Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Supplemental Information Andrew P. Stein, BA1,2, Sandeep Saha, MS3, Jennifer L. Kraninger, BS2, Adam D. Swick, PhD2, Menggang Yu, PhD3, Paul F. Lambert, PhD*,1, and Randall J. Kimple, MD PhD*,2 Departments of Oncology1, Human Oncology2 and Biostatistics3, University of Wisconsin School of Medicine and Public Health Madison, WI 53706, U.S.A. 1 Supplemental Methods We followed the PRISMA statement guidelines throughout all elements of our analysis and manuscript preparation.23 Article selection A systematic literature review was performed using the NIH PubMed search engine to identify articles published through January 31, 2014. We utilized keyword search terms including HPV, oropharyngeal, cancer, tonsillar, and prevalence. Specific search phrases employed were “HPV prevalence in oropharyngeal cancer”, "HPV and tonsillar cancer" and "HPV prevalence in tonsillar cancer". Titles and abstracts of all studies displayed by these broad searches were examined to identify any articles that presented data on the prevalence of HPV in OPSCC by PCR, in situ hybridization (ISH), p16 immunohistochemistry (IHC), or other molecular methods. Studies that met these initial criteria were selected for detailed evaluation of the entire study. Reviewing the reference sections of this initial cohort of articles identified additional relevant papers missed by our PubMed searches. These newly identified articles were subjected to the same process described above whereby the titles and abstracts were examined first, and a portion of the studies were subsequently selected for full review. Exclusion criteria Articles were excluded if they were reviews, did not utilize molecular techniques to determine HPV status, failed to distinguish oropharyngeal cancers from other regions of the head and neck, or were not written in English. To be included in our meta-analysis, all articles needed to present the first and last years that their samples derived from (sample collection period), number of HPV-positive OPSCCs, total number of OPSCCs analyzed, and the country/region where the samples originated. Eighteen articles did not report the sample collection period and three failed to present the number of HPV-positive OPSCCs detected. Before excluding these articles, we contacted the authors to gather the missing information. We received the queried data from 14 of 18 authors related to the sample collection period and two of three regarding the number of HPV-positive OPSCCs detected in their study. If we did not receive the necessary information from the authors, these papers were excluded. Finally, we carefully examined all articles in order to exclude ones with overlapping patient populations (we included the article reporting on the larger number of patients) (Supplemental Table S1). The ultimate decisions for article inclusion/exclusion were made jointly between two of the authors (APS and RJK). Data abstraction and organization The following data was collected from all articles meeting our inclusion criteria: authors, journal, publication year, country, description of patients, anatomical sites of cancers analyzed, sample preservation technique, HPV detection 2 method, sample collection period, overall number of head and neck cancers analyzed, number of cancers that were HPVpositive and breakdown of HPV subtypes (if documented). Some studies employed multiple methods for HPV detection. In these instances we collected data based on the method the article utilized as their standard for evaluating HPV status. To focus our analysis on the prevalence of HPV in OPSCC, we stratified the head and neck cancers reported by each study into oropharyngeal (tonsil, base of tongue, soft palate, and lateral/posterior pharyngeal walls) and nonoropharyngeal (all other sites) subgroups. Our final data included the overall number of HPV-positive OPSCCs out of the total number of OPSCCs analyzed by a specific article. Detailed data extracted from each manuscript is documented in Supplemental Table S2, and the additional information gathered from the authors we contacted is described in the footnotes of this table. Based on the country of origin for the samples analyzed, each study was separated into one of six distinct geographical regions: North America, Europe, Asia, Australia, South America and International. Due to the limited number of articles from Asia (n=11), Australia (n=2), South America (n=2) and International (n=3), we combined these studies into a single category labeled “Other”. To assess changes in the prevalence of HPV-positive OPSCCs over time, we used the median year of each article’s sample collection period (rounded down to the nearest year) to separate articles into four discrete time frames: pre-1995, 1995—1999, 2000—2004 and 2005—present. As shown in Supplemental Table S2, 13 articles separated their samples into multiple collection periods. Therefore, we had a total of 135 data points from the 105 articles. Statistical analysis Due to the small number of articles for individual countries, we could not carry out appropriate statistical analyses examining trends over time for each nation (aside from the United States24). Therefore, we examined broader regions and determined if HPV prevalence was static or changed over time worldwide, in North America and throughout Europe. There were not sufficient articles from specific geographic regions such as Asia, Australia or South America to perform informative statistical analyses on these individual areas. Moreover, we did not evaluate the “Other” category separately as this group contains nations with significant ethnic/geographic diversity. Thus, the primary subgroup analyses were limited to North America and Europe. Additionally, all articles within a particular region were combined together into a single analysis regardless of the detection method utilized (ie: PCR, ISH, p16, etc). The number of articles employing methods other than PCR was too small to perform relevant statistical analyses assessing trends over time for each distinct detection method. 