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Front Biosci (Schol Ed). 2011 Jan 1;3(1):82-97. doi: 10.2741/s134.
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本文引用的文献

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Phase II trial of bevacizumab in recurrent or persistent endometrial cancer: a Gynecologic Oncology Group study.贝伐珠单抗治疗复发性或持续性子宫内膜癌的 II 期临床试验:一项妇科肿瘤学组研究。
J Clin Oncol. 2011 Jun 1;29(16):2259-65. doi: 10.1200/JCO.2010.32.6397. Epub 2011 May 2.
2
Phase II trial of combretastatin A4 phosphate, carboplatin, and paclitaxel in patients with platinum-resistant ovarian cancer.卡铂、紫杉醇联合 Combretastatin A4 磷酸盐治疗铂类耐药卵巢癌的 II 期临床试验
Ann Oncol. 2011 Sep;22(9):2036-2041. doi: 10.1093/annonc/mdq708. Epub 2011 Jan 27.
3
A phase II study of sunitinib in patients with recurrent epithelial ovarian and primary peritoneal carcinoma: an NCIC Clinical Trials Group Study.一项舒尼替尼治疗复发性上皮性卵巢癌和原发性腹膜癌患者的 II 期研究:加拿大国立癌症研究所临床试验组研究。
Ann Oncol. 2011 Feb;22(2):335-40. doi: 10.1093/annonc/mdq357. Epub 2010 Aug 12.
4
Phase II, open-label study of pazopanib or lapatinib monotherapy compared with pazopanib plus lapatinib combination therapy in patients with advanced and recurrent cervical cancer.帕唑帕尼或拉帕替尼单药治疗与帕唑帕尼联合拉帕替尼联合治疗在晚期和复发性宫颈癌患者中的 II 期、开放标签研究。
J Clin Oncol. 2010 Aug 1;28(22):3562-9. doi: 10.1200/JCO.2009.26.9571. Epub 2010 Jul 6.
5
The role of HER2 in cancer therapy and targeted drug delivery.HER2 在癌症治疗和靶向药物递送中的作用。
J Control Release. 2010 Sep 15;146(3):264-75. doi: 10.1016/j.jconrel.2010.04.009. Epub 2010 Apr 10.
6
Notch signaling: emerging molecular targets for cancer therapy.Notch 信号通路:癌症治疗的新兴分子靶点。
Biochem Pharmacol. 2010 Sep 1;80(5):690-701. doi: 10.1016/j.bcp.2010.03.026. Epub 2010 Mar 31.
7
Expression of nuclear Notch3 in cervical squamous cell carcinomas and its association with adverse clinical outcomes.核 Notch3 在宫颈鳞状细胞癌中的表达及其与不良临床结局的关系。
Gynecol Oncol. 2010 Jun;117(3):409-16. doi: 10.1016/j.ygyno.2010.03.004. Epub 2010 Mar 31.
8
The role of microRNAs in ovarian cancer initiation and progression.微小 RNA 在卵巢癌发生和进展中的作用。
J Cell Mol Med. 2010 Sep;14(9):2240-9. doi: 10.1111/j.1582-4934.2010.01058.x.
9
Dasatinib: a potent SRC inhibitor in clinical development for the treatment of solid tumors.达沙替尼:一种在研的 SRC 抑制剂,用于治疗实体瘤。
Cancer Treat Rev. 2010 Oct;36(6):492-500. doi: 10.1016/j.ctrv.2010.02.015. Epub 2010 Mar 11.
10
Disrupting established tumor blood vessels: an emerging therapeutic strategy for cancer.破坏已建立的肿瘤血管:癌症治疗的新策略。
Cancer. 2010 Apr 15;116(8):1859-71. doi: 10.1002/cncr.24975.

女性癌症的治疗进展

Therapeutic advances in women's cancers.

作者信息

Carroll Amy R, Coleman Robert L, Sood Anil K

机构信息

Department of Gynecologic Oncology, M.D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Front Biosci (Schol Ed). 2011 Jan 1;3(1):82-97. doi: 10.2741/s134.

DOI:10.2741/s134
PMID:21196359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3199127/
Abstract

Cytotoxic therapy and surgery have improved outcomes for patients with gynecologic malignancies over the last twenty years, but women's cancers still account for over ten percent of cancer related deaths annually. Insights into the pathogenesis of cancer have led to the development of drugs that target molecular pathways essential to tumor survival including angiogenesis, DNA repair, and apoptosis. This review outlines several of the promising new biologically targeted drugs currently being tested to treat gynecologic malignancies.

摘要

在过去二十年中,细胞毒性疗法和手术改善了妇科恶性肿瘤患者的治疗效果,但女性癌症仍占每年癌症相关死亡人数的10%以上。对癌症发病机制的深入了解促使了针对肿瘤生存所必需的分子途径(包括血管生成、DNA修复和细胞凋亡)的药物的开发。本综述概述了目前正在测试用于治疗妇科恶性肿瘤的几种有前景的新型生物靶向药物。