# Efficacy and Safety of Small Molecule Inhibitor Therapies for Vitiligo: A Systematic Review

**Authors:** Alireza Jafarzadeh, Mohammad Amin Darvishi, Mina Khosravi, Masoumeh Roohaninasab, Azadeh Goodarzi

PMC · DOI: 10.1002/hsr2.71842 · Health Science Reports · 2026-02-22

## TL;DR

This study reviews the effectiveness and safety of small molecule inhibitors for treating vitiligo in different age groups, finding promising results but highlighting the need for more long-term safety data.

## Contribution

The paper provides a systematic review of JAKI and SMI therapies for vitiligo, comparing their efficacy and safety across age groups.

## Key findings

- Ritlecitinib showed significant improvements in VASI scores, especially when combined with NB-UVB phototherapy.
- Tofacitinib achieved up to 75% repigmentation in sun-exposed areas and pediatric populations.
- Upadacitinib and Baricitinib showed efficacy but were associated with adverse events, including a nonfatal stroke.

## Abstract

The latest advances in the treatment of vitiligo involve the introduction of Janus kinase inhibitors (JAKI) and small molecule inhibitors (SMI). These modern treatment modalities target specific inflammatory pathways that can improve outcomes for vitiligo in adults, adolescents, and children.

We did a literature search among PubMed, Scopus, and Web of Science, utilizing PRISMA guidelines. Articles included in the study were those reporting systemic medications using JAKI and SMI for vitiligo, categorized into subgroups of children (2–12), adolescents (12–18), and adults (over 18). We extracted information based on patient demographics, treatment regimens, efficacy outcomes, adverse effects, and follow‐up data.

After screening 987 studies, a total of 25 articles met the inclusion criteria and were included. The analysis demonstrated that JAKI, as well as the phosphodiesterase‐4 Inhibitor (PDE4 Inhibitor), apremilast, showed notable efficacy in the treatment of vitiligo across various age groups. Among these, ritlecitinib was the most extensively studied, showing significant improvements in both Facial‐VASI and Total‐VASI scores, especially when combined with NB‐UVB phototherapy. Tofacitinib demonstrated up to 75% repigmentation, particularly in sun‐exposed areas and pediatric populations, with higher efficacy noted when used alongside phototherapy. Upadacitinib showed ≥ 35% improvement in Facial‐VASI scores, though higher doses were associated with increased adverse events, including a serious nonfatal ischemic stroke. Baricitinib led to > 50% VASI improvement in 70.6% of patients when combined with NB‐UVB. Apremilast showed partial disease control and up to 61.5% repigmentation, though it was generally less effective than corticosteroids in halting progression.

JAKI and SMIs appear to be promising treatment options for vitiligo in adults, adolescents, and children, offering better efficacy than traditional treatments. However, some treatments like Apremilast had conflicting results about efficacy in vitiligo. Although these are notable findings, further research is required to establish their long‐term safety, particularly in children and adolescents.

## Linked entities

- **Chemicals:** ritlecitinib (PubChem CID 118115473), tofacitinib (PubChem CID 9926791), upadacitinib (PubChem CID 58557659), baricitinib (PubChem CID 44205240), apremilast (PubChem CID 10151715)
- **Diseases:** vitiligo (MONDO:0008661)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, PIK3C2A (phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha) [NCBI Gene 5286] {aka CPK, OCSKD, PI3-K-C2(ALPHA), PI3-K-C2A, PI3K-C2-alpha, PI3K-C2alpha}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PDE4A (phosphodiesterase 4A) [NCBI Gene 5141] {aka DPDE2, PDE4, PDE46}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CXCL11 (C-X-C motif chemokine ligand 11) [NCBI Gene 6373] {aka H174, I-TAC, IP-9, IP9, SCYB11, SCYB9B}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** skin repigmentation (MESH:D012871), syncope (MESH:D013575), oral ulcers (MESH:D019226), acral lesions (MESH:C000721267), headache (MESH:D006261), inflammation (MESH:D007249), respiratory infection (MESH:D012141), Injuries to the (MESH:D014947), anxiety (MESH:D001007), uterine leiomyoma (OMIM:150699), abdominal pain (MESH:D015746), T-VASI (MESH:D014820), head and neck injuries (MESH:D006258), benign (MESH:D009369), insomnia (MESH:D007319), immune-mediated disease (MESH:C567355), diarrhea (MESH:D003967), fatigue (MESH:D005221), GI discomfort (MESH:D006470), nonmelanoma skin cancers (MESH:D012878), common cold (MESH:D003139), depigmented lesions (MESH:D009059), nausea (MESH:D009325), weight gain (MESH:D015430), rash (MESH:D005076), Behcet's disease (MESH:D001528), depigmenting disorder (MESH:D009358), pruritus (MESH:D011537), arm injuries (MESH:D001134), psoriasis (MESH:D011565), psoriatic arthritis (MESH:D015535), hearing impairment (MESH:D034381), phenomenon (MESH:D009222), death (MESH:D003643), hypertension (MESH:D006973), vitiligo lesions (OMIM:606579), GI symptoms (MESH:D012816), laboratory abnormalities (MESH:D007757), dizziness (MESH:D004244), AEs (MESH:D064420), weight loss (MESH:D015431), urinary tract infection (MESH:D014552), arthralgia (MESH:D018771), ischemic stroke (MESH:D002544), gastrointestinal discomfort (MESH:D005767), COVID-19 infection (MESH:D000086382), infection (MESH:D007239), coagulation (MESH:D001778), appetite loss (MESH:D001068), nasopharyngitis (MESH:D009304), coronary artery arteriosclerosis (MESH:D003324), invasive lobular breast carcinoma (MESH:D001943), Depression (MESH:D003866), abdominal discomfort (MESH:D000007), renal function impairment (MESH:D007674), nausea, vomiting (MESH:D020250), alopecia areata (MESH:D000506), atopic dermatitis (MESH:D003876), herpes zoster (MESH:D006562), erythema (MESH:D004890)
- **Chemicals:** Upadacitinib (MESH:C000613732), axitinib (MESH:D000077784), brepocitinib (MESH:C000630838), idelalisib (MESH:C552946), Tofacitinib (MESH:C479163), triglyceride (MESH:D014280), betamethasone (MESH:D001623), ABBV-181 (MESH:C000719868), uric acid (MESH:D014527), tamoxifen (MESH:D013629), pimecrolimus (MESH:C117268), imatinib (MESH:D000068877), BIOSKIN (MESH:C437163), methylprednisolone (MESH:D008775), methotrexate (MESH:D008727), cyclic adenosine monophosphate (MESH:D000242), ruxolitinib (MESH:C540383), fulvestrant (MESH:D000077267), NB (MESH:D009556), everolimus (MESH:D000068338), tacrolimus (MESH:D016559), Apremilast (MESH:C505730), JNJ-64052981 (-), deucravacitinib (MESH:C000628674), dasatinib (MESH:D000069439), lipid (MESH:D008055), ropsacitinib (MESH:C000720458), erlotinib (MESH:D000069347), Abrocitinib (MESH:C000634427), halometasone (MESH:C036518), filgotinib (MESH:C584571), fedratinib (MESH:C528327), Baricitinib (MESH:C000596027), Ritlecitinib (MESH:C000614924)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12928105/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928105/full.md

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Source: https://tomesphere.com/paper/PMC12928105