Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer
An etiological role of high risk human papillomavirus (HPV) in the development of cervical cancer has been well established. Hence, attention of researchers has been focused on the role of HPV in pathogenesis of other malignancies, such as head and neck cancers. An analysis of epidemiological data o...
Gespeichert in:
| Veröffentlicht in: | Experimental Oncology |
|---|---|
| Datum: | 2016 |
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | English |
| Veröffentlicht: |
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
2016
|
| Schlagworte: | |
| Online Zugang: | https://nasplib.isofts.kiev.ua/handle/123456789/137990 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| Zitieren: | Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer / V.A. Bychkov, E.G. Nikitina, M.K. Ibragimova, E.V. Kaigorodova, E.L. Choinzonov, N.V. Litviakov // Experimental Oncology. — 2016 — Т. 38, № 2. — С. 68–72. — Бібліогр.: 34 назв. — англ. |
Institution
Digital Library of Periodicals of National Academy of Sciences of Ukraine| id |
nasplib_isofts_kiev_ua-123456789-137990 |
|---|---|
| record_format |
dspace |
| spelling |
Bychkov, V.A. Nikitina, E.G. Ibragimova, M.K. Kaigorodova, E.V. Choinzonov, E.L. Litviakov, N.V. 2018-06-17T20:28:22Z 2018-06-17T20:28:22Z 2016 Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer / V.A. Bychkov, E.G. Nikitina, M.K. Ibragimova, E.V. Kaigorodova, E.L. Choinzonov, N.V. Litviakov // Experimental Oncology. — 2016 — Т. 38, № 2. — С. 68–72. — Бібліогр.: 34 назв. — англ. 1812-9269 https://nasplib.isofts.kiev.ua/handle/123456789/137990 An etiological role of high risk human papillomavirus (HPV) in the development of cervical cancer has been well established. Hence, attention of researchers has been focused on the role of HPV in pathogenesis of other malignancies, such as head and neck cancers. An analysis of epidemiological data on the prevalence of HPV infection among healthy people and patients with precancerous lesions and/or cancer is an important step in understanding the role of HPV in head and neck carcinogenesis. More and more data demonstrate the impact of HPV infection on disease outcome. HPVpositive patients have been shown to have better responses to radiotherapy and better overall and diseasefree survival than HPVnegative patients. This review presents data of the metaanalysis based on a large number of original studies on HPV prevalence in patients with precancerous lesions and in patients with oral, oropharyngeal and laryngeal cancers as well as findings on the impact of HPV infection on survival of these patients. This research is supported by Tomsk State University Competitiveness Improvement Program. The study was conducted with financial support from the Council for Grants of the President of the Russian Federation for the state support of young philosophy doctors, agreements of SC № 14.120.14.168-MD. en Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України Experimental Oncology Reviews Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer Article published earlier |
| institution |
Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| collection |
DSpace DC |
| title |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer |
| spellingShingle |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer Bychkov, V.A. Nikitina, E.G. Ibragimova, M.K. Kaigorodova, E.V. Choinzonov, E.L. Litviakov, N.V. Reviews |
| title_short |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer |
| title_full |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer |
| title_fullStr |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer |
| title_full_unstemmed |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer |
| title_sort |
comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer |
| author |
Bychkov, V.A. Nikitina, E.G. Ibragimova, M.K. Kaigorodova, E.V. Choinzonov, E.L. Litviakov, N.V. |
| author_facet |
Bychkov, V.A. Nikitina, E.G. Ibragimova, M.K. Kaigorodova, E.V. Choinzonov, E.L. Litviakov, N.V. |
| topic |
Reviews |
| topic_facet |
Reviews |
| publishDate |
2016 |
| language |
English |
| container_title |
Experimental Oncology |
| publisher |
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України |
| format |
Article |
| description |
An etiological role of high risk human papillomavirus (HPV) in the development of cervical cancer has been well established. Hence, attention of researchers has been focused on the role of HPV in pathogenesis of other malignancies, such as head and neck cancers. An analysis of epidemiological data on the prevalence of HPV infection among healthy people and patients with precancerous lesions and/or cancer is an important step in understanding the role of HPV in head and neck carcinogenesis. More and more data demonstrate the impact of HPV infection on disease outcome. HPVpositive patients have been shown to have better responses to radiotherapy and better overall and diseasefree survival than HPVnegative patients. This review presents data of the metaanalysis based on a large number of original studies on HPV prevalence in patients with precancerous lesions and in patients with oral, oropharyngeal and laryngeal cancers as well as findings on the impact of HPV infection on survival of these patients.
