Abstract
Background Vandetanib is an oral tyrosine kinase inhibitor of VEGFR-2/3, EGFR and RET, which has demonstrated clinical activity as a single agent and in combination with taxanes. We explored the efficacy, safety and toxicity of docetaxel and vandetanib in women with recurrent ovarian cancer (OC). Methods Women with refractory or progressive OC were randomised 1:1 to docetaxel (75 mg/m2, IV) + vandetanib (100 mg daily, PO, D + V) or docetaxel (75 mg/m2, D). Up to three additional cytotoxic regimens for recurrence and prior anti-angiogenic agents (as primary therapy) were allowed. The primary end-point was progression free survival (PFS). The study had 84% power to detect a PFS hazard ratio of 0.65, using a one-sided P of 0.1. This corresponds to an increase in median PFS from 3.6 months to 5.6 months. Patients progressing on D were allowed to receive single agent vandetanib (D → V). Results 131 Patients were enrolled; two were excluded. 16% had received prior anti-angiogenic therapy. The median PFS estimates were 3.0 mos (D + V) versus 3.5 (D); HR: 0.99 (80% CI: 0.79-1.26). 61 Patients on D + V were assessable for toxicity; 20(33%) had treatment-related Grade (G) 4 events, primarily haematologic. Similarly, 17 (27%) of 64 patients receiving D had G4 events, primarily haematologic. 27 Evaluable patients crossed-over to V. 1/27(4%) experienced a G4 event. G3 diarrhoea was observed in 4% D → V patients. Median OS was 14 mos (D + V) versus 18 mos (D → V); HR(OS): 1.25 (80% CI: 0.93-1.68). Crossover vandetanib response was 4% (1/27 evaluable patients). High plasma IL-8 levels were associated with response to D + V. Conclusions Combination docetaxel + vandetanib did not prolong PFS relative to docetaxel alone in OC patients. No unexpected safety issues were identified.
Original language | English (US) |
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Pages (from-to) | 1638-1648 |
Number of pages | 11 |
Journal | European Journal of Cancer |
Volume | 50 |
Issue number | 9 |
DOIs | |
State | Published - Jun 2014 |
Keywords
- Chemotherapy
- Clinical trial
- Epithelial cancer
- Fallopian tube cancer
- Ovarian cancer
- Primary peritoneal cancer
- Randomised phase II
- Taxanes
- Vandetanib
ASJC Scopus subject areas
- Oncology
- Cancer Research