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Original article
peer-reviewed

Laryngeal Squamous Cell Carcinoma Survival in the Context of Human Papillomavirus: A Systematic Review and Meta-analysis



Abstract

Background: Head and neck (H&N) squamous cell carcinoma (SCC) is a significant contributor to worldwide mortality and morbidity. Human papillomavirus (HPV) has been linked with H&N cancer and HPV-positive H&N SCC have been shown to have better survival outcomes.

Objective: To evaluate the effect of human papillomavirus (HPV) on laryngeal carcinoma (LSCC) survival outcomes and prognosis.

Method: A systematic review and meta-analysis were performed using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. LSCC was confirmed based on histopathology, and HPV status was confirmed by either polymerase chain reaction, immunohistochemistry, and/or in-situ hybridization.

Results: There were 1214 studies which were identified, of which 14 studies were eligible for our review. A total of 2,578 cases of LSCC were included in analysis with 413 (16.0%) HPV-positive. Overall survival (OS) was not significant for HPV-positive LSCC in first five years (year one: OR 1.44 p=0.13; year two: OR 1.24 p=0.30; year three: OR 1.01 p=0.97; year four: OR 1.13 p=0.63; year five: OR 1.01 p=0.98). Disease-free survival (DFS) was similarly not significant for HPV-positive LSCC (year one: OR 1.08 p=0.68; year two: OR 1.22, p=0.31; year three: OR 1.13, p=0.69; year four: OR 0.93, p=0.80 and year five: OR 1.42, p=0.30). When studies are sub-divided into global regions, Chinese studies had better HPV-positive survival compared to North American studies in year five (OR 1.84 vs OR 0.46, p=0.04).

Conclusion: This is the first study of its kind to evaluate the survival impact of HPV-positive LSCC patients. Unlike oropharyngeal cancer, HPV status does not make a difference to OS or DFS in LSCC. This supports data that HPV is not a prognostic factor in squamous carcinoma of the larynx.

Introduction

Squamous cell carcinoma of the head and neck is a significant contributor to worldwide morbidity and mortality. There are more than 500,000 new cases worldwide reported annually [1]. Laryngeal squamous cell carcinoma (LSCC) is the second most common head and neck malignancy worldwide with 151,000 new cases per year worldwide [2-3]. While there is a great amount of evidence that suggests alcohol and tobacco are causative agents in developing LSCC, there are increasing incidences of LSCC in non-smokers and non-drinkers [4-6].

There is great variation in reporting the incidence of HPV-positive LSCC in literature, however, a recent meta-analysis reports incidence at roughly 25% with minor variation depending on methods of testing [7]. While it is regarded that HPV-positive oropharyngeal squamous carcinoma has better survival outcomes, there is no evidence the same holds true for LSCC.

The aim of this study is to conduct a systematic review and meta-analysis to evaluate and quantify the effect of human papillomavirus (HPV) on survival outcome of LSCC and to assess regional variation across the globe.

Materials & Methods

Search strategy and selection criteria:

Using the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines, this study was conducted [8]. Electronic search of Medline, Embase, Cochrane Methodology Register, Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, Database of Abstracts of Reviews and Effectiveness, ACP Journal Club, and NHS Economic Evaluation Database was conducted from their respective conception to January 2017.

Utilising both MeSH terms and keywords, the search was conducted to ensure ideal sensitivity. The terms “larynx”, “squamous cell carcinoma” and “human papilloma virus (HPV)” along with their relevant variations were used. Relevant studies were identified by two independent reviewers (Na.A. and Ni.A.) and were extracted for further evaluations.

Inclusion criteria included histologically confirmed LSCC and HPV-DNA or p16 status was confirmed by polymerase chain reaction (PCR), immunohistochemistry (IHC), and/or in-situ hybridization (ISH). Studies were excluded if they did not provide overall survival (OS) or disease-free survival (DFS) comparing HPV-positive and HPV-negative LSCC. Search was limited to papers with minimum length of follow up of one year, English language, and human subjects. Abstracts, case-reports, conference presentation and any papers without original data were excluded.

