Table 4 Antineoplastic drugs significantly associated with vitiligo and their drug categories.
From: Real world pharmacovigilance study of antineoplastic drug related vitiligo risks
Medications investigated | Mechanism of action |
---|---|
L01A—ALKYLATING AGENTS | |
L01AB—Alkyl sulfonates | |
L01AB01—Busulfan | Forms DNA cross-links by alkylation, leading to DNA damage and apoptosis of rapidly dividing cells |
L01AX—Other alkylating agents | |
L01AX03—Temozolomide | Methylates DNA at the O6 and N7 positions of guanine, causing DNA strand breaks and tumor cell death |
L01B—ANTIMETABOLITES | |
L01BA—Folic acid analogues | |
L01BA04—Pemetrexed | Inhibits folate-dependent enzymes involved in nucleotide synthesis, blocking DNA and RNA synthesis and leading to cell death |
L01E—PROTEIN KINASE INHIBITORS | |
L01EC—B-Raf serine-threonine kinase (BRAF) inhibitors | |
L01EC02—Dabrafenib | Selectively inhibits mutant BRAF V600 kinases, blocking the MAPK/ERK signaling pathway and reducing tumor cell proliferation |
L01EC03—Encorafenib | Inhibits BRAF V600 mutant kinases, suppressing MAPK pathway signaling and inhibiting tumor cell growth |
L01EE—Mitogen-activated protein kinase (MEK) inhibitors | |
L01EE01—Trametinib | Inhibits MEK1 and MEK2 activation and kinase activity, disrupting the MAPK/ERK pathway and decreasing tumor cell proliferation |
L01EF—Cyclin-dependent kinase (CDK) inhibitors | |
L01EF02—Ribociclib | Selectively inhibits CDK4 and CDK6, preventing phosphorylation of Rb protein and causing cell cycle arrest in the G1 phase |
L01EF03—Abemaciclib | Inhibits CDK4 and CDK6, leading to decreased Rb phosphorylation and inducing cell cycle arrest at the G1 phase |
L01F—MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES | |
L01FF—PD-1/PD-L1 (Programmed cell death protein 1/death ligand 1) inhibitors | |
L01FF01—Nivolumab | Blocks PD-1 receptors on T cells, enhancing immune responses against tumors by preventing PD-1/PD-L1 interaction |
L01FF02—Pembrolizumab | Inhibits PD-1 on T cells, blocking PD-1/PD-L1 interaction and enhancing anti-tumor immune responses |
L01FF05—Atezolizumab | Targets PD-L1, blocking its interaction with PD-1 and B7.1, thereby enhancing T-cell-mediated immune responses against tumor cells |
L01FX—Other monoclonal antibodies and antibody drug conjugates | |
L01FX04—Ipilimumab | Blocks CTLA-4 on T cells, enhancing T-cell activation and proliferation by preventing inhibitory signaling |
L01FX09—Mogamulizumab | Targets CCR4 on malignant T cells, inducing antibody-dependent cellular cytotoxicity and depleting CCR4-positive cells |
L01X—OTHER ANTINEOPLASTIC AGENTS | |
L01XL—Antineoplastic cell and gene therapy | |
L01XL02—Talimogene laherparepvec | An oncolytic virus that selectively replicates in tumor cells and expresses GM-CSF, leading to tumor cell lysis and enhanced anti-tumor immunity |