评估LSIL活检女性发生高级别鳞状上皮内病变(HSIL+)的风险:一项基于机器学习的研究

IF 3.1 2区 医学 Q3 IMMUNOLOGY Infectious Agents and Cancer Pub Date : 2024-12-05 DOI:10.1186/s13027-024-00625-z
Dongmei Li, Zhichao Wang, Yan Liu, Meiyuan Zhou, Bo Xia, Lin Zhang, Keming Chen, Yong Zeng
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引用次数: 0

摘要

目的:本研究旨在分析经阴道镜活检初步诊断为低级别鳞状上皮内病变(LSIL)患者高级别鳞状上皮内病变(HSIL+)漏诊的相关因素,并建立评估HSIL+漏诊风险的预测模型。方法:我们对505例经阴道镜活检诊断为LSIL后行环电切除手术(LEEP)的患者进行回顾性分析。采用Logistic回归来确定与HSIL+漏诊相关的人口学和病理学参数。此外,还采用了几种机器学习方法来构建和评估风险预测模型的性能。结果:HSIL+的总漏诊率为15.2%。确定的独立危险因素为HPV16/18感染(OR 2.071;95% ci 1.039-4.127;p = 0.039), TCT≥ASC-H (OR 4.147;95% ci 1.392-12.355;p = 0.011), TZ3 (OR 1.966;95% ci 1.003-3.853;p = 0.049)和阴道镜印模G2 (OR 3.627;95% ci 1.350-9.743;p = 0.011)。在测试的模型中,决策树算法的准确率为94.7%,灵敏度为80.0%,特异性为96.9%,验证集中的曲线下面积(AUC)为0.936,表现出较好的性能。结论:LSIL患者HSIL漏诊的关键独立危险因素包括HPV16/18感染、TCT≥ASC-H、TZ3、阴道镜印模G2。决策树模型为准确预测HSIL+的漏诊风险,促进早期干预和管理提供了一种具有成本效益、可靠性和临床价值的工具。
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Assessing the risk of high-grade squamous intraepithelial lesions (HSIL+) in women with LSIL biopsies: a machine learning-based study.

Objective: This study aims to analyze factors associated with the missed diagnosis of high-grade squamous intraepithelial lesions (HSIL+) in patients initially diagnosed with low-grade squamous intraepithelial lesions (LSIL) through colposcopic biopsy and to develop a predictive model for assessing the risk of missed HSIL+.

Methods: We conducted a retrospective analysis of 505 patients who underwent loop electrical excision procedure (LEEP) following an LSIL diagnosis by colposcopic biopsy. Logistic regression was used to identify demographic and pathological parameters associated with missed diagnoses of HSIL+. Additionally, several machine learning methods were employed to construct and assess the performance of the risk prediction models.

Results: The overall rate of missed diagnoses for HSIL+ was 15.2%. Independent risk factors identified were HPV16/18 infection (OR 2.071; 95% CI 1.039-4.127; p = 0.039), TCT ≥ ASC-H (OR 4.147; 95% CI 1.392-12.355; p = 0.011), TZ3 (OR 1.966; 95% CI 1.003-3.853; p = 0.049) and Colposcopic impression G2 (OR 3.627; 95% CI 1.350-9.743; p = 0.011). Among the models tested, the Decision Tree algorithm demonstrated superior performance with an accuracy of 94.7%, sensitivity of 80.0%, specificity of 96.9%, and an area under the curve (AUC) of 0.936 in the validation set.

Conclusion: Key independent risk factors for the missed diagnosis of HSIL  in patients with LSIL include HPV16/18 infection, TCT ≥ ASC-H, TZ3, and colposcopic impression G2. The Decision Tree model offers a cost-effective, reliable, and clinically valuable tool for accurately predicting the risk of missed diagnosis of HSIL+, facilitating early intervention and management.

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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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