HPV and RAD51 as Prognostic Factors for Survival in Inoperable Oral and Oropharyngeal Cancer in Patients Unfit for Chemotherapy Treated with Hyperfractionated Radiotherapy

. 2023 Feb 14 ; 59 (2) : . [epub] 20230214

Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid36837562

Grantová podpora
NV19-08-00383 Ministry of Health Czech Republic
27 RVO-FNOs/2021

INTRODUCTION: The incidence of advanced oral cavity and oropharyngeal cancers is generally high. Treatment outcomes for patients, especially those unfit for comprehensive cancer treatment, are unsatisfactory. Therefore, the search for factors to predict response to treatment and increase overall survival is underway. OBJECTIVE: This study aimed to analyze the presence of 32 HPV genotypes in tumor samples of 34 patients and the effect of HPV status and RAD51 on overall survival. METHOD: Tumor samples of 34 patients with locally advanced oropharyngeal or oral cavity cancer treated with accelerated radiotherapy in monotherapy were analyzed using reverse hybridization and immunohistochemistry for the presence of HPV and RAD51. Its effect on overall survival was examined. RESULTS: Only two types of HPV were identified-HPV 16 (dominant) and HPV 66 (two samples). The HPV positivity was associated with a borderline insignificant improvement in 2-year (p = 0.083), 5-year (p = 0.159), and overall survival (p = 0.083). Similarly, the RAD51 overexpression was associated with borderline insignificant improvement in 2-year (p = 0.083) and 5-year (p = 0.159) survival. CONCLUSION: We found no statistically significant differences but detected trends toward improvement in the survival of HPV-positive and RAD51 overexpressing patients unfit for surgical treatment or chemotherapy treated with hyperfractionated radiotherapy. The trends, however, indicate that in a larger group of patients, the effects of these two parameters would likely be statistically significant.

Zobrazit více v PubMed

Warnakulasuriya S. Global Epidemiology of Oral and Oropharyngeal Cancer. Oral Oncol. 2009;45:309–316. doi: 10.1016/j.oraloncology.2008.06.002. PubMed DOI

Vrînceanu D., Dumitru M., Ştefan A.A., Mogoantă C.A., Sajin M. Giant pleomorphic sarcoma of the tongue base—A cured clinical case report and literature review. Rom. J. Morphol. Embryol. 2020;61:1323–1327. doi: 10.47162/RJME.61.4.34. PubMed DOI PMC

Chow L.T., Broker T.R., Steinberg B.M. The Natural History of Human Papillomavirus Infections of the Mucosal Epithelia. APMIS. 2010;118:422–449. doi: 10.1111/j.1600-0463.2010.02625.x. PubMed DOI

SVOD. [(accessed on 17 January 2023)]. Available online: https://www.svod.cz.

R Core Team R: The R Project for Statistical Computing. [(accessed on 12 February 2023)]. Available online: https://www.r-project.org/

Therneau T.M., Grambsch P.M. Modeling Survival Data: Extending the Cox Model. Springer; New York, NY, USA: 2000.

Kassambara A., Kosinski M., Biecek P., Fabian S. Survminer: Drawing Survival Curves Using “ggplot2”. [(accessed on 12 February 2023)]. Available online: https://cran.r-project.org/web/packages/survminer/index.html.

Lê S., Josse J., Husson F. FactoMineR: AnRPackage for Multivariate Analysis. J. Stat. Softw. 2008;25:1–18. doi: 10.18637/jss.v025.i01. DOI

Kassambara A., Mundt F. Factoextra: Extract and Visualize the Results of Multivariate Data Analyses. [(accessed on 12 February 2023)]. Available online: https://cran.r-project.org/web/packages/factoextra/index.html.

Di Gravio E.J., Lang P., Kim H.A.J., Chinnery T., Mundi N., MacNeil S.D., Mendez A., Yoo J., Fung K., Mymryk J.S., et al. Modern Treatment Outcomes for Early T-Stage Oropharyngeal Cancer Treated with Intensity-Modulated Radiation Therapy at a Tertiary Care Institution. Radiat. Oncol. 2020;15:1–9. doi: 10.1186/s13014-020-01705-1. PubMed DOI PMC

Fakhry C., Zhang Q., Nguyen-Tan P.F., Rosenthal D., El-Naggar A., Garden A.S., Soulieres D., Trotti A., Avizonis V., Ridge J.A., et al. Human Papillomavirus and Overall Survival after Progression of Oropharyngeal Squamous Cell Carcinoma. J. Clin. Oncol. 2014;32:3365–3373. doi: 10.1200/JCO.2014.55.1937. PubMed DOI PMC

