Association of Vitiligo With Tumor Response in Patients With Metastatic Melanoma Treated With Pembrolizumab
IMPORTANCE: Vitiligo is an autoimmune skin disorder that reacts against melanocytes. The association of vitiligo with tumor response in patients with melanoma who undergo immunotherapy has been reported but is still controversial. OBJECTIVE: To prospectively evaluate the appearance of vitiligo in pa...
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creator | Hua, Camille Boussemart, Lise Mateus, Christine Routier, Emilie Boutros, Céline Cazenave, Hugo Viollet, Roxane Thomas, Marina Roy, Séverine Benannoune, Naima Tomasic, Gorana Soria, Jean-Charles Champiat, Stéphane Texier, Matthieu Lanoy, Emilie Robert, Caroline |
description | IMPORTANCE: Vitiligo is an autoimmune skin disorder that reacts against melanocytes. The association of vitiligo with tumor response in patients with melanoma who undergo immunotherapy has been reported but is still controversial. OBJECTIVE: To prospectively evaluate the appearance of vitiligo in patients receiving pembrolizumab, a monoclonal antibody directed against the programmed death cell receptor. DESIGN, SETTING, AND PARTICIPANTS: This prospective observational study was conducted from January 1, 2012, through September 24, 2013, in a single tertiary care hospital with a unit dedicated to patients with melanoma. Sixty-seven patients with metastatic melanoma who received pembrolizumab treatment in the context of a phase 1 study were included and screened for the emergence of vitiligo. Data were collected from January 1, 2012, to February 28, 2014, and analyzed from February through December 2014. MAIN OUTCOMES AND MEASURES: Objective tumor response with regard to the occurrence of vitiligo in patients receiving pembrolizumab therapy. Correlation between vitiligo occurrence and overall survival was also estimated using the Kaplan-Meier product-limit method and compared with a log-rank test. To prevent guarantee- or lead-time bias, a landmark analysis approach after 12, 16, and 20 weeks of treatment was retained. RESULTS: Of the 67 patients included in the study, 17 (25%) developed vitiligo during pembrolizumab treatment and 50 (75%) did not. An objective (complete or partial) response to treatment was associated with a higher occurrence of vitiligo (12 of 17 [71%] vs 14 of 50 [28%]; P = .002). The time to onset of vitiligo ranged from 52 to 453 (median, 126) days from the start of treatment. Of the 17 patients with vitiligo, 3 (18%) had a complete response, 9 (53%) had a partial response, 3 (18%) had stable disease, and 2 (12%) had progressive disease at the final follow-up. All the patients treated with pembrolizumab who developed vitiligo were alive at the time of analysis, with a median follow-up of 441 days. CONCLUSIONS AND RELEVANCE: Vitiligo, a clinically visible immune-related adverse event could be associated with clinical benefit in the context of pembrolizumab treatment. |
doi_str_mv | 10.1001/jamadermatol.2015.2707 |
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The association of vitiligo with tumor response in patients with melanoma who undergo immunotherapy has been reported but is still controversial. OBJECTIVE: To prospectively evaluate the appearance of vitiligo in patients receiving pembrolizumab, a monoclonal antibody directed against the programmed death cell receptor. DESIGN, SETTING, AND PARTICIPANTS: This prospective observational study was conducted from January 1, 2012, through September 24, 2013, in a single tertiary care hospital with a unit dedicated to patients with melanoma. Sixty-seven patients with metastatic melanoma who received pembrolizumab treatment in the context of a phase 1 study were included and screened for the emergence of vitiligo. Data were collected from January 1, 2012, to February 28, 2014, and analyzed from February through December 2014. MAIN OUTCOMES AND MEASURES: Objective tumor response with regard to the occurrence of vitiligo in patients receiving pembrolizumab therapy. Correlation between vitiligo occurrence and overall survival was also estimated using the Kaplan-Meier product-limit method and compared with a log-rank test. To prevent guarantee- or lead-time bias, a landmark analysis approach after 12, 16, and 20 weeks of treatment was retained. RESULTS: Of the 67 patients included in the study, 17 (25%) developed vitiligo during pembrolizumab treatment and 50 (75%) did not. An objective (complete or partial) response to treatment was associated with a higher occurrence of vitiligo (12 of 17 [71%] vs 14 of 50 [28%]; P = .002). The time to onset of vitiligo ranged from 52 to 453 (median, 126) days from the start of treatment. Of the 17 patients with vitiligo, 3 (18%) had a complete response, 9 (53%) had a partial response, 3 (18%) had stable disease, and 2 (12%) had progressive disease at the final follow-up. All the patients treated with pembrolizumab who developed vitiligo were alive at the time of analysis, with a median follow-up of 441 days. CONCLUSIONS AND RELEVANCE: Vitiligo, a clinically visible immune-related adverse event could be associated with clinical benefit in the context of pembrolizumab treatment.