Carboplatin and Pegylated Liposomal Doxorubicin for Advanced Ovarian Cancer: Preliminary Activity Results of the MITO-2 Phase III Trial

被引:23
|
作者
Pignata, S.
Scambia, G. [3 ]
Savarese, A. [4 ]
Breda, E. [5 ]
Sorio, R. [6 ]
Pisano, C.
Lorusso, D. [3 ]
Cognetti, F. [4 ]
Lombardi, A. Vernaglia
Gebbia, V. [7 ]
Scollo, P. [8 ]
Morabito, A. [1 ]
Signoriello, G. [2 ]
Perrone, F. [1 ]
机构
[1] Univ Naples 2, Ist Nazl Tumori, Unite Sperimentazioni Clin, Naples, Italy
[2] Univ Naples 2, Dipartimento Med & Salute Pubbl, Naples, Italy
[3] Univ Cattolica Sacro Cuore, Rome, Italy
[4] Ist Regina Elena, I-00161 Rome, Italy
[5] Osped S Giovanni Fatebenefratelli, Rome, Italy
[6] CRO, Aviano, Italy
[7] Univ Palermo, Palermo, Italy
[8] Azienda Osped Cannizzaro, Catania, Italy
关键词
Anthracyclines; Pegylated liposomal doxorubicin; Ovarian cancer; Carboplatin; Paclitaxel; RECURRENT EPITHELIAL OVARIAN; QUALITY-OF-LIFE; 1ST-LINE TREATMENT; SURVIVAL ADVANTAGE; INTERGROUP TRIAL; CISPLATIN; CHEMOTHERAPY; PACLITAXEL; CYCLOPHOSPHAMIDE; COMBINATION;
D O I
10.1159/000178760
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Based on the efficacy of pegylated liposomal doxorubicin (PLD) in relapsed ovarian cancer, we are conducting a phase III study comparing carboplatin plus either paclitaxel or PLD as first-line therapy in advanced ovarian cancer. Because of limited phase I and II data on PLD plus carboplatin in this setting, we conducted an interim activity analysis. Patients and Methods: Patients with stage 1c-IV epithelial ovarian cancer were randomized to carboplatin AUC 5 plus either paclitaxel 175 mg/m(2) or PLD 30 mg/m(2) every 3 weeks for 6 cycles. The interim activity analysis was planned according to a single-stage phase II design with an auspicated 50% response rate; 50 patients eligible for response assessment were required. Response was defined according to RECIST (Response Evaluation Criteria in Solid Tumors). Results: A complete response was achieved in 14 patients (28%) and a partial response in 20 (40%), which produced an overall response rate of 68%. The activity exceeded the minimum required for study continuation. Stable disease was reported in an additional 10 patients (20%). Conclusions: The adopted schedule of PLD plus carboplatin demonstrates activity as a first-line treatment for advanced ovarian cancer. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:49 / 54
页数:6
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