Neoadjuvant Talimogene Laherparepvec for the Treatment of Metastatic Melanoma
Wide local excision of the left ear melanoma was performed with a 2-cm margin of resection along with sentinel lymph node biopsy of two level II cervical nodes. Postoperatively, positron emission tomography-computed tomography (PET-CT) was notable for new hypermetabolic lymphadenopathy in the poster...
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description | Wide local excision of the left ear melanoma was performed with a 2-cm margin of resection along with sentinel lymph node biopsy of two level II cervical nodes. Postoperatively, positron emission tomography-computed tomography (PET-CT) was notable for new hypermetabolic lymphadenopathy in the posterior cervical triangle as well as an FDG avid nodular soft tissue density anterior to the parotid gland; both of which were felt to represent recurrent disease. After lengthy discussions with the patient along with multidisciplinary conference consultation, the patient was screened and enrolled into the neoadjuvant T-VEC trial (NCT02211131) comparing neoadjuvant intralesional T-VEC followed by surgery to surgery alone for patients with stage IIIB-IVM1a metastatic melanoma. The virus has been altered by functionally deleting the nonessential ICP34.5 and ICP47 virulence genes thus limiting the virus's effect on human cells and increasing its ability for replication and tumor cell lysis.2 When combined with the insertion and encoding of the GM-CSF gene, this leads to both an immunogenic and viral oncolytic effect on melanoma cells (Fig. 2). In 2006, results were published from a Phase I study of an oncolytic HSV-1-expressing GM-CSF (OncoVEXGM-CSF) administered via intratumoral injection in patients with refractory cutaneous/subcutaneous breast, head and neck, gastrointestinal, or melanoma metastases.3 Of the nine patients with melanoma included in the study, five had flattening or shrinkage of the injected lesion with treatment and four had evidence of tumor necrosis on biopsy. The treatment was generally well tolerated, even with multiple treatments, with the most common adverse reactions being local inflammatory... |
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Postoperatively, positron emission tomography-computed tomography (PET-CT) was notable for new hypermetabolic lymphadenopathy in the posterior cervical triangle as well as an FDG avid nodular soft tissue density anterior to the parotid gland; both of which were felt to represent recurrent disease. After lengthy discussions with the patient along with multidisciplinary conference consultation, the patient was screened and enrolled into the neoadjuvant T-VEC trial (NCT02211131) comparing neoadjuvant intralesional T-VEC followed by surgery to surgery alone for patients with stage IIIB-IVM1a metastatic melanoma. The virus has been altered by functionally deleting the nonessential ICP34.5 and ICP47 virulence genes thus limiting the virus's effect on human cells and increasing its ability for replication and tumor cell lysis.2 When combined with the insertion and encoding of the GM-CSF gene, this leads to both an immunogenic and viral oncolytic effect on melanoma cells (Fig. 2). In 2006, results were published from a Phase I study of an oncolytic HSV-1-expressing GM-CSF (OncoVEXGM-CSF) administered via intratumoral injection in patients with refractory cutaneous/subcutaneous breast, head and neck, gastrointestinal, or melanoma metastases.3 Of the nine patients with melanoma included in the study, five had flattening or shrinkage of the injected lesion with treatment and four had evidence of tumor necrosis on biopsy. The treatment was generally well tolerated, even with multiple treatments, with the most common adverse reactions being local inflammatory...</description><identifier>ISSN: 0003-1348</identifier><identifier>EISSN: 1555-9823</identifier><identifier>DOI: 10.1177/000313481708300720</identifier><identifier>PMID: 28738934</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Cancer surgery ; Clinical trials ; Drug therapy ; Granulocytes ; Herpesvirus 1, Human - immunology ; Humans ; Lymph Node Excision - methods ; Lymphatic Metastasis ; Lymphatic system ; Male ; Medical prognosis ; Melanoma ; Melanoma - diagnostic imaging ; Melanoma - drug therapy ; Melanoma - pathology ; Melanoma - surgery ; Metastases ; Metastasis ; Middle Aged ; Neck ; Neck Dissection - methods ; Neoadjuvant Therapy - methods ; Neoplasm Invasiveness - pathology ; Neoplasm Staging ; Oncolytic Virotherapy - methods ; Patients ; Positron