Data extraction and critical appraisal:

Two independent investigators (Na.A. and Ni.A.) extracted data, with discrepancies between reviewers resolved by consensus. The senior investigators (N.S. and R.C.) reviewed final results.

Statistical analysis:

Meta-analysis was performed with Review Manager (Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014) using pooled OS and DFS of HPV-positive and HPV-negative LSCC [9]. Data was pooled using the DerSimionian and Laird’s random effect model at one, two, three, four, and five years post-diagnosis [10]. To assess publication bias, Egger’s linear regression test was utilized and heterogeneity was assessed and quantified using the I2 statistics to measure percentage variability among summary indices [11-12]. Statistical significance was set at 0.05.

Results

Through the search of the nine databases, 1214 studies were identified. After excluding studies with duplicated cohorts, irrelevant studies, and studies with data not extractable, 14 studies were analyzed for statistical analysis. All the studies were case-control with two prospective studies, while the remaining 12 were retrospective. Bias was assessed using Egger’s test for publication bias and no publication bias was identified [11]. PRISMA guideline study selection is shown in Figure 1, with a description of studies in Table 1.

Author Year Country n Study Period Study Design Prospective Detection of HPV Sample p16 HPV DNA
Rivera-Pena 2016 USA (Puerto Rico) 83 1993-2005 Case-control Retrospective PCR FF NR Y
Hernandez 2016 USA 101 1993-2004 Case-control Retrospective IHC PE Y NR
Atighechi 2016 Iran 44 2007-2012 Case-control Retrospective PCR PE NR Y
Young 2015 Australia 307 2002-2012 Case-control Retrospective IHC, ISH PE Y Y
Wang 2015 USA 356 1995-2009 Case-control Retrospective PCR, IHC PE Y Y
Larque 2015 Spain 45 NR Case-control Retrospective PCR, IHC FF, PE Y Y
Xu 2014 China 674 2006-NR Case-control Prospective IHC FF, PE Y Y
Lassen 2014 Denmark 479 1992-2012 Case-control Retrospective IHC PE Y NR
Chung 2014 Multicentre 181 NR Case-control Prospective IHC, ISH PE Y NR
Jiang 2013 China 71 1997-2008 Case-control Retrospective IHC, ISH PE NR NR
Stephen 2012 USA 79 NR Case-control Retrospective PCR PE NR Y
Duray 2010 Belgium 67 2001-2007 Case-control Retrospective PCR, IHC PE Y Y
Morshed 2010 Poland 93 1999-2002 Case-control Retrospective PCR, IHC PE NR Y
Clayman 1994 USA 78 Prior to 1989 Case-control Retrospective PCR PE NR Y

Overall, 2578 LSCC cases were included in this analysis with 413 (16.0%) cases positive for HPV with 2051 (91.6%) male. HPV rates differed greatly between regions, as is summarised in Table 2. There was no difference noted in terms of OS of HPV-positive male (OR 0.63, 95% CI 0.20-1.92, p=0.41, I2=75%). Majority of LSCC were smokers (n=1252, 85.6%) and alcohol drinkers (n=703, 61.1%). Also, most of LSCC were well differentiated (61.2%) and only the minority were poorly differentiated (15.7%). In terms of tumor classification, there was an even spread between the grades (T1: 27.6%, T2: 22.1%, T3: 35.4, T4: 14.9%). Most of the LSCC had no regional node involvement (58.6%). Most patients were treated with the combination of radiotherapy and/or chemotherapy (42.4%), while 30.9% had surgery alone and 26.7% had surgery with chemotherapy and/or radiotherapy (Table 3).

