The emerging risk of oropharyngeal and oral cavity cancer in HPV-related subsites in young people in Brazil

The emerging risk of oropharyngeal and oral cavity cancer in HPV-related subsites in young people in Brazil
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DOI:
10.1371/journal.pone.0232871
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发表时间:
2020-05-14
期刊:
影响因子:
3.7
通讯作者:
Toporcov, Tatiana Natasha
Toporcov, Tatiana Natasha
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Menezes, Fabricio dos Santos;Dias de Oliveira Latorre, Maria do Rosario;Toporcov, Tatiana Natasha

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人乳头瘤病毒(HPV)是导致口咽、扁桃体和舌根癌发病率上升的原因(即,HPV相关子网站)。HPV引发了亚洲、欧洲、北美和大洋洲口咽和口腔癌(OPC/OCC)流行病学的变化。因此,HPV相关亚位点的癌症发病率正在增加,而其他HPV无关亚位点的癌症发病率正在下降。在南美洲,虽然HPV阳性肿瘤的发病率逐渐增加,但OPC/OCC患者中HPV的患病率很低。为了阐明这一发病趋势的巨大变化是否也发生在这一人群中,我们估计了HPV对巴西圣保罗市OPC/OCC发病趋势的负担。在这项基于人群的研究中,我们根据HPV相关和HPV无关的亚位点对OPC/OCC进行分类。我们使用泊松回归来评估按性别和年龄组分层的年龄标准化发病率(ASR),并检查年龄-时期-队列效应。在HPV相关(n = 5,898; 38.3%)和HPV无关(n = 9,493; 61.7%)子位点中诊断出15,391例OPC/OCC。总体而言,除了年轻男性和女性的HPV相关OPC/OCC每年分别增加3.8%和8.6%外,大多数子位点的ASR在所有年龄组和性别中均下降。在出生队列效应分析中,我们发现在最近的出生队列中,两种性别的HPV相关OPC/OCC的风险都在增加;然而,这种风险在HPV无关的子位点中急剧下降。我们的数据表明,年轻人中出现HPV相关OPC/OCC的风险,这支持该群体的预防性HPV疫苗接种。
Human papillomavirus (HPV) is responsible for the rise in the incidence of cancer in the oropharynx, tonsils, and base of the tongue (i.e., HPV-related subsites). HPV triggered the changes in the epidemiology of oropharyngeal and oral cavity cancer (OPC/OCC) in Asia, Europe, North America, and Oceania. Hence, the incidence of cancer in HPV-related subsites is augmenting, while that in other HPV-unrelated subsites is decreasing. In South America, although the incidence of HPV-positive tumors has gradually increased, there is an atypically low prevalence of HPV in people with OPC/OCC. To clarify whether this dramatic shift in incidence trends also occurred in this population, we estimated the burden of HPV on the incidence trends of OPCs/OCCs in Sao Paulo city in Brazil. In this population-based study, we categorized OPCs/OCCs by HPV-related and HPV-unrelated subsites. We used Poisson regression to assess the age-standardized incidence rates (ASRs) stratified by sex and age groups, as well as to examine the age-period-cohort effects. There were 15,391 cases of OPCs/OCCs diagnosed in HPV-related (n = 5,898; 38.3%) and HPV-unrelated (n = 9,493; 61.7%) subsites. Overall, the ASRs decreased for most subsites, for both sexes and for all age groups, except for HPV-related OPC/OCC in young males and females, which increased by 3.8% and 8.6% per year, respectively. In the birth-cohort-effect analysis, we identified an increasing risk for HPV-related OPC/OCC in both sexes in recent birth cohorts; however, this risk was sharply decreased in HPV-unrelated subsites. Our data demonstrate an emerging risk for HPV-related OPC/OCC in young people, which supports prophylactic HPV vaccination in this group.