Management of side effects of immune checkpoint blockade by anti-CTLA-4 and anti-PD-1 antibodies in metastatic melanoma
Summary CTLA‐4 and PD‐1 are potential targets for tumor‐induced downregulation of lymphocytic immune responses. Immune checkpoint‐modifying monoclonal antibodies oppose these effects, inducing T cell‐mediated immune responses to various tumors including melanoma. Both anti‐CTLA‐4 and anti‐PD‐1 antib...
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Veröffentlicht in: | Journal der Deutschen Dermatologischen Gesellschaft 2016-07, Vol.14 (7), p.662-681 |
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description | Summary
CTLA‐4 and PD‐1 are potential targets for tumor‐induced downregulation of lymphocytic immune responses. Immune checkpoint‐modifying monoclonal antibodies oppose these effects, inducing T cell‐mediated immune responses to various tumors including melanoma. Both anti‐CTLA‐4 and anti‐PD‐1 antibodies modify the interaction between tumor, antigen‐presenting cells, and T lymphocytes. With respect to overall survival, clinical studies have shown a major benefit for the anti‐CTLA‐4 antibody ipilimumab as well as the two anti‐PD‐1 antibodies nivolumab and pembrolizumab. Following approval of ipilimumab in 2011, the latter two achieved market authorization in the summer of 2015.Immune responses thus induced and enhanced inevitably entail autoimmune phenomena, affecting various organs to varying degrees. Knowledge of these side effects is crucial with regard to prevention and management by treating physicians. Typically occurring early on and presenting with pronounced and persistent diarrhea, colitis represents a major and severe side effect. Other immune‐mediated disorders include dermatitis, hypophysitis, thyroiditis, hepatitis, iridocyclitis as well as other less common autoimmune phenomena. Early recognition and initiation of treatment can reduce risks and sequelae for patients.This review describes the mechanisms of action of immune checkpoint blockade as well as its clinical effects in metastatic melanoma, with a detailed focus on the spectrum of adverse events and their therapeutic management. |
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CTLA‐4 and PD‐1 are potential targets for tumor‐induced downregulation of lymphocytic immune responses. Immune checkpoint‐modifying monoclonal antibodies oppose these effects, inducing T cell‐mediated immune responses to various tumors including melanoma. Both anti‐CTLA‐4 and anti‐PD‐1 antibodies modify the interaction between tumor, antigen‐presenting cells, and T lymphocytes. With respect to overall survival, clinical studies have shown a major benefit for the anti‐CTLA‐4 antibody ipilimumab as well as the two anti‐PD‐1 antibodies nivolumab and pembrolizumab. Following approval of ipilimumab in 2011, the latter two achieved market authorization in the summer of 2015.Immune responses thus induced and enhanced inevitably entail autoimmune phenomena, affecting various organs to varying degrees. Knowledge of these side effects is crucial with regard to prevention and management by treating physicians. Typically occurring early on and presenting with pronounced and persistent diarrhea, colitis represents a major and severe side effect. Other immune‐mediated disorders include dermatitis, hypophysitis, thyroiditis, hepatitis, iridocyclitis as well as other less common autoimmune phenomena. Early recognition and initiation of treatment can reduce risks and sequelae for patients.This review describes the mechanisms of action of immune checkpoint blockade as well as its clinical effects in metastatic melanoma, with a detailed focus on the spectrum of adverse events and their therapeutic management.</description><identifier>ISSN: 1610-0379</identifier><identifier>EISSN: 1610-0387</identifier><identifier>DOI: 10.1111/ddg.13047</identifier><identifier>PMID: 27373241</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Antibodies, Monoclonal - adverse effects ; Antineoplastic Agents ; autoimmune side effects ; CTLA-4 antibody ; CTLA-4 Antigen - antagonists & inhibitors ; Drug-Related Side Effects and Adverse Reactions - therapy ; Humans ; immune checkpoint blockade ; Immunoglobulins ; Ipilimumab ; Melanoma ; Melanoma - drug therapy ; Metastasis ; PD-1 antibody ; side effect management ; Skin Neoplasms - drug therapy ; T cell receptors</subject><ispartof>Journal der Deutschen Dermatologischen Gesellschaft, 2016-07, Vol.14 (7), p.662-681</ispartof><rights>2016 Deutsche Dermatologische Gesellschaft (DDG). Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4407-7e25db49b15c872f38f2e2bd1c2ce75c1b9444e50e0bd74aaa19f905c5c302a63</citedby><cites>FETCH-LOGICAL-c4407-7e25db49b15c872f38f2e2bd1c2ce75c1b9444e50e0bd74aaa19f905c5c302a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fddg.13047$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fddg.13047$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27373241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kähler, Katharina C.</creatorcontrib><creatorcontrib>Hassel, Jessica C.</creatorcontrib><creatorcontrib>Heinzerling, Lucie</creatorcontrib><creatorcontrib>Loquai, Carmen</creatorcontrib><creatorcontrib>Mössner, Rotraut</creatorcontrib><creatorcontrib>Ugurel, Selma</creatorcontrib><creatorcontrib>Zimmer, Lisa</creatorcontrib><creatorcontrib>Gutzmer, Ralf</creatorcontrib><creatorcontrib>“Cutaneous Side Effects” Committee of the Work Group Dermatological Oncology (ADO)</creatorcontrib><creatorcontrib>for the “Cutaneous Side Effects” Committee of the Work Group Dermatological Oncology (ADO)</creatorcontrib><title>Management of side effects of immune checkpoint blockade by anti-CTLA-4 and anti-PD-1 antibodies in metastatic melanoma</title><title>Journal der Deutschen Dermatologischen Gesellschaft</title><addtitle>JDDG: Journal der Deutschen Dermatologischen Gesellschaft</addtitle><description>Summary
CTLA‐4 and PD‐1 are potential targets for tumor‐induced downregulation of lymphocytic immune responses. Immune checkpoint‐modifying monoclonal antibodies oppose these effects, inducing T cell‐mediated immune responses to various tumors including melanoma. Both anti‐CTLA‐4 and anti‐PD‐1 antibodies modify the interaction between tumor, antigen‐presenting cells, and T lymphocytes. With respect to overall survival, clinical studies have shown a major benefit for the anti‐CTLA‐4 antibody ipilimumab as well as the two anti‐PD‐1 antibodies nivolumab and pembrolizumab. Following approval of ipilimumab in 2011, the latter two achieved market authorization in the summer of 2015.Immune responses thus induced and enhanced inevitably entail autoimmune phenomena, affecting various organs to varying degrees. Knowledge of these side effects is crucial with regard to prevention and management by treating physicians. Typically occurring early on and presenting with pronounced and persistent diarrhea, colitis represents a major and severe side effect. Other immune‐mediated disorders include dermatitis, hypophysitis, thyroiditis, hepatitis, iridocyclitis as well as other less common autoimmune phenomena. Early recognition and initiation of treatment can reduce risks and sequelae for patients.This review describes the mechanisms of action of immune checkpoint blockade as well as its clinical effects in metastatic melanoma, with a detailed focus on the spectrum of adverse events and their therapeutic management.</description><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antineoplastic Agents</subject><subject>autoimmune side effects</subject><subject>CTLA-4 antibody</subject><subject>CTLA-4 Antigen - antagonists & inhibitors</subject><subject>Drug-Related Side Effects and Adverse Reactions - therapy</subject><subject>Humans</subject><subject>immune checkpoint blockade</subject><subject>Immunoglobulins</subject><subject>Ipilimumab</subject><subject>Melanoma</subject><subject>Melanoma - drug therapy</subject><subject>Metastasis</subject><subject>PD-1 antibody</subject><subject>side effect management</subject><subject>Skin Neoplasms - drug therapy</subject><subject>T cell receptors</subject><issn>1610-0379</issn><issn>1610-0387</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtv1DAURi0Eog9Y8AdQJDawSOvn2FlWMzAFDYVFAakby4-b4k4ST-NE7fx73Ek7CyQkvPF3pXOPbH0IvSH4hORz6v31CWGYy2fokMwILjFT8vk-y-oAHaV0gzEVCuOX6IBKJhnl5BDdfTWduYYWuqGIdZGChwLqGtyQHubQtmMHhfsNbr2JIUO2iW5tMmW3hemGUM4vV2clz9lP8_dFSXbJRh8gFaErWhhMGswQXI6N6WJrXqEXtWkSvH68j9GPTx8v5-fl6tvy8_xsVTrOsSwlUOEtrywRTklaM1VToNYTRx1I4YitOOcgMGDrJTfGkKqusHDCMUzNjB2j95N308fbEdKg25AcNPkVEMekicLZKxTj_4MSNSOcqIy--wu9iWPf5Y_sKKYYrWimPkyU62NKPdR604fW9FtNsH4oTufi9K64zL59NI62Bb8nn5rKwOkE3IUGtv826cVi-aQsp42QBrjfb5h-rWfZKvSvi6UWP6_Y1Zdzpi_YHwi9rx8</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Kähler, Katharina C.</creator><creator>Hassel, Jessica C.