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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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