Toward nodal staging of axillary lymph node basins through intradermal administration of fluorescent imaging agents
Identifieur interne : 001E93 ( Pmc/Checkpoint ); précédent : 001E92; suivant : 001E94Toward nodal staging of axillary lymph node basins through intradermal administration of fluorescent imaging agents
Auteurs : Funda Meric-Bernstam [États-Unis] ; John C. Rasmussen [États-Unis] ; Savitri Krishnamurthy [États-Unis] ; I-Chih Tan [États-Unis] ; Banghe Zhu [États-Unis] ; Jamie L. Wagner [États-Unis] ; Gildy V. Babiera [États-Unis] ; Elizabeth A. Mittendorf [États-Unis] ; Eva M. Sevick-Muraca [États-Unis]Source :
- Biomedical Optics Express [ 2156-7085 ] ; 2013.
Abstract
As part of a proof-of-concept study for future delivery of targeted near-infrared fluorescent (NIRF) tracers, we sought to assess the delivery of micrograms of indocyanine green to all the axillary lymph nodes following intraparenchymal breast injections and intradermal arm injections in 20 subjects with advanced breast carcinoma and undergoing complete axillary lymph node dissection. Lymphatic vessels and nodes were assessed
Url:
DOI: 10.1364/BOE.5.000183
PubMed: 24466486
PubMed Central: 3891331
Affiliations:
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Toward nodal staging of axillary lymph node basins through intradermal administration of fluorescent imaging agents</title>
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<series><title level="j">Biomedical Optics Express</title>
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<front><div type="abstract" xml:lang="en"><p>As part of a proof-of-concept study for future delivery of targeted near-infrared fluorescent (NIRF) tracers, we sought to assess the delivery of micrograms of indocyanine green to all the axillary lymph nodes following intraparenchymal breast injections and intradermal arm injections in 20 subjects with advanced breast carcinoma and undergoing complete axillary lymph node dissection. Lymphatic vessels and nodes were assessed <italic>in vivo</italic>
. <italic>Ex vivo</italic>
images demonstrated that 87% of excised lymph nodes, including 81% of tumor-positive lymph nodes, were fluorescent. Future clinical studies using microdose amounts of tumor-targeting NIRF contrast agents may demonstrate improved surgical intervention with reduced morbidity.</p>
</div>
</front>
</TEI>
<pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Biomed Opt Express</journal-id>
<journal-id journal-id-type="iso-abbrev">Biomed Opt Express</journal-id>
<journal-id journal-id-type="publisher-id">BOE</journal-id>
<journal-title-group><journal-title>Biomedical Optics Express</journal-title>
</journal-title-group>
<issn pub-type="epub">2156-7085</issn>
<publisher><publisher-name>Optical Society of America</publisher-name>
</publisher>
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<article-id pub-id-type="doi">10.1364/BOE.5.000183</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Optics in Cancer Research</subject>
</subj-group>
<subj-group subj-group-type="article-type"><subject>Research-Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Toward nodal staging of axillary lymph node basins through intradermal administration of fluorescent imaging agents</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Meric-Bernstam</surname>
<given-names>Funda</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff5"><sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Rasmussen</surname>
<given-names>John C.</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff5"><sup>5</sup>
</xref>
<xref ref-type="corresp" rid="cor1"><sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Krishnamurthy</surname>
<given-names>Savitri</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Tan</surname>
<given-names>I-Chih</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Zhu</surname>
<given-names>Banghe</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wagner</surname>
<given-names>Jamie L.</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Babiera</surname>
<given-names>Gildy V.</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Mittendorf</surname>
<given-names>Elizabeth A.</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sevick-Muraca</surname>
<given-names>Eva M.</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<aff id="aff1"><label>1</label>
Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030<country>USA</country>
</aff>
<aff id="aff2"><label>2</label>
Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030<country>USA</country>
</aff>
<aff id="aff3"><label>3</label>
Center for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine at the University of Texas Health Science Center at Houston, Houston, TX 77030<country>USA</country>
</aff>
<aff id="aff4"><label>4</label>
Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030<country>USA</country>
</aff>
<aff id="aff5"><label>5</label>
These authors contributed equally to this work</aff>
</contrib-group>
<author-notes><corresp id="cor1"><label>*</label>
<email xlink:href="john.rasmussen@uth.tmc.edu">john.rasmussen@uth.tmc.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="epub"><day>13</day>
<month>12</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="collection"><day>01</day>
<month>1</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>13</day>
<month>12</month>
<year>2013</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the
. </pmc-comment>
<volume>5</volume>
<issue>1</issue>
<fpage>183</fpage>
<lpage>196</lpage>
<history><date date-type="received"><day>30</day>
<month>8</month>
<year>2013</year>
</date>
<date date-type="rev-recd"><day>28</day>
<month>11</month>
<year>2013</year>
</date>
<date date-type="accepted"><day>04</day>
<month>12</month>
<year>2013</year>
</date>
</history>
<permissions><copyright-statement>© 2013 Optical Society of America</copyright-statement>
<copyright-year>2013</copyright-year>
<copyright-holder>Optical Society of America</copyright-holder>
</permissions>
<abstract><p>As part of a proof-of-concept study for future delivery of targeted near-infrared fluorescent (NIRF) tracers, we sought to assess the delivery of micrograms of indocyanine green to all the axillary lymph nodes following intraparenchymal breast injections and intradermal arm injections in 20 subjects with advanced breast carcinoma and undergoing complete axillary lymph node dissection. Lymphatic vessels and nodes were assessed <italic>in vivo</italic>
. <italic>Ex vivo</italic>
images demonstrated that 87% of excised lymph nodes, including 81% of tumor-positive lymph nodes, were fluorescent. Future clinical studies using microdose amounts of tumor-targeting NIRF contrast agents may demonstrate improved surgical intervention with reduced morbidity.</p>
</abstract>
<kwd-group kwd-group-type="OCIS"><title>OCIS codes: </title>
<kwd>(100.2960) Image analysis</kwd>
<kwd>(170.0110) Imaging systems</kwd>
<kwd>(170.1610) Clinical applications</kwd>
<kwd>(170.3880) Medical and biological imaging</kwd>
</kwd-group>
<funding-group><award-group id="sp1"><funding-source>National Center for Research Resources (NCRR)<named-content content-type="doi">10.13039/100000097</named-content>
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<award-id>3 UL1RR024148</award-id>
</award-group>
<award-group id="sp2"><funding-source>National Institutes of Health (NIH)<named-content content-type="doi">10.13039/100000002</named-content>
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<award-id>U54 CA136404</award-id>
</award-group>
<award-group id="sp3"><funding-source>The Univeristy of Texas MD Anderson Cancer Center Support Grant</funding-source>
<award-id>P30 CA016672</award-id>
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</article-meta>
</front>
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<affiliations><list><country><li>États-Unis</li>
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<tree><country name="États-Unis"><noRegion><name sortKey="Meric Bernstam, Funda" sort="Meric Bernstam, Funda" uniqKey="Meric Bernstam F" first="Funda" last="Meric-Bernstam">Funda Meric-Bernstam</name>
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<name sortKey="Tan, I Chih" sort="Tan, I Chih" uniqKey="Tan I" first="I-Chih" last="Tan">I-Chih Tan</name>
<name sortKey="Wagner, Jamie L" sort="Wagner, Jamie L" uniqKey="Wagner J" first="Jamie L." last="Wagner">Jamie L. Wagner</name>
<name sortKey="Zhu, Banghe" sort="Zhu, Banghe" uniqKey="Zhu B" first="Banghe" last="Zhu">Banghe Zhu</name>
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