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首页> 外文期刊>Gynecologic Oncology: An International Journal >Efficacy of pegylated liposomal doxorubicin (PLD) plus carboplatin in ovarian cancer patients who recur within six to twelve months: a phase II study.
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Efficacy of pegylated liposomal doxorubicin (PLD) plus carboplatin in ovarian cancer patients who recur within six to twelve months: a phase II study.

机译:聚乙二醇化脂质体阿霉素(PLD)加卡铂在6至12个月内复发的卵巢癌患者中的疗效:II期研究。

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OBJECTIVES: Pegylated liposomal doxorubicin is one of the preferred alternatives for ovarian cancer patients with early relapse (<6 months) and taxane/carboplatin for late relapse (>12 months), but the optimal therapy for the partially platinum-sensitive (6-12 months) population has not been defined. This single-arm phase II trial was designed to assess the efficacy of pegylated liposomal doxorubicin (PLD)/carboplatin in ovarian cancer patients who relapse between 6 and 12 months after initial treatment with platinum-based chemotherapy. METHODS: Ovarian cancer patients who previously completed a course of therapy with paclitaxel/carboplatin were administered PLD 30 mg/m(2) followed by carboplatin AUC 5 mg/mL/minute every 4 weeks. RESULTS: Fifty-eight patients were enrolled in the study and 54 were eligible for the efficacy analysis, of whom most (75%) received at least 6 cycles of PLD/carboplatin. The objective response rate was 46% (4% CR and 42% PR), with an additional 33% experiencing disease stabilization >6 months. For those patients with measurable CA-125, the response rate was 66% (28% CR and 38% PR), with an additional 18% experiencing disease stabilization >6 months. Median time-to-progression was 10 months (1.5-25). Median overall survival was 19.1 months (2.2-38.9). The most frequent adverse effects were neutropenia, thrombocytopenia, and constipation. CONCLUSIONS: The combination of PLD/carboplatin is efficacious and well tolerated in women with partially platinum-sensitive ovarian cancer and represents a valuable alternative for patients who relapse within 6-12 months of completing paclitaxel/carboplatin chemotherapy.
机译:目的:聚乙二醇脂质体阿霉素是早期复发(<6个月)和紫杉烷/卡铂治疗晚期复发(> 12个月)的卵巢癌患者的首选替代药物,但对部分铂敏感的最佳疗法(6-12个月)人口尚未定义。这项单臂II期试验旨在评估聚乙二醇化脂质体阿霉素(PLD)/卡铂在卵巢癌患者中的疗效,这些患者在铂类化学疗法初始治疗后6到12个月复发。方法:先前完成紫杉醇/卡铂治疗的卵巢癌患者每4周接受PLD 30 mg / m(2),然后接受卡铂AUC 5 mg / mL / min。结果:有58名患者入选了该研究,其中54例符合疗效分析标准,其中大多数(75%)接受了至少6个周期的PLD /卡铂治疗。客观缓解率为46%(CR为4%,PR为42%),另外33%的患者疾病稳定时间> 6个月。对于那些具有可测量的CA-125的患者,缓解率为66%(CR为28%,PR为38%),另有18%的患者病情稳定超过6个月。进展时间中位数为10个月(1.5-25)。中位总生存期为19.1个月(2.2-38.9)。最常见的不良反应是中性粒细胞减少症,血小板减少症和便秘。结论:PLD /卡铂联合治疗对部分铂敏感的卵巢癌女性有效且耐受性良好,对于完成紫杉醇/卡铂化疗后6-12个月内复发的患者而言,是一种有价值的替代选择。

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