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   <subfield code="a">Feasibility of extension of platinum-free interval with weekly bolus topotecan and subsequent platinum retreatment outcomes in recurrent ovarian cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Christopher Bryant, Sanjeev Kumar, Whitney Spannuth, Jay Shah, Adnan Munkarah, Gunter Deppe, Ronald Alvarez, Robert Morris]</subfield>
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   <subfield code="a">Purpose: The goal of this study was to evaluate the outcomes and response in a cohort of patients with presumed platinum-sensitive disease who were subsequently retreated with platinum after receiving weekly bolus topotecan at the time of initial recurrence. Methods: A retrospective review of our institutional databases identified a cohort of platinum-sensitive women with recurrent ovarian and peritoneal carcinoma. Antitumor responses and toxicities were assessed for patients retreated with platinum-based chemotherapy following weekly bolus topotecan (4mg/m2). Results: Twenty-six patients (median age 63years, range 45-80years) were identified. Advanced stage (III/IV) ovarian carcinoma was most common (96%). Residual disease after primary cytoreductive surgery was less than 1cm in 65% of the cohort. Platinum retreatment was well tolerated. Grade 3 neutropenia occurred most commonly (8%) without any episodes of grade 4 myelotoxicity. Fatigue (12%) and hypersensitivity reaction (15%) were the most common non-hematologic toxicities during platinum retreatment. Of the 26 patients, 5 (19%) had a complete response, 5 (19%) had a partial response, 10 (39%) had stable disease, and 6 (23%) had progressive disease. Thirty-nine percent of patients with stable or progressive disease during weekly bolus topotecan responded to subsequent platinum retreatment. Response to platinum retreatment, treatment-free interval, and platinum-free interval was significant prognosticators for survival (P&lt;0.05). Conclusion(s): The results of this retrospective analysis suggest that weekly bolus topotecan, as intervening non-platinum, may result in acceptable toxicities and response rates during platinum retreatment in platinum-sensitive relapsed ovarian or peritoneal carcinoma.</subfield>
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   <subfield code="a">Springer-Verlag, 2010</subfield>
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   <subfield code="a">Recurrent ovarian cancer</subfield>
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   <subfield code="a">Bryant</subfield>
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   <subfield code="u">Wayne State University, Barbara Ann Karmanos Cancer Institute, Harper Professional Building, 4160 John R Street, Suite 2126, 48201, Detroit, MI, USA</subfield>
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   <subfield code="a">Kumar</subfield>
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   <subfield code="u">Wayne State University, Barbara Ann Karmanos Cancer Institute, Harper Professional Building, 4160 John R Street, Suite 2126, 48201, Detroit, MI, USA</subfield>
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