Rapid infusion rituximab is well tolerated in patients with primary CNS lymphoma.

Q1 Medicine
CNS Oncology Pub Date : 2018-07-01 Epub Date: 2018-09-17 DOI:10.2217/cns-2018-0001
Lisa Modelevsky, Richard Tizon, Samantha N Reiss, Marcel Smith, Rachel Garonce, Thomas Kaley
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引用次数: 4

Abstract

Aim: To establish the safety and feasibility of rapidly infusing rituximab over 90 min in patients with primary CNS lymphoma (PCNSL).

Patients & methods: We retrospectively reviewed all patients with PCNSL who received rapid rituximab infusions (RRI) from January 2016 to January 2017. Primary end point was incidence of infusion reactions.

Results & conclusion: 11 patients received a total of 44 RRIs. Rituximab was dosed at 500 or 750 mg/m2. Premedication included acetaminophen and diphenhydramine. No infusion reactions occurred during any RRI. Two infusions were administered with steroids for neurologic symptoms at baseline (4.5%). Rapid administration of rituximab was safe and feasible for patients with PCNSL and at the higher doses received.

快速输注利妥昔单抗在原发性中枢神经系统淋巴瘤患者中耐受性良好。
目的:探讨利妥昔单抗在原发性中枢神经系统淋巴瘤(PCNSL)患者中快速输注90 min的安全性和可行性。患者和方法:我们回顾性分析了2016年1月至2017年1月接受快速利妥昔单抗输注(RRI)的所有PCNSL患者。主要终点为输液反应发生率。结果与结论:11例患者共接受44个RRIs。利妥昔单抗剂量为500或750 mg/m2。前用药包括对乙酰氨基酚和苯海拉明。在任何RRI期间均未发生输注反应。两次输注类固醇治疗神经系统症状(4.5%)。快速给药利妥昔单抗对PCNSL患者是安全可行的,且剂量较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
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