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替伊莫单抗治疗方案的治疗安排

Logistics of therapy with the ibritumomab tiuxetan regimen.

作者信息

Meredith Ruby F

机构信息

Department of Radiation Oncology, University of Alabama Medical Center, Birmingham, AL, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2006;66(2 Suppl):S35-8. doi: 10.1016/j.ijrobp.2006.06.009.

Abstract

Radioimmunotherapy is an important new modality for treating patients with B-cell non-Hodgkin's lymphoma (NHL). Clinical trials have shown the safety and efficacy of agents that deliver radiation directly to malignant cells by attaching the (131)I or (90)Y radionuclide to monoclonal antibodies against CD20. In clinical trials, (90)Y ibritumomab tiuxetan has produced rates of response as high as 83% in patients with relapsed or refractory CD20+ NHL. The ibritumomab tiuxetan regimen is conveniently given in an outpatient setting over the course of 7-9 days. This article describes the logistics for initiating treatment, coordinating a multidisciplinary team, identifying eligible patients, and delivering the imaging and therapeutic doses of ibritumomab tiuxetan. The standard radiation safety procedures to protect family members and healthcare professionals involved in the care of patients treated with (90)Y ibritumomab tiuxetan are also reviewed. Treatment with the ibritumomab tiuxetan regimen involves only standard precautions needed to minimize radiation exposure to other persons.

摘要

放射免疫疗法是治疗B细胞非霍奇金淋巴瘤(NHL)患者的一种重要新方法。临床试验已证明,通过将(131)I或(90)Y放射性核素附着于抗CD20单克隆抗体上,可将辐射直接传递至恶性细胞的药物的安全性和有效性。在临床试验中,(90)Y替伊莫单抗在复发或难治性CD20 + NHL患者中产生的缓解率高达83%。替伊莫单抗方案在门诊环境中7 - 9天内即可方便地给药。本文介绍了开始治疗的流程、协调多学科团队、确定 eligible 患者以及给予替伊莫单抗的成像和治疗剂量的相关事宜。还回顾了保护参与(90)Y替伊莫单抗治疗患者护理的家庭成员和医护人员的标准辐射安全程序。替伊莫单抗方案的治疗仅涉及将辐射暴露降至最低所需的标准预防措施。 (注:eligible未翻译,因文档中未给出该词的释义。)

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