Real world pharmacovigilance study of antineoplastic drug related vitiligo risks.

Publication date: Jul 02, 2025

Vitiligo, a depigmentation disorder, significantly impacts the well-being of affected individuals. The induction of vitiligo by pharmacological agents is a critical concern, with prior research establishing a link between antineoplastic medications and the onset of vitiligo. This study aims to assess the reported association between vitiligo and antineoplastic drugs using the FAERS. The study encompassed FAERS reports spanning the years 2004 to 2024. Medical Dictionary for Regulatory Activities (MedDRA) was used to identify cases of vitiligo. The Reporting Odds Ratio, Proportional Reporting Ratio, Bayesian Confidence Propagation Neural Network, and Empirical Bayes Geometric Mean were calculated to assess the reported associations between available drugs and vitiligo. A significant statistical association was considered when a drug signal met the criteria of all four algorithms. Our analysis of the FAERS database revealed 533 adverse event (AE) reports implicating antineoplastic drugs in the development of vitiligo, with a higher prevalence among females compared to males. The 18-65 age group accounted for the majority of cases, with the United States contributing the most reports. Malignant melanoma was the most frequently reported underlying condition. Nivolumab and Pembrolizumab were the most commonly implicated drugs, with 147 and 126 reports, respectively. Disproportionality analysis identified 14 antineoplastic drugs with a significant association with vitiligo-related AEs, including the monoclonal antibody Mogamulizumab, immune checkpoint inhibitor Ipilimumab, and oncolytic virus Talimogene Laherparepvec, with Mogamulizumab exhibiting the highest correlation. These findings underscore the necessity for heightened clinical vigilance regarding the safety profiles of specific medications. This study represents the inaugural investigation into the real-world incidence of antineoplastic drug-induced vitiligo utilizing the FAERS database. Our findings reveal a strong association between vitiligo and immunomodulatory therapies, including immune checkpoint inhibitors and monoclonal antibodies. There is an imperative need for vigilant patient monitoring during the clinical administration of these agents to promptly identify and address potential AEs such as vitiligo.

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Concepts Keywords
Dictionary Adolescent
Drugs Adult
Immunomodulatory Adverse event
Malignant Aged
Years Antineoplastic Agents
Antineoplastic Agents
Antineoplastic drug
Bayes Theorem
Databases, Factual
Drug-induced vitiligo
FAERS
Female
Humans
Male
Middle Aged
Pharmacovigilance
Pharmacovigilance study
Vitiligo
Vitiligo
Young Adult

Semantics

Type Source Name
disease MESH vitiligo
drug DRUGBANK Methionine
disease MESH Malignant melanoma
drug DRUGBANK Nivolumab
drug DRUGBANK Pembrolizumab
drug DRUGBANK Mogamulizumab
drug DRUGBANK Ipilimumab
drug DRUGBANK Talimogene laherparepvec
disease MESH psychological well being
pathway REACTOME Immune System
disease MESH pathogenesis
drug DRUGBANK Coenzyme M
drug DRUGBANK L-Tyrosine
pathway REACTOME Melanin biosynthesis
disease MESH drug interactions
disease MESH adverse drug reactions
drug DRUGBANK Phosphatidyl serine
disease MESH small cell lung cancer
pathway KEGG Small cell lung cancer
disease MESH cancer
disease MESH renal cancer
disease MESH Emergency
drug DRUGBANK Ribociclib
drug DRUGBANK Atezolizumab
drug DRUGBANK Imatinib
drug DRUGBANK Cyclophosphamide
drug DRUGBANK Vemurafenib
drug DRUGBANK Fludarabine
disease MESH Death
drug DRUGBANK Trametinib
drug DRUGBANK Dabrafenib
drug DRUGBANK Capecitabine
drug DRUGBANK Bevacizumab
disease MESH Recurrences
drug DRUGBANK Timonacic
drug DRUGBANK Encorafenib
drug DRUGBANK Temozolomide
drug DRUGBANK Busulfan
drug DRUGBANK Pemetrexed
drug DRUGBANK Abemaciclib
drug DRUGBANK Methotrexate
drug DRUGBANK Palbociclib
drug DRUGBANK Ruxolitinib
drug DRUGBANK Rituximab
drug DRUGBANK Cabozantinib
drug DRUGBANK Carboplatin
drug DRUGBANK Pazopanib
drug DRUGBANK Trastuzumab
drug DRUGBANK Ixazomib
disease MESH Oxidative stress
drug DRUGBANK Oxygen
disease MESH obesity
disease MESH breast cancer
pathway KEGG Breast cancer
disease MESH lung cancer
disease MESH Syndrome
pathway KEGG Melanoma
disease MESH immune tolerance
disease MESH tumor immune evasion
disease MESH COVID 19
drug DRUGBANK Bismuth subgallate
pathway REACTOME Apoptosis
drug DRUGBANK Guanine
drug DRUGBANK Folic Acid
disease MESH contact dermatitis
drug DRUGBANK Teprotumumab
drug DRUGBANK Sugammadex
disease MESH mycosis fungoides
drug DRUGBANK Diethylstilbestrol
disease MESH infection
disease MESH shock
drug DRUGBANK Natural alpha interferon
disease MESH skin disease
disease MESH autoimmunity
drug DRUGBANK Cemiplimab
disease MESH junctional epidermolysis bullosa
disease MESH halo nevi
pathway REACTOME Interferon Signaling
drug DRUGBANK Telbivudine
pathway REACTOME Reproduction

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