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The following table summarizes the hormone receptor status at entry for all randomized patients in trials and Trial showed that Anastrozole and tamoxifen had similar objective tumor response rates and time to tumor progression see Table 12 and Figures 5 and 6. Table 12 below summarizes the results of trial and trial for the primary efficacy endpoints. Results from the secondary endpoints were supportive of the results of the primary efficacy endpoints. There were too few deaths occurring across treatment groups of both trials to draw conclusions on overall survival differences. Anastrozole was studied in two controlled clinical trialsa North American study;Trenbolone, a predominately European study in postmenopausal women with advanced breast cancer who had disease progression following tamoxifen therapy for either advanced or early breast cancer. Some of the patients had also received previous cytotoxic treatment. Most Buying legal Trenbolone online were ER-positive; a smaller fraction were ER-unknown or ER-negative; the ER-negative Trenbolone were eligible only if they had a positive response to tamoxifen. Eligible patients Trenbolone acetate measurable and non-measurable disease were randomized to receive either a single daily dose of 1 mg or 10 mg of Anastrozole or megestrol acetate 40 mg four times a day. The studies were double-blinded with respect to Anastrozole. Time to progression and objective response only patients with measurable disease could be considered partial responders rates were the primary efficacy variables. The rate of prolonged more than 24 weeks stable disease, the rate of progression, and survival were also calculated. Both trials included over patients; demographics and other baseline characteristics were similar for the three treatment groups in each trial. Patients in the trial had responded better to prior tamoxifen treatment.

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