|
| issn |
1812-9269 |
| url |
https://nasplib.isofts.kiev.ua/handle/123456789/137990 |
| citation_txt |
Comprehensive meta-analytical summary on human papillomavirus association with head and neck cancer / V.A. Bychkov, E.G. Nikitina, M.K. Ibragimova, E.V. Kaigorodova, E.L. Choinzonov, N.V. Litviakov // Experimental Oncology. — 2016 — Т. 38, № 2. — С. 68–72. — Бібліогр.: 34 назв. — англ. |
| work_keys_str_mv |
AT bychkovva comprehensivemetaanalyticalsummaryonhumanpapillomavirusassociationwithheadandneckcancer AT nikitinaeg comprehensivemetaanalyticalsummaryonhumanpapillomavirusassociationwithheadandneckcancer AT ibragimovamk comprehensivemetaanalyticalsummaryonhumanpapillomavirusassociationwithheadandneckcancer AT kaigorodovaev comprehensivemetaanalyticalsummaryonhumanpapillomavirusassociationwithheadandneckcancer AT choinzonovel comprehensivemetaanalyticalsummaryonhumanpapillomavirusassociationwithheadandneckcancer AT litviakovnv comprehensivemetaanalyticalsummaryonhumanpapillomavirusassociationwithheadandneckcancer |
| first_indexed |
2025-11-26T01:39:37Z |
| last_indexed |
2025-11-26T01:39:37Z |
| _version_ |
1850603389437607936 |
| fulltext |
68 Experimental Oncology 38, 68–72, 2016 (June)
COMPREHENSIVE META-ANALYTICAL SUMMARY ON HUMAN
PAPILLOMAVIRUS ASSOCIATION WITH HEAD AND NECK CANCER
V.A. Bychkov1–3, *, E.G. Nikitina1,2, M.K. Ibragimova1, E.V. Kaigorodova1–3, E.L. Choinzonov1,3,, N.V. Litviakov1,2
1Tomsk Cancer Research Institute, Tomsk 634050, Russian Federation
2National Research Tomsk State University, Tomsk 634050, Russian Federation
3Siberian State Medical University, Tomsk 634050, Russian Federation
An etiological role of high risk human papillomavirus (HPV) in the development of cervical cancer has been well established. Hence,
attention of researchers has been focused on the role of HPV in pathogenesis of other malignancies, such as head and neck cancers.
An analysis of epidemiological data on the prevalence of HPV infection among healthy people and patients with precancerous lesions
and/or cancer is an important step in understanding the role of HPV in head and neck carcinogenesis. More and more data de
monstrate the impact of HPV infection on disease outcome. HPVpositive patients have been shown to have better responses
to radiotherapy and better overall and diseasefree survival than HPVnegative patients. This review presents data of the meta
analysis based on a large number of original studies on HPV prevalence in patients with precancerous lesions and in patients with
oral, oropharyngeal and laryngeal cancers as well as findings on the impact of HPV infection on survival of these patients.
Key Words: metaanalysis, human papillomavirus, head and neck cancer, survival.
Members of the Papillomaviridae family play
an important role in the development of certain types
of human malignancies, such as oropharyngeal and
anogenital cancers [1, 2]. Head and neck cancer (HNC)
is the fifth most common type of cancer and the sixth
most common cause of cancer death worldwide. About
550,000 new cases are reported worldwide annually [3].
The HPV involvement in oral and oropharyngeal
carcinogenesis was suggested based on viral tropism
to the epithelial cells and oncogenic potential of high
risk HPV genotypes in the pathogenesis of anogenital
neoplasia, particularly in cervical squamous cell car-
cinoma and the morphological similarities between
oropharyngeal and genital epithelia [4–9].
Almost 90% of HNC cases are of squamous epithe-
lial cell origin that could be characterized by a multistep
and multifactorial pathogenesis [10–12]. It has been
shown that besides smoking and alcohol use, some
infectious pathogens, such as human papillomavirus
(HPV) may act as a carcinogenic factor for HNC of cer-
tain locations, particularly the oropharynx [13, 14].
To evaluate the etiological role of HPV, it is impor-
tant to understand whether the prevalence of HPV
DNA become higher during malignant transformation
of normal epithelium to dysplasia, then to carcinoma
in situ and finally to invasive cancer. A large amount
of the data giving evidence of HPV DNA in head and
neck squamous cell carcinoma (HNSCC) has been ac-
cumulated and a systematic review and meta-analyses
of these data should be performed. Since most of the
original studies were conducted using small number
of samples, the meta-analysis is an effective statistical
tool, which depends less on specific initial data than
on each study individually, thus solving the problem
of low statistical power of each individual study.
