Combination therapy of in vitro‐expanded natural killer T cells and α‐galactosylceramide‐pulsed antigen‐presenting cells in patients with recurrent head and neck carcinoma
The aim of this clinical trial was to investigate the feasibility of intra‐arterial infusion of in vitro‐expanded Vα24 natural killer T (NKT) cells combined with submucosal injection of α‐galactosylceramide (KRN7000; αGalCer)‐pulsed antigen‐presenting cells (APC). A phase I clinical study was carrie...
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creator | Kunii, Naoki Horiguchi, Shigetoshi Motohashi, Shinichiro Yamamoto, Heizaburo Ueno, Naoyuki Yamamoto, Seiji Sakurai, Daiju Taniguchi, Masaru Nakayama, Toshinori Okamoto, Yoshitaka |
description | The aim of this clinical trial was to investigate the feasibility of intra‐arterial infusion of in vitro‐expanded Vα24 natural killer T (NKT) cells combined with submucosal injection of α‐galactosylceramide (KRN7000; αGalCer)‐pulsed antigen‐presenting cells (APC). A phase I clinical study was carried out in patients with head and neck squamous cell carcinoma (HNSCC). Patients with locally recurrent HNSCC refractory to standard therapy were eligible. Eight patients received super‐selective transcatheter intra‐arterial infusion of activated Vα24 NKT cells into tumor‐feeding arteries and nasal submucosal injections of αGalCer‐pulsed APC twice with a 1‐week interval. Vα24 NKT cell‐specific immune responses, safety, and antitumor effects were evaluated. The number of Vα24 NKT cells and interferon‐γ‐producing cells in peripheral blood mononuclear cells increased in seven out of eight patients enrolled. Grade 3 toxicity with a pharyngocutaneous fistula related to local tumor reduction was observed in one patient and mild adverse events with grade 1–2 symptoms occurred in seven patients. Regarding the clinical responses, three cases exhibited a partial but significant response, four were classified as stable disease, and one patient continued to develop progressive disease. The use of the intra‐arterial infusion of activated Vα24 NKT cells and the submucosal injection of αGalCer‐pulsed APC has been shown to induce significant antitumor immunity and had beneficial clinical effects in the management of advanced HNSCC. The use of such therapeutic modalities may be helpful in the management of tumors and therefore needs to be explored in further detail. The clinical trial registration number was UMIN000000722. (Cancer Sci 2009; 100: 1092–1098) |
doi_str_mv | 10.1111/j.1349-7006.2009.01135.x |
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A phase I clinical study was carried out in patients with head and neck squamous cell carcinoma (HNSCC). Patients with locally recurrent HNSCC refractory to standard therapy were eligible. Eight patients received super‐selective transcatheter intra‐arterial infusion of activated Vα24 NKT cells into tumor‐feeding arteries and nasal submucosal injections of αGalCer‐pulsed APC twice with a 1‐week interval. Vα24 NKT cell‐specific immune responses, safety, and antitumor effects were evaluated. The number of Vα24 NKT cells and interferon‐γ‐producing cells in peripheral blood mononuclear cells increased in seven out of eight patients enrolled. Grade 3 toxicity with a pharyngocutaneous fistula related to local tumor reduction was observed in one patient and mild adverse events with grade 1–2 symptoms occurred in seven patients. Regarding the clinical responses, three cases exhibited a partial but significant response, four were classified as stable disease, and one patient continued to develop progressive disease. The use of the intra‐arterial infusion of activated Vα24 NKT cells and the submucosal injection of αGalCer‐pulsed APC has been shown to induce significant antitumor immunity and had beneficial clinical effects in the management of advanced HNSCC. The use of such therapeutic modalities may be helpful in the management of tumors and therefore needs to be explored in further detail. The clinical trial registration