</creator><creator>Heinzerling, Lucie</creator><creator>Loquai, Carmen</creator><creator>Mössner, Rotraut</creator><creator>Ugurel, Selma</creator><creator>Zimmer, Lisa</creator><creator>Gutzmer, Ralf</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QP</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201607</creationdate><title>Management of side effects of immune checkpoint blockade by anti-CTLA-4 and anti-PD-1 antibodies in metastatic melanoma</title><author>Kähler, Katharina C. ; Hassel, Jessica C. ; Heinzerling, Lucie ; Loquai, Carmen ; Mössner, Rotraut ; Ugurel, Selma ; Zimmer, Lisa ; Gutzmer, Ralf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4407-7e25db49b15c872f38f2e2bd1c2ce75c1b9444e50e0bd74aaa19f905c5c302a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antineoplastic Agents</topic><topic>autoimmune side effects</topic><topic>CTLA-4 antibody</topic><topic>CTLA-4 Antigen - antagonists & inhibitors</topic><topic>Drug-Related Side Effects and Adverse Reactions - therapy</topic><topic>Humans</topic><topic>immune checkpoint blockade</topic><topic>Immunoglobulins</topic><topic>Ipilimumab</topic><topic>Melanoma</topic><topic>Melanoma - drug therapy</topic><topic>Metastasis</topic><topic>PD-1 antibody</topic><topic>side effect management</topic><topic>Skin Neoplasms - drug therapy</topic><topic>T cell receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kähler, Katharina C.</creatorcontrib><creatorcontrib>Hassel, Jessica C.</creatorcontrib><creatorcontrib>Heinzerling, Lucie</creatorcontrib><creatorcontrib>Loquai, Carmen</creatorcontrib><creatorcontrib>Mössner, Rotraut</creatorcontrib><creatorcontrib>Ugurel, Selma</creatorcontrib><creatorcontrib>Zimmer, Lisa</creatorcontrib><creatorcontrib>Gutzmer, Ralf</creatorcontrib><creatorcontrib>“Cutaneous Side Effects” Committee of the Work Group Dermatological Oncology (ADO)</creatorcontrib><creatorcontrib>for the “Cutaneous Side Effects” Committee of the Work Group Dermatological Oncology (ADO)</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal der Deutschen Dermatologischen Gesellschaft</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kähler, Katharina C.</au><au>Hassel, Jessica C.</au><au>Heinzerling, Lucie</au><au>Loquai, Carmen</au><au>Mössner, Rotraut</au><au>Ugurel, Selma</au><au>Zimmer, Lisa</au><au>Gutzmer, Ralf</au><aucorp>“Cutaneous Side Effects” Committee of the Work Group Dermatological Oncology (ADO)</aucorp><aucorp>for the “Cutaneous Side Effects” Committee of the Work Group Dermatological Oncology (ADO)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of side effects of immune checkpoint blockade by anti-CTLA-4 and anti-PD-1 antibodies in metastatic melanoma</atitle><jtitle>Journal der Deutschen Dermatologischen Gesellschaft</jtitle><addtitle>JDDG: Journal der Deutschen Dermatologischen Gesellschaft</addtitle><date>2016-07</date><risdate>2016</risdate><volume>14</volume><issue>7</issue><spage>662</spage><epage>681</epage><pages>662-681</pages><issn>1610-0379</issn><eissn>1610-0387</eissn><abstract>Summary
CTLA‐4 and PD‐1 are potential targets for tumor‐induced downregulation of lymphocytic immune responses. Immune checkpoint‐modifying monoclonal antibodies oppose these effects, inducing T cell‐mediated immune responses to various tumors including melanoma. Both anti‐CTLA‐4 and anti‐PD‐1 antibodies modify the interaction between tumor, antigen‐presenting cells, and T lymphocytes. With respect to overall survival, clinical studies have shown a major benefit for the anti‐CTLA‐4 antibody ipilimumab as well as the two anti‐PD‐1 antibodies nivolumab and pembrolizumab. Following approval of ipilimumab in 2011, the latter two achieved market authorization in the summer of 2015.Immune responses thus induced and enhanced inevitably entail autoimmune phenomena, affecting various organs to varying degrees. Knowledge of these side effects is crucial with regard to prevention and management by treating physicians. Typically occurring early on and presenting with pronounced and persistent diarrhea, colitis represents a major and severe side effect. Other immune‐mediated disorders include dermatitis, hypophysitis, thyroiditis, hepatitis, iridocyclitis as well as other less common autoimmune phenomena. Early recognition and initiation of treatment can reduce risks and sequelae for patients.This review describes the mechanisms of action of immune checkpoint blockade as well as its clinical effects in metastatic melanoma, with a detailed focus on the spectrum of adverse events and their therapeutic management.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>27373241</pmid><doi>10.1111/ddg.13047</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies, Monoclonal - adverse effects Antineoplastic Agents autoimmune side effects CTLA-4 antibody CTLA-4 Antigen - antagonists & inhibitors Drug-Related Side Effects and Adverse Reactions - therapy Humans immune checkpoint blockade Immunoglobulins Ipilimumab Melanoma Melanoma - drug therapy Metastasis PD-1 antibody side effect management Skin Neoplasms - drug therapy T cell receptors |
title | Management of side effects of immune checkpoint blockade by anti-CTLA-4 and anti-PD-1 antibodies in metastatic melanoma |
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