Background: A randomized trial conducted by the Gyneco-logic Oncology Group (GOG, study #111) in the United States showed a better outcome for patients with advanced ovarian cancer on the paclitaxel–cisplatin regimen than for those on a standard cyclophosphamide–cisplatin regimen. Before considering the paclitaxel–cisplatin regimen as the new “standard, ” a group of European and Canadian inves-tigators planned a confirmatory phase III trial. Methods: This intergroup trial recruited 680 patients with broader selection criteria than the GOG #111 study and administered paclitaxel as a 3-hour instead of a 24-hour infusion; progres-sion-free survival was the primary end point. Patient sur-vival was analyzed by use of the Kaplan–Meier technique. ...
Purpose: To compare taxane maintenance chemotherapy, paclitaxel (P) and paclitaxel poliglumex (PP), ...
The aim of the study was to evaluate the role of epidoxorubicin plus paclitaxel combination (ET) vs ...
PURPOSE: This phase III randomized trial (NCT00954174) tested the null hypothesis that paclitaxel an...
Two independent and consecutive randomized clinical trials, conducted by the American Gynecological ...
Background Topotecan has single-agent activity in recurrent ovarian cancer. It was evaluated in a no...
Item does not contain fulltextBACKGROUND: Weekly paclitaxel/carboplatin might improve survival in pl...
PURPOSE: This was a multicentric, open, randomized, phase II study of single-agent paclitaxel and ox...
PURPOSE: To evaluate the impact of two different intraperitoneal (IP) chemotherapy regimens on progr...
Objective: Suboptimally debulked patients with advanced ovarian cancer who are treated with a combin...
A recent phase III trial compared the efficacy of cisplatin-topotecan (a topoisomerase I inhibitor) ...
International audienceIMPORTANCE: Single-agent carboplatin is often proposed instead of a convention...
PURPOSE: To assess whether six courses of paclitaxel are effective as consolidation treatment in pat...
Purpose: Carboplatin/paclitaxel is the standard first-line chemotherapy for patients with advanced o...
Purpose: To compare taxane maintenance chemotherapy, paclitaxel (P) and paclitaxel poliglumex (PP), ...
The aim of the study was to evaluate the role of epidoxorubicin plus paclitaxel combination (ET) vs ...
PURPOSE: This phase III randomized trial (NCT00954174) tested the null hypothesis that paclitaxel an...
Two independent and consecutive randomized clinical trials, conducted by the American Gynecological ...
Background Topotecan has single-agent activity in recurrent ovarian cancer. It was evaluated in a no...
Item does not contain fulltextBACKGROUND: Weekly paclitaxel/carboplatin might improve survival in pl...
PURPOSE: This was a multicentric, open, randomized, phase II study of single-agent paclitaxel and ox...
PURPOSE: To evaluate the impact of two different intraperitoneal (IP) chemotherapy regimens on progr...
Objective: Suboptimally debulked patients with advanced ovarian cancer who are treated with a combin...
A recent phase III trial compared the efficacy of cisplatin-topotecan (a topoisomerase I inhibitor) ...
International audienceIMPORTANCE: Single-agent carboplatin is often proposed instead of a convention...
PURPOSE: To assess whether six courses of paclitaxel are effective as consolidation treatment in pat...
Purpose: Carboplatin/paclitaxel is the standard first-line chemotherapy for patients with advanced o...
Purpose: To compare taxane maintenance chemotherapy, paclitaxel (P) and paclitaxel poliglumex (PP), ...
The aim of the study was to evaluate the role of epidoxorubicin plus paclitaxel combination (ET) vs ...
PURPOSE: This phase III randomized trial (NCT00954174) tested the null hypothesis that paclitaxel an...