Human papillomavirus genotype distribution in cervical cancer cases in Spain. Implications for prevention


Por: Alemany, L, Perez, C, Tous, S, Llombart-Bosch, A, Lloveras, B, Lerma, E, Guarch, R, Andujar, M, Pelayo, A, Alejo, M, Ordi, J, Klaustermeier, J, Velasco, J, Guimera, N, Clavero, O, Castellsague, X, Quint, W, Munoz, N, Bosch, FX, de Sanjose, S

Publicada: 1 mar 2012
Resumen:
Objective. Human papillomavirus (HPV) genotype distribution in invasive cervical cancer (ICC) is critical to guide the introduction and to assess the impact of HPV prophylactic vaccines. This study aims to provide specific information for Spain. Methods. 1043 histological confirmed ICC cases diagnosed from 1940 to 2007 from six Spanish regions were assembled. HPV DNA detection was performed by SPF10 broad-spectrum PCR followed by deoxyribonucleic acid enzyme immunoassay and genotyping by reverse hybridization line probe assay (LiPA(25)) (version 1). Results. Of 1043 ICC cases, 904 were HPV DNA positive (adjusted prevalence: 89.1%). The eight most common types, in decreasing order, were HPV 16, 18, 33, 31, 45, 35, 52 and 56, accounting for more than 90% of cases. HPV 16 and 18 contributed to 72.4% of all HPV positive ICC cases. In cervical adenocarcinomas, this contribution increased up to 94%. HPV 16 and 18 relative contributions showed a stable pattern over the 60 year study period. HPV 45, 18 and 16-positive ICC cases presented at younger ages than cases with other HPV types (adjusted mean age: 43.8, 45.2, 52.6 and 57.7 years, respectively). Conclusions. HPV 16 and 18 accounted together for a 72.4% of positive cases, with no statistically significant changes in their relative contributions over the last decades. In 94% of cervical adenocarcinomas we identified at least one of the two HPV types included in the current vaccines (HPV 16/18). Results suggest a major impact of HPV vaccines on reduction of ICC burden in Spain in the HPV vaccinated cohorts. (C) 2011 Elsevier Inc. All rights reserved.

Filiaciones:
Alemany, L:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

 CIBER Epidemiol & Salad Publ CIBERESP, Barcelona, Spain

Perez, C:
 Hosp San Agustin, Aviles, Asturias, Spain

Tous, S:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

Llombart-Bosch, A:
 Univ Valencia, Valencia, Spain

Lloveras, B:
 Hosp del Mar, Barcelona, Spain

Lerma, E:
 Hosp Santa Creu & Sant Pau, Barcelona, Spain

Guarch, R:
 Hosp Virgen Camino, Pamplona, Spain

Andujar, M:
 Complejo Hosp Univ Insular Maternoinfantil, Las Palmas Gran Canaria, Spain

Pelayo, A:
 Hosp Clin San Carlos, Madrid, Spain

Alejo, M:
 Hosp Gen LHospitalet, Barcelona, Spain

Ordi, J:
 Univ Barcelona, Hosp Clin, CRESIB, Barcelona, Spain

Klaustermeier, J:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

 CIBER Epidemiol & Salad Publ CIBERESP, Barcelona, Spain

Velasco, J:
 Hosp San Agustin, Aviles, Asturias, Spain

Guimera, N:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

Clavero, O:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

Castellsague, X:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

 CIBER Epidemiol & Salad Publ CIBERESP, Barcelona, Spain

Quint, W:
 DDL Diagnost Lab, Voorburg, Netherlands

Munoz, N:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

Bosch, FX:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

de Sanjose, S:
 Catalan Inst Oncol, Inst Catala Oncol, IDIBELL, Barcelona, Spain

 CIBER Epidemiol & Salad Publ CIBERESP, Barcelona, Spain
ISSN: 00908258





GYNECOLOGIC ONCOLOGY
Editorial
ACADEMIC PRESS INC ELSEVIER SCIENCE, 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 124 Número: 3
Páginas: 512-517
WOS Id: 000300751900024
ID de PubMed: 22119990

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