</description><identifier>ISSN: 2168-6068</identifier><identifier>EISSN: 2168-6084</identifier><identifier>DOI: 10.1001/jamadermatol.2015.2707</identifier><identifier>PMID: 26501224</identifier><language>eng</language><publisher>United States: American Medical Association</publisher><subject>Adult ; Aged ; Antibodies, Monoclonal, Humanized - pharmacology ; Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Female ; Follow-Up Studies ; Humans ; Male ; Melanoma - drug therapy ; Melanoma - pathology ; Middle Aged ; Neoplasm Metastasis ; Prospective Studies ; Skin Neoplasms - drug therapy ; Skin Neoplasms - pathology ; Survival Rate ; Time Factors ; Treatment Outcome ; Vitiligo - etiology ; Young Adult</subject><ispartof>JAMA dermatology (Chicago, Ill.), 2016-01, Vol.152 (1), p.45-51</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a378t-831a0a8ea9db0d499a99e0da19e61a1c2394c53b9e3d0c3765eef3c0bf88958b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jamanetwork.com/journals/jamadermatology/articlepdf/10.1001/jamadermatol.2015.2707$$EPDF$$P50$$Gama$$H</linktopdf><linktohtml>$$Uhttps://jamanetwork.com/journals/jamadermatology/fullarticle/10.1001/jamadermatol.2015.2707$$EHTML$$P50$$Gama$$H</linktohtml><link.rule.ids>64,314,776,780,3327,27901,27902,76231,76234</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26501224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hua, Camille</creatorcontrib><creatorcontrib>Boussemart, Lise</creatorcontrib><creatorcontrib>Mateus, Christine</creatorcontrib><creatorcontrib>Routier, Emilie</creatorcontrib><creatorcontrib>Boutros, Céline</creatorcontrib><creatorcontrib>Cazenave, Hugo</creatorcontrib><creatorcontrib>Viollet, Roxane</creatorcontrib><creatorcontrib>Thomas, Marina</creatorcontrib><creatorcontrib>Roy, Séverine</creatorcontrib><creatorcontrib>Benannoune, Naima</creatorcontrib><creatorcontrib>Tomasic, Gorana</creatorcontrib><creatorcontrib>Soria, Jean-Charles</creatorcontrib><creatorcontrib>Champiat, Stéphane</creatorcontrib><creatorcontrib>Texier, Matthieu</creatorcontrib><creatorcontrib>Lanoy, Emilie</creatorcontrib><creatorcontrib>Robert, Caroline</creatorcontrib><title>Association of Vitiligo With Tumor Response in Patients With Metastatic Melanoma Treated With Pembrolizumab</title><title>JAMA dermatology (Chicago, Ill.)</title><addtitle>JAMA Dermatol</addtitle><description>IMPORTANCE: Vitiligo is an autoimmune skin disorder that reacts against melanocytes. The association of vitiligo with tumor response in patients with melanoma who undergo immunotherapy has been reported but is still controversial. OBJECTIVE: To prospectively evaluate the appearance of vitiligo in patients receiving pembrolizumab, a monoclonal antibody directed against the programmed death cell receptor. DESIGN, SETTING, AND PARTICIPANTS: This prospective observational study was conducted from January 1, 2012, through September 24, 2013, in a single tertiary care hospital with a unit dedicated to patients with melanoma. Sixty-seven patients with metastatic melanoma who received pembrolizumab treatment in the context of a phase 1 study were included and screened for the emergence of vitiligo. Data were collected from January 1, 2012, to February 28, 2014, and analyzed from February through December 2014. MAIN OUTCOMES AND MEASURES: Objective tumor response with regard to the occurrence of vitiligo in patients receiving pembrolizumab therapy. Correlation between vitiligo occurrence and overall survival was also estimated using the Kaplan-Meier product-limit method and compared with a log-rank test. To prevent guarantee- or lead-time bias, a landmark analysis approach after 12, 16, and 20 weeks of treatment was retained. RESULTS: Of the 67 patients included in the study, 17 (25%) developed vitiligo during pembrolizumab treatment and 50 (75%) did not. An objective (complete or partial) response to treatment was associated with a higher occurrence of vitiligo (12 of 17 [71%] vs 14 of 50 [28%]; P = .002). The time to onset of vitiligo ranged from 52 to 453 (median, 126) days from the start of treatment. Of the 17 patients with vitiligo, 3 (18%) had a complete response, 9 (53%) had a partial response, 3 (18%) had stable disease, and 2 (12%) had progressive disease at the final follow-up. All the patients treated with pembrolizumab who developed vitiligo were alive at the time of analysis, with a median follow-up of 441 days. CONCLUSIONS AND RELEVANCE: Vitiligo, a clinically visible immune-related adverse event could be associated with clinical benefit in the context of pembrolizumab treatment.