3 HPV prevalence was calculated for each article by dividing the number of patients with HPV-positive OPSCCs by the total number of OPSCCs analyzed. Prevalence values were categorized into four time frames (pre-1995, 1995— 1999, 2000—2004 and 2005—present) on the basis of the median year of the study’s sample collection period. An analysis of variance (ANOVA) model with time frame used as a four-level categorical variable and weighted by the total number of OPSCCs analyzed in each paper was utilized to model the time trends of HPV in OPSCC. This analysis included all articles for the worldwide analysis (articles=105, total OPSCCs=9541), with sub-analyses performed for North America (articles=40, total OPSCCs=2844) and Europe (articles=47, total OPSCCs=4812). The p-values generated from this analysis reflect the overall trend of HPV-positivity across the four time frames within each of these regions (pvalue for trend). A more detailed evaluation was then performed to assess the differences in HPV prevalence between every adjoining time frame from pre-1995 to 2005—present for North America and Europe. All analyses were performed using the procedure PROC MIXED from SAS/STAT software (version 9.3). Plots were generated by the ggplot2 package in R (version 3.0.2), and geographical maps were created with Google Fusion Tables (©2014 Google- Imagery ©2014 NASA, TerraMetrics). Every statistical test was two-sided, and a p-value less than 0.05 was considered statistically significant. Finally, we examined the present day prevalence of HPV in OPSCC within individual countries. Due to the limited number of articles (less than three) for each country in the 2005—present time frame, we collated data from studies with median year for sample collection between 2000—present. From all articles within one country, we aggregated the total number of OPSCCs analyzed as well as the number of HPV-positive OPSCCs detected. The proportion of HPV-positive OPSCCs and 95% confidence intervals were generated and plotted for each country using Graphpad Prism v6.0d. 4 Supplemental Tables Table S1. Final group of articles excluded from this meta-analysis. Article Reason for Exclusion Country Region Shahnaz Begum et al, 200553 Failure to report sample collection period United States North America United States North America United States North America United States North America United States North America United States North America United States North America United States North America Czech Republic Europe Denmark Europe Denmark Europe England Europe France Europe Germany Europe Germany Europe Odey C. Ukpo et al, 201151 RD Chernok et al, 200955 Justine M. Ritchie et al, 200356 Seth R. Schwartz et al, 200158 Anthony C. Nichols et al, 200959 Jose Jiron et al, 201461 Maura Gillison et al, 200827 R. Tachezy et al, 200563 Pernille Lassen et al, 200965 Pernille Lassen et al, 201367 AG Schache et al, 201352 Jean Lacau St Huily et al, 201169 Jens P. Klussmann et al, 200371 Jens P. Klussmann et al, 200373 Overlapping patient population with James S. Lewis et al, 201054 Overlapping patient population with James S. Lewis et al, 201054 Overlapping patient population with Elaine M. Smith et al, 200457 Failure to provide number of HPVpositive OPSCCs detected Overlapping patient population with Anthony C. Nichols et al, 201060 Overlapping patient population with Seema Sethi et al, 201262 Overlapping patient population with D’Souza et al, 200728 Overlapping patient population with Jan Klozar et al, 200864 Overlapping patient population with Pernille Lassen et al, 201066 Overlapping patient population with Pernille Lassen et al, 201066 and Pernille Lassen et al, 201168 Overlapping patient population with AG Schache et al, 201115 Overlapping patient population with Jean Lacau St Guily et al, 201170 Overlapping patient population with Niklas Reimers et al, 200772 Overlapping patient population with Jens P. Klussmann et al, 200174 Claus Wittekindt et al, 200575 Failure to report sample collection period Germany Europe Gerald Niedobitek et al, 199076 Failure to report sample collection period Germany Europe Italy Europe Spain Europe Sweden Europe Sweden Europe Sweden Europe Sweden Europe Gianna Badaracco et al, 200077 Ignacio Alvarez Alvarez et al, 199779 Signe Friesland et al, 200180 Hanna Mellin et al, 200082 Hanna Mellin et al, 200383 Anders Nasman et al, 201284 Overlapping patient population with Aldo Venuti et al, 200478 Overlapping patient population with JP Rodrigo et al, 201417 Overlapping patient population with Lalle Hammarstedt et al, 200681 Overlapping patient population with Lalle Hammarstedt et al, 200681 Overlapping patient population with Lalle Hammarstedt et al, 200681 Overlapping patient population with Lalle Hammarstedt et al, 200681 and Anders Nasman et al, 200918 5 Anders Nasman et al, 201385 Hanna Mellin Dahlstrand et al, 200586 Jos M.J.A.A. Streatmans et al, 200988 