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In conclusion, our cumulative experience with IP therapy has
demonstrated sustained improvement in median OS (HR, 0.76) without
an impact on long-term disease-specific mortality
at the expense of increased complexity, toxicity, and cost. Similar
gains
in OS have been observed with other approaches,
including IV therapy that incorporates dose-dense weekly paclitaxel,
especially
in high-risk patients with larger-volume residual
disease.8
Important questions remain regarding patient selection (in terms of the
extent of residual disease), mechanism of action,
treatment modifications, timing, optimal number of
IP cycles, and integration with targeted agents. Some of these questions
will be addressed in the context of GOG-0252, and
it remains to be seen whether better IV chemotherapy might match the
outcomes
previously associated with IP chemotherap
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