Therapeutic human papilloma virus vaccination in patients at risk for cervical dysplasia.

IF 1.6 Q3 OBSTETRICS & GYNECOLOGY
Minerva obstetrics and gynecology Pub Date : 2024-04-01 Epub Date: 2022-10-04 DOI:10.23736/S2724-606X.22.05141-7
Ashley M Florence, Joshua Fogel, Makayla Mozey, Shachi Dave, Heidi O'Dell, Mary Fatehi
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引用次数: 0

Abstract

Background: Shared decision making between patients and their healthcare providers is recommended for use of the human papillomavirus (HPV) vaccine Gardasil 9 (9v-HPV) in women ages 27-45 years. We studied HPV vaccination as a treatment modality for patients undergoing colposcopy older than age 26 years who tested positive for high-risk subtypes of HPV (HR-HPV).

Methods: A retrospective study (N.=155) was performed for patients that were evaluated for cervical dysplasia who tested positive for HR-HPV and received the 9v-HPV vaccine prior to repeat cervical cancer screening with co-testing. Demographic information, risk factors for cervical dysplasia, and treatment outcomes were assessed for response to vaccination as treatment.

Results: Repeat co-testing was negative for HR-HPV in 76 patients (49%) and was positive in 79 patients (51%). A greater percentage of Hispanic patients cleared the virus and Black patients had a greater percentage of persistent HR-HPV on repeat co-testing (P=0.047). When comparing those who cleared the virus and those who had persistent HR-HPV, there were no differences observed for associated risk factors for dysplasia, HPV subtype, cytology or colposcopy results, vaccine dosing interval, or total number of vaccine doses received.

Conclusions: While the HPV vaccine is effective for prevention of infection by high-risk strains of HPV, it remains unclear whether 9v-HPV vaccine should be recommended as a treatment option in exposed patients beyond age 26. We recommend healthcare providers discuss usefulness of 9v-HPV vaccine with their unvaccinated patients 27 years and older at risk for cervical dysplasia.

为有宫颈发育不良风险的患者接种治疗性人类乳头瘤病毒疫苗。
背景:建议 27-45 岁的女性在使用人类乳头瘤病毒 (HPV) 疫苗加卫苗 9 (9v-HPV) 时由患者及其医疗保健提供者共同决策。我们对接受阴道镜检查的 26 岁以上、HPV(HR-HPV)高危亚型检测呈阳性的患者将 HPV 疫苗接种作为一种治疗方式进行了研究:我们对宫颈发育不良的患者进行了一项回顾性研究(n=155),这些患者的HR-HPV检测结果呈阳性,并在接受宫颈癌复查和联合检测之前接种了9v-HPV疫苗。对人口统计学信息、宫颈发育不良的风险因素和治疗结果进行了评估,以了解接种疫苗作为治疗的反应:结果:76 名患者(49%)的重复联合检测结果为 HR-HPV 阴性,79 名患者(51%)的重复联合检测结果为阳性。在重复联合检测中,西班牙裔患者清除病毒的比例更高,黑人患者持续感染 HR-HPV 的比例更高(P=0.047)。在比较清除病毒者和HRHPV持续存在者时,没有观察到发育不良的相关风险因素、HPV亚型、细胞学或阴道镜检查结果、疫苗接种间隔或接种疫苗的总剂数存在差异:虽然 HPV 疫苗能有效预防高危 HPV 株的感染,但对于 26 岁以上的暴露患者,是否应推荐将 9v-HPV 疫苗作为一种治疗选择,目前仍不清楚。我们建议医疗服务提供者与 27 岁及以上未接种疫苗的宫颈发育不良高危患者讨论 9v-HPV 疫苗是否有用。
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来源期刊
Minerva obstetrics and gynecology
Minerva obstetrics and gynecology OBSTETRICS & GYNECOLOGY-
CiteScore
2.90
自引率
11.10%
发文量
191
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