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聚山梨酯 80 在肿瘤学领域的安全性。

Safety of Polysorbate 80 in the Oncology Setting.

机构信息

Division of Hematology/Oncology, Department of Medicine, University of Tennessee Health Science Center and West Cancer Center, Memphis, TN, USA.

Division of Hematology and Oncology, University of Alabama Birmingham, Birmingham, AL, USA.

出版信息

Adv Ther. 2018 Jun;35(6):754-767. doi: 10.1007/s12325-018-0707-z. Epub 2018 May 23.

Abstract

Polysorbate 80 is a synthetic nonionic surfactant used as an excipient in drug formulation. Various products formulated with polysorbate 80 are used in the oncology setting for chemotherapy, supportive care, or prevention, including docetaxel, epoetin/darbepoetin, and fosaprepitant. However, polysorbate 80, like some other surfactants, is not an inert compound and has been implicated in a number of systemic and injection- and infusion-site adverse events (ISAEs). The current formulation of intravenous fosaprepitant has been associated with an increased risk of hypersensitivity systemic reactions (HSRs). Factors that have been associated with an increased risk of fosaprepitant-related ISAEs include the site of administration (peripheral vs. central venous), coadministration of anthracycline-based chemotherapy, number of chemotherapy cycles or fosaprepitant doses, and concentration of fosaprepitant administered. Recently, two polysorbate 80-free agents have been approved: intravenous rolapitant, which is a neurokinin 1 (NK-1) receptor antagonist formulated with the synthetic surfactant polyoxyl 15 hydroxystearate, and intravenous HTX-019, which is a novel NK-1 receptor antagonist free of synthetic surfactants. Alternative formulations will obviate the polysorbate 80-associated ISAEs and HSRs and should improve overall management of chemotherapy-induced nausea and vomiting.Funding Heron Therapeutics, Inc.

摘要

聚山梨酯 80 是一种合成的非离子表面活性剂,用作药物制剂中的赋形剂。含有聚山梨酯 80 的各种产品在肿瘤学领域用于化疗、支持性护理或预防,包括多西他赛、促红细胞生成素/达贝泊汀和福沙匹坦。然而,聚山梨酯 80 与一些其他表面活性剂一样,并非惰性化合物,已被牵涉到许多全身性和注射部位及输注部位不良事件(ISAEs)。目前的福沙匹坦静脉制剂与过敏反应全身性反应(HSRs)的风险增加有关。与福沙匹坦相关 ISAEs 风险增加相关的因素包括给药部位(外周与中央静脉)、联合使用蒽环类化疗药物、化疗周期或福沙匹坦剂量数,以及给予的福沙匹坦浓度。最近,两种不含聚山梨酯 80 的药物已获得批准:静脉注射的罗拉匹坦,它是一种与合成表面活性剂聚氧乙烯 15 羟基硬脂酸酯一起配制的神经激肽 1(NK-1)受体拮抗剂,以及静脉注射的 HTX-019,它是一种新型的、不含合成表面活性剂的 NK-1 受体拮抗剂。替代制剂将消除与聚山梨酯 80 相关的 ISAEs 和 HSRs,并应改善化疗引起的恶心和呕吐的整体管理。

资助方

Heron Therapeutics,Inc.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2185/6015121/4b8c73dfd058/12325_2018_707_Fig1_HTML.jpg

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