The role of bevacizumab as an adjuvant to surgery in recurrent laryngeal papillomatosis: a systematic review of recurrence event outcomes.

IF 2.2
Christian Eliud Galindo Salazar, Victor Roman Sanchez Balderas, Juan Manuel Shiguetomi Medina, María Fernandez Olvera, Juan José Reyes Fortanelli, Gerardo Josue Rangel Ramirez
{"title":"The role of bevacizumab as an adjuvant to surgery in recurrent laryngeal papillomatosis: a systematic review of recurrence event outcomes.","authors":"Christian Eliud Galindo Salazar, Victor Roman Sanchez Balderas, Juan Manuel Shiguetomi Medina, María Fernandez Olvera, Juan José Reyes Fortanelli, Gerardo Josue Rangel Ramirez","doi":"10.1007/s00405-025-09616-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Recurrent laryngeal papillomatosis (RPL) is a disease characterized by the formation of papillomas in the larynx, which can compromise the airway, representing a life-threatening risk. Despite surgical management, the disease presents a high recurrence rate, which motivates the search for adjuvant therapies such as Bevacizumab. This study evaluates the effectiveness of Bevacizumab in reducing recurrence rates and prolonging intervals between surgeries.</p><p><strong>Methods: </strong>A systematic review was performed in PubMed, BVS and Cochrane database, including studies published between 2014 and 2024. Randomized clinical trials and observational studies evaluating Bevacizumab in pediatric and adult patients with PLR were included. The quality of the evidence was assessed with GRADE. Four systematic reviews were included as references for discussion; however, they were excluded because they were not primary studies.</p><p><strong>Results: </strong>Ten studies were included with a total of 173 patients, 69 of whom received Bevacizumab. The age range of treated patients was 0 months to 86 years. Bevacizumab doses ranged from 5-15 mg/kg based on weight, 25mg/ml based on concentration and a single event 400 mg single dose. Before treatment, the recurrence rate ranged from 1-26 surgeries/year and the interval between surgeries ranged from 1 week to 4.34 +- 1.446 months. After treatment, recurrence decreased to 0 to 4 surgeries/year and the intervals extended from 3 months to 14.81 +-12.421 months. The most common side effects, especially with systemic administration, included respiratory complications (glottic stenosis, dysphonia, dyspnea, stridor, aphonia), systemic disturbances (hypertension, mild proteinuria, headache, dysgeusia) and hematological effects (thrombocytopenia). One case of malignant transformation of the lesion was also reported. \"follow-up time ranged from 3 months to 5 years.</p><p><strong>Conclusions: </strong>Bevacizumab is a promising adjuvant therapy for the management of PLR, with significant benefits in reducing recurrence rates and surgical intervals. However, the quality of the available evidence is medium to low, and randomized controlled trials are required to validate its safety and efficacy. Its use should be considered with caution, especially in systemic administration.</p>","PeriodicalId":520614,"journal":{"name":"European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s00405-025-09616-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Recurrent laryngeal papillomatosis (RPL) is a disease characterized by the formation of papillomas in the larynx, which can compromise the airway, representing a life-threatening risk. Despite surgical management, the disease presents a high recurrence rate, which motivates the search for adjuvant therapies such as Bevacizumab. This study evaluates the effectiveness of Bevacizumab in reducing recurrence rates and prolonging intervals between surgeries.

Methods: A systematic review was performed in PubMed, BVS and Cochrane database, including studies published between 2014 and 2024. Randomized clinical trials and observational studies evaluating Bevacizumab in pediatric and adult patients with PLR were included. The quality of the evidence was assessed with GRADE. Four systematic reviews were included as references for discussion; however, they were excluded because they were not primary studies.

Results: Ten studies were included with a total of 173 patients, 69 of whom received Bevacizumab. The age range of treated patients was 0 months to 86 years. Bevacizumab doses ranged from 5-15 mg/kg based on weight, 25mg/ml based on concentration and a single event 400 mg single dose. Before treatment, the recurrence rate ranged from 1-26 surgeries/year and the interval between surgeries ranged from 1 week to 4.34 +- 1.446 months. After treatment, recurrence decreased to 0 to 4 surgeries/year and the intervals extended from 3 months to 14.81 +-12.421 months. The most common side effects, especially with systemic administration, included respiratory complications (glottic stenosis, dysphonia, dyspnea, stridor, aphonia), systemic disturbances (hypertension, mild proteinuria, headache, dysgeusia) and hematological effects (thrombocytopenia). One case of malignant transformation of the lesion was also reported. "follow-up time ranged from 3 months to 5 years.

Conclusions: Bevacizumab is a promising adjuvant therapy for the management of PLR, with significant benefits in reducing recurrence rates and surgical intervals. However, the quality of the available evidence is medium to low, and randomized controlled trials are required to validate its safety and efficacy. Its use should be considered with caution, especially in systemic administration.

贝伐单抗作为复发性喉乳头状瘤病手术辅助的作用:复发事件结果的系统回顾。
背景:复发性喉乳头状瘤病(RPL)是一种以喉乳头状瘤形成为特征的疾病,可危及气道,具有危及生命的危险。尽管手术治疗,疾病呈现高复发率,这促使寻找辅助治疗,如贝伐单抗。本研究评估贝伐单抗在降低复发率和延长手术间隔方面的有效性。方法:系统回顾PubMed、BVS和Cochrane数据库,包括2014 - 2024年间发表的研究。随机临床试验和观察性研究评估贝伐单抗在儿童和成人PLR患者中的应用。用GRADE评价证据的质量。纳入四篇系统综述作为讨论参考;然而,它们被排除在外,因为它们不是初步研究。结果:纳入10项研究,共173例患者,其中69例接受贝伐单抗治疗。治疗患者年龄范围为0个月至86岁。贝伐单抗的剂量范围为5- 15mg /kg(基于体重),25mg/ml(基于浓度),单次剂量为400mg。治疗前复发率为1 ~ 26例/年,手术间隔为1周~ 4.34 + ~ 1.446个月。治疗后复发率降至0 ~ 4例/年,间隔时间由3个月延长至14.81 +-12.421个月。最常见的副作用,尤其是全身给药,包括呼吸系统并发症(声门狭窄、发音困难、呼吸困难、喘鸣、发音困难)、全身障碍(高血压、轻度蛋白尿、头痛、发音困难)和血液学影响(血小板减少)。本文还报道了1例病变的恶性转化。随访时间从3个月到5年不等。结论:贝伐单抗是一种很有前景的PLR辅助治疗,在减少复发率和手术间隔方面有显著的益处。然而,现有证据的质量为中低,需要随机对照试验来验证其安全性和有效性。它的使用应谨慎考虑,特别是在系统管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信