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۱۲ January 2015….. (TCM)…………… :……
.. It is possible that it would have been possible to combine the two methodologies into a single study, had the study been designed with a wider. or the uptake of TCM in England……….
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A Brief Description of the Structural Assessment Tool (TCM)……….. :……………..
۹٫۱٫۱ Introduction………………….. :…………………….
۹٫۱٫۲ The Information Sys tems and Methods………….. :……………..
۹٫۱٫۳ Finding the Best Model……………….. :……………..
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۹٫۲ Case Study…………………….. :…………………….
. ۹٫۲٫۱ Introduction………………………

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In a prospective randomized trial we compared the clinical benefit of a new schedule of temozolomide with that of the standard treatment schedule (methyl-CCNU) in patients with renal cell carcinoma or transitional cell carcinoma of the urothelial tract. Patients with tumor stage T3N+M0 or T4N0M0 were randomly assigned to receive single-agent temozolomide at a dose of 400 mg/m(2) for up to 12 h followed by a 7-day rest period (temozolomide) or methyl-CCNU at a dose of 100 mg/m(2) administered as a 20-min IV infusion every 14 days for at least 6 months (CCNU). A total of 221 patients were registered and treated, including 111 patients who received single-agent temozolomide and 110 who received methyl-CCNU. During the planned treatment period, 76% of patients in the temozolomide group and 80% in the CCNU group completed the planned treatment (P = 0.36). No significant differences were found in the response rates between the groups (28% and 24%, respectively). Median overall survival in the temozolomide group was 15 months versus 10 months in the CCNU group (P = 0.007). At multivariate analysis, two variables were significantly associated with an increased risk of death: large tumor size (P = 0.002) and CCNU-based therapy (P = 0.011). The 12-h infusion of temozolomide was safe and well tolerated, with

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