Systemic Bevacizumab (Avastin) for Juvenile-Onset Recurrent Respiratory Papillomatosis: A Systematic Review

被引:19
|
作者
Ryan, Marisa A. [1 ]
Leu, Grace R. [2 ]
Upchurch, Patrick A. [3 ,4 ]
Tunkel, David E. [1 ]
Walsh, Jonathan M. [1 ]
Boss, Emily F. [1 ]
机构
[1] Johns Hopkins Univ, Dept Otolaryngol Head & Neck Surg, Baltimore, MD USA
[2] Tufts Univ, Sch Med, Boston, MA 02111 USA
[3] Johns Hopkins Univ, Dept Anesthesiol & Crit Care Med, Baltimore, MD USA
[4] Boston Childrens Hosp, Dept Surg, Boston, MA USA
来源
LARYNGOSCOPE | 2021年 / 131卷 / 05期
关键词
Bevacizumab; Avastin; juvenile onset recurrent respiratory papillomatosis; recurrent respiratory papillomatosis; human papillomavirus; HEREDITARY HEMORRHAGIC TELANGIECTASIA; INTRAVENOUS BEVACIZUMAB; INVOLVEMENT; THERAPY;
D O I
10.1002/lary.29084
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives Juvenile onset recurrent respiratory papillomatosis (JORRP) can cause severe or disseminated disease. Surgical treatment may be inadequate. Systemic bevacizumab has shown initial success for severe JORRP. The objective of this systematic review was to assess usage, effectiveness, and safety of this treatment. Methods We searched PubMed, Embase, and Web of Science for studies of humans with JORRP treated with systemic bevacizumab. Two researchers independently reviewed the studies to determine inclusion and aggregate data on patient characteristics, dosing protocols, treatment response, adverse events, and level of evidence. Results Of 80 identified articles, 12 studies were included detailing 20 distinct cases. At a mean age of 12.8 years (range = 1-43 years) patients received initial dosing of 5 to 10 mg/kg of bevacizumab followed by ongoing doses at a mean 3-week intervals (range = 2-5 weeks). All patients had clinically significant disease reduction with reduced need for surgery. Six patients (30%) had complete response in at least one involved anatomic site. Eleven (55%) required no surgery after initiating treatment. There was recurrence in all four patients whose treatment was stopped, but had rapid improvement with treatment resumption. Six (30%) experienced mild or moderate adverse events. Conclusions Marked improvement in severe JORRP has been reported from systemic bevacizumab. Treatment protocols vary, and treatment discontinuation was not feasible in any reported patient. Based on currently available data, systemic bevacizumab can be considered for severe JORRP as it appears to be well tolerated and effective. A clinical trial could enhance the understanding of its safety and efficacy for this indication.Laryngoscope, 2020
引用
收藏
页码:1138 / 1146
页数:9
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