RNA extended interventional nucleic acid longitudinal study: Clinical performance of Aptima messenger RNA HPV testing in cervical cancer screening with a 9-year follow-up

被引:1
|
作者
Granados, Rosario [1 ,2 ]
Duarte, Joanny A. [1 ,2 ]
Lujan, David R. [1 ,2 ]
Gutierrez-Pecharroman, Ana M. [1 ,2 ]
Solis, Isabel [3 ]
Molpeceres, Lourdes [3 ]
Bajo, Paloma [1 ]
Palencia, Elsa [3 ]
Martin, Nuria [3 ]
机构
[1] Hosp Univ Getafe, Dept Pathol, Carretera Toledo Km 12 5, Madrid 28905, Spain
[2] Univ Europea Madrid, Madrid, Spain
[3] Hosp Univ Getafe, Dept Gynecol, Madrid, Spain
关键词
cervical cancer; clinical performance; longitudinal study; mRNA-based HPV testing; predictive values; REINA; HUMAN-PAPILLOMAVIRUS DETECTION; LIQUID-BASED CYTOLOGY; BASE-LINE; DNA; GUIDELINES;
D O I
10.1002/cncy.22895
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThere is a need for additional longitudinal studies with the Aptima messenger RNA human papillomavirus test (AHPV) to support the safety of extended screening intervals. RNA-based extended interventional nucleic acid (REINA) provides relevant information on the clinical performance of AHPV.MethodsThis is a longitudinal prospective analysis of 1538 participants after AHPV and liquid-based cytology (LBC) co-test complemented with REINA interventional protocol with a second co-test 4 years after negative screening on 2000 women. Diagnostic accuracy and cumulative risks for CIN2+ up to 9 years were calculated for all test combinations.ResultsSensitivity and specificity for CIN2+ were 96.9% and 88.0% for AHPV and 72.3% and 92.0% for LBC. Negative predictive value (NPV) and positive predictive value (PPV) of AHPV were 99.9% and 23.6%. The 5- and 9-year risks of AHPV-negative women were 0.4% and 1.0% (CIN2+) and 0.3% and 0.7% (CIN3+), a 73% and 64% lower risk than with negative LBC (p <= .002). REINA participants with an AHPV-positive result at second co-test after a negative AHPV in first round had a significantly lower 5-year risk of CIN2+ (11.1%) than AHPV-positive women with unknown HPV history (29.5%).ConclusionsCurrently, this constitutes the longest European longitudinal study with AHPV testing in screening population. It reveals 99.9% NPV and a significant protective effect of a previous negative test 5 years after a new HPV infection. These findings support the safety of Aptima for screening intervals beyond 5 years. The risk of disease is lower 9 years after a negative AHPV test than 3 years after a negative LBC. High specificity and PPV of Aptima may benefit controlling overtreatment and colposcopy referrals. This is the first European study to show a safe screening interval of 9 years with messenger RNA (mRNA) human papillomavirus (HPV) Aptima testing with a 99.9% negative predictive value. REINA study demonstrated the protective role of a previous negative Aptima mRNA HPV test with a low 5-year cumulative risk of CIN2+ following a new HPV infection.
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收藏
页码:757 / 767
页数:11
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