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鼻腔鼻窦恶性黑色素瘤。

Sinonasal Malignant Melanoma.

机构信息

Professor Emeritus in Rhinology, UCL, London UK & Honorary Consultant Rhinologist and Anterior Skull Base Surgeon, Royal National Throat, Nose and Ear Hospital, UCLH, London, United Kingdom,

出版信息

Adv Otorhinolaryngol. 2020;84:185-196. doi: 10.1159/000457937. Epub 2020 Jul 30.

Abstract

Sinonasal malignant mucosal melanoma (SNMM) is a rare, aggressive, and capricious tumour accounting for 4% of sinonasal malignancies. Recent studies suggest an increasing frequency. There are few large published series, but all authors report poor outcomes irrespective of treatment of approximately 25% 5-year survival. As a consequence, the American Joint Committee on Cancer (AJCC) have restaged all SNMMs as T3 or greater, irrespective of extent. Surgery remains the principle treatment modality. Survival and recurrence data analysis from a single-centre prospective cohort of 125 cases (all treated surgically with or without radiotherapy) showed 5-year overall survival was 28% and disease-free survival was 23.7%. Local control was achieved for a median of 21 months, with a 5-year disease control rate of 27.7%. However, endoscopically resected cases showed a significant overall survival advantage up to 5 years, confirming that endoscopic resection of SNMM does not adversely affect outcome and may even be beneficial up to 5 years. These findings are supported by other recent series in the literature. Radiotherapy did not improve local control or survival in this study, though there is debate in the literature as to its value. Cervical metastases confer a dramatically worse outcome. Chemotherapy has not previously shown much advantage, but more recently immunologic manipulation with drugs such as ipilimumab have shown promise. Thus far, the mutation status does not appear to affect survival outcomes, but NRAS mutations are relatively frequent and could be targeted in this disease by MEK inhibitors in the future.

摘要

鼻腔鼻窦恶性黏膜黑色素瘤(SNMM)是一种罕见、侵袭性和多变的肿瘤,占鼻腔鼻窦恶性肿瘤的 4%。最近的研究表明其发病率呈上升趋势。虽然有少数大型已发表的系列研究,但所有作者报告的结果都很差,无论治疗情况如何,5 年生存率约为 25%。因此,美国癌症联合委员会(AJCC)将所有 SNMM 重新分期为 T3 或更高,无论其范围如何。手术仍然是主要的治疗方式。对 125 例(均通过手术治疗,或手术联合放疗)单一中心前瞻性队列的生存和复发数据分析显示,5 年总生存率为 28%,无疾病生存率为 23.7%。中位局部控制时间为 21 个月,5 年疾病控制率为 27.7%。然而,经内镜切除的病例在 5 年内具有显著的总体生存优势,证实内镜切除 SNMM 不会对结果产生不利影响,甚至在 5 年内可能有益。这些发现得到了文献中其他最近系列研究的支持。在这项研究中,放疗并没有改善局部控制或生存,但在文献中存在关于其价值的争议。颈部转移会导致预后明显恶化。化疗以前并没有显示出太多优势,但最近使用伊匹单抗等药物进行免疫治疗显示出了希望。到目前为止,突变状态似乎不会影响生存结果,但NRAS 突变相对频繁,未来可能可以通过 MEK 抑制剂针对这种疾病进行靶向治疗。

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