Author Year n HPV + HPV -
CHINA  
Jiang 2013 71 31 (43.7%) 40 (56.3%)
Xu 2014 674 33 (4.9%) 641 (95.1%)
Wang 2015 318 42 (13.2%) 276 ( 86.8%)
  Total 1063 106 (10.0%) 957 (90.0%)
EUROPE  
Morshed 2010 93 33 (35.5%) 60 (64.5%)
Duray 2010 59 44 (74.6%) 15 (25.4%)
Lassen 2014 479 65 (13.6%) 414 (86.4%)
Larque 2015 45 4 (8.9%) 41 (91.1%)
  Total 676 146 (21.6%) 530 (78.4%)
NORTH AMERICA & CENTRAL AMERICA  
Clayman 1994 65 30 (46.2%) 35 (53.8%)
Stephen 2012 77 21 (27.3%) 56 (72.7%)
Hernandez 2016 101 8 (7.9%) 93 (92.1%)
Rivera-Pena 2016 83 41 (49.4%) 42 (50.6%)
  Total 326 100 (30.7%) 226 (69.3%)
OTHERS  
Chung 2014 181 31 (17.1%) 150 (82.9%)
Young 2015 288 19 (6.6%) 269 (93.4%)
Atighechi 2016 44 11 (25.0%) 33 (75.0%)
  Total 513 61 (11.9%) 452 (88.1%)
                    Differentiation Nodal Metastasis Location Treatment  
  Author Year n HPV +ve HPV -ve Mean Age Age Range Male (%) Smoker (%) Alcohol Drinker (%) Well-Moderate Poor N0 N+ Supra-glottis Glottis Sub-glottis Surgery alone Surgery + CRT CRT
  Rivera-Pena 2016 83 41 42 NR NR NR NR NR NR NR NR NR NR NR NR NR NR NR
  Hernandez 2016 101 8 93 NR NR NR NR NR NR NR NR NR NR NR NR NR NR NR
  Atighechi 2016 44 11 33 57.8 NR 90.9 NR NR NR NR NR NR NR NR NR NR NR NR
  Young 2015 288 19 269 66* 36-88 93.9 88.2 NR NR NR 213 94 102 180 16 NR 95 207
  Wang 2015 318 42 276 59* 32-87 98.1 86.1 41.5 282 36 290 28 NR NR NR 228 90 NR
  Larque 2015 45 4 41 65 NR 100.0 NR NR 17 28 NR NR 13 12 16 NR NR NR
  Xu 2014 674 33 641 NR NR 97.0 82.9% 65.0 NR NR 363 311 172 461 31 320 354 NR
  Lassen 2014 479 65 414 NR NR 81.0 NR NR NR NR 156 232 NR NR NR NR NR NR
  Chung 2014 181 31 150 NR NR NR NR NR NR NR NR NR 126 50 5 NR NR NR
  Jiang 2013 71 31 40 61.6 NR 97.2 NR NR 60 11 50 21 32 39 NR 32 39 NR
  Stephen 2012 77 21 56 NR NR 75.3 94.8 97.0 61 15 NR NR 28 28 1 26 NR 51
  Duray 2010 59 44 15 NR NR 97.0 NR NR 66 1 56 11 15 35 NR 67 NR NR
  Morshed 2010 93 33 60 NR NR 83.9 87.9 74.7 79 14 49 44 54 35 4 NR NR NR
  Clayman 1994 65 30 35 60 NR 83.1 NR NR NR NR NR NR NR NR NR 22 23 23
  Total 2578 413 (16.0%) 2165 (84.0%) - - 91.6 85.6 61.1 565 (84.3%) 105 (15.7%) 1177 (61.4%) 741 (38.6%) 542 (37.3%) 840 (57.7%) 73 (5.0%) 695 (44.1%) 601 (38.1%) 281 (17.8%)

In terms of survival, there was no difference noted in terms of OS in the first five years post-diagnosis (Figure 2). However, from year three to five post-diagnosis, there was a significant heterogeneity noted between studies (year three: I2=46%, year four: I2=57%, year five: I2=66%). Similarly, there is no difference noted in DFS in the first five years post-diagnosis. There is also significant heterogeneity in third- and fifth-year post-diagnosis (year 3: I2=62%, year 5: I2=64%). Similarly, there was no significance between DFS in the context of HPV (Figure 3).

 

When OS is stratified based on location, studies from China show better OS of HPV-positive LSCC in fourth and fifth-year post-diagnosis (OR=1.92, p=0.05, and OR=1.84, p=0.05 respectively) compared to North America in the same year (OR=0.63, p=0.39, and OR=0.46, p=0.48). This demonstrates a significant difference noted between the regions in fifth-year post-diagnosis (p=0.04). Looking at heterogeneity within regions, there is a significant heterogeneity noted in third- to fifth-year post-diagnosis (p=0.05, p=0.01, and p<0.01 respectively). The results are summarised in Table 4.

