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聚乙二醇化脂质体阿霉素与卡铂治疗晚期妇科肿瘤:妇科肿瘤协作组卵巢癌研究组(AGO-OVAR)的一项前瞻性I/II期研究

Pegylated liposomal doxorubicin and carboplatin in advanced gynecologic tumors: a prospective phase I/II study of the Arbeitsgemeinschaft Gynaekologische Onkologie Studiengruppe Ovarialkarzinom (AGO-OVAR).

作者信息

du Bois A, Burges A, Meier W, Pfisterer J, Schmalfeldt B, Richter B, Jackisch C, Staehle A, Kimmig R, Elser G

机构信息

HSK, Dr Horst Schmidt Klinik, Department of Gynecology & Gynecologic Oncology, Wiesbaden, Germany.

出版信息

Ann Oncol. 2006 Jan;17(1):93-6. doi: 10.1093/annonc/mdj032. Epub 2005 Nov 9.

Abstract

BACKGROUND

Single-agent platinum and single-agent pegylated liposomal doxorubicin (PLD) are both effective in the treatment of gynecologic malignancies. Based on evidence that combination platinum-containing regimens offer superior efficacy versus single-agent regimens, we conducted this study to determine the maximum tolerated dose (MTD) of PLD in combination with carboplatin.

PATIENTS AND METHODS

In this phase I/II dose-finding study, six courses of PLD (20, 30, 40 or 50 mg/m2) and carboplatin (AUC 6) were administered every 28 days to women with advanced gynecologic malignancies. Three to six patients were treated at each dose level; an additional 12 patients were treated at the MTD.

RESULTS

PLD 40 mg/m2 was identified as the MTD when administered with carboplatin. Five of 18 patients experienced a dose-limiting toxicity at the MTD; two patients had grade 3/4 neutropenia, and one each had grade 3 emesis and grade 3 thrombocytopenia and thrombosis. No patient developed cardiotoxicity. In 11 patients evaluable for response, there were two complete responses, two partial responses and four patients with stable disease.

CONCLUSIONS

The MTD for PLD when administered in combination with carboplatin is 40 mg/m2. This regimen is well tolerated and offers promising activity in women with advanced gynecologic malignancies.

摘要

背景

单药铂类和单药聚乙二醇化脂质体阿霉素(PLD)在妇科恶性肿瘤治疗中均有效。基于含铂联合方案比单药方案疗效更优的证据,我们开展了本研究以确定PLD与卡铂联合使用时的最大耐受剂量(MTD)。

患者与方法

在这项I/II期剂量探索研究中,每28天给晚期妇科恶性肿瘤女性患者给予六个疗程的PLD(20、30、40或50mg/m²)和卡铂(AUC 6)。每个剂量水平治疗3至6名患者;另外12名患者在MTD剂量水平接受治疗。

结果

PLD与卡铂联合使用时,40mg/m²被确定为MTD。18名患者中有5名在MTD剂量水平出现剂量限制性毒性;2名患者出现3/4级中性粒细胞减少,1名患者出现3级呕吐,1名患者出现3级血小板减少和血栓形成。无患者发生心脏毒性。在11名可评估反应的患者中,有2例完全缓解,2例部分缓解,4例病情稳定。

结论

PLD与卡铂联合使用时的MTD为40mg/m²。该方案耐受性良好,对晚期妇科恶性肿瘤女性患者具有良好的活性。

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