It should be noted that each meta-analysis de-
termines its own inclusion criteria; therefore, the
following results of evaluation are rather complemen-
tary than contradictory and allow the studied problem
to be described more adequately. The meta-analyses,
described in the present article are mainly focused
on the following points:
• prevalence of HPV in HNSCC tissues, which is ex-
pressed as a percentage, usually with 95% confi-
dence interval (CI);
• the odds ratio (OR) — the ratio of the probability
of presence the studied risk factors in the HPV-
positive patients compared with HPV-negative ones;
• survival of HPV-positive patients. Typically, the surviv-
al rate is estimated, using the Kaplan — Meier analysis
and it is quantitatively assessed as a percentage
survival of each group or calculated risk ratio of ad-
verse outcome (hazard ratio — HR) in the presence
of HPV-infection. The lower HR value, the difference
in survival between HPV-positive and HPV-negative
patients is higher.
The main aim of this review was to summarize all
certain segments of available information with the
focus on infection prevalence, risk of HPV-associated
HNC, and also progression and survival of virus-
positive and virus-negative individuals.
The prevalence of HPV in head and neck pre-
cancerous lesions. There are two types of precan-
cerous lesions in the oral cavity mucosa: leukoplakia
and erythroplakia [15]. Based on published data [2],
the incidence of HPV DNA in leukoplakia was 31.1%
(300/964 cases). The predominant HPV types were
HPV-6 and HPV-11 (HPV-6/-11, 55.8%) followed
by HPV-16/-18 (28.2%). Only a few cases of erythro-
plakia have been described in the literature. The au-
thors reported on 32 cases of erythroplakia, 9 of them
had HPV-16 DNA. In addition, Nielsen et al. [16] de-
Submitted: August 08, 2015.
*Correspondence: E-mail: virology@oncology.tomsk.ru
Abbreviation used: DFS — disease-free survival; HNC — head and
neck cancer; HNSCC — head and neck squamous cell carcinoma;
HPV — human papillomavirus; HR — hazard ratio; OOPD — oral cavity
and oropharyngeal dysplasia; OR — odds ratio; OS — overall survival.
Exp Oncol 2016
38, 2, 68–72
REVIEW
Experimental Oncology 38, 68–72, 2016 (June)38, 68–72, 2016 (June) (June) 69
scribed 10 cases with erythroplakia, 50% of them being
HPV-positive. The prevalence of HPV-16/-18 in oral
cavity and oropharyngeal dysplasia (OOPD) has been
recently shown [17].
The meta-analysis was performed using the results
of 22 studies that reported prevalence of HPV-16 and/or
-18 in 458 OOPD cases. The overall prevalence of HPV-
16/-18 in OOPD lesions was 24.5% (95% CI 16.4–36.7).
The individual prevalence for HPV-16 alone was 24.4%.
The prevalence of HPV-16/-18 in oral cavity lesions
was 25.3% (95% CI 14.2–45.2). The odds of HPV-
16/-18 detection in dysplastic lesions in males were
twice that of females (OR 2.44). HPV-16/-18 were
3-fold more frequent in dysplastic lesions (OR 3.29;
95% CI 1.95–5.53) and invasive cancers (OR 3.43;
95% CI 2.07–5.69), than in normal tissue samples.
There were no significant differences in the incidence
of HPV-16/-18 between patients with mild, moderate
and severe dysplastic changes.
Results of the presented meta-analysis support an as-
sumption that the HPV-16/-18 accumulation occurs in the
early stage of oral and oropharyngeal carcinogenesis.
The prevalence of HPV in HNSCC. The high HPV
prevalence in HNSCC explains the abundance of the
reviews with the scope on a particular problem. Most
of the studies took into account the specific anatomic
sites and just very few of them has described HPV
prevalence in HNSCC. The average of HPV prevalence
in HNSCC was 21.9% [20], 25.9% [18], 34.5% [19],
which is described in 3 meta-analyses performed
on a cohort of about 5000 patients (Table 1).
Interestingly, the difference in HPV DNA prevalence
is observed between the cohorts with similar percentage
of patients. It is likely to be caused by different inclusion
criteria used in studies described above. Furthermore,
the following points can also have a considerable effect:
variety of methods used for HPV detection, different
origin of patients, varying percentage of cases with par-
ticular cancer sites. Thus, there is a definite re quisite for
stratification of HNC patient groups depending on the
anatomical site of squamous cell carcinoma.
It was shown that HPV-16 is the most prevalent
genotype among all HNSCCs (73.3% [18], 86.7% [20],
82.5% [21]), followed by HPV-18 and -33 [18, 20].
