Evidence map›Paper›PMID 41327362›Full record

ArticleInfectious agents and cancer2025

Clinical significance of HPV DNA and EGFR mutations in Egyptian NSCLC.

Shaimaa Saeed Mohamed, Zeinab K Hassan, Ahmed M Fahmy, Amira Salah El-Din Youssef, Nasra F Abdel Fattah, Amira I Khater, Hany K Soliman, Mohamed M Hafez

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Article in Infectious agents and cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shaimaa Saeed MohamedVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Zeinab K HassanVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Ahmed M FahmySurgical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Amira Salah El-Din YoussefVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Nasra F Abdel FattahVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Amira I KhaterCancer Epidemiology & Biostatistics Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Hany K SolimanVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Mohamed M HafezVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt. mohamed.hafez@nci.cu.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality worldwide. While molecular profiling particularly EGFR mutation analysis has transformed therapeutic approaches, the role of viral oncogenesis, such as human papillomavirus (HPV) infection and Epstein-Barr virus (EBV), in NSCLC is less well understood. In this study, we investigated the clinical relevance of HPV/EBV infection and EGFR mutations in NSCLC.

methodsThis retrospective study analyzed tumor tissues from 93 patients with NSCLC, as well as lung tissues from 10 normal adjacent samples. HPV-DNA detection and genotyping were performed using PCR-based methods, alongside EBV-DNA analysis. EGFR mutations were assessed via exon-specific PCR amplification. Associations between HPV/EGFR status and clinicopathological parameters were evaluated, and Kaplan–Meier survival analysis was used to assess overall survival (OS) according to molecular profiles.

resultsHPV-DNA was detected in 31.2% of NSCLC tumors, while EBV-DNA was identified in 2.15%, with no positivity in normal adjacent tissues. HPV 16 was the most prevalent genotype, especially among adenocarcinoma (AC) cases. EGFR mutations were found in 20.4% of patients, predominantly in AC, with exon 19 deletions and L858R mutations being the most common. While HPV status showed no significant correlation with most clinical features, a strong inverse association was observed with surgical operability (p < 0.001). Survival analyses revealed that HPV-positive patients had shorter OS compared to HPV-negative counterparts. Patients with EGFR mutations exhibited longer OS, particularly in the HPV-negative subgroup, while the HPV-positive/EGFR-wild type group had the poorest outcomes.

conclusionThis study demonstrates distinct prevalence patterns and prognostic implications of HPV infection and EGFR mutations in NSCLC. EGFR-mutant status correlated with improved survival, while HPV positivity was associated with inoperable disease and poorer outcomes. Further validation in larger cohorts is needed before clinical application. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

AdenocarcinomaEBV-DNAEGFR mutationsHPV-DNAMolecular profilingNSCLCOverall survivalSquamous cell carcinomaViral oncogenesis

Identifiers

PMID41327362
PMCPMC12690842

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