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Updated: Sep 10, 2025

Quantification of Hypopigmentation Activity In Vitro
Published on: March 6, 2019
Targeted therapies induced depigmentation: a review
Zhaoyang Wang1,2, Meng Wang1,2, Tianyu Wang1,2
1Dermatology Hospital of Shandong First Medical University, Jinan, China.
Abstract:
Skin depigmentation or vitiligo-like depigmentation (VLD) is one of the most prevalent cutaneous adverse events during targeted therapies for cancers or autoimmune diseases. The depigmentation is usually with high mental burden and affect the disease treatment, some of which are even clinical markers for good prognosis. This study aimed to explore the underlying immunopathologic mechanisms of VLD induced by targeted therapy for cancer and autoimmune disease as well as vaccine, such as immune checkpoint inhibitors (e.g., programmed death 1/programmed death-ligand 1 and cytotoxic T-lymphocyte antigen-4 inhibitors), v-raf murine sarcoma viral oncogene homolog inhibitors, tyrosine kinase inhibitors, and other targeted agents. Additionally, it examined the clinical presentations, prognostic implications, and management strategies for VLD across oncologic and nononcologic contexts, including cases associated with vaccines and biologics. The development of VLD often correlates with improved therapeutic outcomes, but it presents unique challenges in balancing antitumor efficacy with patients' quality of life. This review integrated insights from oncology, dermatology, and immunology, and underscored the need for multidisciplinary approaches to enhance the understanding, prevention, and management of these complex cutaneous adverse events.
Insights
Vitiligo-like depigmentation (VLD) is a common side effect of targeted cancer therapies, often indicating a positive prognosis. Understanding its immune mechanisms is key for managing patient quality of life alongside treatment efficacy.
Area of Science:
- Integrates oncology, dermatology, and immunology to study cutaneous adverse events.
- Focuses on targeted therapies, including immune checkpoint inhibitors, BRAF, and tyrosine kinase inhibitors.
Background:
- Vitiligo-like depigmentation (VLD) is a frequent cutaneous adverse event in patients receiving targeted therapies for cancer and autoimmune diseases.
- VLD can cause significant psychological distress and impact treatment adherence, despite sometimes being a marker of favorable prognosis.
- The immunopathologic mechanisms underlying VLD induced by various targeted agents remain incompletely understood.
Purpose of the Study:
- To explore the immunopathologic mechanisms of VLD induced by targeted therapies (cancer, autoimmune diseases, vaccines).
- To examine clinical presentations, prognostic implications, and management strategies for VLD.
- To highlight the correlation between VLD and improved therapeutic outcomes, and the challenges in balancing efficacy with quality of life.
Main Methods:
- Comprehensive literature review integrating findings from oncology, dermatology, and immunology.
- Analysis of VLD cases associated with immune checkpoint inhibitors, BRAF inhibitors, tyrosine kinase inhibitors, vaccines, and biologics.
- Examination of clinical data, prognostic significance, and therapeutic management approaches.
Main Results:
- VLD is a prevalent adverse event linked to targeted therapies, often associated with positive treatment responses.
- Specific targeted agents, including immune checkpoint inhibitors, are implicated in VLD development.
- VLD presents challenges in patient quality of life management despite its prognostic value.
Conclusions:
- Understanding the immunopathologic basis of VLD is crucial for optimizing targeted therapy outcomes.
- Multidisciplinary approaches involving oncology, dermatology, and immunology are needed for effective VLD management.
- Further research is required to enhance the prevention and treatment strategies for VLD in diverse clinical settings.
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