Literature DB >> 11772280

Recent advances in the treatment of epithelial ovarian cancer.

M Harries1, S B Kaye.   

Abstract

Ovarian cancer leads to more fatalities than any other form of gynaecological cancer in North America and Europe. Over the last 30 years survival figures have improved somewhat due to improvements in diagnosis, surgery and chemotherapy. Despite these advances, the majority of patients will die from their disease, with the overall 5-year survival being just 30%. The majority of patients with this disease will require treatment with cytotoxic chemotherapy. It is now well established that the platinum agents (cisplatin or carboplatin) are the most important drugs to be included in first-line regimens. More recently, randomised trials have confirmed the benefit of the addition of taxanes to platinum-containing regimens and the standard of care has become the combination of carboplatin and paclitaxel. Several unanswered questions remain regarding the optimal schedule, the optimum duration of treatment, possible benefits to be gained from the addition of other drugs and whether paclitaxel the best taxane. Despite high response rates to first line chemotherapy, the majority of patients with advanced ovarian cancer will relapse and will be candidates for further chemotherapy, which can palliate symptoms and improve survival even in recurrent disease. For a patient relapsing within six months of first-line treatment, studies have shown that there is little point in rechallenge with the same drugs. However, for patients who have a longer treatment-free interval the response rates to rechallenge with platinum is significant. A number of drugs have been shown to have activity in platinum- and taxane-refractory disease and are approved for this and/or other applications. These include topotecan, etoposide, pegylated liposomal doxorubicin, epirubicin, gemcitabine, altretamine, oxaliplatin and vinorelbine. Anti-oestrogens such as tamoxifen have a small but significant response rate. Recurrent ovarian cancer is a good setting to test investigational agents and compounds with promising activity including new platinums and taxoids, as well as a range of new compounds. Non-cytotoxic approaches that are showing promise include therapies designed to overcome drug resistance, signal transduction inhibitors, immunotherapy and gene therapy.

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Year:  2001        PMID: 11772280     DOI: 10.1517/13543784.10.9.1715

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  10 in total

1.  Octreotide enhances the sensitivity of the SKOV3/DDP ovarian cancer cell line to cisplatin chemotherapy in vitro.

Authors:  Yang Shen; Mulan Ren; Yuehua Shi; Yunxia Zhang; Yunlang Cai
Journal:  Exp Ther Med       Date:  2011-08-11       Impact factor: 2.447

2.  The Significance of Adaptation and Coping with Disease among Patients with Diagnosed Gynaecological Cancer in the Context of Disease Acceptance.

Authors:  Sylwia Wieder-Huszla; Joanna Owsianowska; Anita Chudecka-Głaz; Dorota Branecka-Woźniak; Anna Jurczak
Journal:  Int J Environ Res Public Health       Date:  2022-06-13       Impact factor: 4.614

3.  Ovarian tumor growth regression using a combination of vascular targeting agents anginex or topomimetic 0118 and the chemotherapeutic irofulven.

Authors:  Ruud P M Dings; Emily S Van Laar; Jeremy Webber; Yan Zhang; Robert J Griffin; Stephen J Waters; John R MacDonald; Kevin H Mayo
Journal:  Cancer Lett       Date:  2008-04-01       Impact factor: 8.679

4.  δ-Cadinene inhibits the growth of ovarian cancer cells via caspase-dependent apoptosis and cell cycle arrest.

Authors:  Li-Mei Hui; Guo-Dong Zhao; Jian-Jun Zhao
Journal:  Int J Clin Exp Pathol       Date:  2015-06-01

5.  Comparative effectiveness of platinum-based chemotherapy versus taxane and other regimens for ovarian cancer.

Authors:  Xianglin L Du; Rohan C Parikh; David R Lairson; Sharon H Giordano; Putao Cen
Journal:  Med Oncol       Date:  2013-01-10       Impact factor: 3.064

6.  Estrogen receptor alpha expression in ovarian cancer predicts longer overall survival.

Authors:  Agnieszka Halon; Verena Materna; Malgorzata Drag-Zalesinska; Ewa Nowak-Markwitz; Tserenchunt Gansukh; Piotr Donizy; Marek Spaczynski; Maciej Zabel; Manfred Dietel; Hermann Lage; Pawel Surowiak
Journal:  Pathol Oncol Res       Date:  2011-01-06       Impact factor: 3.201

7.  Anti-MUC1 monoclonal antibody (C595) and docetaxel markedly reduce tumor burden and ascites, and prolong survival in an in vivo ovarian cancer model.

Authors:  Li Wang; Hongmin Chen; Mohammad H Pourgholami; Julia Beretov; Jingli Hao; Hongtu Chao; Alan C Perkins; John H Kearsley; Yong Li
Journal:  PLoS One       Date:  2011-09-09       Impact factor: 3.240

8.  Period Analysis of Intraracial Differences in Incidence and Survival Rates in Epithelial Ovarian Cancer.

Authors:  Lili Han; Sulaiya Husaiyin; Jing Liu; Miherinisha Maimaiti; Mayinuer Niyazi; Li Li
Journal:  Comput Math Methods Med       Date:  2021-12-08       Impact factor: 2.238

9.  Chemotherapy drug response in ovarian cancer cells strictly depends on a cathepsin D-Bax activation loop.

Authors:  Roberta Castino; Claudia Peracchio; Alessandra Salini; Giuseppina Nicotra; Nicol F Trincheri; Marina Démoz; Guido Valente; Ciro Isidoro
Journal:  J Cell Mol Med       Date:  2008-07-24       Impact factor: 5.310

Review 10.  Emerging Therapeutics to Overcome Chemoresistance in Epithelial Ovarian Cancer: A Mini-Review.

Authors:  Robert Cornelison; Danielle C Llaneza; Charles N Landen
Journal:  Int J Mol Sci       Date:  2017-10-18       Impact factor: 5.923

  10 in total

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