Chemotherapy of anthracy-clineand taxan-resistant breast cancer


Дәйексөз келтіру

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Аннотация

The article presents the results of evaluation of effectiveness and safety of chemotherapy with capecitabine (Xeloda) as monotherapy or as a component of drug combinations, and assessment of progression-free survival in 83 patients with metastatic breast cancer (MBC). The study confirmed the high efficiency and sufficient tolerance of Xeloda and its combinations in anthracycline-resistant and anthracycline-taxan-resistant MBC patients. This drug can be recommended for extensive use in this unfavorable group of patients.

Толық мәтін

Рұқсат жабық

Авторлар туралы

E. Kovalenko

E. Satirova

E. Artamonova

L. Manzyuk

Әдебиет тізімі

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  3. Gilabert M., et al. Capecitabine after antracycline and taxane Exposure in HER2-negative metastatic breast cancer patients: Response, Survival and Prognostic Factors. QAnticancer Research March 2011;31(3):1079-86.
  4. Girre V., et al. Vinorelbine-5-fluorouracil combination as second line chemotherapy in metastatic breast cancer after anthracycline-taxane combination (AT). Annals of Oncology 2000;11 (Suppl. 4):24.
  5. Pallis A., et al. A multicenter randomizedphase III trial of vinorelbine/gemcitabine doublet versus capecitabine monotherapy in anthracycline-and taxane-pretreated women with metastatic breast cancer. Annals of Oncology 2011;10:1093.
  6. Reichardt P., et al. Capecitabine: The news standart in metastatic breast cancer failing antracycline and taxane-containing chemotherapy? Mature results of a large multicenter phase II trial. Eur J Cancer 2001;37(Suppl. 6):S191, abstr.699.
  7. Reichardt P. et al. Multicenter phase II study of oral capecitabine (Xeloda) in patients with metastatic breast cancer relapsing after treatment with a taxane-containing therapy. Annals of Oncology 2003;14: 1227-33.
  8. Fumoleau P. et al. Capecitabine (Xeloda) in patients with advanced breast cancer (ABC) previously treated with antracyclines and taxanes: results of a large phase II study. Proc Am Soc Clin Oncol 2002;21:62a, abstr.247.

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