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    Home > Medical News > Medical Research Articles > FDA approves Roche's avetin ® combined chemotherapy (caplatinum and yewalcohol) for treatment of patients with advanced ovarian cancer

    FDA approves Roche's avetin ® combined chemotherapy (caplatinum and yewalcohol) for treatment of patients with advanced ovarian cancer

    • Last Update: 2020-06-11
    • Source: Internet
    • Author: User
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    recently, the Swiss Roche Group announced that the U.SFDA(approved an avetin ® (bevazumab) combined chemotherapy (caplatinum and yew alcohol) for the treatment of patients with advanced (III or IV) ovarian cancer after initial surgery, followed by the use of anvitamintinmono therapythis approval is based on the phase III Key ClinicalTrialdata show edgy: patients continue to use avestine monotherapy after receiving acombination chemotherapy, the median progression survival (PFS) reached 18.2 months; 95% CI 0.52 - 0.75, p 0.0001This PFS benefit is based on a fixed treatment cycle (a total of 22 courses of treatment for Amvetin), anavetin has been approved for 10 indications in the United States, involving 6 cancersThe approval is the fourth gynaecological oncology approved by Amvetin in four years, and three other indications include advanced cervical cancer, as well as two types of ovarian cancer that has been given platinumdrug(based on chemotherapy that recurs after chemotherapy)
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