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治疗性疫苗对癌前宫颈病变的有效性和安全性:一项系统评价和荟萃分析。

Effectiveness and Safety of Therapeutic Vaccines for Precancerous Cervical Lesions: A Systematic Review and Meta-Analysis.

作者信息

Cai Shan, Tan Xiaoyu, Miao Ke, Li Dantong, Cheng Si, Li Pei, Zeng Xueyang, Sun Feng

机构信息

Institute of Child and Adolescent Health, School of Public Health, Peking University, Beijing, China.

Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.

出版信息

Front Oncol. 2022 Jun 6;12:918331. doi: 10.3389/fonc.2022.918331. eCollection 2022.

Abstract

OBJECTIVE

This study systematically evaluated the effectiveness and safety of therapeutic vaccines for precancerous cervical lesions, providing evidence for future research.

METHODS

We systematically searched the literature in 10 databases from inception to February 18, 2021. Studies on the effectiveness and safety of therapeutic vaccines for precancerous cervical lesions were included. Then, we calculated the overall incidence rates of four outcomes, for which we used the risk ratio (RR) and 95% confidence interval (95% CI) to describe the effects of high-grade squamous intraepithelial lesions (HSILs) on recurrence.

RESULTS

A total of 39 studies were included, all reported in English, published from 1989 to 2021 in 16 countries. The studies covered 22,865 women aged 15-65 years, with a total of 5,794 vaccinated, and 21 vaccines were divided into six types. Meta-analysis showed that the overall incidence rate of HSIL regression in vaccine therapies was 62.48% [95% CI (42.80, 80.41)], with the highest rate being 72.32% for viral vector vaccines [95% CI (29.33, 99.51)]. Similarly, the overall incidence rates of HPV and HPV16/18 clearance by vaccines were 48.59% [95% CI (32.68, 64.64)] and 47.37% [95% CI (38.00, 56.81)], respectively, with the highest rates being 68.18% [95% CI (45.13, 86.14)] for bacterial vector vaccines and 55.14% [95% CI (42.31, 67.66)] for DNA-based vaccines. In addition, a comprehensive analysis indicated that virus-like particle vaccines after conization reduced the risk of HSIL recurrence with statistical significance compared to conization alone [RR = 0.46; 95% CI (0.29, 0.74)]. Regarding safety, only four studies reported a few severe adverse events, indicating that vaccines for precancerous cervical lesions are generally safe.

CONCLUSION

Virus-like particle vaccines as an adjuvant immunotherapy for conization can significantly reduce the risk of HSIL recurrence. Most therapeutic vaccines have direct therapeutic effects on precancerous lesions, and the effectiveness in HSIL regression, clearance of HPV, and clearance of HPV16/18 is great with good safety. That is, therapeutic vaccines have good development potential and are worthy of further research.

SYSTEMATIC REVIEW REGISTRATION

PROSPERO https://www.crd.york.ac.uk/PROSPERO/, CRD42021275452.

摘要

目的

本研究系统评价了治疗性疫苗对宫颈病变前病变的有效性和安全性,为未来研究提供依据。

方法

我们系统检索了从数据库建立至2021年2月18日的10个数据库中的文献。纳入了关于治疗性疫苗对宫颈病变前病变有效性和安全性的研究。然后,我们计算了四个结局的总体发生率,为此我们使用风险比(RR)和95%置信区间(95%CI)来描述高级别鳞状上皮内病变(HSIL)对复发的影响。

结果

共纳入39项研究,均以英文发表,于1989年至2021年在16个国家发表。这些研究涵盖了22865名年龄在15至65岁之间的女性,其中共有5794人接种了疫苗,21种疫苗分为六种类型。荟萃分析表明,疫苗治疗中HSIL消退的总体发生率为62.48% [95%CI(42.80,80.41)],病毒载体疫苗的发生率最高,为72.32% [95%CI(29.33,99.51)]。同样,疫苗清除HPV和HPV16/18的总体发生率分别为48.59% [95%CI(32.68,64.64)]和47.37% [95%CI(38.00,56.81)],细菌载体疫苗的发生率最高,为68.18% [95%CI(45.13,86.14)],基于DNA的疫苗为55.14% [95%CI(42.31,67.66)]。此外,综合分析表明,与单纯锥切术相比,锥切术后的病毒样颗粒疫苗降低HSIL复发风险具有统计学意义[RR = 0.46;95%CI(0.29,0.74)]。关于安全性,只有四项研究报告了一些严重不良事件,表明宫颈病变前病变疫苗总体上是安全的。

结论

病毒样颗粒疫苗作为锥切术的辅助免疫疗法可显著降低HSIL复发风险。大多数治疗性疫苗对癌前病变有直接治疗作用,在HSIL消退、HPV清除和HPV16/18清除方面有效性高且安全性良好。也就是说,治疗性疫苗具有良好的发展潜力,值得进一步研究。

系统评价注册

PROSPERO https://www.crd.york.ac.uk/PROSPERO/,CRD42021275452

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78c5/9207463/7ba725471fab/fonc-12-918331-g001.jpg

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