Experiences and Outcomes in Olfactory Neuroblastoma Over A Decade at a Tertiary Cancer Center.

IF 0.6 Q4 ONCOLOGY South Asian Journal of Cancer Pub Date : 2022-10-01 DOI:10.1055/s-0041-1739181
Himabindu Korra, Joseph Benjamin Gandi, Prathyusha Nanuvala, Aarathi Ardha
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引用次数: 1

Abstract

Background  Olfactory neuroblastoma is a rare epithelial malignancy arising from the odorant receptors in the nasal mucosa or along the cribriform plate of the ethmoid bone. Clinical presentation includes nasal stuffiness, local pain, epistaxis, anosmia, visual impairment, proptosis, headache, and seizures. Radiologic imaging with CT or MRI, an ophthalmic evaluation, and histopathologic confirmation with immunohistochemistry are parts of the initial diagnostic workup. Although surgery, chemotherapy, and radiation have an equally important role in the management, earlier stages may preferably be treated with surgery or radiotherapy and the later stages with a multimodality approach. Materials and Methods  We conducted a retrospective review of 13 patients diagnosed with olfactory neuroblastoma, registered at Mehdi Nawaz Jung Regional Cancer Center over a decade (2010-2019). We analyzed the age and sex distribution, performance status at presentation, clinical symptomatology, and the Kadish stage. In addition, the therapeutic aspects of patients were studied. Results  The most common presentation noted was nasal stuffiness, followed by epistaxis and proptosis. The majority of patients had good performance status at presentation. Ten patients presented with a Kadish stage C, while the remaining patients presented with Kadish stage B. Cervical nodal metastasis was seen in three patients, four patients received multimodality treatment with neoadjuvant chemoradiotherapy followed by surgery, two patients received neoadjuvant chemotherapy followed by radiation, two patients received only surgery, and one patient received surgery followed by adjuvant radiation. Conformal radiation techniques were used to deliver doses as high as 50 to 66 Gy in 2 Gy per fraction. Two patients presented with distant metastasis during follow-up, one with bone metastasis, and the other with retroperitoneal nodal metastasis; they received palliative chemotherapy and conformal radiation to the primary site. Conclusion  This study concludes that neoadjuvant chemotherapy followed by radiation gives the best outcomes. It has been observed that in multi-modality treatment, radiotherapy played a significant role in improving overall survival and better outcomes. Multidisciplinary discussions provide a better sequencing of management.

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三期肿瘤中心十多年来嗅觉神经母细胞瘤的治疗经验和结果。
嗅觉神经母细胞瘤是一种罕见的上皮恶性肿瘤,起源于鼻黏膜或筛骨筛网板上的气味受体。临床表现包括鼻塞、局部疼痛、鼻出血、嗅觉丧失、视力障碍、眼球突出、头痛和癫痫发作。CT或MRI放射成像,眼科检查和免疫组织化学组织病理学确认是初步诊断的一部分。虽然手术、化疗和放疗在治疗中同样重要,但早期阶段最好采用手术或放疗治疗,晚期采用多模式治疗。材料和方法我们对在Mehdi Nawaz Jung地区癌症中心登记的十多年(2010-2019)中诊断为嗅觉神经母细胞瘤的13例患者进行了回顾性研究。我们分析了年龄和性别分布、表现状况、临床症状和卡迪什分期。此外,还对患者的治疗方面进行了研究。结果最常见的临床表现为鼻塞,其次为鼻出血和鼻突出。大多数患者在就诊时表现良好。10例患者为卡迪什C期,其余患者为卡迪什b期。3例患者宫颈淋巴结转移,4例患者接受新辅助放化疗后手术,2例患者接受新辅助化疗后放疗,2例患者仅接受手术,1例患者接受手术后辅助放疗。采用适形辐射技术,以每分数2戈瑞的比例提供高达50至66戈瑞的剂量。2例患者在随访中出现远处转移,1例为骨转移,1例为腹膜后淋巴结转移;他们接受姑息性化疗和原发部位的适形放疗。结论新辅助化疗加放疗治疗效果最佳。据观察,在多模式治疗中,放疗在提高总生存率和改善预后方面发挥了重要作用。多学科讨论提供了更好的管理顺序。
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CiteScore
1.00
自引率
0.00%
发文量
80
审稿时长
35 weeks
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