Human papillomavirus genotype attribution in invasive cervical cancer: a retrospective cross-sectional worldwide study

宫颈癌 医学 基因分型 基因型 人乳头瘤病毒 人乳头瘤病毒疫苗 肿瘤科 HPV感染 内科学 癌症 病毒学 基因 生物 遗传学
作者
Sílvia de Sanjosé,Wim Quint,Laia Alemany,D.T. Geraets,Joellen Klaustermeier,Belén Lloveras,Sara Tous,Ana Félix,Luis Eduardo Bravo,Hai Rim Shin,Carlos S. Vallejos,Patricia Alonso de Ruı́z,Marcus Aurelho de Lima,Núria Guimerà,Omar Clavero,María Alejo,Antonio Llombart‐Bosch,Cheng-Yang Chou,Sílvio Tatti,Elena Kasamatsu,Ermina Iljazović,Michael Odida,Renato Luiz Prado,Muhieddine Seoud,Magdalena Grce,Alp Usubütün,Asha Jain,Gustavo Adolfo Hernandez Suarez,Luis Estuardo Lombardi,Aekunbiola Banjo,Clara Menéndez,Efren J. Domingo,Julio Velasco,Ashrafun Nessa,Saibua Chichareon,You‐Lin Qiao,Enrique Lerma,Suzanne M. Garland,Toshiyuki Sasagawa,Annabelle Ferrera,Doudja Hammouda,Luciano Mariani,Adela Pelayo,I Steiner,Esther Oliva,Chris J.L.M. Meijer,Waleed Al-Jassar,Eugénia Cruz,Thomas Wright,A Puras,Cecilia Llave,Maria Tzardi,Θεόδωρος Αγοραστός,Victoria García-Barriola,Christine Clavel,Jaume Ordi,Miguel Andújar,Xavier Castellsagué,Gloria Inés Sánchez,Andrzej Nowakowski,Jacob Bornstein,Núbia Muñóz,F. Xavier Bosch
出处
期刊:Lancet Oncology [Elsevier]
卷期号:11 (11): 1048-1056 被引量:2124
标识
DOI:10.1016/s1470-2045(10)70230-8
摘要

Summary

Background

Knowledge about the distribution of human papillomavirus (HPV) genotypes in invasive cervical cancer is crucial to guide the introduction of prophylactic vaccines. We aimed to provide novel and comprehensive data about the worldwide genotype distribution in patients with invasive cervical cancer.

Methods

Paraffin-embedded samples of histologically confirmed cases of invasive cervical cancer were collected from 38 countries in Europe, North America, central South America, Africa, Asia, and Oceania. Inclusion criteria were a pathological confirmation of a primary invasive cervical cancer of epithelial origin in the tissue sample selected for analysis of HPV DNA, and information about the year of diagnosis. HPV detection was done by use of PCR with SPF-10 broad-spectrum primers followed by DNA enzyme immunoassay and genotyping with a reverse hybridisation line probe assay. Sequence analysis was done to characterise HPV-positive samples with unknown HPV types. Data analyses included algorithms of multiple infections to estimate type-specific relative contributions.

Findings

22 661 paraffin-embedded samples were obtained from 14 249 women. 10 575 cases of invasive cervical cancer were included in the study, and 8977 (85%) of these were positive for HPV DNA. The most common HPV types were 16, 18, 31, 33, 35, 45, 52, and 58 with a combined worldwide relative contribution of 8196 of 8977 (91%, 95% CI 90–92). HPV types 16 and 18 were detected in 6357 of 8977 of cases (71%, 70–72) of invasive cervical cancer. HPV types 16, 18, and 45 were detected in 443 of 470 cases (94%, 92–96) of cervical adenocarcinomas. Unknown HPV types that were identified with sequence analysis were 26, 30, 61, 67, 69, 82, and 91 in 103 (1%) of 8977 cases of invasive cervical cancer. Women with invasive cervical cancers related to HPV types 16, 18, or 45 presented at a younger mean age than did those with other HPV types (50·0 years [49·6–50·4], 48·2 years [47·3–49·2], 46·8 years [46·6–48·1], and 55·5 years [54·9–56·1], respectively).

Interpretation

To our knowledge, this study is the largest assessment of HPV genotypes to date. HPV types 16, 18, 31, 33, 35, 45, 52, and 58 should be given priority when the cross-protective effects of current vaccines are assessed, and for formulation of recommendations for the use of second-generation polyvalent HPV vaccines. Our results also suggest that type-specific high-risk HPV-DNA-based screening tests and protocols should focus on HPV types 16, 18, and 45.

Funding

Spanish grants from Instituto de Salud Carlos III, Agència de Gestió d'Ajuts Universitaris i de Recerca, Marató de TV3 Foundation, and unrestricted grants from GlaxoSmithKline Biologicals, Sanofi Pasteur MSD, and Merck.
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