Objective
Compared to conventional intravenous platinum and taxane-based chemotherapy for ovarian cancer, both intraperitoneal chemotherapy and more frequent dose-dense intravenous chemotherapy have been associated with improved survival in some studies. We examined the utilization and toxicity of these three methods of chemotherapy delivery in women with ovarian cancer.
Methods
We performed a population-based study and analyzed data on women with ovarian cancer who underwent primary surgery followed by platinum and taxane-based chemotherapy from 2009â2013 who were recorded in the MarketScan database. Adjuvant chemotherapy was classified as: intraperitoneal chemotherapy, dose-dense chemotherapy (weekly administration of chemotherapy), or standard chemotherapy (every 3 weeks). Hospitalizations and emergency department visits for chemotherapy-associated complications and costs were recorded and compared using Ï2 tests.
Results
A total of 5,892 patients, including 4,135 (70.2%) who received standard chemotherapy, 859 (14.6%) who received intraperitoneal chemotherapy, and 898 (15.2%) treated with dose-dense chemotherapy were identified. From 2009 to 2013, use of intraperitoneal chemotherapy remained constant (16.3% to 16.3%) while use of dose-dense therapy increased (8.7% to 18.1%) (P<0.001). Hospitalizations for chemotherapy-associated complications occurred in 21.3% of women receiving standard chemotherapy, 34.7% of patients treated with intraperitoneal therapy, and in 25.2% of those receiving dose-dense treatment (P<0.001), while emergency department visits occurred in 18.3%, 26.3%, and 20.3%, respectively (P<0.001). The largest differences in hospitalizations and emergency visits were seen for gastrointestinal toxicities and electrolyte disorders. The per-patient costs of hospitalization were higher for intraperitoneal chemotherapy than other treatment modalities.
Conclusion
Intraperitoneal chemotherapy was used in less than 15% of women with ovarian cancer, while use of dose-dense chemotherapy is increasing. While we did not examine survival, intraperitoneal chemotherapy is significantly more toxic than the other methods of treatment.