McElroy E A, Buckner J C, Lewis J E
Department of Oncology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
Neurosurgery. 1998 May;42(5):1023-7; discussion 1027-8. doi: 10.1097/00006123-199805000-00040.
Esthesioneuroblastoma (olfactory neuroblastoma) is a rare neuroendocrine tumor that arises in the upper nasal cavity from the olfactory epithelium. Little information is available regarding the treatment of these tumors with chemotherapy in the advanced setting. A retrospective review of patients with recurrent esthesioneuroblastoma treated with chemotherapy between 1970 and 1995 at the Mayo Clinic was undertaken to gain more information regarding the efficacy of chemotherapy treatment for these patients.
Ten patients were identified using a computerized data base available at this institution. The clinical and pathological materials, when available, were reviewed, and each tumor reviewed was assigned a Hyams' grade.
There were six men and four women, ranging in age from 22 to 74 years, all of whom had assessable Kadish Stage C disease at the time of chemotherapy treatment. The chemotherapy regimens and clinical follow-up varied during this 25-year time span. The only tumor regression resultant from chemotherapy was observed in patients with high-grade tumors. Two of four patients with high-grade tumors obtained regression from first-line, platinum-based chemotherapy, with a mean duration of regression of 9.3 months (range, 2-13 mo). Survival time from initial diagnosis was 139.5 months (range, 83-168 mo) in patients with low-grade tumors and 32.2 months (range, 5-84 mo) in patients with high-grade tumors. Survival from initial chemotherapy treatment was 44.5 months (range, 3-130 mo) in patients with low-grade tumors and 26.5 months (range, 2-67 mo) in patients with high-grade tumors.
Hyams' grading of esthesioneuroblastoma tumors seems to be important in predicting response to chemotherapy. Despite sensitivity to platinum-based chemotherapy, patients with high-grade tumors in this series had a much more aggressive course than did those with lower-grade tumors. This series suggests that cisplatin-based chemotherapy is active in advanced, high-grade esthesioneuroblastoma and is a reasonable choice in the systemic treatment of these patients.
嗅神经母细胞瘤是一种罕见的神经内分泌肿瘤,起源于鼻腔上部的嗅上皮。关于晚期情况下这些肿瘤化疗治疗的信息很少。对1970年至1995年在梅奥诊所接受化疗的复发性嗅神经母细胞瘤患者进行回顾性研究,以获取更多关于这些患者化疗疗效的信息。
利用该机构现有的计算机数据库识别出10名患者。对现有的临床和病理资料进行回顾,并对每个审查的肿瘤进行海姆斯分级。
有6名男性和4名女性,年龄在22至74岁之间,所有患者在化疗时均有可评估的卡迪什C期疾病。在这25年期间,化疗方案和临床随访各不相同。化疗导致的唯一肿瘤退缩见于高级别肿瘤患者。4名高级别肿瘤患者中有2名从一线铂类化疗中获得退缩,退缩的平均持续时间为9.3个月(范围为2至13个月)。低级别肿瘤患者从初始诊断开始的生存时间为139.5个月(范围为83至168个月),高级别肿瘤患者为32.2个月(范围为5至84个月)。低级别肿瘤患者从初始化疗开始的生存时间为44.5个月(范围为3至130个月),高级别肿瘤患者为26.5个月(范围为2至67个月)。
嗅神经母细胞瘤的海姆斯分级在预测化疗反应方面似乎很重要。尽管对铂类化疗敏感,但该系列中高级别肿瘤患者的病程比低级别肿瘤患者更具侵袭性。该系列表明,基于顺铂的化疗在晚期高级别嗅神经母细胞瘤中具有活性,是这些患者全身治疗的合理选择。