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Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis

机译:原发性神经胶质瘤的临床特征和疾病特异性预后诺模图:基于SEER人群的分析

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摘要

Because the study population with gliosarcoma (GSM) is limited, the understanding of this disease is insufficient. In this study, the authors aimed to determine the clinical characteristics and independent prognostic factors influencing the prognosis of GSM patients and to develop a nomogram to predict the prognosis of GSM patients after craniotomy. A total of 498 patients diagnosed with primary GSM between 2004 and 2015 were extracted from the 18 Registries Research Data of the Surveillance, Epidemiology, and End Results (SEER) database. The median disease-specific survival (DSS) was 12.0 months, and the postoperative 0.5-, 1-, and 3-year DSS rates were 71.4%, 46.4% and 9.8%, respectively. We applied both the Cox proportional hazards model and the decision tree model to determine the prognostic factors of primary GSM. The Cox proportional hazards model demonstrated that age at presentation, tumour size, metastasis state and adjuvant chemotherapy (CT) were independent prognostic factors for DSS. The decision tree model suggested that age <71 years and adjuvant CT were associated with a better prognosis for GSM patients. The nomogram generated via the Cox proportional hazards model was developed by applying the rms package in R version 3.5.0. The C-index of internal validation for DSS prediction was 0.67 (95% confidence interval (CI), 0.63 to 0.70). The calibration curve at one year suggested that there was good consistency between the predicted DSS and the actual DSS probability. This study was the first to develop a disease-specific nomogram for predicting the prognosis of primary GSM patients after craniotomy, which can help clinicians immediately and accurately predict patient prognosis and conduct further treatment.
机译:由于神经胶质肉瘤(GSM)的研究人群有限,因此对该疾病的了解不足。在这项研究中,作者旨在确定影响GSM患者预后的临床特征和独立的预后因素,并开发诺模图以预测开颅手术后GSM患者的预后。从监视,流行病学和最终结果(SEER)数据库的18个注册研究数据中提取了2004年至2015年之间总计498名被诊断为原发GSM的患者。中位疾病特异性生存(DSS)为12.0个月,术后0.5年,1年和3年DSS发生率分别为71.4%,46.4%和9.8%。我们应用Cox比例风险模型和决策树模型来确定主要GSM的预后因素。 Cox比例风险模型表明,就诊年龄,肿瘤大小,转移状态和辅助化疗(CT)是DSS的独立预后因素。决策树模型表明,年龄<71岁和辅助性CT与GSM患者的预后更好相关。通过Cox比例风险模型生成的列线图是通过应用R版本3.5.0中的rms软件包开发的。 DSS预测的内部验证的C指数为0.67(95%置信区间(CI)为0.63至0.70)。一年的校准曲线表明,预测的DSS与实际DSS概率之间具有良好的一致性。这项研究是第一个开发针对疾病的诺模图以预测开颅手术后原发性GSM患者的预后的方法,该方法可以帮助临床医生立即准确地预测患者的预后并进行进一步治疗。

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