Pannone G., Santoro A., Papagerakis S., Lo Muzio L., De Rosa G., Bufo P. The Role of Human Papillomavirus in the Pathogenesis of Head & Neck Squamous Cell Carcinoma: An Overview. Infect. Agents Cancer. 2011;6:4. PubMed PMC

de Villiers E.-M., Fauquet C., Broker T.R., Bernard H.-U., zur Hausen H. Classification of Papillomaviruses. Virology. 2004;324:17–27. doi: 10.1016/j.virol.2004.03.033. PubMed DOI

van Monsjou H.S., van Velthuysen M.L.F., van den Brekel M.W.M., Jordanova E.S., Melief C.J.M., Balm A.J.M. Human Papillomavirus Status in Young Patients with Head and Neck Squamous Cell Carcinoma. Int. J. Cancer. 2011;130:1806–1812. doi: 10.1002/ijc.26195. PubMed DOI

Garden A.S., Kies M.S., Morrison W.H., Weber R.S., Frank S.J., Glisson B.S., Gunn G.B., Beadle B.M., Ang K.K., Rosenthal D.I., et al. Outcomes and Patterns of Care of Patients with Locally Advanced Oropharyngeal Carcinoma Treated in the Early 21st Century. Radiat. Oncol. 2013;8:1–10. doi: 10.1186/1748-717X-8-21. PubMed DOI PMC

Ang K.K., Harris J., Wheeler R., Weber R., Rosenthal D.I., Nguyen-Tân P.F., Westra W.H., Chung C.H., Jordan R.C., Lu C., et al. Human Papillomavirus and Survival of Patients with Oropharyngeal Cancer. N. Engl. J. Med. 2010;363:24–35. doi: 10.1056/NEJMoa0912217. PubMed DOI PMC

Rischin D., Young R.J., Fisher R., Fox S.B., Le Q.-T., Peters L.J., Solomon B., Choi J., O’Sullivan B., Kenny L.M., et al. Prognostic Significance of P16INK4A and Human Papillomavirus in Patients with Oropharyngeal Cancer Treated on TROG 02.02 Phase III Trial. J. Clin. Oncol. 2010;28:4142–4148. doi: 10.1200/JCO.2010.29.2904. PubMed DOI PMC

Zhang X., Ma N., Yao W., Li S., Ren Z. RAD51 Is a Potential Marker for Prognosis and Regulates Cell Proliferation in Pancreatic Cancer. Cancer Cell Int. 2019;19:1–11. doi: 10.1186/s12935-019-1077-6. PubMed DOI PMC

Gachechiladze M., Škarda J., Skanderová D., Überall I., Kolek V., Smičkova P., Vojta P., Vbrková J., Hajdúch M., Shani I., et al. Prognostic Value of Tumor-Infiltrating Lymphocytes (TILs) and Their Association with PD-L1 Expression and DNA Repair Protein RAD51 in Patients with Resected Non-Small Cell Lung Carcinoma. Lung Cancer. 2020;147:30–38. doi: 10.1016/j.lungcan.2020.06.025. PubMed DOI

Wang J., Che W., Wang W., Su G., Zhen T., Jiang Z. CDKN3 Promotes Tumor Progression and Confers Cisplatin Resistance via RAD51 in Esophageal Cancer. Cancer Manag. Res. 2019;11:3253–3264. doi: 10.2147/CMAR.S193793. PubMed DOI PMC

Zhao M., Chen P., Dong Y., Zhu X., Zhang X. Relationship between Rad51 G135C and G172T Variants and the Susceptibility to Cancer: A Meta-Analysis Involving 54 Case-Control Studies. PLoS ONE. 2014;9:e87259. doi: 10.1371/journal.pone.0087259. PubMed DOI PMC

Connell P.P., Jayathilaka K., Haraf D.J., Weichselbaum R.R., Vokes E.E., Lingen M.W. Pilot Study Examining Tumor Expression of RAD51 and Clinical Outcomes in Human Head Cancers. Int. J. Oncol. 2006;28:1113–1119. doi: 10.3892/ijo.28.5.1113. PubMed DOI

Blažek T., Zděblová Čermáková Z., Knybel L., Hurník P., Štembírek J., Resová K., Paračková T., Formánek M., Cvek J., Soumarová R. Dose Escalation in Advanced Floor of the Mouth Cancer: A Pilot Study Using a Combination of IMRT and Stereotactic Boost. Radiat. Oncol. 2021;16:1–9. doi: 10.1186/s13014-021-01842-1. PubMed DOI PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...