Hobbs et al. [22] in a meta-analysis based on 17 studies
with the total of 2012 patients, showed that HPV is most
strongly associated with tonsillar cancer (OR 15.1; 95%
CI 6.8–33.7), is intermediate for oropharyngeal cancer
(OR 4.3; 95% CI 2.1–8.9), and is the weakest for oral
cancer (OR 2.0; 95% CI 1.0–4.2).
It was also shown that HPV status was associ-
ated with p16 expression (adjusted OR 3.00; 95%
CI 0.90–9.70; p = 0.18), and HPV-positive tumors were
less likely to harbor p53 mutations (adjusted OR 0.21;
95% CI 0.04–0.38; p = 0.015) [20].
Survival rate of patients with HPV-positive and
HPV-negative HNSCC cases was studied in three
meta-analyses, and it was shown that HPV-positive
patients had better prognosis: HR for overall survival
(OS) was 0.42 [20], 0.46 [23], and 0.85 [24], and
HR for disease-free survival (DFS) was 0.41 [23] and
0.62 [24] (Table 2).
Table 1. HPV prevalence by different sites of HNC
State HPV prevalence
(95% CI), % Study type N Source
Leukoplakia HPV-6/-11 — 55.8% Review 364 [2]
HPV-16/-18 — 28.2%
Erythroplakia HPV-16 — 28.1% 32
HPV — 50.0% Original study 10 [16]
Dysplasia HPV-16/-18 — 24.5%
(16.4–36.7)
Meta-analysis
of 22 studies
458 [17]
HNC Pooled HPV — 25.9%
(24.7–27.2)
Meta-analysis
of 60 studies
5046 [18]
Pooled HPV — 34.5%
(28.4–40.6)
Meta-analysis
of 62 studies
4852 [19]
Pooled HPV — 21.9%
(21.0–23.0)
Meta-analysis
of 34 studies
5681 [20]
HPV-16 — 86.7%
(85.0–89.0)
Meta-analysis
of 34 studies
5681 [20]
HPV-16 — 82.4% Meta-analysis
of 269 studies
13972 [21]
HPV-16 — 73.3% Meta-analysis
of 60 studies
5046 [18]
Oral cancer Pooled HPV — 23.5%
(21.9–25.1)
Meta-analysis
of 35 studies
2642 [18]
Pooled HPV — 38.1%
(30.0–46.2)
Meta-analysis
of 47 studies
3238 [19]
HPV-16 — 68.2% Meta-analysis
of 35 studies
2642 [18]
Oropharyn-
geal cancer
Pooled HPV — 35.6%
(32.6–38.7)
Meta-analysis
of 27 studies
969 [18]
Pooled HPV — 47.7%
(42.9–52.3)
Meta-analysis
of 269 studies
5396 [21]
Pooled HPV — 63.8% Original study 323 [28]
HPV-16 — 86.7% Meta-analysis
of 27 studies
969 [18]
HPV-16 — 96.1% Original study 323 [28]
Laryngeal
cancer
Pooled HPV — 24.0%
(21.8–26.3)
Meta-analysis
of 35 studies
1435 [18]
Pooled HPV — 28.0%
(23.5–32.9)
Meta-analysis
of 55 studies
2559 [34]
HPV-16 — 69.2% Meta-analysis
of 35 studies
1435 [18]
HPV-16 — 19.8%
(15.7–24.6)
Meta-analysis
of 55 studies
2559 [34]
The prevalence of HPV in oral cancer. Several
meta-analyzes demonstrated the prevalence of HPV
in the oral cancer [18, 19, 23]. According to these
data, the HPV prevalence in oral cancer was ap-
proximately the same as in other HNC sites (23.5%).
Other data demonstrate much higher prevalence
(38.1% of cases). HPV-16 was detected in 68.2% and
HPV-18 in 34.1% (see Table 1).
The pooled HR for oral cancer was 0.32 (95%
CI 0.16–0.68), that is mean, the OS rate in HPV-positive
patients was 3 times higher than in HPV-negative ones
(see Table 2).
The prevalence of HPV in oropharyngeal can-
cer. An independent population-based study in the
United States (n = 271) showed that the population-
level incidence of HPV-positive oropharyngeal cancers
increased by 225% from 1984 to 2004 (from 0.8 per
100,000 to 2.6 per 100,000), and incidence for HPV-
negative cancers declined by 50% [25]. It is estimated
that by 2020, the annual number of HPV-positive oro-
pharyngeal cancers will exceed the annual number
of cervical cancers.
