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口服依托泊苷延长给药用于铂类化疗后12个月内难治或复发的卵巢癌患者的II期研究。

Phase II study of prolonged oral etoposide in patients with ovarian cancer refractory to or relapsing within 12 months after platinum-containing chemotherapy.

作者信息

de Wit R, van der Burg M E, van den Gaast A, Logmans A, Stoter G, Verweij J

机构信息

Department of Medical Oncology, Rotterdam Cancer Institute/Dr. Daniel den Hoed Kliniek, The Netherlands.

出版信息

Ann Oncol. 1994 Sep;5(7):656-7. doi: 10.1093/oxfordjournals.annonc.a058942.

Abstract

PATIENTS AND METHODS

Twenty-eight patients with ovarian cancer refractory to or relapsing within 12 months after cisplatin-containing chemotherapy were treated with etoposide 50 mg/m2 daily for 21 days, followed by a 7-day break.

RESULTS

Of 25 evaluable patients, 4 achieved partial responses (16%, 95% confidence interval 5%-36%) of 4, 4, 7, and 10 months' duration. The platinum treatment-free intervals for these patients were 2, 9, 7, and 10 months, respectively. Etoposide in this schedule was generally well tolerated, with myelosuppression as the major toxicity, resulting in a median dose intensity over all cycles of 83% (range 47%-100%).

CONCLUSIONS

Prolonged oral etoposide is moderately active both in relapsed and platinum-refractory ovarian cancer, and a schedule of 50 mg/m2 days 1-21, every 4 weeks is fairly well tolerated in this usually heavily pretreated and elderly patient population.

摘要

患者与方法

28例对含顺铂化疗难治或在含顺铂化疗后12个月内复发的卵巢癌患者,接受依托泊苷50mg/m²每日给药,共21天,随后休息7天。

结果

25例可评估患者中,4例获得部分缓解(16%,95%置信区间5%-36%),缓解持续时间分别为4、4、7和10个月。这些患者的无铂治疗间期分别为2、9、7和10个月。该方案中的依托泊苷总体耐受性良好,主要毒性为骨髓抑制,所有周期的中位剂量强度为83%(范围47%-100%)。

结论

延长口服依托泊苷对复发和铂类难治性卵巢癌均有中度活性,对于通常经过多次治疗且年龄较大的患者群体,每4周1-21天50mg/m²的给药方案耐受性相当良好。

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