Regions No. of studies OR 95%CI p-value I2 Hetrogeneity (p-value)
Year 1            
China 2 1.27 0.41-3.88 0.68 0% 0.57
Europe 2 1.25 0.65-2.37 0.50 0% 0.36
N. America & C. America 4 0.97 0.18-5.18 0.97 63% 0.04*
Others 3 2.24 0.78-6.48 0.14 0% 0.93
Between Subgroups       0.78 6% 0.38
Year 2            
China 2 2.14 0.83-5.49 0.11 0% 0.47
Europe 2 0.61 0.09-3.96 0.61 68% 0.08
N. America & C. America 4 0.96 0.32-2.87 0.95 61% 0.05*
Others 3 1.21 0.61-2.43 0.59 0% 0.85
Between Subgroups       0.57 23% 0.23
Year 3            
China 2 1.60 0.77-3.31 0.21 0% 0.69
Europe 2 0.67 0.14-3.29 0.63 59% 0.12
N. America & C. America 4 0.62 0.17-2.20 0.46 75% <0.01
Others 3 1.07 0.44-2.57 0.89 35% 0.22
Between Subgroups       0.54 46% 0.05*
Year 4            
China 2 1.92 0.99-3.73 0.05* 0% 0.76
Europe 2 0.63 0.16-2.44 0.51 47% 0.17
N. America & C. America 4 0.63 0.10-3.78 0.61 85% <0.01*
Others 3 1.28 0.68-1.89 0.60 45% 0.16
Between Subgroups       0.39 57% 0.01*
Year 5            
China 3 1.84 1.00-3.36 0.05* 0% 0.41
Europe 3 0.62 0.36-1.08 0.09 5% 0.35
N. America & C. America 3 0.46 0.06-3.86 0.48 89% <0.01*
Others 3 1.70 0.59-4.93 0.33 52% 0.13
Between Subgroups       0.04* 66% <0.01*

Discussion

The pathogenesis of HPV and its effect on patient treatment and survival outcomes is an area of great importance in head and neck oncology. This study evaluates the current literature with regards to the pathogenesis of HPV as it relates specifically to laryngeal cancer and suggests that unlike in oropharyngeal cancer, HPV in the larynx has little to no effect on survival outcome.

HPV consists of double-stranded DNA genomes with more than 100 genotypes, of which more than 24 genotypes are detected in head and neck cancers [13-17]. HPV produces the malignant transformation of cells by producing E6 and E7 proteins that act together to lock cells in a forward replication phase [18]. As a result, HPV-positive oropharyngeal SCC (OSCC) is different to their HPV-negative counterparts, in that they have different patterns of dissemination and lower incident of metachronous primary tumors [19]. This may explain why HPV-positive OSCC have better responses to chemotherapy and radiotherapy, such that the latest American Joint Committee on Cancer (AJCC) divided staging for OSCC into different categories based in HPV status in the eight edition [20].

HPV has a propensity for tumorigenesis in the tonsillar crypts, which are deep recesses with a discontinuous basement membrane, and vasculature, which may explain the early propensity for lymphovascular invasion and early regional nodal spread [21-22]. This contrasts with laryngeal epithelium which is squamous epithelium with less abundant lymphatics particularly in the glottis [21-22].

While there is a large body of literature looking at HPV in oropharyngeal cancer, little research has focused on laryngeal pathology with regards to HPV. In this study, we demonstrate that there is no difference in survival in the context of OS and DFS based on HPV status. This suggests that HPV is not a significant driver of LSCC, and as such HPV status has limited clinical relevance in LSCC.