70 Experimental Oncology 38, 68–72, 2016 (June)
In the meta-analysis of Kreimer et al. [18], the fre-
quency of HPV detection was significantly higher in oro-
pharyngeal cancer (35.6% of 969 cases) compared
to oral cancer (23.5% of 2642 cases) and laryngeal
cancer (24.0% of 1435 cases). HPV-16 was detected
in 86.7% of patients with oropharyngeal cancer and
HPV-18 in 2.8% of patients (see Table 1).
Table 2. Impact of HPV-infection on survival rate of HNC patients
State Survival type Rate Study type N Source
HNC OS HR 0.42 Meta-analysis
of 34 studies
5682 [20]
OS HR 0.46
(0.37–0.57)
Meta-analysis
of 32 studies
3575 [23]
DFS HR 0.41
(0.27–0.64)
Meta-analysis
of 16 studies
1422 [23]
OS HR 0.85
(0.7–1.0)
Meta-analysis
of 19 studies
1990 [24]
DFS HR 0.62
(0.5–0.8)
Meta-analysis
of 9 studies
626 [24]
Oral
cancer
OS HR 0.32
(0.16–0.68)
Meta-analysis
of 2 studies
n/a [23]
DFS HR 0.62
(0.13–2.98)
Meta-analysis
of 3 studies
n/a [23]
Oropha-
ryngeal
cancer
OS HR 0.72
(0.5–1.0)
Meta-analysis
of 4 studies
224 [24]
DFS HR 0.51
(0.4–0.7)
Meta-analysis
of 5 studies
293 [24]
OS HR 0.47
(0.35–0.62)
Meta-analysis
of 17 studies
n/a [23]
DFS HR 0.37
(0.22–0.63)
Meta-analysis
of 8 studies
n/a [23]
3-year OS
(HPV-positive
vs HPV-nega-
tive), %
82.4 (77.2–87.6)
vs 57.1
(48.1–66.1)
Original study 323 [28]
3-year pro-
gression-
free survival
(HPV-positive
vs HPV-nega-
tive), %
73.7 (67.7–79.8)
vs 43.4
(34.4–52.4)
Original study 323 [28]
n/a — not available.
A meta-analysis of Mehanna et al. [21] based
on 269 studies (1970–2008) included 5396 patients
with oropharyngeal cancer and 13,972 patients with
non-oropharyngeal cancer. The overall pooled HPV
prevalence in patients with oropharyngeal cancer was
47.7% (95% CI 42.9–52.5). Overall HPV prevalence
in oropharyngeal cancer increased significantly over
time in Europe (p < 0.004) and in North America (p <
0.002) from 40.5% (95% CI 35.1–46.1) in the 54 stu-
dies that recruited patients before 2000 to 64.3% (95%
CI 56.7–71.3) in cohorts recruited between 2000 and
2004 (22 studies) and to 72.2% (95% CI 52.9–85.7)
from 2004–2008 (4 studies) (see Table 1). These
findings were consistent with the data obtained
by Chaturvedi et al. [25]. Overall HPV prevalence dif-
fered by geographic region. The overall prevalence was
35.3% in Europe, 50.7% in North America and 32.2%
in all other regions (p = 0.008). For oropharyngeal can-
cer, HPV-16 was positive in 1353 (95.7%) of 1414 cases.
Overall HPV prevalence in non-oropharyngeal
cancer was 21.8% (95% CI 18.9–25.1), and there ap-
peared to be statistically insignificant, declining trend
over time. Thus, the pooled HPV prevalence was 22.2%
before 2000 (95% CI 18.4–26.4), compared with 17.2%
(95% CI 11.9–24.4) between 2000 and 2004 and 6.1%
(95% CI 0.7–39) from 2004 to 2008. No statistically
significant difference between the regions was found.
The HPV-16 was detected in 1626 (73.9%) out of the
2199 HPV-positive patients with oropharyngeal cancer.
Gillison et al. [26] reported that the major risk factors
for HPV-positive oropharyngeal cancer are: high lifetime
number of both oral and vaginal sexual partners, early
age of sexual debut, anogenital warts and the con-
sumption of marijuana. HPV-negative oropharyngeal
cancer is strongly associated with tobacco and alcohol
consumption, older age and poor oral hygiene.
According to a meta-analysis of Ragin et al. [24],
HPV-positive patients with oropharyngeal cancer had
a 28% lower risk of dying compared with HPV-negative
patients (HR 0.72; 95% CI 0.5–1.0) (see Table 2). Similar
findings were published in a prospective analysis of data
from clinical trials [27]. In order to evaluate other fa-
vorable prognostic factors associated with HPV status
of the tumor, Ang et al. [28] analyzed survival rates
of patients with oropharyngeal squamous cell carcinoma.
