首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Pegylated liposomal doxorubicin HCL (PLD; Caelyx/Doxil(R)): Experience with long-term maintenance in responding patients with recurrent epithelial ovarian cancer.
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Pegylated liposomal doxorubicin HCL (PLD; Caelyx/Doxil(R)): Experience with long-term maintenance in responding patients with recurrent epithelial ovarian cancer.

机译:聚乙二醇化脂质体阿霉素盐酸盐(PLD; Caelyx / Doxil(R)):长期维持治疗复发性上皮性卵巢癌患者的经验。

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BACKGROUND: We hypothesized that a response to pegylated liposomal doxorubicin (PLD, Caelyx/Doxil) followed by maintenance is beneficial and safe in recurrent ovarian cancer. PATIENTS AND METHODS: Sixteen patients have received PLD for more than 1 year for recurrent ovarian (14) or fallopian tube (2) cancer. All had stable disease or better responses to PLD + carboplatin (5) or topotecan (9) doublets or to PLD alone (2). PLD maintenance therapy 30-40 mg/m(2) was given every 4-8 weeks. This analysis focuses on cardiac status, overall tolerance, and time to recurrence. RESULTS: Termination of PLD was due to progression in all patients. Noteworthy was the lack of cumulative myelosuppression and, with one exception, clinical cardiac toxicity. This patient was hospitalized with cardiogenic shock and fever complicating grade 4 pancytopenia from topotecan ten months after discontinuation of PLD. Seven patients continue to receive PLD after a median of 1680 mg/m(2) (1180-2460 mg/m(2)). Four of these had documented relapses after 3-6 years on maintenance occurring in the setting of lengthening of the treatment interval. Maintenance PLD was reinstituted after 'reinduction' with a platinum. CONCLUSIONS: PLD appears to be safe as long-term maintenance in ovarian cancer and may be important for a continued response.
机译:背景:我们假设对聚乙二醇化脂质体阿霉素(PLD,Caelyx / Doxil)的继之以维持治疗对复发性卵巢癌是有益且安全的。患者和方法:16例因复发性卵巢癌(14)或输卵管癌(2)接受了PLD超过1年。所有患者均对PLD +卡铂(5)或拓扑替康(9)联用或仅对PLD(2)有稳定的疾病或更好的反应。每4-8周进行一次PLD维持疗法30-40 mg / m(2)。该分析的重点是心脏状态,总体耐受性和复发时间。结果:PLD的终止归因于所有患者的进展。值得注意的是缺乏累积性骨髓抑制,除了一个例外,是临床心脏毒性。该患者在停药10个月后因心源性休克和发烧而住院,并伴有拓扑替康的4级全血细胞减少症。中位数1680 mg / m(2)(1180-2460 mg / m(2))之后,有7名患者继续接受PLD。在延长治疗间隔的情况下,其中四项已记录在维持3-6年后复发。在用铂“还原”后重新建立了维护PLD。结论:PLD作为卵巢癌的长期维持治疗似乎是安全的,并且对于持续反应可能很重要。

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