Dermatology Research Centre, The University of Queensland, School of Medicine, Translational Research Institute, Brisbane, Queensland, Australia.
Dermatology Research Centre, The University of Queensland, School of Medicine, Translational Research Institute, Brisbane, Queensland, Australia2The University of Queensland, Institute for Molecular Biosciences, Brisbane, Queensland, Australia.
JAMA Dermatol. 2014 Oct;150(10):1079-82. doi: 10.1001/jamadermatol.2014.436.
Recent advances in targeting BRAFV600E mutations, which occur in roughly 50% of melanomas and 70% of benign nevi, have improved response rates and survival in patients with melanoma. With increased survival, the importance of other comorbidities increases and requires consideration in long-term management. This case report discusses dynamic dermoscopic nevus changes that occur during dabrafenib therapy and offers some conclusions regarding BRAF mutations and the changes.
A man in his 30s had been monitored with whole-body dermoscopy at roughly 7-month intervals as part of a nevus surveillance study. Fourteen months after his initial visit, metastases were found, and the patient entered a clinical trial of dabrafenib with or without trametinib therapy. Continued dermoscopic monitoring for the next 12 months revealed that approximately 50% of the existing acquired melanocytic nevi involuted, while the remaining nevi did not change. Biopsy findings from 1 unchanged and 1 involuted nevus showed BRAF wild type in the unchanged nevus, BRAFV600E mutation in the involuting nevus, and no malignant histopathologic characteristics in either one.
Our observations indicate that a previously suggested hypothesis regarding involuting nevi in BRAF inhibitor therapy is correct: Nevi that involute while a patient is undergoing BRAF V600E inhibitor therapy possess the BRAF V600E mutation, while others that grow or remain unchanged are wild type. However larger-scale trials are required to gather conclusive data and create a more complete clinical picture.
针对 BRAFV600E 突变的靶向治疗取得了新进展,这种突变约发生于 50%的黑色素瘤和 70%的良性痣中,改善了黑色素瘤患者的反应率和存活率。随着存活率的提高,其他合并症的重要性也在增加,这需要在长期管理中加以考虑。本病例报告讨论了达布拉非尼治疗期间动态皮肤镜下痣的变化,并对 BRAF 突变和这些变化提供了一些结论。
一名 30 多岁的男性一直在进行全身皮肤镜监测,作为痣监测研究的一部分,大约每 7 个月监测一次。初次就诊后 14 个月发现转移,患者参加了达布拉非尼联合或不联合曲美替尼治疗的临床试验。在接下来的 12 个月里,持续的皮肤镜监测显示,大约 50%的现有的获得性黑素细胞痣消退,而其余的痣没有变化。1 个未改变和 1 个消退的痣的活检结果显示,未改变的痣为 BRAF 野生型,消退的痣为 BRAFV600E 突变,两者均无恶性组织病理学特征。
我们的观察表明,关于 BRAF 抑制剂治疗中消退痣的一个先前提出的假说是正确的:在接受 BRAF V600E 抑制剂治疗的过程中消退的痣具有 BRAF V600E 突变,而其他生长或保持不变的痣则为野生型。然而,需要更大规模的试验来收集确凿的数据并创建更完整的临床图像。