Department of Dermatology, Osaka University Graduate School of Medicine, Suita, Japan.
Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.
J Dermatol. 2020 Apr;47(4):423-425. doi: 10.1111/1346-8138.15256. Epub 2020 Feb 6.
Mucosal melanoma of the nasal cavity is a rare disease that has been consistently associated with poor outcome. While complete surgical excision offers the only prospect of a cure, it is associated with a high risk of surgical morbidity due to the challenging anatomical location, and most patients still develop incurable metastatic disease. The efficacy of immunotherapy on mucosal melanoma is lower in comparison with cutaneous melanoma, and mucosal melanoma rarely has BRAF mutations. Although preclinical data have shown that combination treatment with immune checkpoint inhibitors and radiotherapy (RT) improve the response, there have been few reports on the combination of RT and anti-programmed death 1 therapy for mucosal melanoma of the nasal cavity. We retrospectively investigated 10 cases of mucosal melanoma of the nasal cavity in which combined treatment was applied. The local control (LC) rate of the primary lesion and regional lymph nodes was favorably 100%. On the other hand, the median progression-free survival (PFS) time was 29.6 weeks (range, 2-82). The 6-month PFS rate was 60%. Although severe mucositis occurred in one patient, the incidence of treatment-related adverse events was not significantly increased. RT with anti-programmed death 1 antibody therapy for mucosal melanoma of the nasal cavity was tolerable and had the potential to improve LC and PFS.
鼻腔黏膜黑色素瘤是一种罕见疾病,其预后一直较差。虽然完全手术切除是治愈的唯一希望,但由于解剖位置的挑战性,手术发病率很高,大多数患者仍会发展为无法治愈的转移性疾病。与皮肤黑色素瘤相比,免疫疗法对黏膜黑色素瘤的疗效较低,而且黏膜黑色素瘤很少有 BRAF 突变。虽然临床前数据表明,免疫检查点抑制剂联合放疗(RT)可提高疗效,但关于 RT 联合抗程序性死亡 1 治疗鼻腔黏膜黑色素瘤的报道很少。我们回顾性研究了 10 例接受联合治疗的鼻腔黏膜黑色素瘤患者。原发灶和区域淋巴结的局部控制(LC)率为 100%。另一方面,中位无进展生存期(PFS)为 29.6 周(范围,2-82)。6 个月的 PFS 率为 60%。虽然 1 例患者发生严重黏膜炎,但治疗相关不良事件的发生率并未显著增加。RT 联合抗程序性死亡 1 抗体治疗鼻腔黏膜黑色素瘤是可耐受的,并有提高 LC 和 PFS 的潜力。