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本文引用的文献

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FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer.FOLFIRINOX 对比吉西他滨治疗转移性胰腺癌。
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TP53INP1 decreases pancreatic cancer cell migration by regulating SPARC expression.TP53INP1 通过调节 SPARC 的表达抑制胰腺癌迁移。
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A Cancer and Leukemia Group B phase II study of sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma (CALGB 80603).一项曾接受治疗的转移性胰腺腺癌患者中马来酸舒尼替尼的癌症和白血病组 B 期 II 期研究(CALGB 80603)。
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Gene expression levels as predictive markers of outcome in pancreatic cancer after gemcitabine-based adjuvant chemotherapy.基于吉西他滨的辅助化疗后胰腺癌中基因表达水平作为预后预测标志物。
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Hypoxia inducible BHLHB2 is a novel and independent prognostic marker in pancreatic ductal adenocarcinoma.缺氧诱导因子 BHLHB2 是胰腺导管腺癌的一个新的独立预后标志物。
Biochem Biophys Res Commun. 2010 Oct 22;401(3):422-8. doi: 10.1016/j.bbrc.2010.09.070. Epub 2010 Sep 21.
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Adjuvant chemotherapy with fluorouracil plus folinic acid vs gemcitabine following pancreatic cancer resection: a randomized controlled trial.胰腺癌切除术后氟尿嘧啶加亚叶酸辅助化疗与吉西他滨的随机对照试验。
JAMA. 2010 Sep 8;304(10):1073-81. doi: 10.1001/jama.2010.1275.
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Gemcitabine plus sorafenib in patients with advanced pancreatic cancer: a phase II trial of the University of Chicago Phase II Consortium.吉西他滨联合索拉非尼治疗晚期胰腺癌患者:芝加哥大学二期联盟的一项二期临床试验。
Invest New Drugs. 2012 Feb;30(1):382-6. doi: 10.1007/s10637-010-9526-z. Epub 2010 Aug 28.
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CD10+ pancreatic stellate cells enhance the progression of pancreatic cancer.CD10+ 胰腺星状细胞促进胰腺癌的进展。
Gastroenterology. 2010 Sep;139(3):1041-51, 1051.e1-8. doi: 10.1053/j.gastro.2010.05.084. Epub 2010 Jun 8.
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Phase III study comparing gemcitabine plus cetuximab versus gemcitabine in patients with advanced pancreatic adenocarcinoma: Southwest Oncology Group-directed intergroup trial S0205.吉西他滨联合西妥昔单抗对比吉西他滨治疗晚期胰腺腺癌的 III 期研究:西南肿瘤协作组指导下的多中心临床试验 S0205。
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Gemcitabine plus bevacizumab compared with gemcitabine plus placebo in patients with advanced pancreatic cancer: phase III trial of the Cancer and Leukemia Group B (CALGB 80303).吉西他滨联合贝伐珠单抗对比吉西他滨联合安慰剂治疗晚期胰腺癌患者:癌症和白血病 B 组(CALGB 80303)的 III 期试验。
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展望未来:胰腺癌管理中的生物标志物

Looking to the future: biomarkers in the management of pancreatic adenocarcinoma.

作者信息

Spratlin Jennifer L, Mulder Karen E

机构信息

Department of Oncology, Cross Cancer Institute, School of Cancer, Imaging and Engineering Sciences, Faculty of Medicine and Dentistry, University of Alberta, 11560 University Avenue, Edmonton, Alberta, T6G 1Z2, Canada.

出版信息

Int J Mol Sci. 2011;12(9):5895-907. doi: 10.3390/ijms12095895. Epub 2011 Sep 14.

DOI:10.3390/ijms12095895
PMID:22016635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3189759/
Abstract

The incidence and mortality of pancreas cancer converge. There has been little advancement in the treatment of pancreas cancer since the acceptance of gemcitabine as the standard therapy. Unfortunately, the efficacy of gemcitabine is dismal. While there is much discussion for the development of biomarkers to help direct therapy in this area, there is little action to move them into clinical practice. Herein, we review potential pancreatic cancer biomarkers and discuss the limitations in their implementation.

摘要

胰腺癌的发病率和死亡率趋于一致。自吉西他滨被接受为标准治疗方法以来,胰腺癌的治疗进展甚微。不幸的是,吉西他滨的疗效不佳。虽然关于开发生物标志物以指导该领域治疗的讨论很多,但将其应用于临床实践的行动却很少。在此,我们综述了潜在的胰腺癌生物标志物,并讨论了其应用中的局限性。