Netupitant / palonosetron (NEPA);Akynzeo®)联合用药预防接受蒽环类化疗的乳腺癌患者的恶心和呕吐

A. G. Kedrova, A. I. Berishvili
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引用次数: 0

摘要

化疗引起的恶心和呕吐是癌症治疗过程中常见的问题,特别是在蒽环类/环磷酰胺化疗的乳腺癌患者中。Netupitant / palonosetron (NEPA);Akynzeo®是两种药物的固定剂量组合(netupitant,一种神经激肽1受体拮抗剂;还有帕洛诺司琼(一种血清素3受体拮抗剂),它针对诱导呕吐的两种不同信号通路。尼妥吡坦/帕洛诺司琼被批准用于预防急性和延迟化疗引起的成人恶心和呕吐,在化疗前口服或静脉输注单剂量。在临床试验中,在化疗前接受奈吡坦/帕洛诺司琼(与皮质类固醇地塞米松联合使用)的患者中,有很高比例的患者在化疗后5天内没有出现呕吐,不需要救援药物,也没有明显的恶心。该药物组合的口服和静脉制剂均具有良好的耐受性。因此,奈吡坦/帕洛诺司琼是一种简单、方便、有效的药物组合,可预防化疗患者急性和迟发性血液疗法引起的恶心和呕吐,具有中高致吐潜能。
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Netupitant/palonosetron (NEPA; Akynzeo®) combination in prevention of the nausea and vomiting in patients with breast cancer receiving anthracyclinbased chemotherapy
Chemotherapy-induced nausea and vomiting is a common problem during cancer treatment, especially in breast cancer patients with anthracycline/cyclophosphamide (ас) chemotherapy. Netupitant/palonosetron (NEPA; Akynzeo®) is a fixed-dose combination of two drugs (netupitant, a neurokinin 1 receptor antagonist; and palonosetron, a serotonin 3 receptor antagonist) which target two diferent signalling pathways involved in the induction of vomiting. Approved for use in the prevention of acute and delayed chemotherapy-induced nausea and vomiting in adults, netupitant/palonosetron is given orally or via intravenous infusion as a single dose prior to chemotherapy. In clinical trials, high proportions of patients who received netupitant/palonosetron (used in combination with the corticosteroid dexamethasone) prior to chemotherapy reported no vomiting, no requirement for rescue medication, and no signifcant nausea in the 5 days post chemotherapy. Both the oral and intravenous formulations of the drug combination are well tolerated. Thus, netupitant/palonosetron is a simple, convenient and efective drug combination for the prevention of acute and delayed xhemotherapy-induced nausea and vomiting in patients receiving chemotherapy that has a moderate to high emetogenic potential.
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来源期刊
Opuholi Zenskoj Reproduktivnoj Sistemy
Opuholi Zenskoj Reproduktivnoj Sistemy Medicine-Obstetrics and Gynecology
CiteScore
0.50
自引率
0.00%
发文量
38
审稿时长
10 weeks
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