A total of 63.8% of patients with oropharyngeal cancer
(206 of 323) had HPV-positive tumors, and 198 (96.1%)
of 206 were positive for HPV-16. Kaplan — Meier
analysis revealed that HPV-positive cancer patients had
better overall and DFS compared with HPV-negative
patients (p < 0.001). 3-year OS was 82.4% (95%
CI 77.2–87.6) in HPV-positive patients and 57.1% (95%
CI 48.1–66.1) in HPV-negative patients. The 3-year DFS
rates were 73.7% (95% CI 67.7–79.8) and 43.4% (95%
CI 34.4–52.4), respectively.
In the multivariable analysis, the age, race, perfor-
mance status, tumor stage, nodal stage, and number
of pack-years of tobacco smoking were also significant
determinants of the OS and DFS.
Tumors were evaluated for the expression of not only
HPV, but also for p16, a known biomarker of HPV infec-
tion. The presence of HPV and p16 expression in tumors
were in good agreement (κ = 0.80; 95% CI 0.73–0.87).
Using p16 expression as a stratification factor, the dif-
ferences in the OS and DFS rates, that were consistent
with those based on HPV status, were shown. Thus, the
3-year survival rate was 83.6% in patients with p16-
positive expression and 51.3% (95% CI 41.5–61.0) in the
patients with p16-negative expression.
Recursive-partitioning analysis showed that the
HPV status of the tumor was the major determinant
of OS, followed by the number of pack-years of tobacco
smoking and then nodal stage for HPV-positive tumors,
or tumor stage for HPV-negative tumors.
In a meta-analysis by O’Rorke et al. [23], the au-
thors examined the difference in OS between the HPV-
positive and HPV-negative patients with oropharyngeal
cancer and found that the pooled HR was 0.47 (95%
CI 0.35–0.62) (see Table 2).
The prevalence of HPV in laryngeal cancer. In a me-
ta-analysis stratified by anatomical site, Kreimer et al. [18]
reported that the prevalence of HPV in laryngeal squamous
cell carcinomas was 24.0% (of a total of 1435 cases)
and found HPV-16 positivity in 69.2% of cases and HPV-
Experimental Oncology 38, 68–72, 2016 (June)38, 68–72, 2016 (June) (June) 71
18 positivity in 17.0% of ca ses. Meta-analysis by Tor-
rente et al. [29] demonstrated the same HPV prevalence
(24.0%; 95% CI 21.8–26.3) in laryngeal cancer patients.
The authors paid attention to the fact that the overall HPV
prevalence in normal laryngeal mucosa was not deter-
mined because sampling methods for HPV detection
in healthy cells were not standardized, and prevalence
estimates remained inconsistent.
The reported incidence of HPV infection in normal
laryngeal mucosa has been as high as 19.0% [30–33].
These results suggest that the number of HPV-positive
cancers observed might reflect the prevalence of latent
HPV infections in the vocal cord epithelium.
Li et al. [34] performed a systemic review and meta-
analysis based on 55 studies that tested the presence
of HPV in laryngeal cancer patients. It was reported
that HPV DNA was detected in 28.0% of the 2559 cases
of laryngeal carcinoma (95% CI 23.5–32.9%) (see
Table 1). The prevalence of high risk HPV types was
significantly higher than that of low risk HPV types
(26.6% vs 3.7%). The most common HPV type
was HPV-16, with a summary prevalence of 19.8%
(95% CI 15.7–24.6). The remaining most frequently
identified HPV types were HPV-18 (6.2% of cases;
95% CI 4.0–9.5), HPV-33 (3.3%; 95% CI 2.1–5.1),
HPV-31 (2.4%; 95% CI 1.3–4.4), HPV-6 (4.3%; 95%
CI 2.4–7.7) and HPV-11 (2.3%; 95% CI 1.2–4.4).
Analyses stratified by cancer location showed
that laryngeal cancers in the glottis region had the
highest HPV prevalence (35.2%; 95% CI 28.2–42.8),
followed by those in the supraglottic region (30.5%;
95% CI 24.0–37.8) and the subglottic region (27.5%;
95% CI 17.5–40.4). The microenvironment of the
glottis might favor HPV infection, because the squa-
mocolumnar junction in the ventricle is similar to the
cervical transformation zone.
The estimated HPV prevalence among laryngeal
cancers might vary with respect to the analyzed popu-
lation, HPV detection methods and tumor charac-
teristics. The prevalence of high risk HPV was found
to be much higher than that of low risk HPV types.
Various HPV prevalences in laryngeal cancers were
observed in different geographical regions (range;
25.6–35.6%). Studies from South America reported
a higher rate of HPV infection compared with that ob-
served in Asia, North America and Europe.
