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Comparison of the clinical and analytical performance of Alinity m HR HPV and cobas 4800 HPV assays in a population-based screening setting
ID
Oštrbenk Valenčak, Anja
(
Avtor
),
ID
Bertram, Alexander
(
Avtor
),
ID
Gröning, Arndt
(
Avtor
),
ID
Poljak, Mario
(
Avtor
)
PDF - Predstavitvena datoteka,
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(410,13 KB)
MD5: CB9387F10C8815051B44C79AFB12F311
URL - Izvorni URL, za dostop obiščite
https://www.sciencedirect.com/science/article/pii/S1386653221001189
Galerija slik
Izvleček
Background: The recently launched Abbott Alinity m HR HPV (Alinity) assay separately identifies high-risk human papillomavirus (hrHPV) genotypes HPV16, HPV18, and HPV45, and reports 11 other genotypes as two aggregates. Methods: Clinical and analytical performance of Alinity was compared with the cobas 4800 HPV assay on 4,334 women aged 20–64 years attending routine, population-based organized cervical cancer screening during 2009/ 2010. After 36 months, they were invited to participate in the second screening round (2012–2014) and later followed-up through centralized national cervical cancer screening registry. Results: In women 30 and older, the clinical sensitivity for cervical intraepithelial neoplasia grade 2+ (CIN2+) was 100.0% (95% CI, 88.2–100.0%) for Alinity and 100.0% (95% CI, 88.2–100.0%) for cobas, and for CIN3+ 100.0% (95% CI, 78.9–100.0%) for both assays. The clinical specificity for ≤ CIN1 in women 30 and older was 92.4% (95% CI, 91.4–93.3%) and 92.9% (95% CI, 91.9–93.7%), respectively. The assays demonstrated excellent overall agreement for hrHPV detection (97.9%) and genotype-specific agreement for HPV16 (99.6%), HPV18 (99.8%), and other hrHPV (98.1%). Overall positive agreement and positive agreements for HPV16, HPV18, and other hrHPV genotypes were 84.3%, 89.1%, 73.2%, and 82.3%. Based on a 5-year CIN3+ risk, slightly more HPV-positive women would require referral to immediate colposcopy after testing with Alinity vs. cobas (4.1% vs. 3.8%; p = 0.470), but significantly fewer Alinity-tested women would need a 6- to 12-month follow-up visit compared with those tested with cobas (5.0% vs. 8.6%; p < 0.0001). Conclusions: Alinity and cobas have comparable clinical performance and showed excellent overall and genotypespecific agreement. The Alinity’s extended genotyping ability could help predict the 5-year CIN3+ risk and costsaving management of HPV-screen-positive women.
Jezik:
Angleški jezik
Ključne besede:
cervical cancer
,
human papillomavirus
,
screening
,
validation
,
alinity
,
cobas
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2021
Št. strani:
6 str.
Številčenje:
Vol. 140, art. 104851
PID:
20.500.12556/RUL-138708
UDK:
618.1
ISSN pri članku:
1873-5967
DOI:
10.1016/j.jcv.2021.104851
COBISS.SI-ID:
95845379
Datum objave v RUL:
10.08.2022
Število ogledov:
996
Število prenosov:
113
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Journal of clinical virology
Založnik:
Elsevier
ISSN:
1873-5967
COBISS.SI-ID:
23214341
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
rak materničnega vratu
,
humani papiloma virus
,
presejanje
Projekti
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Abbott Molecular
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
University of Ljubljana, Faculty of Medicine, Institute of Microbiology and Immunology
Financer:
EC - European Commission
Program financ.:
H2020
Številka projekta:
847845
Naslov:
Risk-based screening for cervical cancer
Akronim:
RISCC
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