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A case series of low dose bevacizumab and chemotherapy in heavily pretreated patients with epithelial ovarian cancerAbstract: We treated 15 patients, mostly with platinum resistant EOC, who had received a median of four prior cytotoxic regimens, with bevacizumab 5–7.5?mg/kg q21 days in combination with either carboplatin (n?=?8), oral cyclofosfamide (n?=?5) or weekly paclitaxel (n?=?2). Bevacizumab was administered until disease progression. Tumor response was assessed by CA125 and fusion 18?F-FDG PET/contrast enhanced CT.The median number of bevacizumab cycles was 21 (range 3–59). The median baseline CA125 was 272 U/ml and decreased to 15.2 U/ml at nadir. Tumor response was 4 complete response (CR) (26.7%) and 7 partial response (PR) (46.7%) by chemotherapy (CT), with an overall response rate of 73.4% (95% CI, 51.0 – 95.8) according to Response Evaluation Criteria In Solid Tumors (RECIST), and 6 CR (40%) and 4 PR (26.7%) by PET, for an overall metabolic response rate of 67% (95%CI, 42.8 – 90.6) according to PET Response Criteria in Solid Tumors (PERCIST). Median progression free survival (PFS) was 21?months and median overall survival (OS) was 24?months. Grade 3 adverse events related to bevacizumab were hypertension (n?=?2), proteinuria (n?=?1) and epistaxis (n?=?5). Treatment was delayed in five patients for nasal bleeding or uncontrolled hypertension.Low-dose bevacizumab and chemotherapy was well tolerated and active in a heavily pretreated population of advanced EOC. Further studies should assess the activity of low dose bevacizumab in EOC.
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