Emission Tomography Computed Tomography ; Prognosis ; Risk Assessment ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - diagnostic imaging ; Skin Neoplasms - drug therapy ; Skin Neoplasms - pathology ; Skin Neoplasms - surgery ; Tomography ; Treatment Outcome ; Tumors</subject><ispartof>The American surgeon, 2017-07, Vol.83 (7), p.266-268</ispartof><rights>2017 Southeastern Surgical Congress</rights><rights>Copyright Southeastern Surgical Congress Jul 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-330d6b59ab9047dd4a867fe9a842f95bc3cc43c42d71bc230ca9da6004dec5bc3</citedby><cites>FETCH-LOGICAL-c415t-330d6b59ab9047dd4a867fe9a842f95bc3cc43c42d71bc230ca9da6004dec5bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/000313481708300720$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/000313481708300720$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21818,27923,27924,43620,43621</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28738934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stiles, Zachary E.</creatorcontrib><creatorcontrib>Fleming, Martin D.</creatorcontrib><creatorcontrib>Luce, Edward A.</creatorcontrib><creatorcontrib>Deneve, Jeremiah L.</creatorcontrib><title>Neoadjuvant Talimogene Laherparepvec for the Treatment of Metastatic Melanoma</title><title>The American surgeon</title><addtitle>Am Surg</addtitle><description>Wide local excision of the left ear melanoma was performed with a 2-cm margin of resection along with sentinel lymph node biopsy of two level II cervical nodes. Postoperatively, positron emission tomography-computed tomography (PET-CT) was notable for new hypermetabolic lymphadenopathy in the posterior cervical triangle as well as an FDG avid nodular soft tissue density anterior to the parotid gland; both of which were felt to represent recurrent disease. After lengthy discussions with the patient along with multidisciplinary conference consultation, the patient was screened and enrolled into the neoadjuvant T-VEC trial (NCT02211131) comparing neoadjuvant intralesional T-VEC followed by surgery to surgery alone for patients with stage IIIB-IVM1a metastatic melanoma. The virus has been altered by functionally deleting the nonessential ICP34.5 and ICP47 virulence genes thus limiting the virus's effect on human cells and increasing its ability for replication and tumor cell lysis.2 When combined with the insertion and encoding of the GM-CSF gene, this leads to both an immunogenic and viral oncolytic effect on melanoma cells (Fig. 2). In 2006, results were published from a Phase I study of an oncolytic HSV-1-expressing GM-CSF (OncoVEXGM-CSF) administered via intratumoral injection in patients with refractory cutaneous/subcutaneous breast, head and neck, gastrointestinal, or melanoma metastases.3 Of the nine patients with melanoma included in the study, five had flattening or shrinkage of the injected lesion with treatment and four had evidence of tumor necrosis on biopsy. The treatment was generally well tolerated, even with multiple treatments, with the most common adverse reactions being local inflammatory...</description><subject>Cancer surgery</subject><subject>Clinical trials</subject><subject>Drug therapy</subject><subject>Granulocytes</subject><subject>Herpesvirus 1, Human - immunology</subject><subject>Humans</subject><subject>Lymph Node Excision - methods</subject><subject>Lymphatic Metastasis</subject><subject>Lymphatic system</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Melanoma</subject><subject>Melanoma - diagnostic imaging</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - pathology</subject><subject>Melanoma - surgery</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neck</subject><subject>Neck Dissection - methods</subject><subject>Neoadjuvant Therapy - methods</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Neoplasm Staging</subject><subject>Oncolytic Virotherapy - methods</subject><subject>Patients</subject><subject>Positron Emission Tomography Computed Tomography</subject><subject>Prognosis</subject><subject>Risk Assessment</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - diagnostic imaging</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - surgery</subject><subject>Tomography</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0003-1348</issn><issn>1555-9823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kMtOwzAQRS0EoqXwAyxQJDZsQu3YeS1RxUtqYVPW0cSetKmSuNhOJf4eRy0IgVjNjObMnatLyCWjt4yl6ZRSyhkXGUtpxilNI3pExiyO4zDPIn5MxgMQDsSInFm78aNIYnZKRlGW8iznYkwWL6hBbfoddC5YQlO3eoUdBnNYo9mCwe0OZVBpE7g1BkuD4Fr0qK6CBTqwDlwtfdtAp1s4JycVNBYvDnVC3h7ul7OncP76-Dy7m4dSsNiFnFOVlHEOZU5FqpSALEkrzCETUZXHpeRSCi5FpFJWyohTCbmCxNtXKIf1hNzsdbdGv_doXdHWVmLjXaDubcHyiDOfRMI8ev0L3ejedN7dQCUxpxmjnor2lDTaWoNVsTV1C-ajYLQYwi7-hu2Prg7Sfdmi-j75StcD0z1gYYU__v4v-QkQQIZd</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Stiles, Zachary E.