{"title":"Rapid infusion rituximab for maintenance therapy: is it feasible?","authors":"Jolly Patel, Melissa Ho, Viet Ho, Celeste Bello, Benjamin Djulbegovic, Lubomir Sokol, Gene Wetzstein","doi":"10.1155/2013/629283","DOIUrl":null,"url":null,"abstract":"<p><p>Rituximab is an anti-CD-20 monoclonal antibody used in the management of lymphoproliferative disorders. The use of maintenance rituximab has improved progression free survival and overall survival in follicular lymphomas. Although rapid rituximab infusions have been studied extensively, there is little data on the use of rapid infusions during maintenance therapy for low grade lymphomas. The primary objective of this retrospective analysis was to evaluate the incidence of Grade 3 and 4 toxicities with maintenance rapid infusion rituximab according to the Common Terminology Criteria for Adverse Events version 4 (CTC v. 4). Secondary objectives included evaluating all grade infusion related adverse events and correlation of adverse events with varying schedules of rituximab maintenance therapy. All patients who received rapid infusion rituximab as maintenance therapy for low grade lymphoma between December 2007 and November 2011 were included. Rapid rituximab infusions were administered over 90 minutes. Demographic, laboratory and clinical data were collected. A total of 109 patients received 647 rapid rituximab infusions. Three patients experienced an adverse reaction which resulted in one grade 1 infusion reaction and three grade 3 infusion reactions. No patients required hospitalization. All 3 patients received pharmacological and/or supportive care to relieve symptoms associated with the reaction. </p>","PeriodicalId":18102,"journal":{"name":"Leukemia Research and Treatment","volume":"2013 ","pages":"629283"},"PeriodicalIF":0.0000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/629283","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Leukemia Research and Treatment","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2013/629283","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/10/31 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
Abstract
Rituximab is an anti-CD-20 monoclonal antibody used in the management of lymphoproliferative disorders. The use of maintenance rituximab has improved progression free survival and overall survival in follicular lymphomas. Although rapid rituximab infusions have been studied extensively, there is little data on the use of rapid infusions during maintenance therapy for low grade lymphomas. The primary objective of this retrospective analysis was to evaluate the incidence of Grade 3 and 4 toxicities with maintenance rapid infusion rituximab according to the Common Terminology Criteria for Adverse Events version 4 (CTC v. 4). Secondary objectives included evaluating all grade infusion related adverse events and correlation of adverse events with varying schedules of rituximab maintenance therapy. All patients who received rapid infusion rituximab as maintenance therapy for low grade lymphoma between December 2007 and November 2011 were included. Rapid rituximab infusions were administered over 90 minutes. Demographic, laboratory and clinical data were collected. A total of 109 patients received 647 rapid rituximab infusions. Three patients experienced an adverse reaction which resulted in one grade 1 infusion reaction and three grade 3 infusion reactions. No patients required hospitalization. All 3 patients received pharmacological and/or supportive care to relieve symptoms associated with the reaction.
利妥昔单抗是一种抗cd -20单克隆抗体,用于淋巴细胞增生性疾病的治疗。使用维持性利妥昔单抗可改善滤泡性淋巴瘤的无进展生存期和总生存期。尽管快速输注利妥昔单抗已被广泛研究,但在低级别淋巴瘤的维持治疗中使用快速输注的数据很少。本回顾性分析的主要目的是根据不良事件通用术语标准第4版(CTC v. 4)评估维持快速输注利妥昔单抗3级和4级毒性的发生率。次要目标包括评估所有级别输注相关的不良事件以及不良事件与不同的利妥昔单抗维持治疗方案的相关性。所有在2007年12月至2011年11月期间接受快速输注利妥昔单抗作为维持治疗的低级别淋巴瘤患者被纳入研究。快速输注利妥昔单抗超过90分钟。收集了人口统计学、实验室和临床数据。109例患者接受647次利妥昔单抗快速输注。3例患者出现不良反应,1例为1级输液反应,3例为3级输液反应。没有病人需要住院治疗。所有3例患者均接受药理学和/或支持性治疗,以缓解与反应相关的症状。