Skip to main content
main-content

01.12.2017 | Research article | Ausgabe 1/2017 Open Access

BMC Cancer 1/2017

Cancer incidence in Germany attributable to human papillomavirus in 2013

Zeitschrift:
BMC Cancer > Ausgabe 1/2017
Autoren:
Nina Buttmann-Schweiger, Yvonne Deleré, Stefanie J. Klug, Klaus Kraywinkel
Abbreviations
CI5
Cancer in five continents
DCO
Cancer cases notified from death certificate only
EU
European Union
HPV
Human papillomavirus
IARC
International Agency for Research on Cancer
ICD-O-3
International Classification of Diseases for Oncology
NOS
Not otherwise specified
OP
Oropharynx
PAF
Population attributable fraction
SCC
Squamous cell carcinoma
STIKO
German Standing Committee on Vaccination
UK
United Kingdom
US
United States of America
WHO
World Health Organization
ZfKD
German Centre for Cancer Registry Data at the Robert Koch Institute

Background

Persistent infection with Human Papillomavirus (HPV) is considered a necessary cause in the etiology of virtually all cases of invasive cervical cancer [ 1]. In Germany, 4600 women were diagnosed with invasive cervical cancer in 2012 [ 2]. Increasing evidence further suggests HPV to be causally related to squamous cell carcinomas of another five cancer sites: the penis, vulva, vagina, anus and subsites of the oropharynx. It is estimated that a total of 120,000 new cancer cases in men and in women in more developed countries could be avoided if exposure to HPV was prevented [ 3].
Monitoring of HPV-associated disease remains crucial as two prophylactic HPV-vaccines have been licensed in Germany in 2006 and are recommended since 2007 by the German Standing Committee on Vaccination (STIKO). In 2014, the recommended age for vaccinating girls was lowered from 12–17 years to 9–14 years [ 4]. With the introduction of the HPV-vaccine and implementation in the German vaccination schedule, cervical cancer might become a largely preventable disease. The current vaccines are highly effective in preventing infections with HPV-types 16 and 18, the types that cause most cervical and anal cancers as well as anogenital pre-cancers [ 5]. High vaccine efficacy in protection against HPV-16/18 infections in oral sites has been demonstrated [ 6]. A newly developed nonavalent HPV-vaccine was recently licensed in the European Union (EU), which further prevents infection with HPV-31, 33, 45, 52, and 58 [ 7] that may cause about 15% of cervical cancers [ 8].
We used the nationwide pool of German population-based cancer registry data to assess the baseline incidence of HPV-associated cancer in our population for the year 2013, yet before quantifiable effects from HPV-vaccination on cancer incidence can be anticipated. Thus, our analyses provide the basis for a continuous monitoring of the effects of HPV-vaccination on cancer incidence at the population-level. This also applies to HPV-associated cancer in men, as a positive effect from vaccinating girls on HPV-related outcomes in men is expected [ 9]. Potential future discussions on vaccinating boys against HPV might be triggered by the findings of this study.

Methods

Classification of potentially HPV-associated cancer and estimation of the HPV-attributable fraction

