Acessibilidade / Reportar erro

Survival Outcome in True Carcinoma of Unknown Primary (tCUP) with p16 + Cervical Metastasis

Abstract

Introduction

Age and lymph node ratio have been attributed as independent predictors for survival and recurrence in carcinoma of unknown primary (CUP).

Objective

The purpose of this study was to analyze the prognostic value of p16 overexpression for CUP in the absence of true primary (TP).

Methods

The study involved 43 patients who underwent therapeutic lymph node dissection (LND) from 2000 to 2015 after all the diagnostic work up for CUP. Immunohistochemistry for p16 overexpression was performed. Cox proportional hazard regression analysis was used to analyze the prognostic impact on 5-year overall survival (OS) and recurrence-free survival (RFS).

Results

The male-to-female ratio was 5.1:1, with a median age of 62 years. The clinicopathological data, except for p16 overexpression, did not differ significantly in terms of 5-year OS and RFS. The Cox regression analysis proposed p16 positivity to be an independent prognosticator of regional recurrence-free survival (RRFS) (hazard ratio [HR] 6.180, p = 0.21). The median time to recurrence and death were 10 and 25 months, respectively.

Conclusion

Cervical metastasis with p16 overexpression is a significant prognostic factor of improved RFS after surgery in CUP. The prognostic significance of lymph node p16 positivity should be further studied.

Keywords
unknown primary; neoplasm metastasis; head and neck neoplasms

Introduction

Carcinoma of unknown primary (CUP) is a rare disease among head and neck cancers, accounting for only 3 to 7% of cases.11 Miller FR, Karnad AB, Eng T, Hussey DH, Stan McGuff H, Otto RA. Management of the unknown primary carcinoma: long-term follow-up on a negative PET scan and negative panendoscopy. Head Neck 2008;30(01):28–34,22 Galloway TJ, Ridge JA. Management of Squamous Cancer Metastatic to Cervical Nodes With an Unknown Primary Site. J Clin Oncol 2015;33(29):3328–3337 Carcinoma of unknown primary is defined as cervical metastasis without any evidence of the primary tumor despite comprehensive history, clinical examination, morphologic/ metabolic imaging, examination under anesthesia (EUA) and direct biopsies.33 Pavlidis N, Khaled H, Gaafar R. A mini review on cancer of unknown primary site: A clinical puzzle for the oncologists. J Adv Res 2015;6(03):375–382,44 Pavlidis N, Pentheroudakis G, Plataniotis G. Cervical lymph node metastases of squamous cell carcinoma from an unknown primary site: a favourable prognosis subset of patients with CUP. Clin Transl Oncol 2009;11(06):340–348 The primary tumor may remain undetected in 5 to 10% of cases after all the diagnostic work up.55 Guntinas-Lichius O, Peter Klussmann J, Dinh S, et al. Diagnostic work-up and outcome of cervical metastases from an unknown primary. Acta Otolaryngol 2006;126(05):536–544 Subclinical dormancy or early spontaneous regression are the possible carcinogenic theories responsible for no identification of the primary site.66 Challis GB, Stam HJ. The spontaneous regression of cancer. A review of cases from 1900 to 1987. Acta Oncol 1990;29(05):545–550,77 van de Wouw AJ, Jansen RL, Speel EJ, Hillen HF. The unknown biology of the unknown primary tumour: a literature review. Ann Oncol 2003;14(02):191–196 The metastatic lymph nodes (LNs) most commonly contain squamous cell carcinoma (53–80%) followed by undifferentiated carcinomas (13–14%) and adenocarcinomas (13%).88 Boscolo-Rizzo P, Da Mosto MC, Gava A, Marchiori C. Cervical lymph node metastases from occult squamous cell carcinoma: analysis of 82 cases. ORL J Otorhinolaryngol Relat Spec 2006;68 (04):189–194,99 Koivunen P, Laranne J, Virtaniemi J, et al. Cervical metastasis of unknown origin: a series of 72 patients. Acta Otolaryngol 2002; 122(05):569–574,1010 Villeneuve H, Després P, Fortin B, et al. Cervical lymph node metastases from unknown primary cancer: a single-institution experience with intensity-modulated radiotherapy. Int J Radiat Oncol Biol Phys 2012;82(05):1866–1871,1111 Haas I, Hoffmann TK, Engers R, Ganzer U. Diagnostic strategies in cervical carcinoma of an unknown primary (CUP). Eur Arch Otorhinolaryngol 2002;259(06):325–333 The rarity of the disease has led to a wide range of small retrospective studies using various diagnostic criteria and treatment strategies.1212 Müller von der Grün J, Bon D, Rödel C, Balermpas P. Patterns of care analysis for head & neck cancer of unknown primary site: a survey inside the German society of radiation oncology (DEGRO). Strahlenther Onkol 2018;194(08):750–758 There is increasing evidence on the prevalence of human papillomavirus (HPV)-related squamous cell carcinoma of unknown primary (SCCUP) showing better outcomes in terms of treatment response and survival while demonstrating a weaker association with smoking and alcohol.1313 O’Rorke MA, Ellison MV, Murray LJ, Moran M, James J, Anderson LA. Human papillomavirus related head and neck cancer survival: a systematic review and meta-analysis. Oral Oncol 2012;48(12): 1191–1201,1414 Dixon PR, Au M, Hosni A, et al. Impact of p16 expression, nodal status, and smoking on oncologic outcomes of patients with head and neck unknown primarysquamous cellcarcinoma. Head Neck 2016;38(09):1347–1353 In HPV-induced CUP, p16INK4 overexpression has been considered a surrogate marker correlated with survival outcomes, but its role as an independent predictor has remained controversial. Interestingly, p16 overexpression is not only the trademark of HPV-driven SCCUP, but it also has a strong association with cutaneous squamous cell carcinoma as well as with branchial cyst. This requires further confirmation of HPV presence by performing in-situ hybridization (ISH) or polymerase chain reaction (PCR) in SCCUP.1515 Rassy E, Nicolai P, Pavlidis N. Comprehensive management of HPV-related squamous cell carcinoma of the head and neck of unknown primary. Head Neck 2019;41(10):3700–3711 The objective of the present study was to evaluate the prognostic value of p16 overexpression in cervical LNs of CUP in terms of overall and RRFS. Apart from that, age and LNR have also been incorporated to determine their role as predictors of survival in CUP.

