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DOI 10.3389/fonc.2025.1669407

Медицинская библиотека · Frontiers in oncology · 2025

Vitiligo associated with ribociclib therapy: a rare case report.

Wang Zirui, Bai Yuanrui, Wu Rihan, Liu Yihui, Dong Chunhui, Chen Ling

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Аннотация

BACKGROUND

Ribociclib, a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor, occupies a pivotal role in the clinical management of metastatic breast cancer, with its hematologic and gastrointestinal toxicities well-established. However, cutaneous adverse reactions induced by this agent-among which vitiligo is particularly prominent-are extremely rare. Herein, we report a case of vitiligo-like lesions induced by ribociclib, aiming to elucidate this underrecognized drug-adverse reaction association and conduct an in-depth analysis of its potential immune-mediated mechanism.

CASE SUMMARY: A 59-year-old woman with ER/PR (90% strong+), HER2-negative metastatic breast cancer developed pruritic hypopigmented patches on her forearms 16 months after initiating ribociclib/letrozole. Dermoscopy revealed complete pigment loss, peripheral hyperpigmentation, and telangiectasia. Wood's lamp examination demonstrated bright blue-white fluorescence, confirming non-segmental vitiligo. No personal/family history of autoimmunity was noted. Topical 0.1% mometasone cream and 0.1% tacrolimus ointment were initiated, with stabilization of existing lesions and no new depigmentation at 2-month follow-up. Ribociclib was maintained due to ongoing tumor control.

CONCLUSIONS

HR-positive metastatic breast cancer patients using ribociclib may develop vitiligo, with individual differences (e.g., over one-year incubation as in this case). Combined with prior reports, it suggests a link between ribociclib and vitiligo. Further clinical observations and studies are needed to confirm causality, and pre-use risk explanations to patients are advisable.

Для цитирования: Wang Zirui, Bai Yuanrui, Wu Rihan, Liu Yihui, Dong Chunhui, Chen Ling. Vitiligo associated with ribociclib therapy: a rare case report.. Frontiers in oncology. 2025. DOI: 10.3389/fonc.2025.1669407.
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