Literature DB >> 25859831

Dose-dense approaches to ovarian cancer treatment.

Noriyuki Katsumata1.   

Abstract

OPINION STATEMENT: Currently, paclitaxel and carboplatin are administered every 3 weeks as the standard agents for the first-line treatment of advanced ovarian cancer. The concept of "dose-dense therapy" is based on the Norton-Simon hypothesis that a shorter interval between the doses of cytotoxic agents is more effective in reducing tumor burden than dose escalation. The results of phase III clinical trials demonstrating the superiority of weekly paclitaxel administration, compared with a 3-week schedule in breast cancer in both the metastatic and adjuvant settings support the hypothesis. The Japanese Gynecologic Oncology Group reported the results from a phase III study comparing the conventional paclitaxel and carboplatin every 3-week administration vs dose-dense weekly administration of paclitaxel combined with the every 3-week administration of carboplatin in advanced epithelial ovarian cancer, Fallopian tube, or primary peritoneal cancer. The median progression-free survival (PFS), the primary endpoint of this study, was substantially improved in the dose-dense treatment group (28 vs 17.2 months, hazard ratio [HR]: 0.71, 95% CI: 0.58-0.88, P = 0.0015), and the overall survival (OS) at 3 years was also higher in the dose-dense treatment group (72 · 1%) than in the conventional treatment group (65.1%; HR 0.75, 0.57-0.98; P = 0 · 03). The long-term outcomes at a median follow-up period of 76.8 months were reported. The median PFS was significantly longer in the dose-dense regimen than in the conventional regimen (28.2 vs 17.5 months; hazard ratio [HR], 0.76; 95% CI, 0.62-0.91; P = 0.0037), and the median OS was 100.5 months (95% CI 65.2-∞) in the dose-dense regimen and 62.2 months (52.1-82.6) in the conventional regimen (HR, 0.79; 95% CI, 0.63-0.99; P = 0.039; log-rank test). Dose-dense treatment offers a potential new standard of care for first-line chemotherapy for patients with advanced epithelial ovarian cancer. Ongoing studies will clarify the best dose, schedule, and route of administration.

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Year:  2015        PMID: 25859831     DOI: 10.1007/s11864-015-0338-4

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  3 in total

Review 1.  First-line therapy in ovarian cancer trials.

Authors:  Tate Thigpen; Andreas duBois; Jessica McAlpine; Philip DiSaia; Keiichi Fujiwara; William Hoskins; Gunnar Kristensen; Robert Mannel; Maurie Markman; Jacobus Pfisterer; Michael Quinn; Nick Reed; Ann Marie Swart; Jonathan Berek; Nicoletta Colombo; Gilles Freyer; Dolores Gallardo; Marie Plante; Andres Poveda; Lawrence Rubinstein; Monica Bacon; Henry Kitchener; Gavin C E Stuart
Journal:  Int J Gynecol Cancer       Date:  2011-05       Impact factor: 3.437

2.  Carboplatin plus paclitaxel once a week versus every 3 weeks in patients with advanced ovarian cancer (MITO-7): a randomised, multicentre, open-label, phase 3 trial.

Authors:  Sandro Pignata; Giovanni Scambia; Dionyssios Katsaros; Ciro Gallo; Eric Pujade-Lauraine; Sabino De Placido; Alessandra Bologna; Beatrice Weber; Francesco Raspagliesi; Pierluigi Benedetti Panici; Gennaro Cormio; Roberto Sorio; Maria Giovanna Cavazzini; Gabriella Ferrandina; Enrico Breda; Viviana Murgia; Cosimo Sacco; Saverio Cinieri; Vanda Salutari; Caterina Ricci; Carmela Pisano; Stefano Greggi; Rossella Lauria; Domenica Lorusso; Claudia Marchetti; Luigi Selvaggi; Simona Signoriello; Maria Carmela Piccirillo; Massimo Di Maio; Francesco Perrone
Journal:  Lancet Oncol       Date:  2014-02-28       Impact factor: 41.316

3.  Long-term results of dose-dense paclitaxel and carboplatin versus conventional paclitaxel and carboplatin for treatment of advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer (JGOG 3016): a randomised, controlled, open-label trial.

Authors:  Noriyuki Katsumata; Makoto Yasuda; Seiji Isonishi; Fumiaki Takahashi; Hirofumi Michimae; Eizo Kimura; Daisuke Aoki; Toshiko Jobo; Shoji Kodama; Fumitoshi Terauchi; Toru Sugiyama; Kazunori Ochiai
Journal:  Lancet Oncol       Date:  2013-08-13       Impact factor: 41.316

  3 in total
  5 in total

1.  Inhibition of enhancer of zeste homolog 2 increases the expression of p16 and suppresses the proliferation and migration of ovarian carcinoma cells in vitro and in vivo.

Authors:  Fangfang Lu; Hong Xu; Qi Wang; Meiyi Li; Jiahua Meng; Yan Kuang
Journal:  Oncol Lett       Date:  2017-12-28       Impact factor: 2.967

2.  Expression of Toll-like receptor 4 in ovarian serous adenocarcinoma and correlation with clinical stage and pathological grade.

Authors:  Xue-Zhen Luo; Qi-Zhi He; Kai Wang
Journal:  Int J Clin Exp Med       Date:  2015-08-15

3.  Expression of the tumor suppressor gene p16, and lymph node metastasis in patients with ovarian cancer.

Authors:  Hongyan Wang; Jingfang Zheng; Qiang Li; Min Zhou; Dongmei Ai; Hui Zhang
Journal:  Oncol Lett       Date:  2017-08-08       Impact factor: 2.967

4.  Targeted Inhibition of miR-221/222 Promotes Cell Sensitivity to Cisplatin in Triple-Negative Breast Cancer MDA-MB-231 Cells.

Authors:  Shujun Li; Qun Li; Jinhui Lü; Qian Zhao; Danni Li; Lei Shen; Zhongrui Wang; Junjun Liu; Dongping Xie; William C Cho; Shaohua Xu; Zuoren Yu
Journal:  Front Genet       Date:  2020-01-14       Impact factor: 4.599

5.  Mathematical model predicts response to chemotherapy in advanced non-resectable non-small cell lung cancer patients treated with platinum-based doublet.

Authors:  Emilia Kozłowska; Rafał Suwiński; Monika Giglok; Andrzej Świerniak; Marek Kimmel
Journal:  PLoS Comput Biol       Date:  2020-10-05       Impact factor: 4.475

  5 in total

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