Materials and Methods

Patient Cohort

In this multicenter, retrospective study, 94 patients with CUP of the head and neck have been treated from 2000 to 2015 at the departments of otorhinolaryngology, head and neck surgery of the Vienna General Hospital (University Hospital of the Medical University of Vienna), Kaiser-Franz-Josef Hospital (Vienna), Hanusch Hospital (Vienna), and Rudolfstiftung Teaching Hospital (Vienna). In order to analyze a homogeneous patient cohort, patients had to fulfill criteria tobe included in our study. Patients hadtobe initially treated with lymph node dissection (LND) followed by adjuvant RT. Thus, patients with primary RT (n = 10, 10.6%), palliative therapy protocol (n = 6, 6.4%) or prematurely terminated therapy (n = 2, 2.1%) were excluded. Another exclusion criterion was the emergence of the primary tumor before completion of treatment. Patients with distant metastases at the time of diagnosis were excluded. Furthermore, sufficient documentation of the performed diagnostic methods was mandatory. Hence, 42 (45.7%) of the 94 CUP patients were included in this study. Based on the median LNR of 0.05 in our cohort, the cut-off of 0.05 was selected to divide the sample into roughly equal sized groups.

Diagnostic Methods

The standard diagnostic algorithm of the Medical University of Vienna comprises a non-invasive and an invasive part. First, a detailed anamnesis, clinical examination including flexible nasopharyngoscopy, ultrasound of the neck, chest X-ray, and computed tomography (CT) or magnetic resonance imaging (MRI) are performed. In addition, the 18F-FDG-PET-CT has become part of the algorithm from 1999 on. Subsequently, fine-needle aspiration cytology (FNAC), panendoscopy, and diagnostic tonsillectomy are carried out.

Treatment Methods

Cervical LN metastases were initially treated with LND. Depending on the spread of LN metastases, unilateral or bilateral ND was performed. Subsequently, all patients with N2/N3 disease without extracapsular extension (ENE) were irradiated either unilaterally or bilaterally using three-dimensional conformal radiation therapy (3D-CRT), intensity-modulated radiation therapy (IMRT), or volumetric modulated arc therapy (VMAT) technique. Furthermore, chemotherapy (CTX) was applied in certain patients based on extracapsular extension of the nodal disease.