</creator><creator>Fleming, Martin D.</creator><creator>Luce, Edward A.</creator><creator>Deneve, Jeremiah L.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><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>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7QL</scope><scope>7RV</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>201707</creationdate><title>Neoadjuvant Talimogene Laherparepvec for the Treatment of Metastatic Melanoma</title><author>Stiles, Zachary E. ; Fleming, Martin D. ; Luce, Edward A. ; Deneve, Jeremiah L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-330d6b59ab9047dd4a867fe9a842f95bc3cc43c42d71bc230ca9da6004dec5bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cancer surgery</topic><topic>Clinical trials</topic><topic>Drug therapy</topic><topic>Granulocytes</topic><topic>Herpesvirus 1, Human - 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Academic</collection><jtitle>The American surgeon</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stiles, Zachary E.</au><au>Fleming, Martin D.</au><au>Luce, Edward A.</au><au>Deneve, Jeremiah L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neoadjuvant Talimogene Laherparepvec for the Treatment of Metastatic Melanoma</atitle><jtitle>The American surgeon</jtitle><addtitle>Am Surg</addtitle><date>2017-07</date><risdate>2017</risdate><volume>83</volume><issue>7</issue><spage>266</spage><epage>268</epage><pages>266-268</pages><issn>0003-1348</issn><eissn>1555-9823</eissn><abstract>Wide local excision of the left ear melanoma was performed with a 2-cm margin of resection along with sentinel lymph node biopsy of two level II cervical nodes. Postoperatively, positron emission tomography-computed tomography (PET-CT) was notable for new hypermetabolic lymphadenopathy in the posterior cervical triangle as well as an FDG avid nodular soft tissue density anterior to the parotid gland; both of which were felt to represent recurrent disease. After lengthy discussions with the patient along with multidisciplinary conference consultation, the patient was screened and enrolled into the neoadjuvant T-VEC trial (NCT02211131) comparing neoadjuvant intralesional T-VEC followed by surgery to surgery alone for patients with stage IIIB-IVM1a metastatic melanoma. The virus has been altered by functionally deleting the nonessential ICP34.5 and ICP47 virulence genes thus limiting the virus's effect on human cells and increasing its ability for replication and tumor cell lysis.2 When combined with the insertion and encoding of the GM-CSF gene, this leads to both an immunogenic and viral oncolytic effect on melanoma cells (Fig. 2). In 2006, results were published from a Phase I study of an oncolytic HSV-1-expressing GM-CSF (OncoVEXGM-CSF) administered via intratumoral injection in patients with refractory cutaneous/subcutaneous breast, head and neck, gastrointestinal, or melanoma metastases.3 Of the nine patients with melanoma included in the study, five had flattening or shrinkage of the injected lesion with treatment and four had evidence of tumor necrosis on biopsy. The treatment was generally well tolerated, even with multiple treatments, with the most common adverse reactions being local inflammatory...</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>28738934</pmid><doi>10.1177/000313481708300720</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cancer surgery Clinical trials Drug therapy Granulocytes Herpesvirus 1, Human - immunology Humans Lymph Node Excision - methods Lymphatic Metastasis Lymphatic system Male Medical prognosis Melanoma Melanoma - diagnostic imaging Melanoma - drug therapy Melanoma - pathology Melanoma - surgery Metastases Metastasis Middle Aged Neck Neck Dissection - methods Neoadjuvant Therapy - methods Neoplasm Invasiveness - pathology Neoplasm Staging Oncolytic Virotherapy - methods Patients Positron Emission Tomography Computed Tomography Prognosis Risk Assessment Sentinel Lymph Node Biopsy Skin Neoplasms - diagnostic imaging Skin Neoplasms - drug therapy Skin Neoplasms - pathology Skin Neoplasms - surgery Tomography Treatment Outcome Tumors |
title | Neoadjuvant Talimogene Laherparepvec for the Treatment of Metastatic Melanoma |
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