number was UMIN000000722. (Cancer Sci 2009; 100: 1092–1098)</description><identifier>ISSN: 1347-9032</identifier><identifier>ISSN: 1349-7006</identifier><identifier>EISSN: 1349-7006</identifier><identifier>DOI: 10.1111/j.1349-7006.2009.01135.x</identifier><identifier>PMID: 19302288</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Combined Modality Therapy ; Dendritic Cells - immunology ; Female ; Flow Cytometry ; Galactosylceramides - immunology ; Galactosylceramides - therapeutic use ; Head and Neck Neoplasms - immunology ; Head and Neck Neoplasms - radiotherapy ; Head and Neck Neoplasms - surgery ; Humans ; Killer Cells, Natural - immunology ; Killer Cells, Natural - transplantation ; Lymphocyte Activation ; Male ; Medical sciences ; Middle Aged ; Neoplasm Recurrence, Local - immunology ; Neoplasm Recurrence, Local - radiotherapy ; Neoplasm Recurrence, Local - surgery ; Original ; Otorhinolaryngology (head neck, general aspects and miscellaneous) ; Otorhinolaryngology. Stomatology ; Patient Selection ; Tumors</subject><ispartof>Cancer science, 2009-06, Vol.100 (6), p.1092-1098</ispartof><rights>2009 Japanese Cancer Association</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5875-5360466ffddfcbea63b95759dfeeacc0d27f3efd86dc6a699899d3e558474a0d3</citedby><cites>FETCH-LOGICAL-c5875-5360466ffddfcbea63b95759dfeeacc0d27f3efd86dc6a699899d3e558474a0d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11158111/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11158111/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1349-7006.2009.01135.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21487805$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19302288$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kunii, Naoki</creatorcontrib><creatorcontrib>Horiguchi, Shigetoshi</creatorcontrib><creatorcontrib>Motohashi, Shinichiro</creatorcontrib><creatorcontrib>Yamamoto, Heizaburo</creatorcontrib><creatorcontrib>Ueno, Naoyuki</creatorcontrib><creatorcontrib>Yamamoto, Seiji</creatorcontrib><creatorcontrib>Sakurai, Daiju</creatorcontrib><creatorcontrib>Taniguchi, Masaru</creatorcontrib><creatorcontrib>Nakayama, Toshinori</creatorcontrib><creatorcontrib>Okamoto, Yoshitaka</creatorcontrib><title>Combination therapy of in vitro‐expanded natural killer T cells and α‐galactosylceramide‐pulsed antigen‐presenting cells in patients with recurrent head and neck carcinoma</title><title>Cancer science</title><addtitle>Cancer Sci</addtitle><description>The aim of this clinical trial was to investigate the feasibility of intra‐arterial infusion of in vitro‐expanded Vα24 natural killer T (NKT) cells combined with submucosal injection of α‐galactosylceramide (KRN7000; αGalCer)‐pulsed antigen‐presenting cells (APC). A phase I clinical study was carried out in patients with head and neck squamous cell carcinoma (HNSCC). Patients with locally recurrent HNSCC refractory to standard therapy were eligible. Eight patients received super‐selective transcatheter intra‐arterial infusion of activated Vα24 NKT cells into tumor‐feeding arteries and nasal submucosal injections of αGalCer‐pulsed APC twice with a 1‐week interval. Vα24 NKT cell‐specific immune responses, safety, and antitumor effects were evaluated. The number of Vα24 NKT cells and interferon‐γ‐producing cells in peripheral blood mononuclear cells increased in seven out of eight patients enrolled. Grade 3 toxicity with a pharyngocutaneous fistula related to local tumor reduction was observed in one patient and mild adverse events with grade 1–2 symptoms occurred in seven patients. Regarding the clinical responses, three cases exhibited a partial but significant response, four were classified as stable disease, and one patient continued to develop progressive disease. The use of the intra‐arterial infusion of activated Vα24 NKT cells and the submucosal injection of αGalCer‐pulsed APC has been shown to induce significant antitumor immunity and had beneficial clinical effects in the management of advanced HNSCC. The use