Cases of cervical cancer with epithelial, squamous cell, basal and transitional cell origin, adenocarcinomas and cystic carcinomas as well as mixed tumors; squamous carcinoma of the anus and oropharynx, the vulva, vagina and penis were classified as potentially HPV-associated carcinoma (Table  1). The International Agency for Research on Cancer (IARC) established a causal role for human papillomavirus in a subset of these carcinoma, defining HPV-associated sites [ 10].
Table 1
HPV-associated cancer sites and morphologic specification
Site
ICD-O-3 topography code
Potentially HPV-associated morphology
ICD-O-3-codes
Cervix
C53
All carcinoma (except for melanoma, mesothelioma, Kaposi sarcoma, lymphoma, leukemia and other myeloproliferative malignant disorders)
8010–8671, 8940–8941
Penis
C60
Squamous cell carcinoma (SCC)
8050–8084
Vulva
C51
SCC
8050–8084
Vagina
C52
SCC
8050–8084
Anus
C21 (incl. C20 with ICD-O-3 8050–8084, 8120–8131)
SCC
8050–8084
Oropharynx, incl. base of tongue and tonsils
C01, C02.4–02.9, C05.1–05.9, C09.0–09.9, C10.0–10.9, C14.0-C14.8
SCC
8050–8084
Pathophysiological knowledge and epidemiologic evidence strongly suggest that the presence of HPV-infection in tumor material is sufficient to infer that HPV-infection caused the cancer. Estimation of the population attributable fraction (PAF) due to HPV was therefore based on the prevalence of viral DNA in squamous cell carcinoma (SCC) cells in the respective sites, as provided from the international literature, preferably from most recent metaanalyses and large tissue sample studies [ 1, 1115]. From the vaginal, penile and anal cancer studies, the HPV-DNA prevalence in European invasive SCC was chosen to derive the HPV-attributional fractions [ 1214]. In oropharyngeal cancer, the HPV-attributional fraction was more specifically derived from the prevalence of the combination of HPV-DNA positivity, mRNA positivity or positivity for a cell surrogate marker of HPV-induced carcinogenic transformation (p16 INK4a overexpression) - a validated and widely used HPV-detection algorithm [ 16]. The oropharynx included the base of tongue, lingual tonsil, overlapping lesions of tongue, tongue not otherwise specified, soft palate, uvula, overlapping lesions of palate and palate not otherwise specified, the tonsils, oropharynx, and other ill-defined sites in lip, oral cavity and pharynx including Waldeyer ring. For the HPV-attributable fraction in vulvar SCC, we used the crude European HPV-prevalence from HPV-DNA positive/p16 INK4a overexpressive keratinizing or warty-basaloid vulvar SCC [ 11].
Namely, all cases of cervical cancer and 88–90% of anal carcinoma with HPV-associated morphologies were considered HPV-attributable. An HPV-attributable proportion of 32% was assumed in penile cancer with HPV-associated morphologies, whereas 81% of vaginal, 18% of vulvar, and 16% of OP cancer with potentially HPV-associated morphologies were considered HPV-attributable (Table  2).
Table 2
Incident anogenital and oropharyngeal cancer cases and estimation of HPV-attributable cancer in Germany, 2013
Cancer site
Incident cases independent of morphology
Incident cases of HPV-associated morphology
(Proportion estimated) a
HPV-attributable fraction PAF
Reference
Estimated HPV-attributable incident cases
(Proportion of overall anogenital and oropharyngeal cancer)
Cervix
4458
4422
(7.1%)
100%
[ 1]
4422
(70.9%)
Vulva
3015
2596
(4.0%)
18%
[ 11]
467
(7.5%)
Vagina
386
275
(9.6%)
81%
[ 13]
223
(3.6%)
Female anus
1142
1030
(5.0%)
90%
[ 14]
927
(14.9%)
Female oropharynx
1371
1249
(7.5%)
16%
[ 15]
200
(3.2%)
Female overall anogenital & oropharynx
10,372
9573
(6.1%)
   
6239
(100%)
Penis
757
704
(6.3%)
32%
[ 12]
225
(16.6%)
Male anus
653
564
(3.9%)
88%
[ 14]
496
(36.5%)
Male oropharynx
4154
3978
(5.8%)
16%
[ 15]
636
(46.9%)
Male overall anogenital & oropharynx
5564
5246
(5.7%)
   
1358
(100%)
a proportion of estimated cases with HPV-associated morphology that were not coded as such, but redistributed from cases of not otherwise specified morphology