Statistical Methods

The IBM SPSS Statistics for Windows, version 24.0 (IBM Corp., Armonk, NY, USA) was used for the statistical analyses. The t-test was performed to analyze the distribution of the age. The Kaplan-Meier analysis was used to determine the impact of clinical variables on 5-year overall survival(OS) and 5-year regional recurrence-free survival (RFS) and corresponding p-values were obtained via log-rank test. Kaplan-Meier curves (►Figures 1 2) were created in GraphPad Prism 8 (GraphPad Software Inc., La Jolla, CA, USA).

Fig. 1
Overall survival for patients having metastatic lymph nodes containing p16 overexpression.

Fig. 2
Regional recurrence-free survival (RRFS) for patients having metastatic lymph nodes containing p16 overexpression.

Results

Patient Characteristics

The median ageof the patients was 62.00 years (range: 44–86) with a male-to-female ratio of 5.1 to 1. Nicotine consumption with an average of 20 cigarettes per day was documented in 67.4% of the patients. More frequent or excessive consumption of alcohol was stated in 62.8% of the patients, whereas cancer family history was positive in 39.5% (►Table 1.)

Table 1
Patient characteristics and details of diagnostic methods

Diagnostic Methods

Radiologically, the head and neck are a were examined by using CT in 88.4% of the patients, while MRI was performed in 51.2% of the cases. The 18F-FDG-PET-CT was applied either before RT or during the examinations/follow up in 65.1% of patients.

FNAC was performed in 27.9% of the patients while panendoscopy was indicated in 90.7% of cases. Due to the lack of documentation in 4 patients, it can be assumed that all patients were examined endoscopically. Tonsillectomy was carried out in 41.9% of the patients while tonsils have already been removed in 44.2% of cases (►Table 1).

Details of the Cervical LN Metastases

The most commonly affected areas of the neck were levels II and III (cumulatively: 81.7%). Lymph node metastases occurred in 57.6% of patients in the territory of level II, while level III was affected in 7.6% of cases. Moreover, LNs were classified according to the American Joint Committee on Cancer (AJCC) as follows: 11.9% of the patients were staged as N1, 21.4% as N2a, 57.1% as N2b, 2.3% as N2c, and 7.1% as N3, respectively. Squamous cell carcinoma (SCC) was found in 100% of cases

In most cases, the tumor was found to be moderately-to-poorly differentiated (G2–G3, cumulatively: 94.1%). (►Table 2).

Table 2
Details of lymph node metastases and treatment methods

P16 Immunohistochemistry and Overexpression

Immunohistochemistry for p16 was performed on LN after dissection using a CINTec p16 Histology Kit (MTM Laboratories; Roche Applied Sciences, Penzberg, Germany) according to the manufacturer’s protocol.1616 Deng Z, Hasegawa M, Aoki K, et al. A comprehensive evaluation of human papillomavirus positive status and p16INK4a overexpression as a prognostic biomarker in head and neck squamous cell carcinoma. Int J Oncol 2014;45(01):67–76 The defined criteria for p1 6 overexpression was ≥ 75% positive cells and at least moderate staining intensity on immunohistochemistry. The cumulative results in our cohort showed 55.8% cases to be positive for p16 overexpression (►Table 2).

Clinical Outcome and Survival Analysis

Within a median follow-up time of 47.00 months, the mortality rate was 32.6%, whereas regional recurrences (RRs) occurred in 28.6% of the patients.

By using a Kaplan-Meier survival analysis, the estimated 5-year OS and RRFS were 67.4% and 71.4%, respectively (►Figures 1, 2). Within the 5-year observation period, the median time until death was 25.00 months, while RR occurred after a median time of 10.00 months.

