• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

B 细胞非霍奇金淋巴瘤患者利妥昔单抗输注相关反应的特征和预测因素。

Characteristics and predictors of infusion-related reactions to rituximab in patients with B-cell non-Hodgkin lymphoma.

机构信息

Department of Pharmacy, King Hussein Cancer Center, Amman, Jordan.

Department of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.

出版信息

J Chemother. 2024 Jul;36(4):291-298. doi: 10.1080/1120009X.2023.2270833. Epub 2023 Oct 20.

DOI:10.1080/1120009X.2023.2270833
PMID:37860948
Abstract

This retrospective study aimed to assess the characteristics and predictors of infusion-related reactions (IRRs) to rituximab in patients with B-cell non-Hodgkin lymphoma (B-NHL). The medical records of adult patients with B-NHL who received their first cycle of rituximab from August 2020 to August 2022 were reviewed. IRRs were defined as any signs experienced by patients during rituximab infusion and graded according to the Common Terminology Criteria for Adverse Events. During the study period, 334 patients were included; among them, 100 patients (30%) developed IRRs (mean age 54.7 (SD 13.2) years). Of the reported IRRs, 90% were grade II reactions, and 10% were grade III reactions. The multivariate analysis identified indolent lymphoma [OR 1.90,  = 0.025], no hydrocortisone as premedication [OR 3.03,  = 0.029], thrombocytopenia [OR 2.55,  = 0.009], and absolute lymphocyte count ≥ 2000 lymphocytes/microL [OR 1.74,  = 0.045] as independent predictors for IRRs.

摘要

这项回顾性研究旨在评估利妥昔单抗输注相关反应(IRR)在 B 细胞非霍奇金淋巴瘤(B-NHL)患者中的特征和预测因素。回顾性分析了 2020 年 8 月至 2022 年 8 月期间接受首次利妥昔单抗治疗的 B-NHL 成年患者的病历。IRR 定义为患者在利妥昔单抗输注期间经历的任何体征,并根据不良事件常用术语标准进行分级。在研究期间,共纳入 334 例患者,其中 100 例(30%)发生 IRR(平均年龄 54.7[SD 13.2]岁)。报告的 IRR 中,90%为 2 级反应,10%为 3 级反应。多因素分析确定惰性淋巴瘤[OR 1.90,=0.025]、无氢化可的松作为预处理[OR 3.03,=0.029]、血小板减少症[OR 2.55,=0.009]和绝对淋巴细胞计数≥2000 个/μL[OR 1.74,=0.045]为 IRR 的独立预测因素。

相似文献

1
Characteristics and predictors of infusion-related reactions to rituximab in patients with B-cell non-Hodgkin lymphoma.B 细胞非霍奇金淋巴瘤患者利妥昔单抗输注相关反应的特征和预测因素。
J Chemother. 2024 Jul;36(4):291-298. doi: 10.1080/1120009X.2023.2270833. Epub 2023 Oct 20.
2
A clinical prediction model for infusion-related reactions to rituximab in patients with B cell lymphomas.B细胞淋巴瘤患者中利妥昔单抗输注相关反应的临床预测模型。
Int J Clin Pharm. 2017 Apr;39(2):380-385. doi: 10.1007/s11096-017-0429-3. Epub 2017 Jan 31.
3
Rituximab: a review of its use in non-Hodgkin's lymphoma and chronic lymphocytic leukaemia.利妥昔单抗:用于非霍奇金淋巴瘤和慢性淋巴细胞白血病的综述
Drugs. 2003;63(8):803-43. doi: 10.2165/00003495-200363080-00005.
4
A Phase II Trial of Rituximab Combined With Pegfilgrastim in Patients With Indolent B-cell Non-Hodgkin Lymphoma.利妥昔单抗联合聚乙二醇化重组人粒细胞刺激因子治疗惰性B细胞非霍奇金淋巴瘤的II期试验
Clin Lymphoma Myeloma Leuk. 2018 Jan;18(1):e51-e60. doi: 10.1016/j.clml.2017.09.003. Epub 2017 Nov 6.
5
Bone marrow involvement is predictive of infusion-related reaction during rituximab administration in patients with B cell lymphoma.骨髓受累可预测 B 细胞淋巴瘤患者接受利妥昔单抗治疗时的输注相关反应。
Support Care Cancer. 2013 Apr;21(4):1145-52. doi: 10.1007/s00520-012-1639-9. Epub 2012 Oct 31.
6
Copanlisib plus rituximab versus placebo plus rituximab in patients with relapsed indolent non-Hodgkin lymphoma (CHRONOS-3): a double-blind, randomised, placebo-controlled, phase 3 trial.Copanlisib 联合利妥昔单抗与安慰剂联合利妥昔单抗治疗复发惰性非霍奇金淋巴瘤(CHRONOS-3):一项双盲、随机、安慰剂对照、3 期临床试验。
Lancet Oncol. 2021 May;22(5):678-689. doi: 10.1016/S1470-2045(21)00145-5. Epub 2021 Apr 10.
7
Adverse drug reactions after intravenous rituximab infusion are more common in hematologic malignancies than in autoimmune disorders and can be predicted by the combination of few clinical and laboratory parameters: results from a retrospective, multicenter study of 374 patients.静脉注射利妥昔单抗后的药物不良反应在血液系统恶性肿瘤中比在自身免疫性疾病中更常见,并且可以通过少数临床和实验室参数的组合来预测:一项对374例患者的回顾性多中心研究结果。
Leuk Lymphoma. 2017 Nov;58(11):2633-2641. doi: 10.1080/10428194.2017.1306648. Epub 2017 Apr 3.
8
Effectiveness of fractionated rituximab in preventing tumor lysis syndrome in aggressive B-cell lymphoma: Insights from real-life clinical practice.分阶段利妥昔单抗预防侵袭性 B 细胞淋巴瘤肿瘤溶解综合征的疗效:来自真实临床实践的见解。
Cancer Rep (Hoboken). 2024 Oct;7(10):e1983. doi: 10.1002/cnr2.1983.
9
Randomized Phase II Trial Comparing Obinutuzumab (GA101) With Rituximab in Patients With Relapsed CD20+ Indolent B-Cell Non-Hodgkin Lymphoma: Final Analysis of the GAUSS Study.比较奥滨尤妥珠单抗(GA101)与利妥昔单抗治疗复发的CD20+惰性B细胞非霍奇金淋巴瘤患者的随机II期试验:GAUSS研究的最终分析
J Clin Oncol. 2015 Oct 20;33(30):3467-74. doi: 10.1200/JCO.2014.59.2139. Epub 2015 Aug 17.
10
A novel rituximab administration protocol to minimize infusion-related adverse reactions in patients with B-cell lymphoma.一种新型利妥昔单抗给药方案,以尽量减少B细胞淋巴瘤患者的输液相关不良反应。
Int J Clin Pharm. 2022 Apr;44(2):366-373. doi: 10.1007/s11096-021-01348-6. Epub 2021 Dec 11.

引用本文的文献

1
Successful Switch to Obinutuzumab in a Rituximab-Intolerant Child with Difficult-to-Treat Idiopathic Nephrotic Syndrome.一名对利妥昔单抗不耐受的难治性特发性肾病综合征儿童成功转换为使用奥妥珠单抗治疗
J Clin Med. 2025 Jan 3;14(1):239. doi: 10.3390/jcm14010239.