Monitoring of HPV-associated morphology in cancer registry data

Population-based cancer registration in Germany is organized by the 16 federal states, six of them merged to a joint registry for East Germany (including Berlin). Continuous registration has commenced in 1970 in the Saarland, but nationwide coverage has not been reached before 2009, when the population-based cancer registry of Baden-Württemberg was implemented. According to our current nationwide estimation, the degree of cancer registration across Germany is high, and 96% (463,611 cases) of the estimated 482,473 new cancer cases in 2013 have actually been recorded in the registries (data not shown). For our analyses, we retrieved incident cases of cervical cancer, penile cancer, vulvar cancer, vaginal cancer, anal cancer, and oropharyngeal cancer from the nationwide data pool for 2013. Site, behavior and histology are coded according to the International Classification of Diseases for Oncology (ICD-O-3).
For the purpose of monitoring, we provide the number of newly diagnosed cases, proportions and rates of cancer with potentially HPV-associated morphologies. Morphology codes of potential HPV-association are shown in Table 1. To correct for missing information on further morphologic specification of cancer cases (ICD-O-3 group 800: neoplasms, not otherwise specified), we redistributed these cases according to the distribution of morphology codes among those cases with further specified morphology (by site, gender and 5-year-age-group), assuming the information on morphology was ‘missing at random’. Cases notified from death certificate only (DCO) represented the majority of morphologically not otherwise specified cases.
Incidence rates from 2013 were age-standardized to the old European standard population (ASIR). 95% confidence intervals of ASIR were calculated using the binomial approximation according to the recommendation of IARC [ 17]. Calculation of the 95% confidence intervals of crude age-specific rates was based on a Poisson-distribution of the cases.

Results

In 2013, 5564 male incident cases and 10,372 female incident cases of invasive anogenital and oropharyngeal cancers were registered in Germany. Overall 9573 incident female cancer cases with potential HPV-associated site and morphology were extracted from the pooled data. Amongst them were 6239 incident cases considered to be attributable to HPV; 4422 cervical cancers (70.9% of all HPV-attributable female cancer cases), 927 anal cancers, 467 vulvar cancers, 223 vaginal cancers, and 200 oropharyngeal cancers. Among the 5246 incident male cancer cases with potential HPV-associated site and morphology, 1358 cases were attributed to HPV. Oropharyngeal cancer constituted the largest group (636 cases; 46.9% of all HPV-attributable male cancer cases) followed by anal cancer (496 cases) and penile cancer (225 cases). Table 2 provides the site-specific results and illustrates our calculations: for vaginal cancer, 386 incident cases were registered in 2013, of which 275 cases were of HPV-associated morphology. A proportion of 9.6% (26 cases) of the 275 cases with HPV-associated morphology were not coded as such, but redistributed from cases morphologically not otherwise specified. Applying the assumed PAF of 81% [ 13], 223 vaginal cancer cases were finally considered attributable to HPV.
Overall, a proportion of 1.6% of an estimated 482,473 new cancer cases in Germany in 2013 was considered HPV-attributable. The number of 9573 female cancer cases and 5246 male cancer cases with potential HPV-associated site and morphology assessed corresponds to approximately 3.1% (male: 2.1%; female: 4.2%) of the overall cancer burden in Germany in the same year. The proportion of incident cases with potentially HPV-associated morphology that were redistributed from cases morphologically not otherwise specified ranged between 3.9% (male anus) and 9.6% (vagina).
The most common cancers in the female and male population were cervical cancer in women and oropharyngeal cancer in men. Non-cervical anogenital cancer with HPV-associated morphology were rare in the German population. Anal cancer with an HPV-associated morphology was however more common in women than in men (Table  3).
Table 3
Age-standardized incidence rate (ASIR) of cancer in men and women with HPV-associated morphology, Germany 2013
 
