Department of Head and Neck Surgery, Tokyo Medical and Dental University, Tokyo, Japan.
Jpn J Clin Oncol. 2024 Aug 14;54(8):847-862. doi: 10.1093/jjco/hyae062.
Olfactory neuroblastoma is a rare sinonasal malignancy arising from the olfactory epithelium that is characterized by skull base involvement and a modest natural history. Because of its rarity and long course, identification of independent prognostic factors is dependent on multivariate analysis of large, long-term data. In this review, we outline evidence for the evaluation and treatment of olfactory neuroblastoma obtained from recent large-scale population-based studies, meta-analyses and multicenter studies. Hyams grade is currently the only pathological grade system for olfactory neuroblastoma. The modified Kadish staging and Dulguerov classification are available for clinical staging. The results of large-scale studies have confirmed Hyams, the modified Kadish and Dulguerov as independent prognostic factors. Surgery followed by radiotherapy provides the best overall survival and recurrence-free survival for resectable disease. The question of whether postoperative radiotherapy should be administered for all cases or only for those at risk of recurrence remains unanswered. Exclusively endoscopic resection is indicated for modified Kadish A/B cases without any increase in the risk of death or recurrence, and is also indicated for modified Kadish C cases if a negative surgical margin is ensured. For more advanced cases, such as those with extensive brain infiltration, the open approach is indicated. Elective nodal irradiation prevents late nodal recurrence of N0 patients. Chemotherapy has failed to show a benefit in survival or disease control. Current needs for olfactory neuroblastoma include the development and validation of refined staging systems suitable for current practice; expansion of indications for endoscopic surgery; less invasive surgery; definitive radiotherapy and novel systemic therapy.
嗅神经母细胞瘤是一种罕见的发生于嗅上皮的鼻腔鼻窦恶性肿瘤,其特征为颅底受累和适度的自然病史。由于其罕见性和较长的病程,独立预后因素的确定依赖于大型、长期数据的多变量分析。在这篇综述中,我们概述了最近的大规模基于人群的研究、荟萃分析和多中心研究中获得的嗅神经母细胞瘤评估和治疗的证据。Hyams 分级目前是嗅神经母细胞瘤唯一的病理分级系统。改良 Kadish 分期和 Dulguerov 分类可用于临床分期。大规模研究的结果证实了 Hyams、改良 Kadish 和 Dulguerov 是独立的预后因素。手术加放疗为可切除疾病提供了最佳的总生存率和无复发生存率。术后放疗是否应应用于所有病例或仅应用于有复发风险的病例,这一问题仍未得到解答。对于改良 Kadish A/B 型病例,如果没有增加死亡或复发的风险,完全内镜切除是指征;如果能确保手术切缘阴性,也适用于改良 Kadish C 型病例。对于更晚期的病例,如广泛脑浸润的病例,应采用开放式手术。选择性淋巴结照射可预防 N0 患者的淋巴结晚期复发。化疗未能显示在生存或疾病控制方面获益。当前嗅神经母细胞瘤的需求包括开发和验证适合当前实践的改良分期系统;扩大内镜手术的适应证;减少侵袭性手术;确定性放疗和新的全身治疗。
Otolaryngol Head Neck Surg. 2020-4-14
JAMA Otolaryngol Head Neck Surg. 2023-9-1
Otolaryngol Head Neck Surg. 2004-5
Laryngorhinootologie. 2006-10
Int J Radiat Oncol Biol Phys. 2010-3-16