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首页> 外文期刊>The oncologist >Efficacy and Safety of Vincristine Sulfate Liposome Injection in the Treatment of Adult Acute Lymphocytic Leukemia
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Efficacy and Safety of Vincristine Sulfate Liposome Injection in the Treatment of Adult Acute Lymphocytic Leukemia

机译:长春新碱硫酸盐脂质体注射液治疗成人急性淋巴细胞白血病的疗效和安全性

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摘要

Acute lymphoblastic leukemia (ALL) is a heterogeneous group of hematologic malignancies that arise from clonal proliferation of immature lymphoid cells in the bone marrow, peripheral blood, and other organs. The vinca alkaloid vincristine is a standard component of chemotherapy regimens used to treat ALL, because of its well-defined mechanism of action, demonstrated anticancer activity, and ability to be combined with other agents. However, the dosage of vincristine is frequently capped because of neurotoxicity concerns, and patients with large body surface areas are, therefore, almost always underdosed. Liposomal formulations have the ability to a??passivelya?? accumulate at sites of increased vasculature permeability and reduce the adverse effects of encapsulated relative to free drug. Vincristine sulfate liposome injection (VSLI) is a sphingomyelin/cholesterol-based liposome-encapsulated formulation that is delivered weekly in a 1-hour infusion. Based on the pharmacokinetics of the liposomal delivery system, vincristine is slowly released from the liposome and delivered into the tissues more efficiently than with the standard preparation, allowing a higher dose. This increase in therapeutic index from reduced toxicity is a valuable difference between the two formulations. VSLI is indicated for the treatment of adults with second or greater relapse and clinically advanced Philadelphia chromosome-negative ALL. For the first time, studies will be able to exploit the delivery of higher and uncapped doses of vincristine in randomized studies comparing first-line chemotherapy with standard vincristine versus VSLI in both ALL and lymphoma to determine whether VSLI is superior to conventional vincristine. Implications for Practice: This review summarizes the development of vincristine sulfate liposome injection, a new formulation of vincristine. The pharmacokinetics of liposomal drug delivery are examined, the limitations and advantages of conventional and liposomal vincristine are compared, and the use of vincristine sulfate liposome injection in clinical trials and case studies is included. Clinicians will be informed of a new chemotherapy agent that is indicated for the treatment of adults with Philadelphia chromosome-negative acute lymphoblastic leukemia, whose disease has relapsed two or more times or whose leukemia has progressed after two or more regimens of antileukemia therapy.
机译:急性淋巴细胞性白血病(ALL)是血液恶性肿瘤的异质性组,其源于骨髓,外周血和其他器官中未成熟淋巴样细胞的克隆增殖。长春花生物碱长春新碱是用于治疗ALL的化疗方案的标准组成部分,因为它的作用机制明确,显示出抗癌活性以及与其他药物合用的能力。然而,由于神经毒性的考虑,长春新碱的剂量经常被限制,因此,体表面积大的患者几乎总是剂量不足。脂质体制剂具有“被动”的能力。聚集在增加的脉管系统通透性的位置,并减少了胶囊化药物相对于游离药物的不良作用。硫酸长春新碱脂质体注射液(VSLI)是一种基于鞘磷脂/胆固醇的脂质体包裹制剂,每周输注1小时。基于脂质体递送系统的药代动力学,长春新碱从脂质体中缓慢释放并比标准制剂更有效地递送到组织中,从而允许更高的剂量。由于降低的毒性而使治疗指数增加是两种制剂之间的宝贵区别。 VSLI适用于治疗具有第二次或更多次复发且临床晚期费城染色体阴性ALL的成人。这项随机对照研究将一线化疗与标准长春新碱对比VSLI在ALL和淋巴瘤中进行比较,从而确定VSLI是否优于常规长春新碱。对实践的意义:该综述总结了长春新碱新制剂硫酸长春新碱脂质体注射剂的开发。检查了脂质体药物递送的药代动力学,比较了常规和脂质体长春新碱的局限性和优点,并包括了在临床试验和案例研究中使用硫酸长春新碱脂质体注射剂。将告知临床医生一种新的化疗药物,该药物可用于治疗费城染色体阴性急性淋巴细胞白血病的成年人,该患者的疾病已复发两次或更多次,或者经过两次或更多次抗白血病治疗后白血病已进展。

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