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晚期前列腺癌的靶向治疗:透过新视角审视

Targeted therapy for advanced prostate cancer: Looking through new lenses.

作者信息

Vogiatzi P, Cassone M, Claudio L, Claudio P P

机构信息

Department of Cancer Biology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

出版信息

Drug News Perspect. 2009 Dec;22(10):593-601. doi: 10.1358/dnp.2009.10.1428872.

DOI:10.1358/dnp.2009.10.1428872
PMID:20140279
Abstract

Prostate cancer is the most common noncutaneous malignancy in men and also the third leading cause of death due to cancer in males. The conventional initial therapy for localized advanced or metastatic disease is hormone or androgen deprivation therapy. Although hormone-based therapies generally result in rapid responses, the disease then progresses to a phase when they fail to control the malignancy despite castrate testosterone levels. Some patients with castration-resistant prostate cancer continue to respond to secondary hormonal manipulations, and docetaxel-based chemotherapy improves median survival to about 18 months. Prostate cancer is termed hormone-refractory when it no longer responds to hormonal therapy. Currently, other therapeutic options, such as radical prostatectomy, radiation therapy or cryotherapy offer improvement in survival mostly in early stages. New therapy approaches based on a deeper understanding of especially metastatic prostate cancer are of vital importance. Here we discuss up-to-date clinical trials of agents with novel targets and present paradigms in prostate cancer vaccine therapy, metastasis suppressor genes, and some provocative findings on combination therapies of cytotoxic agents, which might provide a platform for developing effective treatment for advanced prostate cancer.

摘要

前列腺癌是男性最常见的非皮肤恶性肿瘤,也是男性癌症死亡的第三大主要原因。对于局限性晚期或转移性疾病,传统的初始治疗方法是激素或雄激素剥夺疗法。尽管基于激素的疗法通常会迅速产生反应,但疾病随后会进展到一个阶段,即尽管睾酮水平已被抑制,但这些疗法仍无法控制恶性肿瘤。一些去势抵抗性前列腺癌患者继续对二次激素治疗有反应,基于多西他赛的化疗可将中位生存期提高到约18个月。当前列腺癌不再对激素治疗有反应时,就被称为激素难治性前列腺癌。目前,其他治疗选择,如根治性前列腺切除术、放射治疗或冷冻治疗,大多在早期阶段能提高生存率。基于对尤其是转移性前列腺癌更深入理解的新治疗方法至关重要。在此,我们讨论具有新靶点药物的最新临床试验,并介绍前列腺癌疫苗治疗、转移抑制基因方面的范例,以及关于细胞毒性药物联合治疗的一些引人深思的发现,这些可能为开发晚期前列腺癌的有效治疗方法提供一个平台。

相似文献

1
Targeted therapy for advanced prostate cancer: Looking through new lenses.晚期前列腺癌的靶向治疗:透过新视角审视
Drug News Perspect. 2009 Dec;22(10):593-601. doi: 10.1358/dnp.2009.10.1428872.
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Immunotherapy for prostate cancer - recent progress in clinical trials.前列腺癌免疫疗法——临床试验的最新进展
Clin Adv Hematol Oncol. 2007 Jun;5(6):465-74, 477-9.
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Treatment options in androgen-independent prostate cancer.雄激素非依赖性前列腺癌的治疗选择。
Cancer Invest. 1999;17(2):137-44.
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Overcoming bcl-2- and p53-mediated resistance in prostate cancer.克服前列腺癌中bcl-2和p53介导的耐药性。
Semin Oncol. 1999 Feb;26(1 Suppl 2):112-6.
5
New drugs in prostate cancer.前列腺癌的新药
Curr Opin Urol. 2006 May;16(3):138-45. doi: 10.1097/01.mou.0000193390.69845.bb.
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New molecular targets in advanced prostate cancer.晚期前列腺癌中的新分子靶点
Expert Rev Anticancer Ther. 2006 Jul;6(7):993-1002. doi: 10.1586/14737140.6.7.993.
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Endocrine treatment of prostate cancer.前列腺癌的内分泌治疗
J Steroid Biochem Mol Biol. 2004 Nov;92(4):287-95. doi: 10.1016/j.jsbmb.2004.10.005. Epub 2004 Dec 31.
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Novel targets and approaches in advanced prostate cancer.晚期前列腺癌的新靶点与新方法
Curr Opin Urol. 2007 May;17(3):182-7. doi: 10.1097/MOU.0b013e3280dd8a4f.
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Targeted therapeutic approaches for hormone-refractory prostate cancer.针对激素难治性前列腺癌的靶向治疗方法。
Cancer Treat Rev. 2010 Apr;36(2):122-30. doi: 10.1016/j.ctrv.2009.06.001. Epub 2010 Jan 27.
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Cellular immunotherapies for prostate cancer.前列腺癌的细胞免疫疗法
Biomed Pharmacother. 2007 Jul;61(6):315-22. doi: 10.1016/j.biopha.2006.12.006. Epub 2007 Jan 26.

