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限制使用帕利珠单抗不会导致小儿造血干细胞移植患者的发病率和死亡率增加。

Restrictive Palivizumab Use Does Not Lead to Increased Morbidity and Mortality in Pediatric Hematopoietic Stem Cell Transplantation Patients.

作者信息

Teusink-Cross Ashley, Davies Stella M, Danziger-Isakov Lara, El-Bietar Javier, Grimley Michael S

机构信息

Department of Pharmacy, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Bone Marrow Transplantation and Immune Deficiency, Cincinnati, Ohio.

出版信息

Biol Blood Marrow Transplant. 2016 Oct;22(10):1904-1906. doi: 10.1016/j.bbmt.2016.07.005. Epub 2016 Jul 12.

Abstract

Respiratory syncytial virus (RSV) is a common cause of infection in immunocompromised patients and can lead to significant morbidity and mortality in pediatric hematopoietic stem cell transplantation (HSCT) patients and patients with a primary immune deficiency (PID). Palivizumab is a humanized monoclonal antibody that targets the F glycoprotein on the surface of the RSV virus, preventing RSV replication. Palivizumab was initially licensed for the prevention of RSV infections in children at high risk of severe disease. Since licensure, the American Academy of Pediatrics (AAP) has issued guidelines to help ensure appropriate use of palivizumab in pediatric patients. In the 2014 edition of the guidelines, the AAP recognizes that severe and fatal disease secondary to RSV can be seen in patients receiving chemotherapy or patients who are immunocompromised because of other conditions. However, they recognize that no large clinical trials exist to support the use of palivizumab, and efficacy and safety data in this population are limited. Despite this, the AAP recommends considering prophylaxis for children younger than 24 months who are profoundly immunocompromised during the RSV season. Because of the high cost of palivizumab, the uncertainty of its efficacy as prophylaxis in hospitalized pediatric HSCT and PID patients, and secondary to recent data from our center that suggested immunocompromised patients diagnosed with RSV did not have worse outcomes, we implemented very restrictive criteria for the use of palivizumab in the 2015 to 2016 RSV season in our pediatric HSCT population. Despite these strict criteria, there was no change in the number of patients developing RSV during this season compared with previous seasons, and there was no change in RSV course in those patients developing RSV compared with previous seasons. Restricted use also resulted in a significant dose and cost savings. Based on our experience, we recommend only administering prophylaxis palivizumab to the youngest and most high-risk HSCT patients during the RSV season.

摘要

呼吸道合胞病毒(RSV)是免疫功能低下患者感染的常见原因,可导致儿科造血干细胞移植(HSCT)患者和原发性免疫缺陷(PID)患者出现严重的发病和死亡情况。帕利珠单抗是一种人源化单克隆抗体,可靶向RSV病毒表面的F糖蛋白,阻止RSV复制。帕利珠单抗最初被批准用于预防重症风险高的儿童RSV感染。自获批以来,美国儿科学会(AAP)已发布指南,以帮助确保帕利珠单抗在儿科患者中的合理使用。在2014年版指南中,AAP认识到接受化疗的患者或因其他情况免疫功能低下的患者可能会出现继发于RSV的严重和致命疾病。然而,他们认识到尚无大型临床试验支持使用帕利珠单抗,且该人群中的疗效和安全性数据有限。尽管如此,AAP仍建议考虑对在RSV季节严重免疫功能低下的24个月以下儿童进行预防。由于帕利珠单抗成本高昂,其作为住院儿科HSCT和PID患者预防用药的疗效存在不确定性,且继发于我们中心最近的数据表明,被诊断为RSV的免疫功能低下患者预后并不更差,因此我们在2015至2016年RSV季节对儿科HSCT人群实施了非常严格的帕利珠单抗使用标准。尽管有这些严格标准,但与前几个季节相比,本季节发生RSV的患者数量没有变化,且发生RSV的患者的RSV病程与前几个季节相比也没有变化。限制使用还带来了显著的剂量和成本节省。基于我们的经验,我们建议仅在RSV季节对最年幼和风险最高的HSCT患者给予帕利珠单抗预防用药。

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