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Prognostic validity of a novel American Joint Committee on Cancer Staging Classification for pancreatic neuroendocrine tumors.一种新型美国癌症联合委员会(AJCC)分期分类系统对胰腺神经内分泌肿瘤预后的有效性。
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N Engl J Med. 2011 Feb 10;364(6):514-23. doi: 10.1056/NEJMoa1009290.
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N Engl J Med. 2011 Feb 10;364(6):501-13. doi: 10.1056/NEJMoa1003825.
6
DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors.DAXX/ATRX、MEN1 和 mTOR 通路基因在胰腺神经内分泌肿瘤中经常发生改变。
Science. 2011 Mar 4;331(6021):1199-203. doi: 10.1126/science.1200609. Epub 2011 Jan 20.
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9
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胰腺神经内分泌肿瘤(pNETs)的治疗进展

Advances in the Treatment of Pancreatic Neuroendocrine Tumors (pNETs).

作者信息

Strosberg Jonathan

机构信息

H. Lee Moffitt Cancer Center and Research Institute Department of GI Oncology Tampa, FL.

出版信息

Gastrointest Cancer Res. 2013 Jul;6(4 Suppl 1):S10-2.

PMID:24312683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3849907/
Abstract

Recent clinical trials have led to significant advancements in treatment options for metastatic neuroendocrine tumors of the pancreas. Sunitinib and everolimus have been approved by the Food and Drug Administration for treatment of progressive pancreatic NETs based on phase III trial data demonstrating improvements in progression-free survival. Cytotoxic drugs such as temozolomide and capecitabine have been associated with high radiographic response rates; however data derives primarily from subset analysis of prospective trials and from retrospective series. During the next few years, randomized clinical trials are expected to provide more clarity on the role of somatostatin analogs and cytotoxic drugs. New studies are also evaluating biomarkers that will potentially allow for improved selection of drugs for specific tumor subtypes.

摘要

近期的临床试验已使胰腺转移性神经内分泌肿瘤的治疗选择取得了重大进展。基于III期试验数据显示无进展生存期有所改善,舒尼替尼和依维莫司已获美国食品药品监督管理局批准用于治疗进展性胰腺神经内分泌肿瘤。替莫唑胺和卡培他滨等细胞毒性药物已显示出较高的影像学缓解率;然而,数据主要来自前瞻性试验的亚组分析和回顾性系列研究。在未来几年,随机临床试验有望更明确地阐明生长抑素类似物和细胞毒性药物的作用。新的研究也在评估生物标志物,这可能有助于针对特定肿瘤亚型更好地选择药物。