Peter J.F. Snijders et al, 199290 Harriet C. Hafkamp et al, 200392 Angela Hong et al, 201093 Wei Li et al, 200394 Angela Hong et al, 201096 Zeyi Deng et al, 201197 Kwonoh Park et al, 201399 Overlapping patient population with Lalle Hammarstedt et al, 200681 and Anders Nasman et al, 200918 Overlapping patient population with Lalle Hammarstedt et al, 200681 and Hanna Mellin et al, 200287 Overlapping patient population with Harriet C. Hafkamp et al, 200889 Overlapping patient population with Peter J.F. Snijders et al, 199491 Failure to report sample collection period Overlapping patient population with Angela Hong et al, 201011 Overlapping patient population with Angela Hong et al, 201395 Overlapping patient population with Angela Hong et al, 201011 Overlapping patient population with Zeyi Deng et al, 201398 Overlapping patient population with Miji Lee et al, 2013100 6 Sweden Europe Sweden Europe Netherlands Europe Netherlands Europe Netherlands Europe Australia Other Australia Other Australia Other Japan Other South Korea Other Table S2. Detailed information extracted from each article included in the meta-analysis. North America ‡ Median Year # of HPV+ OPSCCs 28 102 103 104 57 105 106 107 1992 2003 1986, 1992, 1997, 2002 2002 2000 1985 1997 1995 2002 2000 1998 34 25 8/49 (1986), 27/75 (1992), 48/93 (1997), 33/46 (2002) 72 12 2 17 25 26 48 24 54b Ref. # 21 101 12a Total # of OPSCCs Material Detection Method Country 60 30 Fresh frozen FFPE PCR PCR United States United States 263 FFPE PCR United States 100 16 7 48 67 49 102 35 FFPE FFPE Fresh frozen FFPE FFPE FFPE FFPE FFPE United States United States United States United States United States United States United States United States 2002 158 239 FFPE c 108 109 110 2002 1999 1996 38 12 10 62 21 11 FFPE FFPE FFPE 111d 2001 27 42 FFPE 112 62 113 24 41 22 1/5 (1982), 3/7 (1987), 4/7 (1992), 15/20 (1997), 27/33 (2002) 9/24 (2002), 13/23 (2009) 52 81 55 FFPE FFPE FFPE 72 FFPE PCR United States 115 1991 2003 1992 1982, 1987, 1992, 1997, 2002 2002, 2009 ISH PCR Southern blot ISH PCR ISH PCR PCR p16 IHC, ISH, PCR ISH ISH PCR PCR with flight mass spectroscopy PCR PCR PCR 47 ISH United States 116 1989 14 22 PCR United States 117 118 119 2003 1996 1988 206 15 2 323 29 14 ISH PCR PCR United States United States United States 120 2001 13 14 FFPE Fresh frozen, FFPE FFPE Fresh frozen Fresh frozen Fresh frozen, FFPE PCR United States 121 2006 37 50 FFPE 122 123 60e 124 1989 2004 2001 2009 48 23 53 111 79 31 68 162 125 2002 19 23 126 1994 12 34 f 2002 137 169 128 2001 16 22 129 2004 1996, 2002, 2008 2002 1997, 2006 2007 73 8/39 (1996), 43/63 (2002), 44/71 (2008) 12 1/7 (1997), 4/16 (2006) 11 111 FFPE Fresh frozen FFPE FFPE Fresh frozen, FFPE Information not available FFPE Fresh frozen and FFPE FFPE 173 20 23 18 114 127 13 130 14 131 aDr. PCR with flight mass spectroscopy PCR PCR ISH p16 IHC United States United States United States United States United States United States United States United States United States United States United States United States United States ISH, PCR United States PCR United States PCR Canada PCR Canada PCR Canada FFPE PCR Canada FFPE FFPE Fresh frozen PCR p16 IHC, PCR PCR Canada Greenland Mexico Anil Chaturvedi sent us a table outlining the number of HPV-positive OPSCCs detected in each of the four time periods based on the Inno-LiPA assay as this information was not provided for the 1990—1994 or 1995—1999 time periods. 7 bDr. James Lewis provided the sample collection period for a different article.51 He then helped us identify studies with overlapping patient populations from his group’s work to allow us to select the most representative study from his cohort of patients.54 cDr. Maura Gillison provided us with the sample collection period for this study. dDr. Francis Worden provided us with the sample collection period for this study. e Drs. James Rocco and Anthony Nichols provided the sample collection period for a different article.59 Subsequently, they helped us select the most inclusive analysis from studies of their patients to include in our analysis.60 fDrs. Bernard Fortin and Denis Soulieres provided us with the sample collection period for this study. Europe ‡ Median Year # of HPV+ OPSCCs Total # of OPSCCs Material Detection Method 64 2003 50 71 FFPE PCR 132 2004 71 109 FFPE PCR 133 2005 35 44 FFPE PCR 68 66 83 53 5/36 (1992), 12/29 (2005), 17/30 (2008) 9 200 143 PCR England PCR England 135a 1991 2 7 PCR England 136 137 138 70 139 140 2003 1997 1998 2004 1994 1996 69 5 41 146 14 32 138 5 60 314 75 52 p16 IHC, PCR PCR p16 IHC PCR PCR PCR England Finland Finland France France France 141 1996 24 138 PCR France b 1998 1 9 PCR Germany 142 2006 12 24 PCR Germany 143 144 72 145 2000 1998 1999 1998 24 7 30 12 31 16 106 24 PCR PCR PCR PCR Germany Germany Germany Germany 146 2004 13 52 FFPE FFPE Fresh frozen and FFPE FFPE Fresh frozen and FFPE FFPE Fresh frozen FFPE FFPE FFPE FFPE Fresh frozen and FFPE Fresh frozen Fresh frozen and FFPE FFPE Fresh frozen FFPE Fresh frozen Fresh frozen and FFPE p16 IHC p16 IHC 134 1995 1988 1992, 2005, 2008 2005 Czech Republic Czech Republic Czech Republic Denmark Denmark p16 IHC, PCR Germany 147 1996 51 162 PCR Germany, Netherlands 78c 1998 6 14 148 149 150 151 16 17 18 152 2009 2006 1994 1995 1972, 1990 1994, 2004 2004, 2006 2004 153 1999, 2002, 2004, 2006 10 66 17 9 24/63 (1972), 47/74 (1990) 3/166 (1994), 5/82 (2004) 40/52 (2004), 43/46 (2006) 12 15/26 (1999), 18/24 (2002), 22/26 (2004), 16/19 (2006) 7/30 (1974), 12/42 (1984), 48/84 (1994), 32/47 (2001) 60 15 Ref. # 15 74 81 154 155 1974, 1984, 1994, 2001 2003 1997 95 14 FFPE Country PCR Italy 21 120 90 78 137 248 98 69 Fresh frozen and FFPE Fresh frozen FFPE FFPE FFPE FFPE FFPE FFPE FFPE PCR p16 IHC PCR PCR PCR p16 IHC, PCR PCR PCR Italy Italy Italy Italy Norway Spain Sweden Sweden 95 FFPE PCR Sweden 203 FFPE PCR Sweden 77 25 FFPE Fresh frozen PCR PCR Sweden Sweden 8 156 157 87 158 159 160 89 91d 161e 162 10 2002 2003 1994 1986 1994 1995 1996 1987 1997 2003 1990, 1995, 2000, 2005, 2009, 2010 19 153 12 10 14 35 33 12 7 150 2/39 (1990), 3/37 (1995), 6/42 (2000), 12/59 (2005), 24/86 (2009), 18/62 (2010) 45 211 22 25 99 85 81 14 30 711 Fresh frozen FFPE Fresh frozen FFPE FFPE FFPE FFPE FFPE Fresh frozen FFPE PCR p16 IHC, PCR PCR PCR PCR p16 IHC ISH PCR PCR p16 IHC, PCR Sweden Sweden Sweden Sweden Switzerland Switzerland Netherlands Netherlands Netherlands Netherlands 325 Fresh frozen and FFPE p16 IHC, PCR Netherlands Total # of OPSCCs Material Detection Method Country 280 FFPE p16 IHC, PCR Australia 403 p16 IHC, PCR Australia PCR Brazil PCR PCR ISH PCR PCR PCR PCR ISH ISH PCR PCR PCR PCR p16 IHC, ISH, PCR PCR Brazil India India Israel Japan Japan Japan South Korea South Korea South Korea Taiwan Taiwan International aDr. John Field provided us with the sample collection period for this study. Jens Klussmann provided us with the sample collection period for this study. cDr. Aldo Venuti provided us with the sample collection period for this study. dDr. Peter Snijders provided us with the sample collection period for this study. eDr. Ruud Brakenhoff provided us with the sample collection period for this study. bDr. Other Ref. # ‡ Median Year # of HPV+ OPSCCs 11a 1988, 1993, 1998, 2003 95 1996 6/31 (1988), 11/52 (1993), 44/111 (1998), 40/86 (2003) 185 163 2003 6 91 164 165 166b 167 98 168 169c 100 170 171 172 173 174 1995 2010 1999 1984 2008 2003 1986 2005 2002 1998 1998 2001 2001 4 24 13 4 24 23 7 59 20 10 14 69 56 11 105 42 13 48 71 13 89 56 38 111 92 111 FFPE Fresh frozen and FFPE Fresh frozen Fresh frozen FFPE FFPE Fresh frozen FFPE Fresh frozen FFPE FFPE FFPE FFPE FFPE FFPE 175 2003 88 169 FFPE 176 1997 26 142 Fresh frozen aDrs. International International Barbara Rose and Angela Hong provided us with the number of OPSCCs analyzed in each of their discrete time periods since their study only described the percent that were HPV-positive without providing the total number of cancers evaluated. bDr. Rekha Kumar provided us with the sample collection period for this study. cDrs. Hiroyuki Mineta and Kiyoshi Misawa provided us with the sample collection period for this study. ‡ Median year: Median year of each study’s sample collection period. 9 Table S3. Number of articles and OPSCCs analyzed within each country. Country United States Canada Greenland Mexico Czech Republic Denmark England Finland France Germany Germany, Netherlands Italy Norway Spain Sweden Switzerland Netherlands Australia Brazil India Israel Japan South Korea Taiwan International Articles (n) Total OPSCCs (n) 33 5 1 1 3 2 4 2 4 7 2308 495 23 18 224 343 254 65 579 262 1 162 5 1 1 10 2 5 2 2 2 1 3 3 2 3 323 137 248 870 184 1161 683 102 147 13 132 183 203 422 10 References (Numbers 1—52 are the same as in the manuscript) 53. Begum S, Cao D, Gillison M, et al. Tissue distribution of human papillomavirus 16 DNA integration in patients with tonsillar carcinoma. Clin Cancer Res. 2005;11:5694-9. 54. Lewis JS, Jr., Thorstad WL, Chernock RD, et al. p16 positive oropharyngeal squamous cell carcinoma:an entity with a favorable prognosis regardless of tumor HPV status. Am J Surg Pathol. 2010;34:1088-96. 55. Chernock RD, El-Mofty SK, Thorstad WL, et al. HPV-related nonkeratinizing squamous cell carcinoma of the oropharynx: utility of microscopic features in predicting patient outcome. Head Neck Pathol. 2009;3:186-94. 56. Ritchie JM, Smith EM, Summersgill KF, et al. Human papillomavirus infection as a prognostic factor in carcinomas of the oral cavity and oropharynx. Int J Cancer. 2003;104:336-44. 57. Smith EM, Ritchie JM, Summersgill KF, et al. Age, sexual behavior and human papillomavirus infection in oral cavity and oropharyngeal cancers. Int J Cancer. 2004;108:766-72. 58. Schwartz SR, Yueh B, McDougall JK, et al. Human papillomavirus infection and survival in oral squamous cell cancer: a population-based study. Otolaryngol Head Neck Surg. 2001;125:1-9. 59. Nichols AC, Faquin WC, Westra WH, et al. HPV-16 infection predicts treatment outcome in oropharyngeal squamous cell carcinoma. Otolaryngol Head Neck Surg. 2009;140:228-34. 60. Nichols AC, Finkelstein DM, Faquin WC, et al. Bcl2 and human papilloma virus 16 as predictors of outcome following concurrent chemoradiation for advanced oropharyngeal cancer. Clin Cancer Res. 2010;16:2138-46. 61. Jiron J, Sethi S, Ali-Fehmi R, et al. Racial disparities in Human Papillomavirus (HPV) associated head and neck cancer. Am J Otolaryngol. 2014;35:147-53. 62. Sethi S, Ali-Fehmi R, Franceschi S, et al. Characteristics and survival of head and neck cancer by HPV status: a cancer registry-based study. Int J Cancer. 2012;131:1179-86. 63. Tachezy R, Klozar J, Salakova M, et al. HPV and other risk factors of oral cavity/oropharyngeal cancer in the Czech Republic. Oral Dis. 2005;11:181-5. 64. Klozar J, Kratochvil V, Salakova M, et al. HPV status and regional metastasis in the prognosis of oral and oropharyngeal cancer. Eur Arch Otorhinolaryngol. 2008;265 Suppl 1:S75-82. 