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283
ICAR SINONASAL TUMORS
TABLE XXV.3 Evidence surrounding HPV DNA in NPC.
Clinical endpoints
Study
Year LOE Study design Study groups
Conclusion
Isayeva et al. 1735
2012 1
Systematic review
154 NPC (47 HPV + )
Prevalence of HPV
Weighted prevalence of HPV DNA detection in 154 NPC patients is 31.1% (95% CI: 20.3%–44.5%) WHO type I NPC: EBV–/HPV– (56.4%), EBV–/HPV + (21.5%) WHO type II/III: EBV + /HPV– (87.5%)
Thamet al. 1736
2021
2
Systematic review
1919 NPC (1600
Prevalence of
EBV + /HPV–, 141 EBV–/HPV + , 68 EBV + /HPV + , 110 EBV–HPV–) 570 NPC (29 HPV + , 422EBV + )
EBVandHPV
Huang et al. 1651
HPV neither correlates with nor predicts survival in NPC
2022 4
Retrospective
1. LRC 2. Distant control 3. OS
case–control
Wuet al. 1652
2022 4
Retrospective case series
78 NPC (43 EBV + , 12 HPV + , 23 EBV–/HPV–)
OS
1. OS time was not significantly different between the EBV + and HPV + groupsEBV − /HPV– tumors had worst OS 2. Viral status not a significant predictor of OS There was no statistically significant difference in survival between the three groups ( p = 0.61) Viral status was not prognostic for OS OS better among patients with EBV + andHPV + compared to EBV–/HPV– No significant difference in DSS between HPV + and HPV– NPC patients HPV neither correlates with nor predicts survival in NPC 1. p16 overexpression is associated with improved PFS and LRC in patients with EBV-positive NPC 2. p16 expression may complement EBV status in predicting treatment outcomes for NPC patients
Simon et al. 1653
OS
2020 4
Retrospective
98 NPC (66 EBV + , 18 HPV + , 14 EBV/HPV–) 343 NPC (205 EBV + , 21HPV + , 12viral negative, 105 unknown) 150 NPC (93 EBV + , 21 HPV + , 36 EBV–/HPV–) 517 NPC (180 HPV + , 337HPV–) 956 NPC (308 HPV + , 648HPV–) 86 (44EBV + , 35EBV–, seven indeterminate; 40 HPV + , 26 HPV–, 20 no tissue sample; 13 EBV + /HPV + )
case–control
Verma et al. 1654
2020 4
Retrospective case series
OS
Ruuskanen et al. 1737
1. OS 2. DSS
2019 4
Retrospective case series
Wotman
2019 4
Database study [SEER]
DSS
et al. 1655
Verma et al. 1650
2018 4
Database study [NCDB] Retrospective case series
OS
Jiang et al. 1738
2016 4
1. OS 2. PFS 3. LRC
Atighechi et al. 1739
2014 4
Retrospective case series
41 NPC (9 HPV + , 32 HPV–)
1. OS 2. Recurrence
1. HPV type 16 and 18 most common subtypes 2. HPV + patients had better
prognosis and lower recurrence rates
Stenmark et al. 1740
2014 4
Retrospective case series
61NPC(26
1. OS 2. PFS 3. LRC
1. High-risk HPV infection may play an etiologic role in the development of nonendemic EBV–NPC 2. Compared with EBV + NPC,
EBV + /HPV– 18 HPV + /EBV–, 17 EBV–/HPV–)
HPV + and EBV–/HPV– NPC are associated with worse outcomes (Continues)
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