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Comparison of antiemetic effects of granisetron and palonosetron in patients receiving bendamustine-based chemotherapy

机译:格兰司琼与吡喃司琼治疗接受叶模司汀化疗患者的抑制作用比较

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The antiemetic effects and safety of granisetron and palonosetron against chemotherapy-induced nausea and vomiting (CINV) were retrospectively evaluated in patients with non-Hodgkin lymphoma receiving bendamustine-based chemotherapy. A total of 61 patients were eligible for this study.Before starting the bendamustine-based chemotherapy, granisetron or palonosetron were intravenously administered with or without aprepitant and/or dexamethasone. The proportions of patients with complete control (CC) during the overall (during the 6 days after the start of the chemotherapy),acute (up to 2 days), and delayed (3 to 6 days) phases were assessed. CC was defined as complete response with only grade 0–1 nausea, no vomiting, and no use of antiemetic rescue medication. Granisetron or palonosetron alone were administered to 9 and 19 patients, respectively. Aprepitantand/or dexamethasone were combined with granisetron and palonosetron in 28 and 5 patients, respectively. Acute CINV was completely controlled in all patients. Both granisetron monotherapy and palonosetron combination therapy could provide good control of delayed CINV, although the CC ratesduring the delayed and overall phases were not significantly different among mono- and combination therapy of the antiemetics. There was no significant difference in the frequencies of adverse drug events between the granisetron and palonosetron treatment groups. The present study showed thatthe antiemetic efficacy and safety of granisetron-based therapy were non-inferior to those of palonosetron-based therapy. Taken together with treatment costs, granisetron monotherapy would be adequate to prevent CINV in patients with non-Hodgkin lymphoma receiving bendamustine-based chemotherapy.
机译:回顾性评估了对基于Bendamustine的化疗的非霍奇金淋巴瘤患者回顾性评估了格兰司琼和帕康冬菌诱导的化疗诱导的恶心和呕吐(CINV)。共有61名患者有资格参加本研究。在开始弯曲的基础化疗,Granisetron或Palonosetron静脉内施用或没有共用和/或地塞米松。在整个控制期间(化疗开始后的6天),急性(最多2天)和延迟(3至6天)阶段的完全控制(CC)的比例。 CC被定义为只有0级0– 1恶心,没有呕吐,也没有使用止血药物。单独给予Granisetron或Palonosetron,分别给9例和19名患者施用。 48和5名患者分别与Granisetron和PalonoSetron合并了4.4患者。急性Cinv完全控制在所有患者中。 Granisetron单疗法和Palonosetron组合疗法都可以提供对延迟Cinv的良好控制,尽管延迟和整体阶段的延迟和整体阶段在助性和组合治疗中没有显着差异。 Granisetron和Palonosetron治疗组之间的不良药物事件的频率没有显着差异。本研究表明,基于格拉司琼治疗的止吐功效和安全性与基于帕洛尼蛋白静脉的疗法的抗抑制效能和安全性。随着治疗成本和治疗成本一起服用,格兰司琼单疗法将足以防止患有非霍奇金淋巴瘤的患者的CINV,接受基于Bendamustine的化学疗法。

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