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Eruptive naevi in a patient treated with LGX818 for BRAF mutant metastatic melanoma

机译:LGX818治疗BRAF突变转移性黑色素瘤患者的爆发性奈维

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LGX818 is a new-generation BRAF inhibitor (BRAFi) that is currently undergoing phase 3 trials for the treatment of BRAF mutant metastatic melanoma patients (NCT01909453). Cutaneous toxicities associated with the administration of BRAF inhibitors are considered to be induced by the paradoxical activation of the mitogen-activated protein kinase pathway in wild-type BRAF cells. Changes in naevi, including new naevi, hyperpigmentation and fading of existing naevi, have also been reported. In addition, some patients receiving these therapies have developed second primary melanomas. As a consequence, the importance of sequential digital dermoscopy in all patients treated with a BRAFi to detect new primary melanomas has been emphasized. A 61-year-old man with (V600E)BRAF mutant stage IV metastatic melanoma was commenced on the phase 1 trial of LGX818 at 300mg daily in 2013. After 2 months of therapy, the patient was noted to have developed eruptive naevi, fading of existing naevi and darkening of other naevi. Excision of a new pigmented lesion from the back indicated a compound naevus. Immunohistochemistry showed that the naevus cells lacked a BRAF V600E mutation. This is the first reported case of eruptive naevi in a patient treated with LGX818. The absence of the BRAF V600E mutation within a changing naevus supports the theory that BRAFi stimulates the proliferation of wild-type BRAF cells. Close dermatological surveillance is important for all patients treated with any type of BRAFi.
机译:LGX818是新一代BRAF抑制剂(BRAFi),目前正在进行3期试验,用于治疗BRAF突变型转移性黑色素瘤患者(NCT01909453)。与BRAF抑制剂给药有关的皮肤毒性被认为是野生型BRAF细胞中有丝分裂原激活的蛋白激酶途径的反常激活所诱导的。也已经报道了naevi的变化,包括新的naevi,色素沉着和现有naevi的褪色。此外,一些接受这些疗法的患者已发展为第二原发性黑色素瘤。结果,已经强调了在所有接受BRAFi治疗的患者中进行顺序数字皮肤镜检查以检测新发原发性黑色素瘤的重要性。一名(V600E)BRAF突变IV期转移性黑色素瘤的61岁男性于2013年开始每日300mg的LGX818的1期试验中开始治疗。经过2个月的治疗,该患者已发展为爆发性奈维,褪色。现有的naevi和其他naevi的变暗。从背部切除新的色素性病变表明有复合痣。免疫组织化学显示,痣细胞缺乏BRAF V600E突变。这是LGX818治疗的患者中首次报告的纳维火山喷发病例。不断变化的痣内不存在BRAF V600E突变,这支持BRAFi刺激野生型BRAF细胞增殖的理论。对于所有接受任何类型BRAFi治疗的患者而言,严密的皮肤病学监测都很重要。

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