65. Lassen P, Eriksen JG, Hamilton-Dutoit S, et al. Effect of HPV-associated p16INK4A expression on response to radiotherapy and survival in squamous cell carcinoma of the head and neck. J Clin Oncol. 2009;27:1992-8. 11 66. Lassen P, Eriksen JG, Hamilton-Dutoit S, et al. HPV-associated p16-expression and response to hypoxic modification of radiotherapy in head and neck cancer. Radiother Oncol. 2010;94:30-5. 67. Lassen P, Overgaard J, Eriksen JG. Expression of EGFR and HPV-associated p16 in oropharyngeal carcinoma: correlation and influence on prognosis after radiotherapy in the randomized DAHANCA 5 and 7 trials. Radiother Oncol. 2013;108:489-94. 68. Lassen P, Eriksen JG, Krogdahl A, et al. The influence of HPV-associated p16-expression on accelerated fractionated radiotherapy in head and neck cancer: evaluation of the randomised DAHANCA 6&7 trial. Radiother Oncol. 2011;100:49-55. 69. St Guily JL, Clavel C, Okais C, et al. Human papillomavirus genotype distribution in tonsil cancers. Head Neck Oncol. 2011;3:6. 70. St Guily JL, Jacquard AC, Pretet JL, et al. Human papillomavirus genotype distribution in oropharynx and oral cavity cancer in France--The EDiTH VI study. J Clin Virol. 2011;51:100-4. 71. Klussmann JP, Gultekin E, Weissenborn SJ, et al. Expression of p16 protein identifies a distinct entity of tonsillar carcinomas associated with human papillomavirus. Am J Pathol. 2003;162:747-53. 72. Reimers N, Kasper HU, Weissenborn SJ, et al. Combined analysis of HPV-DNA, p16 and EGFR expression to predict prognosis in oropharyngeal cancer. Int J Cancer. 2007;120:1731-8. 73. Klussmann JP, Weissenborn SJ, Wieland U, et al. Human papillomavirus-positive tonsillar carcinomas: a different tumor entity? Med Microbiol Immunol. 2003;192:129-32. 74. Klussmann JP, Weissenborn SJ, Wieland U, et al. Prevalence, distribution, and viral load of human papillomavirus 16 DNA in tonsillar carcinomas. Cancer. 2001;92:2875-84. 75. Wittekindt C, Gultekin E, Weissenborn SJ, et al. Expression of p16 protein is associated with human papillomavirus status in tonsillar carcinomas and has implications on survival. Adv Otorhinolaryngol. 2005;62:72-80. 76. Niedobitek G, Pitteroff S, Herbst H, et al. Detection of human papillomavirus type 16 DNA in carcinomas of the palatine tonsil. J Clin Pathol. 1990;43:918-21. 77. Badaracco G, Venuti A, Morello R, et al. Human papillomavirus in head and neck carcinomas: prevalence, physical status and relationship with clinical/pathological parameters. Anticancer Res. 2000;20:1301-5. 78. Venuti A, Badaracco G, Rizzo C, et al. Presence of HPV in head and neck tumours: high prevalence in tonsillar localization. J Exp Clin Cancer Res. 2004;23:561-6. 12 79. Alvarez Alvarez I, Sanchez Lazo P, Ramos Gonzalez S, et al. Using polymerase chain reaction to human papillomavirus in oral and pharyngolaryngeal carcinomas. Am J Otolaryngol. 1997;18:375-81. 80. Friesland S, Mellin H, Munck-Wikland E, et al. Human papilloma virus (HPV) and p53 immunostaining in advanced tonsillar carcinoma--relation to radiotherapy response and survival. Anticancer Res. 2001;21:529-34. 81. Hammarstedt L, Lindquist D, Dahlstrand H, et al. Human papillomavirus as a risk factor for the increase in incidence of tonsillar cancer. Int J Cancer. 2006;119:2620-3. 82. Mellin H, Friesland S, Lewensohn R, et al. Human papillomavirus (HPV) DNA in tonsillar cancer: clinical correlates, risk of relapse, and survival. Int J Cancer. 2000;89:300-4. 83. Mellin H, Friesland S, Auer G, et al. Human papillomavirus and DNA ploidy in tonsillar cancer--correlation to prognosis. Anticancer Res. 2003;23:2821-8. 84. Nasman A, Romanitan M, Nordfors C, et al. Tumor infiltrating CD8+ and Foxp3+ lymphocytes correlate to clinical outcome and human papillomavirus (HPV) status in tonsillar cancer. PLoS One. 2012;7:e38711. 85. Nasman A, Andersson E, Nordfors C, et al. MHC class I expression in HPV positive and negative tonsillar squamous cell carcinoma in correlation to clinical outcome. Int J Cancer. 2013;132:72-81. 86. Mellin Dahlstrand H, Lindquist D, Bjornestal L, et al. P16(INK4a) correlates to human papillomavirus presence, response to radiotherapy and clinical outcome in tonsillar carcinoma. Anticancer Res. 2005;25:4375-83. 87. Mellin H, Dahlgren L, Munck-Wikland E, et al. Human papillomavirus type 16 is episomal and a high viral load may be correlated to better prognosis in tonsillar cancer. Int J Cancer. 2002;102:152-8. 88. Straetmans JM, Olthof N, Mooren JJ, et al. Human papillomavirus reduces the prognostic value of nodal involvement in tonsillar squamous cell carcinomas. Laryngoscope. 2009;119:1951-7. 89. Hafkamp HC, Manni JJ, Haesevoets A, et al. Marked differences in survival rate between smokers and nonsmokers with HPV 16-associated tonsillar carcinomas. Int J Cancer. 2008;122:2656-64. 90. Snijders PJ, Cromme FV, van den Brule AJ, et al. Prevalence and expression of human papillomavirus in tonsillar carcinomas, indicating a possible viral etiology. Int J Cancer. 1992;51:845-50. 91. Snijders PJ, Steenbergen RD, Top B, et al. Analysis of p53 status in tonsillar carcinomas associated with human papillomavirus. J Gen Virol. 1994;75 ( Pt 10):2769-75. 13 92. Hafkamp HC, Speel EJ, Haesevoets A, et al. A subset of head and neck squamous cell carcinomas exhibits integration of HPV 16/18 DNA and overexpression of p16INK4A and p53 in the absence of mutations in p53 exons 5-8. Int J Cancer. 2003;107:394-400. 93. Hong AM, Dobbins TA, Lee CS, et al. Human papillomavirus predicts outcome in oropharyngeal cancer in patients treated primarily with surgery or radiation therapy. Br J Cancer. 