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Differentiation Versus Grade for Pancreatic Neuroendocrine Neoplasms.
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Endocr Relat Cancer. 2025 Jan 30;32(3). doi: 10.1530/ERC-24-0203. Print 2025 Mar 1.
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Pancreatic Neuroendocrine Neoplasms: Classification and Novel Role of Endoscopic Ultrasound in Diagnosis and Treatment Personalization.胰腺神经内分泌肿瘤:内镜超声在诊断及治疗个体化中的分类及新作用
United European Gastroenterol J. 2025 Feb;13(1):34-43. doi: 10.1002/ueg2.12710. Epub 2024 Nov 14.
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World Medical Association Declaration of Helsinki: Ethical Principles for Medical Research Involving Human Participants.《世界医学协会赫尔辛基宣言:涉及人类受试者的医学研究伦理原则》
JAMA. 2025 Jan 7;333(1):71-74. doi: 10.1001/jama.2024.21972.
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Recurrence and treatment trends of pancreatic neuroendocrine tumors.胰腺神经内分泌肿瘤的复发及治疗趋势
Surgery. 2025 Jan;177:108835. doi: 10.1016/j.surg.2024.05.051. Epub 2024 Oct 4.
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Neuroendocrine Neoplasms.神经内分泌肿瘤。
Prim Care. 2024 Sep;51(3):549-560. doi: 10.1016/j.pop.2024.04.010. Epub 2024 May 23.
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Gastroenteropancreatic neuroendocrine neoplasms: current development, challenges, and clinical perspectives.胃肠胰神经内分泌肿瘤:当前的发展、挑战和临床观点。
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Pancreatic Neuroendocrine Tumors in French VHL Mutation Carriers.法国VHL基因突变携带者中的胰腺神经内分泌肿瘤
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Advancements in medical treatment for pancreatic neuroendocrine tumors: A beacon of hope.胰腺神经内分泌肿瘤的医学治疗进展:希望之光。
World J Gastroenterol. 2024 Mar 28;30(12):1670-1675. doi: 10.3748/wjg.v30.i12.1670.
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Epidemiology of gastroenteropancreatic neuroendocrine neoplasms: a review and protocol presentation for bridging tumor registry data with the Italian association for neuroendocrine tumors (Itanet) national database.胃肠胰神经内分泌肿瘤的流行病学:一项综述及方案介绍,旨在将肿瘤登记处数据与意大利神经内分泌肿瘤学会(Itanet)国家数据库相连接。
Endocrine. 2024 Apr;84(1):42-47. doi: 10.1007/s12020-023-03649-4. Epub 2024 Jan 4.

胰腺神经内分泌肿瘤血清学标志物的临床特征及预后价值:一项单中心回顾性研究

Clinical characteristics and prognostic value of serological markers in pancreatic neuroendocrine tumors: a single-center retrospective study.

作者信息

Wan Renrui, Wang Junfeng, Xie Ping, Wu Xiaochang, Guo Kun

机构信息

Department of Hepatobiliary Surgery, Huzhou Central Hospital (The Affiliated Central Hospital of Huzhou Teachers College, The Fifth School of Clinical Medicine, Zhejiang Chinese Medical University, The Affiliated Huzhou Hospital, Zhejiang University School of Medicine) Huzhou 313000, Zhejiang, P. R. China.

Department of Hepatobiliary Surgery, The Fourth Affiliated Hospital of Zhejiang University School of Medicine Yiwu 322000, Zhejiang, P. R. China.

出版信息

Am J Cancer Res. 2025 Aug 15;15(8):3546-3556. doi: 10.62347/HTDK5833. eCollection 2025.

DOI:10.62347/HTDK5833
PMID:40948524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12432554/
Abstract

OBJECTIVE

To investigate the clinical characteristics, diagnostic methods, treatment strategies and prognostic factors of pancreatic neuroendocrine tumors (pNETs).

METHODS

A retrospective analysis was conducted on 43 pNET patients treated at Huzhou Central Hospital from January 2003 to December 2023. The data included age, gender, function, tumor location, tumor size, pathological characteristics, lymph nodes, metastasis, and treatment. Association of these factors with pNET prognosis was proven by univariate analysis and multivariate analysis.

RESULTS

The incidence of G3 tumors in this group of advanced patients was relatively high (P=0.001). Meanwhile, elevated CA125 was commonly seen in the advanced stage (P=0.045), and surgeries occurred more frequently in the early stage (P=0.003). In addition, the positive expression of CD56 in low-grade tumors was relatively high (P=0.014). The incidence of non-functional tumors larger than 2 cm was high (P=0.015). Univariate Cox regression revealed that tumor size >2 cm, G3 grade, liver metastasis, advanced stage, lymph node metastasis and invasion were risk factors. Multivariate analysis revealed that G3 grade, liver metastasis and advanced stage were independent influencing factors for disease progression.

CONCLUSION

pNETs are heterogeneous tumors. Pathological grade, metastatic status, and serological markers may assist in diagnosis and prognosis assessment, aiding individualized clinical management.

摘要

目的

探讨胰腺神经内分泌肿瘤(pNETs)的临床特征、诊断方法、治疗策略及预后因素。

方法

对2003年1月至2023年12月在湖州市中心医院接受治疗的43例pNET患者进行回顾性分析。数据包括年龄、性别、功能、肿瘤位置、肿瘤大小、病理特征、淋巴结、转移情况及治疗情况。通过单因素分析和多因素分析验证这些因素与pNET预后的相关性。

结果

该组晚期患者中G3肿瘤的发生率相对较高(P=0.001)。同时,晚期患者中CA125升高较为常见(P=0.045),而手术在早期更为频繁(P=0.003)。此外,低级别肿瘤中CD56的阳性表达相对较高(P=0.014)。大于2 cm的无功能肿瘤发生率较高(P=0.015)。单因素Cox回归显示,肿瘤大小>2 cm、G3分级、肝转移、晚期、淋巴结转移及侵犯是危险因素。多因素分析显示,G3分级、肝转移和晚期是疾病进展的独立影响因素。

结论

pNETs是异质性肿瘤。病理分级、转移状态及血清学标志物可能有助于诊断和预后评估,辅助个体化临床管理。