of such therapeutic modalities may be helpful in the management of tumors and therefore needs to be explored in further detail. The clinical trial registration number was UMIN000000722. (Cancer Sci 2009; 100: 1092–1098)</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Combined Modality Therapy</subject><subject>Dendritic Cells - immunology</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Galactosylceramides - immunology</subject><subject>Galactosylceramides - therapeutic use</subject><subject>Head and Neck Neoplasms - immunology</subject><subject>Head and Neck Neoplasms - radiotherapy</subject><subject>Head and Neck Neoplasms - surgery</subject><subject>Humans</subject><subject>Killer Cells, Natural - immunology</subject><subject>Killer Cells, Natural - transplantation</subject><subject>Lymphocyte Activation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - immunology</subject><subject>Neoplasm Recurrence, Local - radiotherapy</subject><subject>Neoplasm Recurrence, Local - surgery</subject><subject>Original</subject><subject>Otorhinolaryngology (head neck, general aspects and miscellaneous)</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Patient Selection</subject><subject>Tumors</subject><issn>1347-9032</issn><issn>1349-7006</issn><issn>1349-7006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk-O0zAUxiMEYobCFZA3sEtw4jixFwiNKv5JI7FgWFuu_dK6k9jBTmbaHUfgCFyBBRfgAByCk-C0UYEVeBHb7_3el_fkL0lQjrM8rmfbLCclT2uMq6zAmGc4zwnNdneS81Pi7uFcpxyT4ix5EMIWY1KVvLyfnOWc4KJg7Dz5tnTdylg5GGfRsAEv-z1yDTL2-5cbM3j389Nn2PXSatAoYqOXLbo2bQseXSEFbRtQTKIfXyO4lq1Ugwv7VkWhzmiIwX5sQ6yVdjBrsFPAQ4B4s-u53ljUxwZiLKBbM2yQBzV6H-9oA1If9C2oa6SkV8a6Tj5M7jUyyj6a90Xy4dXLq-Wb9PLd67fLi8tUUVbTlJIKl1XVNFo3agWyIitOa8p1AyCVwrqoGwKNZpVWlaw4Z5xrApSysi4l1mSRvDjq9uOqA61iS3F-0XvTSb8XThrxd8aajVi7GxEfibL4iQpPZwXvPo4QBtGZMI0tLbgxiKompCgZ-SdYYMpzGp9wkbAjqLwLwUNzaifH039zsRWTCcRkAjG5QxzcIXax9PGf4_wunO0QgSczIIOSbeOlVSacuCIvWc0wjdzzI3drWtj_dwNiefF-OpFfBcTh7g</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Kunii, Naoki</creator><creator>Horiguchi, Shigetoshi</creator><creator>Motohashi, Shinichiro</creator><creator>Yamamoto, Heizaburo</creator><creator>Ueno, Naoyuki</creator><creator>Yamamoto, Seiji</creator><creator>Sakurai, Daiju</creator><creator>Taniguchi, Masaru</creator><creator>Nakayama, Toshinori</creator><creator>Okamoto, Yoshitaka</creator><general>Blackwell Publishing Asia</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200906</creationdate><title>Combination therapy of in vitro‐expanded natural killer T cells and α‐galactosylceramide‐pulsed antigen‐presenting cells in patients with recurrent head and neck carcinoma</title><author>Kunii, Naoki ; Horiguchi, Shigetoshi ; Motohashi, Shinichiro ; Yamamoto, Heizaburo ; Ueno, Naoyuki ; Yamamoto, Seiji ; Sakurai, Daiju ; Taniguchi, Masaru ; Nakayama, Toshinori ; Okamoto, Yoshitaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5875-5360466ffddfcbea63b95759dfeeacc0d27f3efd86dc6a699899d3e558474a0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Combined Modality Therapy</topic><topic>Dendritic Cells - immunology</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Galactosylceramides - immunology</topic><topic>Galactosylceramides - therapeutic use</topic><topic>Head and Neck Neoplasms - immunology</topic><topic>Head and Neck Neoplasms - radiotherapy</topic><topic>Head and Neck Neoplasms - surgery</topic><topic>Humans</topic><topic>Killer Cells, Natural - immunology</topic><topic>Killer Cells, Natural - transplantation</topic><topic>Lymphocyte Activation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - immunology</topic><topic>Neoplasm Recurrence, Local - radiotherapy</topic><topic>Neoplasm Recurrence, Local - surgery</topic><topic>Original</topic><topic>Otorhinolaryngology (head neck, general aspects and miscellaneous)</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Patient