2010;103:1510-7. 94. Li W, Thompson CH, O'Brien CJ, et al. Human papillomavirus positivity predicts favourable outcome for squamous carcinoma of the tonsil. Int J Cancer. 2003;106:553-8. 95. Hong AM, Martin A, Chatfield M, et al. Human papillomavirus, smoking status and outcomes in tonsillar squamous cell carcinoma. Int J Cancer. 2013;132:2748-54. 96. Hong A, Dobbins T, Lee CS, et al. Relationships between epidermal growth factor receptor expression and human papillomavirus status as markers of prognosis in oropharyngeal cancer. Eur J Cancer. 2010;46:2088-96. 97. Deng Z, Hasegawa M, Matayoshi S, et al. Prevalence and clinical features of human papillomavirus in head and neck squamous cell carcinoma in Okinawa, southern Japan. Eur Arch Otorhinolaryngol. 2011;268:1625-31. 98. Deng Z, Hasegawa M, Kiyuna A, et al. Viral load, physical status, and E6/E7 mRNA expression of human papillomavirus in head and neck squamous cell carcinoma. Head Neck. 2013;35:800-8. 99. Park K, Cho KJ, Lee M, et al. p16 immunohistochemistry alone is a better prognosticator in tonsil cancer than human papillomavirus in situ hybridization with or without p16 immunohistochemistry. Acta Otolaryngol. 2013;133:297304. 100. Lee M, Kim SB, Lee SW, et al. Human papillomavirus prevalence and cell cycle related protein expression in tonsillar squamous cell carcinomas of korean patients with clinicopathologic analysis. Korean J Pathol. 2013;47:14857. 101. Evans MF, Matthews A, Kandil D, et al. Discrimination of 'driver' and 'passenger' HPV in tonsillar carcinomas by the polymerase chain reaction, chromogenic in situ hybridization, and p16(INK4a) immunohistochemistry. Head Neck Pathol. 2011;5:344-8. 102. Andrews E, Seaman WT, Webster-Cyriaque J. Oropharyngeal carcinoma in non-smokers and non-drinkers: a role for HPV. Oral Oncol. 2009;45:486-91. 103. Brandsma JL, Abramson AL. Association of papillomavirus with cancers of the head and neck. Arch Otolaryngol Head Neck Surg. 1989;115:621-5. 14 104. Luginbuhl A, Sanders M, Spiro JD. Prevalence, morphology, and prognosis of human papillomavirus in tonsillar cancer. Ann Otol Rhinol Laryngol. 2009;118:742-9. 105. Sedaghat AR, Zhang Z, Begum S, et al. Prognostic significance of human papillomavirus in oropharyngeal squamous cell carcinomas. Laryngoscope. 2009;119:1542-9. 106. Ukpo OC, Pritchett CV, Lewis JE, et al. Human papillomavirus-associated oropharyngeal squamous cell carcinomas: primary tumor burden and survival in surgical patients. Ann Otol Rhinol Laryngol. 2009;118:368-73. 107. Cohen MA, Basha SR, Reichenbach DK, et al. Increased viral load correlates with improved survival in HPV-16-associated tonsil carcinoma patients. Acta Otolaryngol. 2008;128:583-9. 108. 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. 109. Westra WH, Taube JM, Poeta ML, et al. Inverse relationship between human papillomavirus-16 infection and disruptive p53 gene mutations in squamous cell carcinoma of the head and neck. Clin Cancer Res. 2008;14:366-9. 110. El-Mofty SK, Lu DW. Prevalence of human papillomavirus type 16 DNA in squamous cell carcinoma of the palatine tonsil, and not the oral cavity, in young patients: a distinct clinicopathologic and molecular disease entity. Am J Surg Pathol. 2003;27:1463-70. 111. Worden FP, Kumar B, Lee JS, et al. Chemoselection as a strategy for organ preservation in advanced oropharynx cancer: response and survival positively associated with HPV16 copy number. J Clin Oncol. 2008;26:313846. 112. Strome SE, Savva A, Brissett AE, et al. Squamous cell carcinoma of the tonsils: a molecular analysis of HPV associations. Clin Cancer Res. 2002;8:1093-100. 113. Schwartz SM, Daling JR, Doody DR, et al. Oral cancer risk in relation to sexual history and evidence of human papillomavirus infection. J Natl Cancer Inst. 1998;90:1626-36. 114. Ernster JA, Sciotto CG, O'Brien MM, et al. Rising incidence of oropharyngeal cancer and the role of oncogenic human papilloma virus. Laryngoscope. 2007;117:2115-28. 115. Wang XI, Thomas J, Zhang S. Changing trends in human papillomavirus-associated head and neck squamous cell carcinoma. Ann Diagn Pathol. 2012;16:7-12. 15 116. Wilczynski SP, Lin BT, Xie Y, et al. Detection of human papillomavirus DNA and oncoprotein overexpression are associated with distinct morphological patterns of tonsillar squamous cell carcinoma. Am J Pathol. 1998;152:145-56. 117. Ang KK, Harris J, Wheeler R, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med. 2010;363:24-35. 118. Ringstrom E, Peters E, Hasegawa M, et al. Human papillomavirus type 16 and squamous cell carcinoma of the head and neck. Clin Cancer Res. 2002;8:3187-92. 119. Paz IB, Cook N, Odom-Maryon T, et al. Human papillomavirus (HPV) in head and neck cancer. An association of HPV 16 with squamous cell carcinoma of Waldeyer's tonsillar ring. Cancer. 1997;79:595-604. 120. Jo S, Juhasz A, Zhang K, et al. Human papillomavirus infection as a prognostic factor in oropharyngeal squamous cell carcinomas treated in a prospective phase II clinical trial. Anticancer Res. 2009;29:1467-74. 121. Cohen MA, Weinstein GS, O'Malley BW, Jr., et al. Transoral robotic surgery and human papillomavirus status: Oncologic results. Head Neck. 2011;33:573-80. 122. Weinberger PM, Yu Z, Haffty BG, et al. Molecular classification identifies a subset of human papillomavirus--associated oropharyngeal cancers with favorable prognosis. J Clin Oncol. 2006;24:736-47. 