Association of Vitiligo With Tumor Response in Patients With Metastatic Melanoma Treated With Pembrolizumab

被引:520
作者
Hua, Camille [1 ]
Boussemart, Lise [1 ]
Mateus, Christine [1 ]
Routier, Emilie [1 ]
Boutros, Celine [1 ]
Cazenave, Hugo [1 ]
Viollet, Roxane [1 ]
Thomas, Marina [1 ]
Roy, Severine [1 ]
Benannoune, Naima [1 ]
Tomasic, Gorana [2 ]
Soria, Jean-Charles [3 ,4 ]
Champiat, Stephane [3 ,5 ]
Texier, Matthieu [6 ,7 ]
Lanoy, Emilie [6 ,7 ]
Robert, Caroline [1 ,5 ]
机构
[1] Inst Gustave Roussy, Dept Dermatol, Canc Campus,114 Rue Edouard Vaillant, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Dept Pathol, Canc Campus, F-94805 Villejuif, France
[3] Inst Gustave Roussy, Dept Early Clin Dev, Canc Campus, F-94805 Villejuif, France
[4] Univ Paris Sud, Grand Paris, France
[5] Inst Gustave Roussy, INSERM, U981, Canc Campus, Grand Paris, France
[6] Inst Gustave Roussy, Biostat & Epidemiol Unit, F-94805 Villejuif, France
[7] Univ Paris Saclay, Univ Versailles St Quentin En Yvelines, Univ Paris 11, INSERM,Ctr Rech Epidemiol & Sante Populat, Villejuif, France
关键词
MALIGNANT-MELANOMA; PROGNOSTIC-SIGNIFICANCE; CANCER-IMMUNOTHERAPY; AUTOIMMUNE ASPECTS; HYPOPIGMENTATION; DEPIGMENTATION; INTERFERON; REGRESSION; ANTIGEN-4; BLOCKADE;
D O I
10.1001/jamadermatol.2015.2707
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
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.
引用
收藏
页码:45 / 51
页数:7
相关论文
共 30 条
[1]
Regressing cutaneous malignant melanoma and vitiligo-like depigmentation [J].
Arpaia, Nicola ;
Cassano, Nicoletta ;
Vena, Gino A. .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2006, 45 (08) :952-956
[2]
Autoimmunity correlates with tumor regression in patients with metastatic melanoma treated with anti-cytotoxic T-lymphocyte antigen-4 [J].
Attia, P ;
Phan, GQ ;
Maker, AV ;
Robinson, MR ;
Quezado, MM ;
Yang, JC ;
Sherry, RM ;
Topalian, SL ;
Kammula, US ;
Royal, RE ;
Restifo, NP ;
Haworth, LR ;
Levy, C ;
Mavroukakis, SA ;
Nichol, G ;
Yellin, MJ ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :6043-6053
[3]
Final Version of 2009 AJCC Melanoma Staging and Classification [J].
Balch, Charles M. ;
Gershenwald, Jeffrey E. ;
Soong, Seng-jaw ;
Thompson, John F. ;
Atkins, Michael B. ;
Byrd, David R. ;
Buzaid, Antonio C. ;
Cochran, Alistair J. ;
Coit, Daniel G. ;
Ding, Shouluan ;
Eggermont, Alexander M. ;
Flaherty, Keith T. ;
Gimotty, Phyllis A. ;
Kirkwood, John M. ;
McMasters, Kelly M. ;
Mihm, Martin C., Jr. ;
Morton, Donald L. ;
Ross, Merrick I. ;
Sober, Arthur J. ;
Sondak, Vernon K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) :6199-6206
[4]
BARRIERE H, 1984, ANN DERMATOL VENER, V111, P991
[5]
Enhanced survival associated with vitiligo expression during maintenance biotherapy for metastatic melanoma [J].
Boasberg, Peter D. ;
Hoon, Dave S. B. ;
Piro, Lawrence D. ;
Martin, Maureen A. ;
Fujimoto, Akhide ;
Kristedja, Timothy S. ;
Bhachu, Sandeep ;
Ye, Xing ;
Deck, Regina R. ;
O'Day, Steven J. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (12) :2658-2663
[6]
Autoimmunity and treatment outcome in melanoma [J].
Bouwhuis, Marna G. ;
ten Hagen, Timo L. M. ;
Suciu, Stefan ;
Eggermont, Alexander M. M. .
CURRENT OPINION IN ONCOLOGY, 2011, 23 (02) :170-176
[7]
Byrne KT, 2011, ONCOTARGET, V2, P684
[8]
PROGNOSTIC-SIGNIFICANCE OF HYPOPIGMENTATION IN MALIGNANT-MELANOMA [J].
BYSTRYN, JC ;
RIGEL, D ;
FRIEDMAN, RJ ;
KOPF, A .
ARCHIVES OF DERMATOLOGY, 1987, 123 (08) :1053-1055
[9]
MELANOMA AND VITILIGO ARE ASSOCIATED WITH ANTIBODY-RESPONSES TO SIMILAR ANTIGENS ON PIGMENT-CELLS [J].
CUI, J ;
BYSTRYN, JC .
ARCHIVES OF DERMATOLOGY, 1995, 131 (03) :314-318
[10]
New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247