Literature DB >> 26001052

Emerging therapies: angiogenesis inhibitors for ovarian cancer.

Amanda L Jackson1, Eric L Eisenhauer, Thomas J Herzog.   

Abstract

INTRODUCTION: Patients with epithelial ovarian cancer (EOC) have a high rate of recurrence, and overall survival remains at ∼ 25%. There is a need for new treatments that can increase progression free survival and quality of life. Recent clinical trials focus on angiogenesis, VEGFs, and tyrosine kinase inhibitors that play a role in recurrence, metastasis, and ascites in EOC. AREAS COVERED: This review summarizes clinical rationale, mechanisms of action, and clinical data for angiogenesis inhibitors under evaluation in Phase II and III trials for EOC. Anti-angiogenesis agents reviewed in this paper include aflibercept, bevacizumab, cediranib, fosbretabulin, imatinib, nintedanib, pazopanib, saracatinib, sorafenib, sunitinib, and trebananib. EXPERT OPINION: These agents have particular rationale for potential use in EOC due to the molecular changes associated with EOC tumorigenesis, namely a significant increase in angiogenic activity. Due to the costs and toxicities associated with anti-angiogenics, biomarker or molecular signature selection strategy for patients who will most benefit would be ideal but no such strategy has been validated to date.

Entities:  

Keywords:  VEGF; angiogenesis; bevacizumab; fallopian tube cancer; ovarian cancer; primary peritoneal cancer; tyrosine kinase inhibitors

Mesh:

Substances:

Year:  2015        PMID: 26001052     DOI: 10.1517/14728214.2015.1036739

Source DB:  PubMed          Journal:  Expert Opin Emerg Drugs        ISSN: 1472-8214            Impact factor:   4.191


  13 in total

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Review 2.  Ovarian cancer.

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Review 4.  Epithelial ovarian cancer: the molecular genetics of epithelial ovarian cancer.

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Journal:  Ann Oncol       Date:  2016-04       Impact factor: 32.976

Review 5.  Modifying the tumor microenvironment using nanoparticle therapeutics.

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Review 6.  Molecular Characterization of Epithelial Ovarian Cancer: Implications for Diagnosis and Treatment.

Authors:  Veronica Rojas; Kim M Hirshfield; Shridar Ganesan; Lorna Rodriguez-Rodriguez
Journal:  Int J Mol Sci       Date:  2016-12-15       Impact factor: 5.923

7.  miR-205 mediates the inhibition of cervical cancer cell proliferation using olmesartan.

Authors:  Zhang Yue; Zhang Yun-Shan; Xue Feng-Xia
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8.  MicroRNA-27b functions as a new inhibitor of ovarian cancer-mediated vasculogenic mimicry through suppression of VE-cadherin expression.

Authors:  Wenming Liu; Chunping Lv; Bin Zhang; Quansheng Zhou; Zhifei Cao
Journal:  RNA       Date:  2017-04-10       Impact factor: 4.942

9.  Reduced expression of SIRT2 in serous ovarian carcinoma promotes cell proliferation through disinhibition of CDK4 expression.

Authors:  Yanhua Du; Jun Wu; Haiyan Zhang; Shaobo Li; Hong Sun
Journal:  Mol Med Rep       Date:  2017-02-08       Impact factor: 2.952

10.  Bevacizumab and paclitaxel-carboplatin chemotherapy and secondary cytoreduction in recurrent, platinum-sensitive ovarian cancer (NRG Oncology/Gynecologic Oncology Group study GOG-0213): a multicentre, open-label, randomised, phase 3 trial.

Authors:  Robert L Coleman; Mark F Brady; Thomas J Herzog; Paul Sabbatini; Deborah K Armstrong; Joan L Walker; Byoung-Gie Kim; Keiichi Fujiwara; Krishnansu S Tewari; David M O'Malley; Susan A Davidson; Stephen C Rubin; Paul DiSilvestro; Karen Basen-Engquist; Helen Huang; John K Chan; Nick M Spirtos; Raheela Ashfaq; Robert S Mannel
Journal:  Lancet Oncol       Date:  2017-04-21       Impact factor: 41.316

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