123. Lohavanichbutr P, Houck J, Fan W, et al. Genomewide gene expression profiles of HPV-positive and HPVnegative oropharyngeal cancer: potential implications for treatment choices. Arch Otolaryngol Head Neck Surg. 2009;135:180-8. 124. Hess CB, Rash DL, Daly ME, et al. Competing Causes of Death and Medical Comorbidities Among Patients With Human Papillomavirus-Positive vs Human Papillomavirus-Negative Oropharyngeal Carcinoma and Impact on Adherence to Radiotherapy. JAMA Otolaryngol Head Neck Surg. 2014. 125. Chuang AY, Chuang TC, Chang S, et al. Presence of HPV DNA in convalescent salivary rinses is an adverse prognostic marker in head and neck squamous cell carcinoma. Oral Oncol. 2008;44:915-9. 126. Ragin CC, Taioli E, Weissfeld JL, et al. 11q13 amplification status and human papillomavirus in relation to p16 expression defines two distinct etiologies of head and neck tumours. Br J Cancer. 2006;95:1432-8. 127. Thibaudeau E, Fortin B, Coutlee F, et al. HPV Prevalence and Prognostic Value in a Prospective Cohort of 255 Patients with Locally Advanced HNSCC: A Single-Centre Experience. Int J Otolaryngol. 2013;2013:437815. 16 128. Machado J, Reis PP, Zhang T, et al. Low prevalence of human papillomavirus in oral cavity carcinomas. Head Neck Oncol. 2010;2:6. 129. Shi W, Kato H, Perez-Ordonez B, et al. Comparative prognostic value of HPV16 E6 mRNA compared with in situ hybridization for human oropharyngeal squamous carcinoma. J Clin Oncol. 2009;27:6213-21. 130. Chau NG, Perez-Ordonez B, Zhang K, et al. The association between EGFR variant III, HPV, p16, c-MET, EGFR gene copy number and response to EGFR inhibitors in patients with recurrent or metastatic squamous cell carcinoma of the head and neck. Head Neck Oncol. 2011;3:11. 131. Ibieta-Zarco BR, Carrillo-Garcia A, Ponce-de-Leon-Rosales S, et al. Frequency and genotype distribution of multiple human papillomavirus infections in cancer of the head and neck in a Mexican population. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012;114:350-7. 132. Rotnaglova E, Tachezy R, Salakova M, et al. HPV involvement in tonsillar cancer: prognostic significance and clinically relevant markers. Int J Cancer. 2011;129:101-10. 133. Laco J, Nekvindova J, Novakova V, et al. Biologic importance and prognostic significance of selected clinicopathological parameters in patients with oral and oropharyngeal squamous cell carcinoma, with emphasis on smoking, protein p16(INK4a) expression, and HPV status. Neoplasma. 2012;59:398-408. 134. Heath S, Willis V, Allan K, et al. Clinically significant human papilloma virus in squamous cell carcinoma of the head and neck in UK practice. Clin Oncol (R Coll Radiol). 2012;24:e18-23. 135. Snijders PJ, Scholes AG, Hart CA, et al. Prevalence of mucosotropic human papillomaviruses in squamouscell carcinoma of the head and neck. Int J Cancer. 1996;66:464-9. 136. Evans M, Newcombe R, Fiander A, et al. Human Papillomavirus-associated oropharyngeal cancer: an observational study of diagnosis, prevalence and prognosis in a UK population. BMC Cancer. 2013;13:220. 137. Koskinen WJ, Chen RW, Leivo I, et al. Prevalence and physical status of human papillomavirus in squamous cell carcinomas of the head and neck. Int J Cancer. 2003;107:401-6. 138. Lundberg M, Leivo I, Saarilahti K, et al. Increased incidence of oropharyngeal cancer and p16 expression. Acta Otolaryngol. 2011;131:1008-11. 139. Fouret P, Monceaux G, Temam S, et al. Human papillomavirus in head and neck squamous cell carcinomas in nonsmokers. Arch Otolaryngol Head Neck Surg. 1997;123:513-6. 17 140. Charfi L, Jouffroy T, de Cremoux P, et al. Two types of squamous cell carcinoma of the palatine tonsil characterized by distinct etiology, molecular features and outcome. Cancer Lett. 2008;260:72-8. 141. Jung AC, Briolat J, Millon R, et al. Biological and clinical relevance of transcriptionally active human papillomavirus (HPV) infection in oropharynx squamous cell carcinoma. Int J Cancer. 2010;126:1882-94. 142. Hoffmann M, Tribius S, Quabius ES, et al. HPV DNA, E6*I-mRNA expression and p16INK4A immunohistochemistry in head and neck cancer - how valid is p16INK4A as surrogate marker? Cancer Lett. 2012;323:8896. 143. Glombitza F, Guntinas-Lichius O, Petersen I. HPV status in head and neck tumors. Pathol Res Pract. 2010;206:229-34. 144. Fischer M, von Winterfeld F. Evaluation and application of a broad-spectrum polymerase chain reaction assay for human papillomaviruses in the screening of squamous cell tumours of the head and neck. Acta Otolaryngol. 2003;123:752-8. 145. Hoffmann M, Gorogh T, Gottschlich S, et al. Human papillomaviruses in head and neck cancer: 8 yearsurvival-analysis of 73 patients. Cancer Lett. 2005;218:199-206. 146. Semrau R, Duerbaum H, Temming S, et al. Prognostic impact of human papillomavirus status, survivin, and epidermal growth factor receptor expression on survival in patients treated with radiochemotherapy for very advanced nonresectable oropharyngeal cancer. Head Neck. 2013;35:1339-44. 147. Mooren JJ, Gultekin SE, Straetmans JM, et al. P16(INK4A) immunostaining is a strong indicator for highrisk-HPV-associated oropharyngeal carcinomas and dysplasias, but is unreliable to predict low-risk-HPV-infection in head and neck papillomas and laryngeal dysplasias. Int J Cancer. 2014;134:2108-17. 148. Bussu F, Sali M, Gallus R, et al. HPV infection in squamous cell carcinomas arising from different mucosal sites of the head and neck region. Is p16 immunohistochemistry a reliable surrogate marker? Br J Cancer. 2013;108:115762. 