2020
DOI: 10.1186/s12935-020-01512-4
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Cost-effectiveness and accuracy of cervical cancer screening with a high-risk HPV genotyping assay vs a nongenotyping assay in China: an observational cohort study

Abstract: Background: New screening techniques may affect the optimal approaches for the prevention of cervical cancer. We evaluated the cost-effectiveness and accuracy of alternative screening strategies to provide evidence for cervical cancer screening guidelines in China. Methods: In total, 32,306 women were enrolled. The current screening with Cervista ® high-risk human papillomavirus (HR-HPV) nongenotyping and cytology cotesting (Cervista ® cotesting) was compared with PCR-reverse dot blot HR-HPV genotyping and cyt… Show more

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Cited by 7 publications
(5 citation statements)
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“…The HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82, 83, 6, 11, 42, 43, 81) were detected by Polymerase chain reaction-reverse dot blot (PCR-RDB) HPV genotyping kit (YaNeng Biosciences, Shenzhen, China) 34 . This method and kit have been approved by China Food and Drug Administration (Approval number 20020515).…”
Section: Methodsmentioning
confidence: 99%
“…The HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82, 83, 6, 11, 42, 43, 81) were detected by Polymerase chain reaction-reverse dot blot (PCR-RDB) HPV genotyping kit (YaNeng Biosciences, Shenzhen, China) 34 . This method and kit have been approved by China Food and Drug Administration (Approval number 20020515).…”
Section: Methodsmentioning
confidence: 99%
“…However, the accuracy of the examination results of this method is affected by the subjective experience of physicians, which may lead to misdiagnosis (45)(46)(47). HR-HPV testing has become an important screening method for cervical cancer; it not only improves the sensitivity of cytological screening, but also predicts the development of disease in patients with normal cytology or atypical squamous cell lesions, reduces the number of tests in HPV-negative women with abnormal cytology and reduces medical waste (48)(49)(50). In the present study, the two examination methods were applied in the clinical diagnosis of cervical cancer and precancerous lesions.…”
Section: Discussionmentioning
confidence: 99%
“…At the same time, it is usually temporary, with the infection clearing up in approximately 80% of cases within 24 months, whereas the development of CIN and cervical cancer is almost always accompanied by persistent HR-HPV infection. 23,24 Human papillomavirus testing has high sensitivity, and HR-HPV detection has been proven feasible as a primary screening protocol for cervical cancer in China, [25][26][27] although it has a high false-positive rate that may easily lead to unnecessary colposcopy. Meanwhile, LBC has low sensitivity and is influenced by subjective factors, which necessitates the development of a triage method to retain the high sensitivity of HPV detection and simultaneously improve its screening specificity, to effectively reduce unnecessary colposcopy referrals.…”
Section: Discussionmentioning
confidence: 99%