Recent meta-analysis by Ndiaye and colleagues showed HPV prevalence of LSCC is 22.1% (95% CI 16.4-28.3) while another meta-analysis demonstrated that the prevalence was 26.8% or 20.3% depending on whether PCR-testing for HPV was utilized or not [6-7]. This is lower than the incidence of HPV (45.8%; 95% CI 38.9–52.9%) in OSCC in the same study [6]. This demonstrates selective uptake of HPV in oropharynx as compared to larynx, and further suggests that HPV is likely not a strong indicator of LSCC. The prevalence of LSCC in this study (16%) is lower than the two above-mentioned meta-analyses. This may represent an inherent selection bias, as only studies with survival outcome and HPV status were included. As a result, the external validity of the current literature needs to be questioned in terms of providing accurate survival data on LSCC in context of HPV.

Another explanation for the different prevalence of HPV is the heterogeneity between different regional populations. The prevalence HPV-positive LSCC of Chinese cohort is 10%, while the prevalence of the rest of the world is 20.3%. While others have shown similar heterogeneity, their reported prevalence is different to our study. Ndiaye, et al. (2014) show the prevalence of HPV is 28.3% in Asia and 18.8% in North America, while Gama, et al. (2016) show point estimate of 0.246 (95%CI: 0.201-0.298) in North America to 0.399 (95%CI: 0.323-0.479) [6-7]. The lower rates in the Chinese population may, to some extent, account for a higher smoking rate in China, compared to North America.

There was no difference noted between HPV-positive and HPV-negative LSCC in terms OS and DFS. However, there was significant heterogeneity noted in studies. As mentioned previously, the AJCC now considers HPV-positive and HPV-negative OSCC different disease entities [20]. This is because HPV-positive OSCC also has better survival outcomes compared to HPV-negative OSCC [23-25]. However, the same does not seem to follow for LSCC. The difference in HPV prevalence between oropharynx and larynx is still not completely well understood and it is uncertain why HPV affects OSCC and LSCC differently [26].

There is significant regional variation in LSCC survival. This is most pronounced in the fifth year post-diagnosis, where there is a significant difference between the stratified cohorts (Table 4). As mentioned above, Xu, et al. attribute the low prevalence of HPV in Chinese cohorts to high rates of smoking within China which may explain the variability in terms of prevalence and survival of LSCC patients in Chinese cohort [27]. Furthermore, the variability also raises the concern regarding the external validity of various studies performed across the many centers around the world and calls for investigation of the cause of this difference. More molecular and epidemiologic studies are needed to evaluate the relationship of HPV and laryngeal cancers [26].

Limitations

This meta-analysis is limited by the number of studies with adequate data to allow for sub-analysis of outcomes and further multivariate analysis. There were also a limited number of studies from various regions of the world, with North American and Chinese studies accounting for most of the cohort of our meta-analysis. Further research is required to better assess survival outcome of LSCC based on HPV status.

Conclusions

This is the first meta-analysis to compare HPV-positive LSCC with smoking and alcohol-related LSCC and compare survival outcomes. This is the largest laryngeal meta-analysis looking at survival outcomes in laryngeal SCC with 2578 cases. Even though the study showed heterogeneity across regions in the world, particularly North America and China, the study showed that unlike oropharyngeal squamous cell carcinoma, HPV-positive LSCC does not have a better survival outcome compared to smoking and alcohol-related LSCC.


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Original article
peer-reviewed

Laryngeal Squamous Cell Carcinoma Survival in the Context of Human Papillomavirus: A Systematic Review and Meta-analysis


Author Information

Navid Ahmadi Corresponding Author

Faculty of Medicine, UNSW

Nima Ahmadi

Colorectal Surgery, Royal Prince Alfred Hospital

Michael V. Chan

Department of Radiology, Concord Hospital

Ya Ruth Huo

Faculty of Medicine, UNSW

Niranjan Sritharan

ENT Department, Nepean Hospital, Kingswood, AUS

Ronald Chin

ENT Department, St. George Hospital, University of Sydney, Sydney, AUS

ENT Department, Nepean Hospital, Kingswood, AUS


Ethics Statement and Conflict of Interest Disclosures

Human subjects: Consent was obtained by all participants in this study. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.


Original article
peer-reviewed

Laryngeal Squamous Cell Carcinoma Survival in the Context of Human Papillomavirus: A Systematic Review and Meta-analysis


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