Literature DB >> 15934521

Epidermal growth factor receptor inhibitors for the treatment of epithelial ovarian cancer.

Stephanie V Blank1, Richard Chang, Franco Muggia.   

Abstract

The majority of patients with ovarian cancer, especially those who present with stages IIIC and IV, will relapse soon after completion of platinum-based induction treatment. It is imperative to find ways to improve and/or enhance the efficacy of induction and to prolong the duration of the first remission. The epidermal growth factor receptor (EGFR) family has been exploited, and currently, three agents that directly target this group of receptors are in use in the treatment of colorectal, non-small-cell lung and breast cancers. EGFR and HER2/neu are overexpressed in a significant percentage of epithelial ovarian cancers. Thus, it would be reasonable to explore directly targeted therapy in ovarian cancer. Numerous investigational trials involving a variety of EGFR inhibitors in ovarian cancer are ongoing. Our institution has an active phase II clinical study that seeks to define the role of erlotinib (Tarceva) in potentiating first-line chemotherapy, and to determine whether the drug offers a significant contribution as maintenance therapy. It is hoped that data from these and other studies will help investigators to understand more clearly the biology of ovarian cancer and to delineate the role of EGFR inhibitors in the management of ovarian cancer.

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Year:  2005        PMID: 15934521

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN: 0890-9091            Impact factor:   2.990


  9 in total

Review 1.  A terrible beauty: a physician's story of ovarian cancer.

Authors:  Linda J Spano
Journal:  Can Fam Physician       Date:  2007-06       Impact factor: 3.275

2.  Photoimmunotherapy and irradiance modulation reduce chemotherapy cycles and toxicity in a murine model for ovarian carcinomatosis: perspective and results.

Authors:  Imran Rizvi; Tri A Dinh; Weiping Yu; Yuchiao Chang; Margaret E Sherwood; Tayyaba Hasan
Journal:  Isr J Chem       Date:  2012-09       Impact factor: 3.333

3.  Priming with EGFR tyrosine kinase inhibitor and EGF sensitizes ovarian cancer cells to respond to chemotherapeutical drugs.

Authors:  Cong Cao; Shan Lu; Alex Sowa; Rebecca Kivlin; Ashley Amaral; Wenming Chu; Hui Yang; Wen Di; Yinsheng Wan
Journal:  Cancer Lett       Date:  2008-04-08       Impact factor: 8.679

4.  Targeting EGFR and PI3K pathways in ovarian cancer.

Authors:  S Glaysher; L M Bolton; P Johnson; N Atkey; M Dyson; C Torrance; I A Cree
Journal:  Br J Cancer       Date:  2013-09-10       Impact factor: 7.640

5.  Targeted in vivo delivery of EGFR siRNA inhibits ovarian cancer growth and enhances drug sensitivity.

Authors:  Minati Satpathy; Roman Mezencev; Lijuan Wang; John F McDonald
Journal:  Sci Rep       Date:  2016-11-07       Impact factor: 4.379

6.  Cross talk of signals between EGFR and IL-6R through JAK2/STAT3 mediate epithelial-mesenchymal transition in ovarian carcinomas.

Authors:  M Colomiere; A C Ward; C Riley; M K Trenerry; D Cameron-Smith; J Findlay; L Ackland; N Ahmed
Journal:  Br J Cancer       Date:  2008-12-16       Impact factor: 7.640

7.  Photodynamic therapy for gynecological diseases and breast cancer.

Authors:  Natashis Shishkova; Olga Kuznetsova; Temirbolat Berezov
Journal:  Cancer Biol Med       Date:  2012-03       Impact factor: 4.248

8.  Genomic activation of the EGFR and HER2-neu genes in a significant proportion of invasive epithelial ovarian cancers.

Authors:  Joanna Vermeij; Erik Teugels; Claire Bourgain; Ji Xiangming; Peter in 't Veld; Vanessa Ghislain; Bart Neyns; Jacques De Grève
Journal:  BMC Cancer       Date:  2008-01-08       Impact factor: 4.430

9.  Amphiregulin enhances intercellular adhesion molecule-1 expression and promotes tumor metastasis in human osteosarcoma.

Authors:  Ju-Fang Liu; Ya-Ting Tsao; Chun-Han Hou
Journal:  Oncotarget       Date:  2015-12-01
  9 in total

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