Men
Women
 
ASIR
95% CI
ASIR
95% CI
Overall anogenital
2.3
2.2–2.4
14.8
14.4–15.1
Cervix
8.9
8.6–9.2
Penis
1.2
1.1–1.3
Vulva
3.7
3.6–3.9
Vagina
0.4
0.3–0.4
Anus
1.1
1.0–1.2
1.7
1.6–1.8
Oropharynx
7.6
7.4–7.9
2.2
2.0–2.3
Age-standardized incidence rates (European standard population) and corresponding 95% confidence intervals (95%CI) per 100,000 population; HPV-associated morphology codes (ICD-O-3): 8010–8671, 8940–8941 (cervix), 8050–8084 (penis, vulva, vagina, anus, oropharynx)
The age-distribution largely differed by site (Fig.  1a and b). The largest proportion of patients diagnosed below the age of 50 years was seen among cervical cancer cases (42.9%). Almost half of all anal cancer cases and female oropharyngeal cancer patients were 50–64 years of age (39.6% of female anal cancer patients, 41.2% of male anal cancer patients, and 47.0% of female oropharyngeal cancer patients respectively). Penile, vulvar and vaginal cancer patients were comparably older at diagnosis. The age distribution of male oropharyngeal cancer patients closely resembled the one of female oropharyngeal cancer patients (Fig. 1b): 9.1% of men were younger than 50 years (in females: 9.3%), 53.5% were aged 50 to 64 years (in females: 47.0%), 33.7% were aged 65 years to 79 years (in females 34.5%) and 3.7% were 80 years or older (in females: 9.4%).
Correspondingly, crude incidence rates (IR) of cervical cancer were highest in the age groups of 35–49 years and 50–64 years (16.5 per 100,000 and 14.8 per 100,000, respectively) and hereafter declined (Table  4). IR of vulvar, vaginal, anal, and penile cancer increased with increasing age. For oropharyngeal cancer, incidence rates peaked at ages 50–64 years both in men (IR: 24.8 per 100,000) and in women (IR: 6.7 per 100,000) and hereafter declined (Table 4).
Table 4
Age-specific incidence-rates (95% confidence intervals) of female and male cancer with HPV-associated morphology by age-groups, Germany 2013
   
35–49 years
50–64 years
65–79 years
≥80 years
   
IR
95% CI
IR
95% CI
IR
95% CI
IR
95% CI
Women
Cervix
16.5
15.6–17.4
14.8
14.0–15.6
12.4
11.6–13.3
14.1
12.8–15.6
Vulva
3.3
2.9–3.7
6.4
5.9–7.0
15.0
14.1–16.0
24.3
22.6–26.2
Vagina
0.2
0.1–0.3
0.7
0.5–0.9
1.7
1.4–2.1
2.7
2.1–3.4
Anus
1.5
1.3–1.8
4.7
4.2–5.2
4.7
4.2–5.2
5.8
4.9–6.7
Oropharynx
1.3
1.1–1.5
6.7
6.2–7.3
6.4
5.8–7.1
4.1
3.4–4.9
Men
Penis
0.6
0.4–0.8
2.2
1.9–2.5
5.8
5.2–6.4
8.8
7.3–10.4
Anus
1.1
0.9–1.4
2.7
2.4–3.1
2.9
2.5–3.4
4.0
3.1–5.2
Oropharynx
4.0
3.6–4.5
24.8
23.8–25-9
23.4
22.1–24.7
10.0
8.5–11.8
Age-specific incidence rates (IR) and corresponding 95% confidence intervals (95%CI) per 100,000 population