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Microbubble-mediated delivery of human adenoviruses does not elicit innate and adaptive immunity response in an immunocompetent mouse model of prostate cancer.微泡介导的人腺病毒传递在前列腺癌免疫功能正常的小鼠模型中不会引起固有和适应性免疫反应。
J Transl Med. 2019 Jan 11;17(1):19. doi: 10.1186/s12967-019-1771-0.
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Imatinib induces up-regulation of , a metastasis suppressor gene, in human Hepatocarcinoma (HepG2) Cell Line.伊马替尼在人肝癌(HepG2)细胞系中诱导转移抑制基因的上调。
Gastroenterol Hepatol Bed Bench. 2017 Winter;10(1):29-33.
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Genetic variations in a PTEN/AKT/mTOR axis and prostate cancer risk in a Chinese population.
PTEN/AKT/mTOR 轴基因变异与中国人群前列腺癌风险
PLoS One. 2012;7(7):e40817. doi: 10.1371/journal.pone.0040817. Epub 2012 Jul 18.
4
Altered CXCR3 isoform expression regulates prostate cancer cell migration and invasion.CXCR3 异构体表达的改变调节前列腺癌细胞的迁移和侵袭。
Mol Cancer. 2012 Jan 11;11:3. doi: 10.1186/1476-4598-11-3.
5
Targeted inhibition of mitochondrial Hsp90 suppresses localised and metastatic prostate cancer growth in a genetic mouse model of disease.靶向抑制线粒体热休克蛋白 90 可抑制疾病遗传小鼠模型中的局部和转移性前列腺癌生长。
Br J Cancer. 2011 Feb 15;104(4):629-34. doi: 10.1038/bjc.2011.9. Epub 2011 Feb 1.
6
The Akt-inhibitor Erufosine induces apoptotic cell death in prostate cancer cells and increases the short term effects of ionizing radiation.Akt 抑制剂依鲁替尼诱导前列腺癌细胞凋亡,并增强电离辐射的短期作用。
Radiat Oncol. 2010 Nov 16;5:108. doi: 10.1186/1748-717X-5-108.
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Preclinical characterization of mitochondria-targeted small molecule hsp90 inhibitors, gamitrinibs, in advanced prostate cancer.在晚期前列腺癌中,靶向线粒体的小分子 HSP90 抑制剂 gamitrinibs 的临床前特征。
Clin Cancer Res. 2010 Oct 1;16(19):4779-88. doi: 10.1158/1078-0432.CCR-10-1818. Epub 2010 Sep 28.
8
[11C]Choline as pharmacodynamic marker for therapy response assessment in a prostate cancer xenograft model.[11C]胆碱作为前列腺癌异种移植模型治疗反应评估的药效标志物。
Eur J Nucl Med Mol Imaging. 2010 Oct;37(10):1861-8. doi: 10.1007/s00259-010-1493-2. Epub 2010 May 30.