Autoimmune colitis and neutropenia in adjuvant anti-PD-1 therapy for malignant melanoma: efficacy of Vedolizumab, a case report

被引:4
|
作者
d'Apolito, Maria [1 ]
Spagnuolo, Rocco [1 ]
Siciliano, Maria Anna [1 ]
Barbieri, Vito [2 ]
Cosco, Cristina [2 ]
Fiorillo, Lucia [2 ]
Cuomo, Onofrio [1 ]
Zuccala, Valeria [1 ]
Correale, Pierpaolo [3 ]
Pensabene, Licia [4 ]
Rossi, Marco [1 ]
Doldo, Patrizia [1 ]
Tassone, Pierfrancesco [1 ]
Tagliaferri, Pierosandro [1 ]
机构
[1] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med, I-88100 Catanzaro, Italy
[2] AOU Mater Domini, Catanzaro, Italy
[3] Bianchi Melacrino Morelli Grand Metropolitan Hosp, Reggio Di Calabria, Italy
[4] Magna Graecia Univ Catanzaro, Dept Med & Surg Sci, Calabria, Italy
关键词
anti-PD-1; melanoma; autoimmunity; colitis; neutropenia; immune-relate adverse events; irAEs; Pembrolizumab; Vedolizumab; STAGE-III MELANOMA; DOUBLE-BLIND; MAINTENANCE THERAPY; ADVERSE EVENTS; IPILIMUMAB; IMMUNOTHERAPY; INFLIXIMAB; NIVOLUMAB; SURVIVAL; PLACEBO;
D O I
10.1177/20406223211063024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Immune checkpoint inhibitors (ICIs) represent an important advance in the adjuvant treatment of patients with high-risk melanoma. Although the safety profile of anti-programmed cell death protein-1 (PD-1) is fairly acceptable, different immune-related adverse events (irAEs) are described. Herein we report for the first time a notably multidisciplinary combined approach on a malignant melanoma (MM) patient treated with anti-PD-1 antibody in adjuvant setting. In this novel approach, corticosteroid-refractory immune-mediated colitis (IMC) was effectively treated with Vedolizumab, a selective blockade of the alpha 4 beta 7 integrin and corticosteroids were successfully administered for autoimmune neutropenia. Notably, our patient also express HLA-B*35, a potential biomarker for predicting a genetic basis of autoimmune susceptibility. Our experience offers a possible future perspective about the use of Vedolizumab together with immunotherapy in a strategic early approach for high-risk patients genotyped for HLA.
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页数:9
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