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Abstract
Highlights
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- Results are presented for a phase II study of maintenance therapy with sorafenib in the treatment of OC.
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- Median PFS was not significantly superior for sorafenib compared with placebo.
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- Discontinuations due to AEs were more frequent with sorafenib which likely impacted assessment of efficacy.
Background
Sorafenib,
an oral multikinase inhibitor of the VEGFR/PDGFR/ Raf/MEK/ERK pathway,
has shown potential activity in patients with recurrent ovarian cancer
(OC). One strategy to prolong disease control and survival in patients
with OC is maintenance therapy after achieving a complete response. A
double-blind, randomized, placebo-controlled, phase II study to assess
the efficacy and safety of maintenance therapy with sorafenib in the
treatment of OC is presented.
Methods
Patients
with epithelial OC or primary peritoneal cancer in complete remission
were randomized to sorafenib 400 mg BID or matching placebo. The primary
endpoint was progression-free survival (PFS).
Results
Of
246 randomized patients, 93% had OC; baseline characteristics were
balanced between treatment arms. There was no significant difference
between sorafenib and placebo arms for PFS (median 12.7 vs 15.7 months;
hazard ratio 1.09; 95% CI 0.72–1.63), although there was a notable
imbalance in early censoring. The most common ≥ grade 3 adverse events
(AEs) were hand-foot skin reaction (39.0% vs 0.8%) and rash (14.6% vs
0%). More patients receiving sorafenib versus placebo required dose
reductions (67.5% vs 30.1%), resulting in a lower than planned median
daily dose (median 584.6 vs 800.0 mg). Treatment with sorafenib was of
shorter duration (median 17.6 vs 51.9 weeks) with more frequent
discontinuations due to AEs (37.4% vs 6.5%).
Conclusions
Sorafenib
400 mg BID cannot be recommended as maintenance therapy for patients
with OC in complete remission. Assessment of efficacy was limited by the
high rate of dose reductions and early discontinuations.
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