Single agent carboplatin versus carboplatin plus pegylated liposomal doxorubicin in recurrent ovarian cancer: Final survival results of a SWOG (S0200) phase 3 randomized trial

Objectives. Randomized phase 3 trials have demonstrated the utility of a regimen of carboplatin plus pegylated liposomal doxorubicin (PLD) in recurrent ovarian cancer, and have provided provocative data Suggesting a Substantially lower Fisk of carboplatin-associated hypersensitivity if PDL is delivered in combination with the platinum agent. Methods. To further examine both of these clinically-relevant issues, the survival outcome (With longer follow-up) and hypersensitivity reaction profile of a previously reported phase 3 trial that compared single agent carboplatin (AUC 5) to carboplatin (AUC 5) plus PLD (30 mg/m(2)) delivered on an every 4-week schedule in recurrent ovarian cancer (SWOG 0200) were re-analyse. Results. In the limited number of patients (n=61) entered into this phase 3 Study before closure by the SWOG Data Safety and Monitoring Committee due to insufficient accrual, there was an initially reported improvement in outcome associated with the combination regimen. With longer follow-up and additional events there is still a statistically-significant improved progression-free survival (median: 12 versus 8 months, p = 0.02), but the previously observed impact of the two-drug regimen on overall survival is 110 longer apparent (median: 3 1 versus 18 months; p = 0.2). While no hypersensitivity reactions were reported in the carboplatin plus PLD arm (0/31), 9 of 30 patients (30%) of women randomized to single agent carboplatin experienced at) allergic episode (p=0.0008), with 5 being >grade 2 in severity. Conclusion. Despite a favorable impact of carboplatin and PLD on progression-free survival in this trial, the effect on overall Survival is not statistically significant. For currently unknown reasons, administering PLD with carboplatin appears to substantially reduce the incidence of platinum-associated hypersensitivity reactions. (C) 2009 Elsevier Inc. All rights reserved.