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聚乙二醇化脂质体阿霉素联合长春瑞滨治疗转移性乳腺癌:一项I-II期临床研究。

Pegylated liposomal doxorubicin with vinorelbine in metastatic breast carcinoma. A phase I-II clinical investigation.

作者信息

Gebbia Vittorio, Mauceri Gaetano, Fallica Giuseppina, Borsellino Nicolò, Tirrito Maria Lina, Testa Antonio, Varvara Francesca, Colombo Alfredo, Ferrera Patrizia

机构信息

Institute of Internal Medicine, University of Palermo, Palermo, Italy.

出版信息

Oncology. 2002;63(1):23-30. doi: 10.1159/000065716.

Abstract

A multicenter phase I-II trial was carried out with the aim of identifying the dose-limiting toxicity and the maximum tolerated dose of vinorelbine (VNR) in combination with pegylated liposomal doxorubicin at a dose of 20 mg/m(2) every 15 days in patients with metastatic breast carcinoma. In the phase I part of the trial, VNR was given at a dose of 20 mg/m(2) every 15 days to a group of 3 patients. In absence of unacceptable toxicity, VNR was escalated to 25, 30, and 35 mg/m(2) for subsequent groups of 3 patients, until the dose-limiting toxicity was reached. No case of palmar-plantar erythrodysesthesia was recorded in these patients. Grade 4 neutropenia, grade 3 thrombocytopenia, and grade 3 mucositis were the dose-limiting toxicities recorded in patients treated with VNR 35 mg/m(2). These side effects caused a substantial decrease in programmed dose intensity. Therefore 30 mg/m(2) was considered the maximum tolerated dose of VNR in combination with pegylated liposomal doxorubicin 20 mg/m(2), both given every 15 days. These dosages were employed for the treatment of further 18 patients included in phase II of the study. The overall response rate, calculated according to an intention to treat analysis, was 63% (95% CI: 44-80%), with 2 patients achieving a complete response. The median time to progression was 7.0 months or more (range 2-14 months). Median duration of objective responses was 8.4 months or more. The duration of the 2 complete responses was 9 and 14 months, respectively. Median duration of survival was 16.0 months or more (range from 4.0 to >or=24.0). Toxicity was generally mild and easily manageable. Neutropenia and mucositis were the most frequently recorded side effects. A case of palmar-plantar erythrodysesthesia was recorded in phase II of the study. In conclusion, the maximum tolerated dose of VNR in association with pegylated liposomal doxorubicin is 30 mg/m(2) on a bimonthly schedule. Moreover, the combination of VNR and pegylated liposomal doxorubicin is active against metastatic breast carcinoma and is associated with a good toxicity profile. Further studies with this combination regimen are warranted.

摘要

开展了一项多中心I-II期试验,旨在确定长春瑞滨(VNR)与聚乙二醇化脂质体阿霉素联合使用时的剂量限制性毒性和最大耐受剂量,聚乙二醇化脂质体阿霉素剂量为20mg/m²,每15天给药一次,用于治疗转移性乳腺癌患者。在试验的I期部分,对一组3例患者每15天给予剂量为20mg/m²的VNR。在未出现不可接受的毒性反应时,后续每组3例患者的VNR剂量递增至25、30和35mg/m²,直至达到剂量限制性毒性。这些患者中未记录到手足红斑性感觉异常病例。接受35mg/m² VNR治疗的患者记录到的剂量限制性毒性为4级中性粒细胞减少、3级血小板减少和3级粘膜炎。这些副作用导致计划剂量强度大幅下降。因此,30mg/m²被认为是VNR与20mg/m²聚乙二醇化脂质体阿霉素联合使用(均每15天给药一次)时的最大耐受剂量。这些剂量用于治疗研究II期纳入的另外18例患者。根据意向性分析计算的总缓解率为63%(95%CI:44-80%),2例患者实现完全缓解。中位疾病进展时间为7.0个月或更长(范围2-14个月)。客观缓解的中位持续时间为8.4个月或更长。2例完全缓解的持续时间分别为9个月和14个月。中位生存时间为16.0个月或更长(范围4.0至≥24.0)。毒性一般较轻且易于处理。中性粒细胞减少和粘膜炎是最常记录到的副作用。研究II期记录到1例手足红斑性感觉异常病例。总之,VNR与聚乙二醇化脂质体阿霉素联合使用时的最大耐受剂量为每两个月一次的30mg/m²。此外,VNR与聚乙二醇化脂质体阿霉素联合对转移性乳腺癌有活性,且毒性特征良好。有必要对这种联合治疗方案进行进一步研究。

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