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吉西他滨耐药的晚期胰腺癌的治疗选择。

Options for the treatment of gemcitabine-resistant advanced pancreatic cancer.

作者信息

Gounaris Ioannis, Zaki Kamarul, Corrie Pippa

机构信息

Oncology Centre, Cambridge University Hospitals NHS Trust, Cambridge, United Kingdom.

出版信息

JOP. 2010 Mar 5;11(2):113-23.

PMID:20208317
Abstract

CONTEXT

Pancreatic cancer is noteworthy in that the number of patients dying from the disease is roughly equal to the number diagnosed. For more than a decade, gemcitabine has constituted the standard of care for the palliative treatment of the majority of patients who present with metastatic or relapsed disease, although the survival gains are limited. Despite a median survival of less than 6 months, there is a significant proportion of advanced pancreatic cancer patients who progress on gemcitabine that remains fit and these patients are candidates for second-line treatment.

METHODS

The OVID MEDLINE database was searched from 1950 to present using the MeSH terms "pancreatic neoplasms", "drug treatment" and "gemcitabine". After excluding non-relevant results, 31 published studies were identified. These results were supplemented by searching the last three (2007-2009) American Society of Clinical Oncology (ASCO) Proceedings of Annual Meetings for studies published only in abstract form and reviewing reference lists of published articles.

RESULTS AND DISCUSSION

The evidence for second line treatments of metastatic pancreatic cancer consists mostly of single arm, small phase II studies. Oxaliplatin-fluoropyrimidine combinations appear promising and have shown increased survival compared to best supportive care. As the molecular pathways governing pancreatic cancer are unravelled, novel targeted therapies may offer the greatest promise for this disease either given alone, combined with one another, or with cytotoxic agents. The need for further, collaborative research is emphasised.

摘要

背景

胰腺癌值得关注之处在于,死于该疾病的患者数量与被诊断出的患者数量大致相等。十多年来,吉西他滨一直是大多数出现转移性或复发性疾病患者姑息治疗的标准疗法,尽管生存获益有限。尽管中位生存期不到6个月,但仍有相当一部分晚期胰腺癌患者在使用吉西他滨治疗时病情进展,且身体状况尚可,这些患者是二线治疗的候选对象。

方法

使用医学主题词“胰腺肿瘤”“药物治疗”和“吉西他滨”对1950年至今的OVID MEDLINE数据库进行检索。排除不相关结果后,确定了31项已发表的研究。通过检索美国临床肿瘤学会(ASCO)最近三届(2007 - 2009年)年会仅以摘要形式发表的研究,并查阅已发表文章的参考文献列表,对这些结果进行了补充。

结果与讨论

转移性胰腺癌二线治疗的证据主要来自单臂、小型II期研究。奥沙利铂 - 氟嘧啶联合方案似乎很有前景,与最佳支持治疗相比,已显示出生存期延长。随着控制胰腺癌的分子途径被逐步揭示,新型靶向治疗单独使用、相互联合或与细胞毒性药物联合使用,可能为该疾病带来最大的希望。强调了进一步开展合作研究的必要性。

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Options for the treatment of gemcitabine-resistant advanced pancreatic cancer.吉西他滨耐药的晚期胰腺癌的治疗选择。
JOP. 2010 Mar 5;11(2):113-23.
2
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引用本文的文献

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Efficacy of second-line treatment for gemcitabine-refractory unresectable pancreatic cancer in a real-world setting.吉西他滨难治性不可切除胰腺癌二线治疗在真实世界中的疗效
BMC Cancer. 2025 Jul 24;25(1):1209. doi: 10.1186/s12885-025-14601-2.
2
Identification of initial leads directed at the calmodulin-binding region on the Src-SH2 domain that exhibit anti-proliferation activity against pancreatic cancer.鉴定针对Src-SH2结构域上钙调蛋白结合区域的初始先导化合物,这些先导化合物对胰腺癌具有抗增殖活性。
Bioorg Med Chem Lett. 2016 Feb 15;26(4):1237-44. doi: 10.1016/j.bmcl.2016.01.027. Epub 2016 Jan 12.
3
Lipocalin-2 is associated with a good prognosis and reversing epithelial-to-mesenchymal transition in pancreatic cancer.
脂联素-2 与良好的预后相关,并可逆转胰腺癌中的上皮间质转化。
World J Surg. 2013 Aug;37(8):1892-900. doi: 10.1007/s00268-013-2009-6.
4
FOLFIRI regimen in metastatic pancreatic adenocarcinoma resistant to gemcitabine and platinum-salts.FOLFIRI 方案治疗吉西他滨和铂类耐药的转移性胰腺腺癌。
World J Gastroenterol. 2012 Sep 7;18(33):4533-41. doi: 10.3748/wjg.v18.i33.4533.
5
Second-line therapy for gemcitabine-pretreated advanced or metastatic pancreatic cancer.吉西他滨预处理后晚期或转移性胰腺癌的二线治疗。
World J Gastroenterol. 2012 Mar 28;18(12):1357-64. doi: 10.3748/wjg.v18.i12.1357.
6
Exploring protein kinase inhibitors: potentiating gemcitabine efficacy in pancreatic cancer.探索蛋白激酶抑制剂:增强吉西他滨在胰腺癌中的疗效
Pancreas. 2012 Apr;41(3):496-8. doi: 10.1097/MPA.0b013e318230f71a.
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Phase II study of nimotuzumab, a humanized monoclonal anti-epidermal growth factor receptor (EGFR) antibody, in patients with locally advanced or metastatic pancreatic cancer.尼妥珠单抗(一种人源化单克隆抗表皮生长因子受体(EGFR)抗体)治疗局部晚期或转移性胰腺癌的 II 期研究。
Invest New Drugs. 2012 Jun;30(3):1138-43. doi: 10.1007/s10637-010-9619-8. Epub 2010 Dec 21.