In a meta-analysis based on 12 case-control studi es,
Li et al. [34] estimated the association between HPV infec-
tion and the risk of laryngeal cancer. A total of 638 patients
with laryngeal cancer and 419 controls were enrolled.
It was shown that HPV infection significantly increased
the risk of laryngeal cancer (OR 5.39; 95% CI 3.25–8.94),
this OR was higher than that for oropharyngeal cancer
(OR 4.3; 95% CI 2.1–8.9) and oral cancer (OR 2.0; 95%
CI 1.2–3.4) demonstrated by Hobbs et al. [22].
The OR of individual types indicated diffe rences
in the magnitudes of the association for HPV-
16 (6.07; 95% CI 3.44–10.7) and HPV-18 (4.16; 95%
CI 1.87–20.04). For low risk HPV (16 and 11 types) the
OR were not statistically significant.
When estimating survival, O’Rorke et al. [23]
showed that patients with HPV-positive laryngeal squa-
mous cell carcinoma had a 50% lower risk of mortality
compared to HPV-negative patients (HR 0.5; 95%
CI 0.33–0.77) (see Table 2).
CONCLUSION
The prevalence of HPV was found to be greater
in HNC than in dysplasia and HPV virus was most
frequently detected in oropharyngeal cancer among
the different anatomical sites, HPV-16 was the most
prevalent HPV type in HNC.
In spite of tumor location, the risk of dying was
lower and survival was higher in HPV-positive patients
than in HPV-negative patients, indicating that along
with the carcinogenic effect, HPV is able to modulate
the disease and influence on the prognosis.
ACKNOWLEDGMENT
This research is supported by Tomsk State Univer-
sity Competitiveness Improvement Program.
The study was conducted with financial support
from the Council for Grants of the President of the Rus-
sian Federation for the state support of young philoso-
phy doctors, agreements of SC № 14.120.14.168-MD.
REFERENCES
1. Zur Hausen H. Papillomaviruses in human cancer. Appl
Pathol 1987; 5: 19–24.
2. Syrjanen S. Human papillomavirus (HPV) in head and
neck cancer. J Clin Virol 2005; 32S: S59–66.
3. Jemal A, Bray F, Center MM, et al. Global cancer
statistics. CA Cancer J Clin 2011; 61: 69–90.
4. Syrjanen K, Syrjanen S, Lamberg M, et al. Morpho�Morpho�
logical and immunohistochemical evidence suggesting human
papillomavirus (HPV) involvement in oral squamous cell
carcinogenesis. Int J Oral Surg 1983; 12: 418–24.
5. Zur Hausen H. Papillomavirus infections — a major cause
of human cancers. Biochim Biophys Acta 1996; 1288: F55–F78.
6. Zur Hausen H. Papillomavirus and cancer: from basic
studies to clinical application. Nat Rev Cancer 2002; 2: 342–50.
7. Erdmann J. Recent studies attempt to clarify relationship
between oral cancer and human papillomavirus. J Natl Cancer
Inst 2003; 95: 638–9.
8. Nair S, Pillai M. Human papillomavirus and disease
mechanisms: relevance to oral and cervical cancers. Oral Dis
2005; 11: 350–9.
9. Thompson IO, Van Der Bijl P, Van Wyk CW, et al.
A comparative lightmicroscopic, electron�microscopic and
chemical study of human vaginal and buccal epithelium. Arch
Oral Biol 2001; 46: 1091–8.
10. Franceschi S, Levi F, La Vecchia C. Comparison
of the effect of smoking and alcohol drinking between oral and
pharyngeal cancer. Int J Cancer 1999; 83: 1–4.
11. Scully C, Field JK, Tanzawa H. Genetic aberra�
tions in oral or head and neck squamous cell carcinoma
(SCCHN): 1. Carcinogen metabolism, DNA repair and cell
cycle control. Oral Oncol 2000; 36: 256–63.
12. Girja KP, Sundharam BS, Krishnan PA, et al. Bio�Bio�
chemical changes of saliva in tobacco chewers tobacco smo�
kers, alcohol consumers, leukoplakia and oral cancer patients.
Indian J Dent Res 2002; 13: 102–7.
13. Lutzky VP, Moss DJ, Chin D, et al. Biomarkers for
cancers of the head and neck. Clinical Medicine: Ear, Nose
and Throat 2008; 1: 5–15.
72 Experimental Oncology 38, 68–72, 2016 (June)
14. Duray A, Descamps G, Arafa M, et al. High incidence
of high�risk HPV in benign and malignant lesions of the larynx.
Int J Oncol 201; 39: 51–9.
