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拓扑替康在复发性卵巢癌患者中持续输注14天。

Topotecan as a continuous infusion over 14 days in recurrent ovarian cancer patients.

作者信息

Denschlag D, Watermann D, Hörig K, Kissel C, Tempfer C, Gitsch G

机构信息

Department of Gynecology and Obstetrics, University of Freiburg School of Medicine, Freiburg, Germany.

出版信息

Anticancer Res. 2004 Mar-Apr;24(2C):1267-9.

PMID:15154658
Abstract

OBJECTIVE

In recurrent ovarian cancer the topoisomerase-1 inhibitor topotecan shows activity after prior treatment with platinum and taxanes. Overall response rates of up to 38% in combination with an acceptable toxicity profile have been reported. We performed a pilot study to evaluate the therapeutic efficacy and toxicity profile of a low-dose continuous infusion protocol of topotecan.

PATIENTS AND METHODS

Twelve patients with recurrent ovarian cancer and a measurable lesion received a continuous infusion of topotecan (0.4 mg/m2/d) over 14 days, repeated every 28 days. All patients had at least one prior platinum-containing regimen of chemotherapy (range 1-7). Responses were evaluated by ultrasound, computed tomography (CT) scans and/or magnetic resonance imaging (MRI).

RESULTS

A total of 57 (median 5, range 1-12) topotecan treatment cycles were administered. The overall response rate was 2/12 (17%). Four patients had stable disease (33%), among them two patients with platinum-refractory tumors. The median time to progression was 26 (range 20-100) weeks. No grade 3 or 4 hematological toxicities were observed. However, one patient developed a grade 2 allergy leading to discontinuation of topotecan.

CONCLUSION

Treatment of recurrent ovarian cancer with low-dose continuous infusion of topotecan over 14 days demonstrated response rates comparable to other dosing schedules with minimal toxicity in a preliminary series of 12 patients.

摘要

目的

在复发性卵巢癌中,拓扑异构酶-1抑制剂拓扑替康在先前接受铂类和紫杉烷类治疗后显示出活性。据报道,联合使用时总体缓解率高达38%,且毒性特征可接受。我们进行了一项前瞻性研究,以评估拓扑替康低剂量持续输注方案的治疗效果和毒性特征。

患者和方法

12例复发性卵巢癌且有可测量病灶的患者接受拓扑替康持续输注(0.4mg/m²/天),持续14天,每28天重复一次。所有患者至少接受过一种含铂化疗方案(范围为1 - 7种)。通过超声、计算机断层扫描(CT)和/或磁共振成像(MRI)评估疗效。

结果

共进行了57个(中位数为5,范围1 - 12)拓扑替康治疗周期。总体缓解率为2/12(17%)。4例患者病情稳定(33%),其中2例为铂耐药肿瘤患者。中位疾病进展时间为26(范围20 - 100)周。未观察到3级或4级血液学毒性。然而,1例患者出现2级过敏反应,导致拓扑替康停用。

结论

在12例患者的初步系列研究中,拓扑替康14天低剂量持续输注治疗复发性卵巢癌的缓解率与其他给药方案相当,且毒性最小。

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Topotecan as a continuous infusion over 14 days in recurrent ovarian cancer patients.拓扑替康在复发性卵巢癌患者中持续输注14天。
Anticancer Res. 2004 Mar-Apr;24(2C):1267-9.
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