Increased lymphocyte infiltration in patients with head and neck cancer treated with the IRX-2 immunotherapy regimen
Identifieur interne : 000567 ( France/Analysis ); précédent : 000566; suivant : 000568Increased lymphocyte infiltration in patients with head and neck cancer treated with the IRX-2 immunotherapy regimen
Auteurs : Neil L. Berinstein [États-Unis] ; Gregory T. Wolf [États-Unis] ; Paul H. Naylor [États-Unis] ; Lorraine Baltzer [États-Unis] ; James E. Egan [États-Unis] ; Harvey J. Brandwein [États-Unis] ; Theresa L. Whiteside [États-Unis] ; Lynn C. Goldstein [États-Unis] ; Adel El-Naggar [États-Unis] ; Cecile Badoual [France] ; Wolf-Herve Fridman [France] ; J. Michael White [États-Unis] ; John W. Hadden [États-Unis]Source :
- Cancer immunology and immunotherapy [ 0340-7004 ] ; 2012.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
Abstract
Twenty-seven subjects with squamous cell cancer of the head and neck received the neoadjuvant IRX-2 immunotherapy regimen prior to surgery in a Phase 2 trial. Pretreatment tumor biopsies were compared with the primary tumor surgical specimens for lymphocyte infiltration, necrosis and fibrosis, using hematoxylin and eosin stain and immunohistochemistry in 25 subjects. Sections were examined by three pathologists. Relative to pretreatment biopsies, increases in lymphocyte infiltration (LI) were seen using H and E or immunohistochemistry. CD3+ CD4+ T cells and CD20+ B cells were primarily found in the peritumoral stroma and CD3+ CD8+ T cells and CD68+ macrophages were mainly intratumoral. LI in the surgical specimens were associated with reductions in the primary tumor size. Improved survival at 5 years was correlated with high overall LI in the tumor specimens. Neoadjuvant IRX-2 immunotherapy regimen may restore immune responsiveness presumably by mobilizing tumor infiltrating effector lymphocytes and macrophages into the tumor.
Affiliations:
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Pascal:12-0259414Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Increased lymphocyte infiltration in patients with head and neck cancer treated with the IRX-2 immunotherapy regimen</title>
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<series><title level="j" type="main">Cancer immunology and immunotherapy</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antigen presenting cell</term>
<term>Cytokine</term>
<term>Dendritic cell</term>
<term>Head and neck cancer</term>
<term>Human</term>
<term>Immunotherapy</term>
<term>Infiltration</term>
<term>Lymphocyte</term>
<term>Macrophage</term>
<term>Monocyte</term>
<term>Patient</term>
<term>Therapeutic protocol</term>
<term>Treatment</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Lymphocyte</term>
<term>Infiltration</term>
<term>Homme</term>
<term>Malade</term>
<term>Cancer de la tête et du cou</term>
<term>Traitement</term>
<term>Immunothérapie</term>
<term>Protocole thérapeutique</term>
<term>Monocyte</term>
<term>Macrophage</term>
<term>Cellule dendritique</term>
<term>Cellule APC</term>
<term>Cytokine</term>
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<front><div type="abstract" xml:lang="en">Twenty-seven subjects with squamous cell cancer of the head and neck received the neoadjuvant IRX-2 immunotherapy regimen prior to surgery in a Phase 2 trial. Pretreatment tumor biopsies were compared with the primary tumor surgical specimens for lymphocyte infiltration, necrosis and fibrosis, using hematoxylin and eosin stain and immunohistochemistry in 25 subjects. Sections were examined by three pathologists. Relative to pretreatment biopsies, increases in lymphocyte infiltration (LI) were seen using H and E or immunohistochemistry. CD3+ CD4+ T cells and CD20+ B cells were primarily found in the peritumoral stroma and CD3+ CD8<sub>+</sub>
T cells and CD68+ macrophages were mainly intratumoral. LI in the surgical specimens were associated with reductions in the primary tumor size. Improved survival at 5 years was correlated with high overall LI in the tumor specimens. Neoadjuvant IRX-2 immunotherapy regimen may restore immune responsiveness presumably by mobilizing tumor infiltrating effector lymphocytes and macrophages into the tumor.</div>
</front>
</TEI>
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<li>États-Unis</li>
</country>
<region><li>Pennsylvanie</li>
<li>Île-de-France</li>
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<settlement><li>Paris</li>
<li>Pittsburgh</li>
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<tree><country name="États-Unis"><noRegion><name sortKey="Berinstein, Neil L" sort="Berinstein, Neil L" uniqKey="Berinstein N" first="Neil L." last="Berinstein">Neil L. Berinstein</name>
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<name sortKey="Egan, James E" sort="Egan, James E" uniqKey="Egan J" first="James E." last="Egan">James E. Egan</name>
<name sortKey="El Naggar, Adel" sort="El Naggar, Adel" uniqKey="El Naggar A" first="Adel" last="El-Naggar">Adel El-Naggar</name>
<name sortKey="Goldstein, Lynn C" sort="Goldstein, Lynn C" uniqKey="Goldstein L" first="Lynn C." last="Goldstein">Lynn C. Goldstein</name>
<name sortKey="Hadden, John W" sort="Hadden, John W" uniqKey="Hadden J" first="John W." last="Hadden">John W. Hadden</name>
<name sortKey="Michael White, J" sort="Michael White, J" uniqKey="Michael White J" first="J." last="Michael White">J. Michael White</name>
<name sortKey="Naylor, Paul H" sort="Naylor, Paul H" uniqKey="Naylor P" first="Paul H." last="Naylor">Paul H. Naylor</name>
<name sortKey="Whiteside, Theresa L" sort="Whiteside, Theresa L" uniqKey="Whiteside T" first="Theresa L." last="Whiteside">Theresa L. Whiteside</name>
<name sortKey="Wolf, Gregory T" sort="Wolf, Gregory T" uniqKey="Wolf G" first="Gregory T." last="Wolf">Gregory T. Wolf</name>
</country>
<country name="France"><region name="Île-de-France"><name sortKey="Badoual, Cecile" sort="Badoual, Cecile" uniqKey="Badoual C" first="Cecile" last="Badoual">Cecile Badoual</name>
</region>
<name sortKey="Fridman, Wolf Herve" sort="Fridman, Wolf Herve" uniqKey="Fridman W" first="Wolf-Herve" last="Fridman">Wolf-Herve Fridman</name>
</country>
</tree>
</affiliations>
</record>
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