Selection</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kunii, Naoki</creatorcontrib><creatorcontrib>Horiguchi, Shigetoshi</creatorcontrib><creatorcontrib>Motohashi, Shinichiro</creatorcontrib><creatorcontrib>Yamamoto, Heizaburo</creatorcontrib><creatorcontrib>Ueno, Naoyuki</creatorcontrib><creatorcontrib>Yamamoto, Seiji</creatorcontrib><creatorcontrib>Sakurai, Daiju</creatorcontrib><creatorcontrib>Taniguchi, Masaru</creatorcontrib><creatorcontrib>Nakayama, Toshinori</creatorcontrib><creatorcontrib>Okamoto, Yoshitaka</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Kunii, Naoki</au><au>Horiguchi, Shigetoshi</au><au>Motohashi, Shinichiro</au><au>Yamamoto, Heizaburo</au><au>Ueno, Naoyuki</au><au>Yamamoto, Seiji</au><au>Sakurai, Daiju</au><au>Taniguchi, Masaru</au><au>Nakayama, Toshinori</au><au>Okamoto, Yoshitaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combination therapy of in vitro‐expanded natural killer T cells and α‐galactosylceramide‐pulsed antigen‐presenting cells in patients with recurrent head and neck carcinoma</atitle><jtitle>Cancer science</jtitle><addtitle>Cancer Sci</addtitle><date>2009-06</date><risdate>2009</risdate><volume>100</volume><issue>6</issue><spage>1092</spage><epage>1098</epage><pages>1092-1098</pages><issn>1347-9032</issn><issn>1349-7006</issn><eissn>1349-7006</eissn><abstract>The aim of this clinical trial was to investigate the feasibility of intra‐arterial infusion of in vitro‐expanded Vα24 natural killer T (NKT) cells combined with submucosal injection of α‐galactosylceramide (KRN7000; αGalCer)‐pulsed antigen‐presenting cells (APC). A phase I clinical study was carried out in patients with head and neck squamous cell carcinoma (HNSCC). Patients with locally recurrent HNSCC refractory to standard therapy were eligible. Eight patients received super‐selective transcatheter intra‐arterial infusion of activated Vα24 NKT cells into tumor‐feeding arteries and nasal submucosal injections of αGalCer‐pulsed APC twice with a 1‐week interval. Vα24 NKT cell‐specific immune responses, safety, and antitumor effects were evaluated. The number of Vα24 NKT cells and interferon‐γ‐producing cells in peripheral blood mononuclear cells increased in seven out of eight patients enrolled. Grade 3 toxicity with a pharyngocutaneous fistula related to local tumor reduction was observed in one patient and mild adverse events with grade 1–2 symptoms occurred in seven patients. Regarding the clinical responses, three cases exhibited a partial but significant response, four were classified as stable disease, and one patient continued to develop progressive disease. The use of the intra‐arterial infusion of activated Vα24 NKT cells and the submucosal injection of αGalCer‐pulsed APC has been shown to induce significant antitumor immunity and had beneficial clinical effects in the management of advanced HNSCC. The use of such therapeutic modalities may be helpful in the management of tumors and therefore needs to be explored in further detail. The clinical trial registration number was UMIN000000722. (Cancer Sci 2009; 100: 1092–1098)</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>19302288</pmid><doi>10.1111/j.1349-7006.2009.01135.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biological and medical sciences Combined Modality Therapy Dendritic Cells - immunology Female Flow Cytometry Galactosylceramides - immunology Galactosylceramides - therapeutic use Head and Neck Neoplasms - immunology Head and Neck Neoplasms - radiotherapy Head and Neck Neoplasms - surgery Humans Killer Cells, Natural - immunology Killer Cells, Natural - transplantation Lymphocyte Activation Male Medical sciences Middle Aged Neoplasm Recurrence, Local - immunology Neoplasm Recurrence, Local - radiotherapy Neoplasm Recurrence, Local - surgery Original Otorhinolaryngology (head neck, general aspects and miscellaneous) Otorhinolaryngology. Stomatology Patient Selection Tumors |
title | Combination therapy of in vitro‐expanded natural killer T cells and α‐galactosylceramide‐pulsed antigen‐presenting cells in patients with recurrent head and neck carcinoma |
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