Department of Head and Neck Surgery, David Geffen School of Medicine at UCLA (University of California, Los Angeles)2Jonsson Comprehensive Cancer Center, David Geffen School of Medicine at UCLA, Los Angeles3Head and Neck Cancer Program, David Geffen Schoo.
Department of Head and Neck Surgery, David Geffen School of Medicine at UCLA (University of California, Los Angeles).
JAMA Otolaryngol Head Neck Surg. 2014 Dec;140(12):1124-9. doi: 10.1001/jamaoto.2014.2541.
There is a need for larger studies characterizing the effect of tumor grade on survival for patients with esthesioneuroblastoma.
To investigate prognostic factors for survival in patients diagnosed with esthesioneuroblastoma, including emphasis on tumor grade.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective, population-based cohort study of patients in the Surveillance, Epidemiology, and End Results (SEER) tumor registry who were diagnosed with esthesioneuroblastoma from January 1, 1973, to January 1, 2010. The last date of survival follow-up was 2013.
Overall and disease-specific survival.
The cohort included 281 patients with a mean age of 52 years. There were 154 males (54.8%) and 127 females (45.2%). Kaplan-Meier analysis demonstrated an overall and disease-specific survival rate of 61% and 70% at 5 years and 50% and 64% at 10 years, respectively. Multivariable Cox regression analysis showed that advanced tumor grade and modified Kadish stage (hazard ratio, 4.930; 95% CI, 2.635-9.223; P = .001) portended worse disease-specific survival, and radiation therapy (hazard ratio, 0.499; 95% CI, 0.272-0.916; P = .03) improved disease-specific survival. Patients with low-grade tumors (grades I and II) demonstrated an overall and disease-specific survival rate of 84% and 92% at 5 years and 67% and 87% at 10 years, respectively. Multivariable analysis of low-grade tumors only revealed receiving surgery (P = .004) as an independent positive predictor of disease-specific survival. High-grade tumors (grades III and IV) demonstrated overall and disease-specific survival of 40% and 50% at 5 years and 34% and 43% at 10 years, respectively. Multivariable analysis of high-grade tumors showed modified Kadish stage (hazard ratio, 2.025; 95% CI, 1.430-2.866; P < .001) predicted worse disease-specific survival, and radiation therapy (hazard ratio, 0.433; 95% CI, 0.228-0.864; P = .02) independently predicted improved disease-specific survival.
Here, to our knowledge, we report the largest study investigating prognostic factors for survival, with the inclusion of tumor grade, in patients diagnosed with esthesioneuroblastoma. Patients with high-grade tumors had substantially worse survival rates than patients with low-grade tumors. Multivariable analysis revealed only receiving surgery as an independent predictor of disease-specific survival for patients with low-grade tumors, while modified Kadish stage and postoperative radiation therapy were significant factors in predicting disease-specific survival in patients with high-grade tumors. This study highlights the growing evidence that tumor grade should be a key factor in predicting survival in patients with esthesioneuroblastoma, and that adjuvant radiation therapy improves survival rates among patients with high-grade, but not low-grade, tumors.
需要更大规模的研究来描述肿瘤分级对嗅神经母细胞瘤患者生存的影响。
调查影响嗅神经母细胞瘤患者生存的预后因素,包括强调肿瘤分级。
设计、地点和参与者:这是一项基于人群的回顾性队列研究,研究对象来自于监测、流行病学和最终结果(SEER)肿瘤登记处的患者,这些患者于 1973 年 1 月 1 日至 2010 年 1 月 1 日被诊断为嗅神经母细胞瘤。生存随访的最后日期为 2013 年。
总生存率和疾病特异性生存率。
该队列包括 281 名平均年龄为 52 岁的患者。其中男性 154 人(54.8%),女性 127 人(45.2%)。Kaplan-Meier 分析显示,5 年和 10 年的总生存率和疾病特异性生存率分别为 61%和 70%、50%和 64%。多变量 Cox 回归分析显示,高级别肿瘤分级和改良 Kadish 分期(风险比,4.930;95%CI,2.635-9.223;P = .001)预示着疾病特异性生存率更差,放射治疗(风险比,0.499;95%CI,0.272-0.916;P = .03)改善了疾病特异性生存率。低级别肿瘤(I 级和 II 级)患者的 5 年和 10 年总生存率和疾病特异性生存率分别为 84%和 92%、67%和 87%。低级别肿瘤的多变量分析仅显示接受手术(P = .004)是疾病特异性生存率的独立正预测因子。高级别肿瘤(III 级和 IV 级)患者的 5 年和 10 年总生存率和疾病特异性生存率分别为 40%和 50%、34%和 43%。高级别肿瘤的多变量分析显示改良 Kadish 分期(风险比,2.025;95%CI,1.430-2.866;P < .001)预测疾病特异性生存率更差,放射治疗(风险比,0.433;95%CI,0.228-0.864;P = .02)独立预测疾病特异性生存率改善。
在这里,据我们所知,我们报告了最大规模的研究,该研究调查了包括肿瘤分级在内的影响嗅神经母细胞瘤患者生存的预后因素。高级别肿瘤患者的生存率明显低于低级别肿瘤患者。多变量分析显示,只有接受手术是低级别肿瘤患者疾病特异性生存率的独立预测因素,而改良 Kadish 分期和术后放疗是预测高级别肿瘤患者疾病特异性生存率的重要因素。这项研究强调了越来越多的证据表明,肿瘤分级应该是预测嗅神经母细胞瘤患者生存的关键因素,辅助放疗可提高高级别肿瘤患者的生存率,但不能提高低级别肿瘤患者的生存率。