Literature DB >> 22591417

Review of dose-intense platinum and/or paclitaxel containing chemotherapy in advanced and recurrent epithelial ovarian cancer.

Ingrid A Boere1, Maria E L van der Burg.   

Abstract

Ovarian cancer is the most lethal gynecological cancer in women in the western world with a 5-year survival of 49.7%. Advanced stage ovarian cancer is treated both surgically and with chemotherapy, but despite initial high response rates of 60- 75%, many women experience disease recurrence with a dismal prognosis, 5 year overall survival for FIGO stage IIIc and IV disease being only 32 and 18%. In an attempt to improve outcome for both primary and recurrent disease, dose-intense and dose-dense chemotherapy regimens have been investigated. This overview summarizes these results in first and second-line treatment. In first-line treatment, no benefit was found of dose-intense regimes in the majority of the studies, only toxicity was increased. However, results are conflicting with the recent Japanese Gynecologic Oncology Group (JGOG) trial showing an improved progression free and overall survival in patients treated with dose-dense weekly paclitaxel combined with standard 3-weekly carboplatin. For recurrent disease dose-dense weekly combination chemotherapy seems to be very effective in patients with platinum-resistant ovarian cancer. Several phase II studies showed an increase in response rate, progression free survival and overall survival for dose-dense paclitaxel and carboplatin, compared to results of nonplatinum chemotherapy. In platinum-sensitive ovarian cancer, on contrary, the results of weekly paclitaxel and carboplatin seem to be comparable with standard 3-weekly regimens.

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Year:  2012        PMID: 22591417     DOI: 10.2174/138161212802002634

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  7 in total

Review 1.  Chemoresistance and targeting of growth factors/cytokines signalling pathways: towards the development of effective therapeutic strategy for endometrial cancer.

Authors:  Fengjun Guo; Haina Zhang; Zanhui Jia; Manhua Cui; Jingyan Tian
Journal:  Am J Cancer Res       Date:  2018-07-01       Impact factor: 6.166

2.  Cystoid macular edema secondary to paclitaxel therapy for ovarian cancer: A case report.

Authors:  Emma Bassi; Vera Loizzi; Claudio Furino; Rosa Martino; Giovanni Alessio; Cicinelli Ettore; Gennaro Cormio
Journal:  Mol Clin Oncol       Date:  2017-06-21

3.  Three-dimensional collagen type I matrix up-regulates nuclear isoforms of the microtubule associated protein tau implicated in resistance to paclitaxel therapy in ovarian carcinoma.

Authors:  Hilal Gurler; Yi Yu; Jacqueline Choi; Andre A Kajdacsy-Balla; Maria V Barbolina
Journal:  Int J Mol Sci       Date:  2015-02-04       Impact factor: 5.923

4.  A longitudinal analysis with CA-125 to predict overall survival in patients with ovarian cancer.

Authors:  An Jen Chiang; Jiabin Chen; Yu-Che Chung; Huan-Jung Huang; Wen Shiung Liou; Chung Chang
Journal:  J Gynecol Oncol       Date:  2014-01-08       Impact factor: 4.401

Review 5.  Chemoresistance and targeted therapies in ovarian and endometrial cancers.

Authors:  Kevin Brasseur; Nicolas Gévry; Eric Asselin
Journal:  Oncotarget       Date:  2017-01-17

Review 6.  Axonal Transport Impairment in Chemotherapy-Induced Peripheral Neuropathy.

Authors:  Gabriella Nicolini; Marianna Monfrini; Arianna Scuteri
Journal:  Toxics       Date:  2015-08-07

7.  Comparing Paclitaxel-Carboplatin with Paclitaxel-Cisplatin as the Front-Line Chemotherapy for Patients with FIGO IIIC Serous-Type Tubo-Ovarian Cancer.

Authors:  Chen-Yu Huang; Min Cheng; Na-Rong Lee; Hsin-Yi Huang; Wen-Ling Lee; Wen-Hsun Chang; Peng-Hui Wang
Journal:  Int J Environ Res Public Health       Date:  2020-03-26       Impact factor: 3.390

  7 in total

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