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Updated: May 19, 2026

A Melanoma Patient-Derived Xenograft Model
Published on: May 20, 2019
Dynamic changes in nevi of a patient with melanoma treated with vemurafenib: importance of sequential dermoscopy
Abstract:
BACKGROUND Therapy with vemurafenib, an inhibitor of mutated BRAF, yields a response rate of approximately 50% in patients with metastatic melanoma harboring a BRAF V600E mutation. As an adverse effect of vemurafenib, proliferative disorders of keratinocytes, including squamous cell carcinoma, have been described. Low concentration of vemurafenib as present in the epidermis were found to activate wild-type RAF, which, in combination with a preexisting RAS mutation, can promote keratinocyte proliferation. While activating BRAF mutations occur in approximately 50% of melanomas, they are even more frequently observed in melanocytic nevi. OBSERVATION We present the case of a patient with dynamic changes of melanocytic nevi well documented by sequential digital dermoscopy during vemurafenib therapy. A variety of dermoscopic changes were observed. First, nevi involuted, and all of these originally showed a centrally elevated papillomatous and predominant globular pattern. Second, preexisting nevi increased in size, and pigmentation that rendered them atypical. Such lesions were flat and showed a predominant reticular pattern at baseline. Third, multiple new nevi occurred. One example of each of the latter 2 categories was excised and showed wild-type BRAF. CONCLUSION Our findings of changing nevi in a patient treated with vemurafenib highlight the need for sequential skin examinations, including dermoscopy.
Insights
Vemurafenib therapy for melanoma can cause changes in moles, including involution, enlargement, and new mole development. Regular skin checks with dermoscopy are crucial during treatment.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Vemurafenib, a BRAF inhibitor, treats metastatic melanoma with BRAF V600E mutations, achieving ~50% response rates.
- Adverse effects include keratinocyte proliferation, such as squamous cell carcinoma, due to epidermal vemurafenib activating wild-type RAF.
- BRAF mutations are common in melanoma (~50%) and even more frequent in melanocytic nevi.
Purpose of the Study:
- To document dynamic changes in melanocytic nevi during vemurafenib therapy.
- To highlight the importance of sequential skin examinations in patients receiving vemurafenib.
Main Methods:
- Case report of a patient undergoing vemurafenib therapy.
- Sequential digital dermoscopy to monitor nevus changes.
- Excision and molecular analysis (BRAF mutation status) of selected nevi.
Main Results:
- Observed involution of papillomatous nevi with globular patterns.
- Observed enlargement and atypical pigmentation in flat, reticular nevi.
- Observed development of new nevi; excised lesions showed wild-type BRAF.
Conclusions:
- Vemurafenib therapy can induce significant dynamic changes in melanocytic nevi.
- These changes necessitate vigilant, sequential skin surveillance, including dermoscopy, in patients on vemurafenib.
- Understanding these effects is crucial for differentiating treatment-related changes from melanoma progression.
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