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Prospective study on nanoparticle albumin-bound paclitaxel in advanced breast cancer: clinical results and biological observations in taxane-pretreated patients

机译:纳米粒子白蛋白结合紫杉醇在晚期乳腺癌中的前瞻性研究:紫杉烷预处理患者的临床结果和生物学观察

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Background: There is a deep need to improve the care of metastatic breast cancer (MBC) patients, since even today it remains an incurable disease. Taxanes are considered the most effective cytotoxic drugs for the treatment of MBC, both in monotherapy and in combined schedules, but the need for synthetic solvents contributes to the severe toxicities and may have a negative impact on the efficacy. Nanoparticle albumin-bound paclitaxel ( Nab -paclitaxel) is a colloidal suspension of paclitaxel and human serum albumin initially developed to avoid the toxicities associated with conventional taxanes. Patients and methods: The aim of this prospective, single-center open-label, noncomparative study was to evaluate the efficacy and safety of nab -paclitaxel in MBC patients pretreated with taxanes. The patients were treated with nab -paclitaxel as a single agent, 260?mg/m2 on day 1 of each 3-week cycle or 125?mg/m2 weekly. The primary endpoint was the overall response rate (ORR). Secondary objectives were duration of response, clinical benefit rate, progression-free survival (PFS), overall survival, and safety. Results: A total of 42 patients (median age 48?years, median Eastern Cooperative Oncology Group performance status 0, triple-negative MBC 19%, all pretreated with a taxane-based therapy, mainly in advanced disease) were enrolled in the study. The ORR was 23.8%, including one complete response (2.4%) and nine partial responses (21.4%); the disease control rate was 50%. The median duration of response was 7.2?months. After a median follow-up of 9?months, the median PFS was 4.6?months. ORR and PFS were similar irrespective of the previous chemotherapy lines, metastatic sites, and biomolecular expression. Nab -paclitaxel was well tolerated, and the most frequent treatment-related toxicities were mild to moderate (grades 1–2). Conclusion: This real-life study shows that nab -paclitaxel has a significant antitumor activity and a manageable safety profile in patients pretreated with taxanes and experiencing a treatment failure after at least one line of chemotherapy.
机译:背景:迫切需要改善转移性乳腺癌(MBC)患者的护理,因为即使在今天,它仍然是无法治愈的疾病。紫杉烷在单一疗法和联合疗法中均被认为是治疗MBC的最有效的细胞毒性药物,但对合成溶剂的需求会导致严重的毒性,并可能对疗效产生负面影响。纳米粒子结合白蛋白的紫杉醇(Nab-紫杉醇)是紫杉醇和人血清白蛋白的胶体悬浮液,最初是为避免与常规紫杉烷类药物相关的毒性而开发的。患者和方法:这项前瞻性,单中心,开放性,非对照性研究的目的是评估nab-紫杉醇对紫杉烷预处理的MBC患者的疗效和安全性。患者以nab-紫杉醇作为单药治疗,每个3周周期的第1天为260?mg / m 2 或每周125?mg / m 2 。主要终点是总体缓解率(ORR)。次要目标是反应持续时间,临床受益率,无进展生存期(PFS),总体生存期和安全性。结果:共纳入42例患者(中位年龄48岁,东部合作肿瘤小组中位状态为0,三阴性MBC为19%,均接受紫杉烷类药物治疗,主要针对晚期疾病)。 ORR为23.8%,包括1个完全缓解(2.4%)和9个部分缓解(21.4%);疾病控制率为50%。中位反应持续时间为7.2个月。在中位随访9个月之后,中位PFS为4.6个月。不论以前的化疗方案,转移部位和生物分子表达如何,ORR和PFS都相似。纳布紫杉醇耐受性良好,与治疗相关的最常见毒性为轻度至中度(1-2级)。结论:这项现实生活研究表明,nab-紫杉醇在接受紫杉烷类药物预处理并经历至少一轮化疗后治疗失败的患者中具有显着的抗肿瘤活性和可控的安全性。

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