Discussion

Overall, the 6239 incident female HPV-attributable cancer cases and 1358 incident male HPV-attributable cancer cases relate to approximately 1.6% HPV-attributable incident cancer cases of the 482,473 new cancer cases in Germany in the same year.
Similar estimates have been reported in other populations of the western world [ 18, 19]. Despite methodological differences in selection of HPV-prevalence estimates, different contribution of cancers related to other risk factors (such as tobacco smoking or alcohol consumption) on the overall and site specific cancer burden, and potentially different degrees of completeness of cancer registry data, our estimates are comparable with recent 2010 figures from the United Kingdom (UK) (1.6%) [ 18], Australia (1.5%) [ 19], and the approximately 2.0% HPV-associated cancers in Europe, proposed in a recent synthesis on the global burden of infection-associated cancer [ 3]. The latter was based on the GLOBOCAN-database provided by IARC, which provides incidence figures by cancer site and country, but not further specified by morphology. Hence, our more conservative approach of applying the HPV-attributable fractions on cases that were of potential HPV-associated morphology only, resulted in somewhat lower estimates of HPV-related disease burden compared to the European estimates provided by DeMartel et al. [ 3].
An aspect that limits precision of our results is introduced by using HPV-attributable fractions from the international literature and their application to our national incidence.
Population-based cancer registries neither collect information on HPV in tumor tissue nor on other individual risk factors such as smoking. Hence, the proportion of HPV-attributable cases, which were derived mostly from recent metaanalyses or large case series, might be over- or underestimated. As prevalence of HPV is likely to vary by country, age, gender (in case of oropharyngeal and anal cancer) and time, the actual HPV-prevalence among cancer cases in Germany might deviate from the prevalence estimates we presumed. In oropharyngeal cancer, previous studies from Germany that were included in a recent metaanalysis [ 20] and one recent German study based on a clinical sample reported higher HPV-prevalence as the European estimate of 16% provided by Castellsague et al. [ 15, 21]. Differences in methods of HPV-testing usually hamper precise comparisons of HPV-prevalence over time and study population – an important advantage of the highly standardized study protocol and the single-centre HPV-DNA detection and genotyping in the study by Castellsagué et al. The authors further describe an increasing proportion of HPV-positive oropharyngeal cancer cases over time (worldwide): only about 10% of oropharyngeal cancer cases diagnosed in the 1990s were HPV-DNA-positive and mRNA-positive/p16-positive. In oropharyngeal cancer cases diagnosed in 2010–2012, one third was HPV-DNA-positive and mRNA-positive/p16-positive [ 15]. It is not clear if HPV-prevalence in the German population is increasing, but recent data indirectly suggests that the observed increase of OP-SCC in the younger population in countries with declining smoking prevalence might be explained by increasing HPV-prevalence [ 2224]. Given the changing epidemiology of HPV-positive oropharyngeal cancer over time, our numbers might underestimate the actual HPV-attributable fraction. Rising HPV-prevalence may also partly explain the increasing trends in vulva cancer which we recently described for Germany [ 25].
The quality of epidemiological cancer registry data limits registry-based studies in general, and also needs to be considered in our study: An aspect of uncertainty is introduced by potentially incomplete registration of incident cases in some registries, leading to underestimation. However, nine German federal states had achieved sufficient data quality and completeness to be included in the IARC publication “Cancer in five continents (CI5)” for the years 2003–2007, which can be regarded as a reference for high quality registries [ 26]. Since 2009, incident cancer cases are registered nationwide and quality has well improved. A comparison of the estimated nationwide incidence indicates that we might have also underestimated the incidence of anogenital and oropharyngeal cancer by up to 5%. The relatively high proportion of cases notified from death certificate only (DCO) (3–10% by cancer site considered in our analysis) similarly suggests certain underreporting in German cancer registries. Another source of bias was introduced by missing information on morphologically not otherwise specified cancer in some cases: overall, 6.1% of morphologically HPV-associated cases in women and 5.7% in men were estimated due to missing information on morphology (including DCO).
In recent studies of penile, anal, vaginal and vulvar cancer, the histological term “warty” or “basaloid/warty” carcinoma has been used to characterize HPV-associated carcinoma [ 1114]. Only recently, this term was introduced in the updated World Health Organization (WHO)-classification of tumours of the penis, and a new code (8054/3) for this entity was suggested [ 27]. The former code for “not otherwise specified keratinizing squamous cell carcinoma (8071/3 keratinizing SCC, NOS)” was omitted. At present, the cancer registry data based on ICD-O-3 classification does not yet provide this specific information. This limitation also applies to the issue of monitoring time trends at the other anogenital sites. The PAF for basaloid/warty cancer would be much higher than the PAFs we applied (e.g. an attributable fraction of 57% in warty/basaloid vulvar SCC compared to 18% in all invasive vulvar cancer [ 11]), however applied to fewer cases with HPV-associated morphology. Further morphology-, age- and site-specific analyses of pathology records are in preparation to verify our literature-based assumption on the HPV-attributable proportions in SCC.
Due to missing information on site specific HPV-prevalence in the general German population [ 28] our PAF-estimates are based upon HPV-prevalence in tumor tissue from international studies and therefore should be considered an approximation. Prevalence in tumor tissue might not necessarily be causally related to cancer development, especially if other risk factors are present. Tobacco-smoking constitutes another major risk factor for anogenital and oropharyngeal cancer, as well as immunodeficiency with HIV-positivity or immunosuppression following organ transplantation [ 2932].
It should be mentioned, that our estimates only take invasive tumors into account, while especially for the cervix, a large number of high-grade dysplastic lesions contribute to the HPV-related disease burden, demanding invasive treatment. Similar to other published estimates on HPV-related disease burden, we did not consider these cases in our analyses.
HPV-associated anogenital cancer and oropharyngeal cancer substantially contribute to the burden of cancer. In the United States of America (US), cancer with HPV-associated site and morphology account for 2% of male cancer cases and 3.3% of female cancer cases [ 33]. Our estimates of 5246 incident male cases and 9573 female cases relate to 2.1% and 4.2%, respectively. Moreover, in the Western world, the incidence in HPV-associated cancers in younger age-groups increases [ 22, 25, 3436]. Successfully implemented HPV-vaccinations programs should reverse these trends during the next decades.
For long-term monitoring of time trends (over 2–4 decades), a focus on cancer sites with high HPV-attributable fractions in younger age-groups (35–49 years) might be reasonable, though effects can first be expected to become observable in the more distant future: In Germany, HPV vaccination commenced in 2007 for 12–17 year old girls. As the oldest vaccinated women from the birth cohort of 1990 will not reach age 35 until 2023, it will be 2038 before the 35–49 age-group consists entirely of potentially vaccinated women.
The attributable fraction method may however not be suitable for monitoring time trends in the incidence of HPV-attributable cancers for sites with low attributional fractions, such as vulvar cancer and the oropharyngeal cancers group. Using vulvar cancer as an example, 18% of all vulvar cancers diagnosed in 2013 were attributed to HPV infection; 82% were attributed to other causes. If HPV vaccination decreases the incidence of HPV-attributable vulvar cancer in future years, this will hardly become apparent in the overall estimates, and the effect of the vaccine especially in low-PAF cancers in absolute terms will be underestimated without regular monitoring of the prevalence of HPV DNA in cancer cells. A decreasing proportion of cancer with HPV-associated morphology at respective sites would be expected. The newly emerging clinical cancer registries in Germany (according to the Law on the Further Development of the Early Detection of Cancer and Quality Assurance Through Clinical Cancer Registries [ 37]) might provide another anchor for concomitant projects to continuously monitor the cancer incidence and HPV-prevalence in cancer for short and medium term effects from HPV-vaccination in Germany in the near future.