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal, Humanized - pharmacology</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - pathology</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><subject>Prospective Studies</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - pathology</subject><subject>Survival Rate</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Vitiligo - etiology</subject><subject>Young Adult</subject><issn>2168-6068</issn><issn>2168-6084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkMFO3DAQhi1UBCvgBTigHHvZZRwnjn1crVqKBCpCCxyjSTKh3sbx1nYO7dPjVSitLx7NfL89-hi74rDiAPx6hxY78hajG1Y58HKVV1AdsUXOpVpKUMWnj1qqU3YRwg7SUQCF4CfsNJcl8DwvFuznOgTXGozGjZnrs2cTzWBeXfZi4o9sO1nns0cKezcGysyYPSSSxhjm-T1FDDG12lQOODqL2dYTRupm4IFs491g_kwWm3N23OMQ6OL9PmNPX79sN9-Wd99vbjfruyWKSsWlEhwBFaHuGugKrVFrgg65JsmRt7nQRVuKRpPooBWVLIl60ULTK6VL1Ygz9nl-d-_dr4lCrK0JLQ1pQXJTqHmVFEkBskyonNHWuxA89fXeG4v-d82hPriu_3ddH1zXB9cpePX-x9RY6j5if80m4HIGUv7ftJCFFly8AauQh-Q</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Hua, Camille</creator><creator>Boussemart, Lise</creator><creator>Mateus, Christine</creator><creator>Routier, Emilie</creator><creator>Boutros, Céline</creator><creator>Cazenave, Hugo</creator><creator>Viollet, Roxane</creator><creator>Thomas, Marina</creator><creator>Roy, Séverine</creator><creator>Benannoune, Naima</creator><creator>Tomasic, Gorana</creator><creator>Soria, Jean-Charles</creator><creator>Champiat, Stéphane</creator><creator>Texier, Matthieu</creator><creator>Lanoy, Emilie</creator><creator>Robert, Caroline</creator><general>American Medical Association</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>7X8</scope></search><sort><creationdate>20160101</creationdate><title>Association of Vitiligo With Tumor Response in Patients With Metastatic Melanoma Treated With Pembrolizumab</title><author>Hua, Camille ; 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The association of vitiligo with tumor response in patients with melanoma who undergo immunotherapy has been reported but is still controversial. OBJECTIVE: To prospectively evaluate the appearance of vitiligo in patients receiving pembrolizumab, a monoclonal antibody directed against the programmed death cell receptor. DESIGN, SETTING, AND PARTICIPANTS: This prospective observational study was conducted from January 1, 2012, through September 24, 2013, in a single tertiary care hospital with a unit dedicated to patients with melanoma. Sixty-seven patients with metastatic melanoma who received pembrolizumab treatment in the context of a phase 1 study were included and screened for the emergence of vitiligo. Data were collected from January 1, 2012, to February 28, 2014, and analyzed from February through December 2014. MAIN OUTCOMES AND MEASURES: Objective tumor response with regard to the occurrence of vitiligo in patients receiving pembrolizumab therapy. Correlation between vitiligo occurrence and overall survival was also estimated using the Kaplan-Meier product-limit method and compared with a log-rank test. To prevent guarantee- or lead-time bias, a landmark analysis approach after 12, 16, and 20 weeks of treatment was retained. RESULTS: Of the 67 patients included in the study, 17 (25%) developed vitiligo during pembrolizumab treatment and 50 (75%) did not. An objective (complete or partial) response to treatment was associated with a higher occurrence of vitiligo (12 of 17 [71%] vs 14 of 50 [28%]; P = .002). The time to onset of vitiligo ranged from 52 to 453 (median, 126) days from the start of treatment. Of the 17 patients with vitiligo, 3 (18%) had a complete response, 9 (53%) had a partial response, 3 (18%) had stable disease, and 2 (12%) had progressive disease at the final follow-up. All the patients treated with pembrolizumab who developed vitiligo were alive at the time of analysis, with a median follow-up of 441 days. CONCLUSIONS AND RELEVANCE: Vitiligo, a clinically visible immune-related adverse event could be associated with clinical benefit in the context of pembrolizumab treatment.</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>26501224</pmid><doi>10.1001/jamadermatol.2015.2707</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antibodies, Monoclonal, Humanized - pharmacology Antibodies, Monoclonal, Humanized - therapeutic use Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Female Follow-Up Studies Humans Male Melanoma - drug therapy Melanoma - pathology Middle Aged Neoplasm Metastasis Prospective Studies Skin Neoplasms - drug therapy Skin Neoplasms - pathology Survival Rate Time Factors Treatment Outcome Vitiligo - etiology Young Adult |
title | Association of Vitiligo With Tumor Response in Patients With Metastatic Melanoma Treated With Pembrolizumab |
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