Abstract
Immunotherapy leads to significantly prolonged survival of patients with metastatic melanoma. Autoimmune side effects including colitis, dermatitis, and endocrine abnormalities are common in patients treated with ipilimumab [anti-CTLA4 (cytotoxic T-lymphocyte-associated protein 4)]. Antibodies such as pembrolizumab that interfere with the PD-1 (programmed cell death 1)/PD-L1 pathway show greater efficacy and less toxicity than ipilimumab. Here we report 2 cases of pembrolizumab-induced uveitis associated with complete or partial tumor response. We suggest that uveitis may serve as a surrogate marker for a tumor response to therapy with pembrolizumab.
MeSH terms
-
Aged
-
Antibodies, Monoclonal, Humanized / adverse effects
-
Antibodies, Monoclonal, Humanized / therapeutic use*
-
Autoimmunity
-
CTLA-4 Antigen / immunology
-
Humans
-
Immunotherapy / methods*
-
Ipilimumab / therapeutic use
-
Male
-
Melanoma / drug therapy*
-
Melanoma / secondary
-
Middle Aged
-
Neoplasms, Unknown Primary / drug therapy*
-
Programmed Cell Death 1 Receptor / immunology*
-
Skin Neoplasms / drug therapy*
-
Skin Neoplasms / secondary
-
Treatment Outcome
-
Uveitis / diagnosis*
-
Uveitis / etiology
Substances
-
Antibodies, Monoclonal, Humanized
-
CTLA-4 Antigen
-
CTLA4 protein, human
-
Ipilimumab
-
PDCD1 protein, human
-
Programmed Cell Death 1 Receptor
-
pembrolizumab