Department of Hepato-Biliary Surgery, Shenzhen Third People's Hospital, The Second Affiliated Hospital, Southern University of Science and Technology, Shenzhen, 518055, China.
Department of Ultrasonography, Shenzhen Third People's Hospital, The Second Affiliated Hospital, Southern University of Science and Technology, Shenzhen, 518055, China.
BMC Cancer. 2021 May 18;21(1):567. doi: 10.1186/s12885-021-08337-y.
Primary hepatic neuroendocrine tumors (PH-NETs) are extremely rare and unknown. Because of its rarity, its prognosis features and influencing factors are not well established.
Data of 140 patients with PH-NETs diagnosed in the SEER database from 1975 to 2016 were collected. The demographics and clinic-pathological features were described. By using propensity-score matching (PSM) analysis, three associated cohorts were selected to describe the malignancy of PH-NETs and univariate analysis was conducted. Then, multivariate Cox analyses were performed and a predicting nomograph was constructed. C-index, receiver operating characteristic (ROC) curve and calibration curves were used to evaluate the predictive value of nomogram.
The overall survival outcomes of PH-NETs were superior to hepatocellular carcinoma (HCC) with a mean survival time 30.64 vs 25.11 months (p = 0.052), but inferior to gastrointestinal tract neuroendocrine tumors in situ (GI-NETs in situ) with a mean survival time 30.64 vs 41.62 months (p = 0.017). With reference to gastrointestinal neuroendocrine tumors with liver metastasis (GI-NETs-LM), GI-NETs-LM had better outcomes in short time (1-year survival rate: 64.75% vs 56.43%) but was worse in long time (5-year survival rate: 8. 63% vs 18.57%). Multivariate Cox analyses showed that tumor grade and surgery were two independent factors for prognosis of the patients (p < 0.00). Tumor grade and surgery were used to construct the predicting nomogram. The C-index was 0.79 (95%CI = 0.75-0.83). The area under curve (AUC) values in ROC were 0.868 in 1-year and 0.917 in 3-year survival and the calibration curves showed good consistency.
The overall prognosis PH-NETs is generally favorable, better than HCC and GI-NETs-LM in long term. Preoperative biopsy and complete pathological diagnosis were recommended. Radical surgical intervention including transplantation was the first choice in PH-NETs therapy.
原发性肝神经内分泌肿瘤(PH-NETs)非常罕见,尚未被完全认识。由于其罕见性,其预后特征和影响因素尚未明确。
收集 1975 年至 2016 年间 SEER 数据库中诊断为 PH-NETs 的 140 例患者的数据。描述患者的人口统计学和临床病理特征。通过倾向评分匹配(PSM)分析,选择三个相关队列来描述 PH-NETs 的恶性程度,并进行单因素分析。然后进行多变量 Cox 分析,并构建预测列线图。使用 C 指数、接收者操作特征(ROC)曲线和校准曲线来评估列线图的预测价值。
PH-NETs 的总体生存结果优于肝细胞癌(HCC),平均生存时间为 30.64 个月比 25.11 个月(p=0.052),但劣于原位胃肠道神经内分泌肿瘤(GI-NETs 原位),平均生存时间为 30.64 个月比 41.62 个月(p=0.017)。与肝转移的胃肠道神经内分泌肿瘤(GI-NETs-LM)相比,GI-NETs-LM 在短期内(1 年生存率:64.75%比 56.43%)有更好的结果,但在长期(5 年生存率:8.63%比 18.57%)则更差。多变量 Cox 分析表明,肿瘤分级和手术是影响患者预后的两个独立因素(p<0.00)。肿瘤分级和手术用于构建预测列线图。C 指数为 0.79(95%CI=0.75-0.83)。ROC 曲线下面积(AUC)值在 1 年和 3 年生存分别为 0.868 和 0.917,校准曲线显示出良好的一致性。
PH-NETs 的总体预后通常较好,长期预后优于 HCC 和 GI-NETs-LM。建议在治疗前进行活检和完整的病理诊断。根治性手术干预包括移植是 PH-NETs 治疗的首选。