Conclusions

Our estimates of the cancer burden at HPV-related sites along with the HPV-attributable fractions provide a baseline assessment of the HPV-related cancer burden in Germany and contribute to future evaluation of long-term HPV-vaccination effects on the population level. With population-based clinical cancer-registration, future monitoring of HPV-associated cancer in Germany is feasible with more accuracy and precision than using global estimates.

Acknowledgements

We especially thank Hiltraud Kajüter, Claudia Lübbers and Sandy Fischer at the cancer registry of North Rhine-Westphalia for their support and we thank all population-based cancer registries in Germany for providing the comprehensive data sets. Included data were namely from the registries of Baden-Württemberg, Bavaria, Bremen, Hamburg, Lower Saxony, North Rhine-Westphalia, Rhineland-Palatinate, Schleswig-Holstein, Hesse, Saarland, and the Common Cancer Registry of the Federal States of Mecklenburg-Western Pomerania, Saxony, Saxony-Anhalt, Brandenburg, Berlin, and Thuringia.

Funding

This study did not receive any specific funding.

Availability of data and materials

Due to ethical restrictions, the dataset supporting the conclusions of this article may only be obtained from the German Centre for Cancer Registry Data (ZfKD) at the Robert Koch Institute by request. Researchers may submit an application form and a data user agreement to access the minimized anonymous dataset [ 38]. Details for acquiring the data are available at www.​krebsdaten.​de.

Ethics approval and consent to participate

Only anonymized data was used for analyses, therefore no informed consent, and no ethical approval was required.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Literatur
Über diesen Artikel

Weitere Artikel der Ausgabe 1/2017

BMC Cancer 1/2017 Zur Ausgabe

Neu im Fachgebiet Onkologie

Mail Icon II Newsletter

Bestellen Sie unseren kostenlosen Newsletter Update Onkologie und bleiben Sie gut informiert – ganz bequem per eMail.

Bildnachweise