. The presence of lymph node metastases is a vital prognostic predictor, and accurate identification by imaging has important implications for disease staging, prognosis, and clinical outcome. Sentinel lymph node (SLN) mapping procedures are limited by a lack of intraoperative visualization tools that can aid accurate determination of disease spread and delineate nodes from adjacent critical neural and vascular structures. Newer methods for circumventing these issues can exploit a variety of imaging tools, including biocompatible particle-based platforms coupled with portable device technologies for use with image-guided surgical and interventional procedures. We describe herein a clinically-translated, integrin-targeting platform for use with both PET and optical imaging that meets a number of key design criteria for improving SLN tissue localization and retention, target-to-background ratios, and clearance from the site of injection and the body. The use of such agents for selectively probing critical cancer targets may elucidate important insights into cellular and molecular processes that govern metastatic disease spread. Coupled with portable, real-time optical camera systems, we show that pre-operative PET imaging findings for mapping metastatic disease in clinically-relevant larger-animal models can be readily translated into the intraoperative setting for direct visualization of the draining tumor lymphatics and fluorescent SLN/s with histologic correlation. The specificity of this platform, relative to the standard-of-care radiotracer, (18)F-FDG, for potentially discriminating metastatic disease from inflammatory processes is also discussed in the setting of surgically-based or interventionally-driven therapies.

Indexed as

NanocapsulesSubtraction TechniqueAnimalsContrast MediaHumansNeoplasmsPositron-Emission TomographySilicon DioxideSurgery, Computer-AssistedContrast MediaNanocapsulesSilicon Dioxide

Identifiers

PMID23138852
PMCPMC4428677
OpenAlexW2156069838

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.