15. Axell T, Pindborg JJ, Smith CJ, et al. Oral white
lesions with special reference to precancerous and tobacco�
related lesions: conclusions of an international symposium
held in Uppsala, Sweden, May 18–21, 1994. J Oral Pathol
Med 1996; 25: 49–54.
16. Nielsen H, Norrild B, Vedtofte P, et al. Human pap�Human pap�
illomavirus in oral premalignant lesions. Eur J Cancer Part
B: Oral Oncol 1996; 32: 264–70.
17. Jayaprakash V, Reid M, Hatton E, et al. Human papil�
lomavirus types 16 and 18 in epithelial dysplasia of oral cavity
and oropharynx: a meta�analysis, 1985–2010. Oral Oncol
2011; 47: 1048–54.
18. Kreimer AR, Clifford GM, Boyle P, et al. Human pap�
illomavirus types in head and neck squamous cell carcinomas
worldwide: a systematic review. Cancer Epidemiol Biomarkers
Prev 2005; 14: 467–75.
19. Termine N, Panzarella V, Falaschini S, et al. HPV
in oral squamous cell carcinoma vs head and neck squamous
cell carcinoma biopsies: a meta�analysis (1988–2007). Ann
Oncol 2008; 19: 1681–90.
20. Dayyani F, Etzel CJ, Liu M, et al. Meta�analysis of the
impact of human papillomavirus (HPV) on cancer risk and
overall survival in head and neck squamous cell carcinomas
(HNSCC). Head Neck Oncol 2010; 29: 2–15.
21. Mehanna H, Beech T, Nicholson T, et al. Prevalence
of human papillomavirus in oropharyngeal and nonoro�
pharyngeal head and neck cancer — systematic review and
meta�analysis of trends by time and region. Head Neck 2013;
35: 747–55.
22. Hobbs CG, Sterne JA, Bailey M, et al. Human papil�Human papil�
lomavirus and head and neck cancer: a systematic review and
meta�analysis. Clin Otolaryngol 2006; 31: 259–66.
23. O’Rorke MA, Ellison MV, Murray LJ, et al. Human pa�
pillomavirus related head and neck cancer survival: a sys tematic
review and meta�analysis. Oral Oncol 2012; 48: 1191–201.
24. Ragin CCR, Taioli E. Survival of squamous cell
carcinoma of the head and neck in relation to human papil�
lomavirus infection: review and meta�analysis. Int J Cancer
2007; 121: 1813–20.
25. Chaturvedi AK, Engels EA, Pfeiffer RM, et al. Human
papillomavirus and rising oropharyngeal cancer incidence
in the United States. J Clin Oncol 2011; 29: 4294–301.
26. Gillison ML, Zhang Q, Jordan R, et al. Tobacco smo�
king and increased risk of death and progression for patients
with p16�positive and p16�negative oropharyngeal cancer.
J Clin Oncol 2012; 30: 2102–11.
27. Fakhry C, Westra WH, Li S, et al. Improved survival
of patients with human papillomavirus�positive head and neck
squamous cell carcinoma in a prospective clinical trial. J Natl
Cancer Inst 2008; 100: 261–9.
28. Ang KK, Harris J, Wheeler R, et al. Human papil�
lomavirus and survival of patients with oropharyngeal cancer.
N Engl J Med 2010; 363: 24–35.
29. Torrente MC, Rodrigo JP, Haigentz M, et al. Human
papillomavirus infections in laryngeal cancer. Head Neck
2011; 33: 581–6.
30. Fukushima K, Ogura H, Watanabe S, et al. Human
papillomavirus type 16 DNA detected by the polymerase chain
reaction in non�cancer tissues of the head and neck. Eur Arch
Otorhinolaryngol 1994; 251: 109–12.
31. Rihkanen H, Peltomaa J, Syrjanen S. Prevalence
of human papillomavirus (HPV) DNA in vocal cords without
laryngeal papillomas. Acta Otolaryngol 1994; 114: 348–51.
32. Garcia�Milian R, Hernandez H, Panade L, et al. De�De�
tection and typing of human papillomavirus DNA in benign
and malignant tumours of laryngeal epithelium. Acta Otolar�
yngol 1998; 118: 754–8.
33. Smith EM, Summersgill KF, Allen J, et al. Human
papillomavirus and risk of laryngeal cancer. Ann Otol Rhinol
Laryngol 2000; 109: 1069–76.
34. Li X, Gao L, Li H, et al. Human papillomavirus
infection and laryngeal cancer risk: a systematic review and
meta�analysis. J Infect Dis 2013; 207: 479–88.
Copyright © Experimental Oncology, 2016
|