Risk of residual/recurrent cervical diseases in HPV-positive women post-conization depends on HPV integration status.

IF 2.8 2区 医学 Q3 IMMUNOLOGY Infectious Agents and Cancer Pub Date : 2025-01-28 DOI:10.1186/s13027-025-00637-3
Wenyu Lin, Yuxuan Huang, Yan Zhang, Lixiang Huang, Hongning Cai, Guanxiang Huang, Ye Li, Qiaoyu Zhang, Huifeng Xue, Binhua Dong, Pengming Sun
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Abstract

Background: It is crucial to identify post-operative patients with HPV infection who are at high risk for residual/recurrent disease. This study aimed to evaluate the association between HPV integration and clinical outcomes in HPV-positive women after cervical conization, as well as to identify HPV integration breakpoints.

Methods: This retrospective study analyzed data of 791 women who underwent cervical conization for cervical intraepithelial neoplasia grades 2-3 (CIN2-3) between September 2019 and September 2023, sourced from the Fujian and Hubei cervical lesion screening cohorts. Among these, 73 women with HPV infection post-conization underwent HPV integration test within 3 months after a positive HPV test. HPV integration test was performed using the high-throughput viral integration detection (HIVID), a sensitive method for genome-wide survey of HPV integration breakpoints.

Results: Among the 73 participants with HPV infection post-conization, 10 cases (13.7%) were positive for HPV integration. The logistic regression analysis showed a higher residual/recurrent lesions risk in patients with HPV integration (OR = 3.917, p = 0.048). According to the Kaplan-Meier analysis, age ≥ 45 years (p = 0.016) and HPV integration (p = 0.035) were associated with a higher risk of residual/recurrent CIN at the 1-year follow-up. HPV 52 accounted for the majority of HPV integration genotype (3/10, 30.0%). Surprisingly, HPV 16 had the highest number of HPV average integration sequencing reads (n = 129), followed by HPV 31, 58, 52, 59, 35, and 39. The study also identified 13 HPV breakpoints, including TP63, TLR4, USP10, etc. CONCLUSIONS: HPV integration was identified as an independent risk factor for residual/recurrent CIN in HPV-positive women post-conization. Women with positive HPV integration should pay attention to careful post-treatment follow-up.

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HPV阳性妇女宫颈病变残留/复发的风险取决于HPV整合状态。
背景:确定HPV感染术后残留/复发风险高的患者至关重要。本研究旨在评估宫颈锥化后HPV阳性妇女HPV整合与临床结果之间的关系,并确定HPV整合断点。方法:本回顾性研究分析了2019年9月至2023年9月期间因宫颈上皮内瘤变2-3级(CIN2-3)接受宫颈锥切术的791名妇女的数据,这些数据来自福建和湖北宫颈病变筛查队列。其中,73名HPV感染后锥突的妇女在HPV检测阳性后3个月内接受了HPV整合检测。采用高通量病毒整合检测(HIVID)进行HPV整合检测,这是一种对HPV整合断点进行全基因组调查的灵敏方法。结果:73例术后HPV感染患者中,HPV整合阳性10例(13.7%)。logistic回归分析显示HPV整合患者的残留/复发病变风险较高(OR = 3.917, p = 0.048)。根据Kaplan-Meier分析,年龄≥45岁(p = 0.016)和HPV整合(p = 0.035)与1年随访时残留/复发CIN的高风险相关。HPV整合基因型以HPV 52型为主(3/10,30.0%)。令人惊讶的是,HPV 16具有最多的HPV平均整合测序读数(n = 129),其次是HPV 31、58、52、59、35和39。该研究还确定了13个HPV断点,包括TP63、TLR4、USP10等。结论:HPV整合被确定为HPV阳性妇女锥化后残留/复发CIN的独立危险因素。HPV整合阳性的妇女应注意仔细的治疗后随访。
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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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