149. Granata R, Miceli R, Orlandi E, et al. Tumor stage, human papillomavirus and smoking status affect the survival of patients with oropharyngeal cancer: an Italian validation study. Ann Oncol. 2012;23:1832-7. 150. Licitra L, Perrone F, Bossi P, et al. High-risk human papillomavirus affects prognosis in patients with surgically treated oropharyngeal squamous cell carcinoma. J Clin Oncol. 2006;24:5630-6. 18 151. Fallai C, Perrone F, Licitra L, et al. Oropharyngeal squamous cell carcinoma treated with radiotherapy or radiochemotherapy: prognostic role of TP53 and HPV status. Int J Radiat Oncol Biol Phys. 2009;75:1053-9. 152. Marklund L, Nasman A, Ramqvist T, et al. Prevalence of human papillomavirus and survival in oropharyngeal cancer other than tonsil or base of tongue cancer. Cancer Med. 2012;1:82-8. 153. Attner P, Du J, Nasman A, et al. The role of human papillomavirus in the increased incidence of base of tongue cancer. Int J Cancer. 2010;126:2879-84. 154. Nordfors C, Grun N, Tertipis N, et al. CD8(+) and CD4(+) tumour infiltrating lymphocytes in relation to human papillomavirus status and clinical outcome in tonsillar and base of tongue squamous cell carcinoma. Eur J Cancer. 2013;49:2522-30. 155. Dahlgren L, Mellin H, Wangsa D, et al. Comparative genomic hybridization analysis of tonsillar cancer reveals a different pattern of genomic imbalances in human papillomavirus-positive and -negative tumors. Int J Cancer. 2003;107:244-9. 156. Hansson BG, Rosenquist K, Antonsson A, et al. Strong association between infection with human papillomavirus and oral and oropharyngeal squamous cell carcinoma: a population-based case-control study in southern Sweden. Acta Otolaryngol. 2005;125:1337-44. 157. Attner P, Nasman A, Du J, et al. Survival in patients with human papillomavirus positive tonsillar cancer in relation to treatment. Int J Cancer. 2012;131:1124-30. 158. Dahlgren L, Dahlstrand HM, Lindquist D, et al. Human papillomavirus is more common in base of tongue than in mobile tongue cancer and is a favorable prognostic factor in base of tongue cancer patients. Int J Cancer. 2004;112:1015-9. 159. Lindel K, Beer KT, Laissue J, et al. Human papillomavirus positive squamous cell carcinoma of the oropharynx: a radiosensitive subgroup of head and neck carcinoma. Cancer. 2001;92:805-13. 160. Fischer CA, Zlobec I, Green E, et al. Is the improved prognosis of p16 positive oropharyngeal squamous cell carcinoma dependent of the treatment modality? Int J Cancer. 2010;126:1256-62. 161. van Houten VM, Snijders PJ, van den Brekel MW, et al. Biological evidence that human papillomaviruses are etiologically involved in a subgroup of head and neck squamous cell carcinomas. Int J Cancer. 2001;93:232-5. 19 162. Rietbergen MM, Martens-de Kemp SR, Bloemena E, et al. Cancer stem cell enrichment marker CD98: A prognostic factor for survival in patients with human papillomavirus-positive oropharyngeal cancer. Eur J Cancer. 2014;50:765-73. 163. Lopez RV, Levi JE, Eluf-Neto J, et al. Human papillomavirus (HPV) 16 and the prognosis of head and neck cancer in a geographical region with a low prevalence of HPV infection. Cancer Causes Control. 2014;25:461-71. 164. Miguel RE, Villa LL, Cordeiro AC, et al. Low prevalence of human papillomavirus in a geographic region with a high incidence of head and neck cancer. Am J Surg. 1998;176:428-9. 165. Bahl A, Kumar P, Dar L, et al. Prevalence and trends of human papillomavirus in oropharyngeal cancer in a predominantly north Indian population. Head Neck. 2013. 166. Kumar RV, Kadkol SS, Daniel R, et al. Human papillomavirus, p53 and cyclin D1 expression in oropharyngeal carcinoma. Int J Oral Maxillofac Surg. 2003;32:539-43. 167. Niv A, Sion-Vardi N, Gatot A, et al. Identification and typing of human papillomavirus (HPV) in squamous cell carcinoma of the oral cavity and oropharynx. J Laryngol Otol. 2000;114:41-6. 168. Mizumachi T, Kano S, Sakashita T, et al. Improved survival of Japanese patients with human papillomavirus-positive oropharyngeal squamous cell carcinoma. Int J Clin Oncol. 2013;18:824-8. 169. Mineta H, Ogino T, Amano HM, et al. Human papilloma virus (HPV) type 16 and 18 detected in head and neck squamous cell carcinoma. Anticancer Res. 1998;18:4765-8. 170. Song JS, Kim MS, Park JW, et al. Expression of human papillomavirus-related proteins and its clinical implication in tonsillar squamous cell carcinoma. Korean J Pathol. 2012;46:177-86. 171. Na, II, Kang HJ, Cho SY, et al. EGFR mutations and human papillomavirus in squamous cell carcinoma of tongue and tonsil. Eur J Cancer. 2007;43:520-6. 172. Chien CY, Su CY, Fang FM, et al. Lower prevalence but favorable survival for human papillomavirusrelated squamous cell carcinoma of tonsil in Taiwan. Oral Oncol. 2008;44:174-9. 173. Kuo KT, Hsiao CH, Lin CH, et al. The biomarkers of human papillomavirus infection in tonsillar squamous cell carcinoma-molecular basis and predicting favorable outcome. Mod Pathol. 2008;21:376-86. 174. Posner MR, Lorch JH, Goloubeva O, et al. Survival and human papillomavirus in oropharynx cancer in TAX 324: a subset analysis from an international phase III trial. Ann Oncol. 2011;22:1071-7. 20 175. Rischin D, Young RJ, Fisher R, et al. Prognostic significance of p16INK4A and human papillomavirus in patients with oropharyngeal cancer treated on TROG 02.02 phase III trial. J Clin Oncol. 2010;28:4142-8. 176. Herrero R, Castellsague X, Pawlita M, et al. Human papillomavirus and oral cancer: the International Agency for Research on Cancer multicenter study. J Natl Cancer Inst. 2003;95:1772-83. 21