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To assess the safety and efficacy of the combination of oral etoposide and intravenous irinotecan in patients with platinum-resistant and taxane-pretreated ovarian cancer.Eligible patients (age, 20–75years; platinum-free interval, ≤28weeks) with an adequate organ function received oral etoposide (50mg/m 2 once a day) from day 1 to day 21 and intravenous irinotecan (70mg/m 2 ) on days...
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