The emergence of distant metastases was observed in 3 patients (7%) (►Table 3). The distribution of metastases localization was: lung (n = 1), bones (n = 1), and liver and bones (n = 1). Moreover, generalized metastases were found in two patients during the autopsy. Primary tumor has emerged in 6 patients (oropharynx = 4, hypopharynx = 1, larynx = 1) in the follow-up. The occurrence of the primary tumor has led to a 5-year OS of 55.6% (p = 0.50). Furthermore, distant metastases had a significantly worsening impact on the 5-year OS (p = -0.005). A univariate Cox-regression analysis was performed to determine the impact of potential prognosticators affecting the 5-year OS and RFS. Tumor grade, nodal disease volume, distant metastasis, and the emergence of the primary tumor in subsequent course of treatment or follow-up did not adversely affect survival. Only p16 overexpression has been documented as the potential factor improving 5-year RFS (HR =6.180, p = 0.021) (►Table 4). A LNR>0.05 has shown adverse outcome in both OS and RFS (HR 1.725 and 1.720, respectively) when compared with LNR < 0.05.

Table 3
Outcome analysis
Table 4
Kaplan-Meier and Cox regression analyses

Discussion

The prognostic value of p16 overexpression in head and neck cancers has been well documented in the background of HPV-driven oropharyngeal primary tumors presenting with cervical metastasis.1717 Mork J, Lie AK, Glattre E, et al. Human papillomavirus infection as a risk factor for squamous-cell carcinoma of the head and neck. N Engl J Med 2001;344(15):1125–1131,1818 D’Souza G, Kreimer AR, Viscidi R, et al. Case-control study of human papillomavirus and oropharyngeal cancer. N Engl J Med 2007;356(19):1944–1956 The recent AJCC 8th edition TNM classification has demarcated HPV mediated p1 6 positive (+) from non-HPV p16 negative (-) oropharyngeal carcinomas for better prognostic categorization.1919 Lydiatt WM, Patel SG, O’Sullivan B, et al. Head and Neck cancers-major changes in the American Joint Committee on cancer eighth edition cancer staging manual. CA Cancer J Clin 2017;67(02): 122–137 Despite the scarcity of randomized controlled trials and prospective studies, multiple prognostic factors have been identified from retrospective series, including HPV (p16 +) oropharyngeal SCC, patient’s age, nodal disease volume, extra nodal extension, and p53 status.2020 Keller LM, Galloway TJ, Holdbrook T, et al. p16 status, pathologic and clinical characteristics, biomolecular signature, and longterm outcomes in head and neck squamous cell carcinomas of unknown primary. Head Neck 2014;36(12):1677–1684,2121 Axelsson L, Nyman J, Haugen-Cange H, et al. Prognostic factors for head and neck cancer of unknown primary including the impact of human papillomavirus infection. J Otolaryngol Head Neck Surg 2017;46(01):45,2222 Jensen DH, Hedback N, Specht L, et al. Human papillomavirus in head and necksquamous cell carcinoma of unknownprimary is a common event and a strong predictor of survival. PLoS One 2014; 9(11):e110456,2323 Schroeder L, Wichmann G, Willner M, et al. Antibodies against human papillomaviruses as diagnostic and prognostic biomarker in patients with neck squamous cell carcinoma from unknown primary tumor. Int J Cancer 2018;142(07):1361–1368,2424 Graboyes EM, Sinha P, Thorstad WL, Rich JT, Haughey BH. Management of human papillomavirus-related unknown primaries of the head and neck with a transoral surgical approach. Head Neck 2015;37(11):1603–1611 Advanced age, high nodal disease volume, p1 6 negativity, and macroscopic extra nodal extension (≥ 2 mm) are considered to be the predictors of poor survival.2020 Keller LM, Galloway TJ, Holdbrook T, et al. p16 status, pathologic and clinical characteristics, biomolecular signature, and longterm outcomes in head and neck squamous cell carcinomas of unknown primary. Head Neck 2014;36(12):1677–1684,2121 Axelsson L, Nyman J, Haugen-Cange H, et al. Prognostic factors for head and neck cancer of unknown primary including the impact of human papillomavirus infection. J Otolaryngol Head Neck Surg 2017;46(01):45,2525 Bersani C, Sivars L, Haeggblom L, et al. Targeted sequencing of tonsillar and base of tongue cancer and human papillomavirus positive unknown primary of the head and neck reveals prognostic effects of mutated FGFR3. Oncotarget 2017;8(21): 35339–35350,2626 Sivars L, Näsman A, Tertipis N, et al. Human papillomavirus and p53 expression in cancer of unknown primary in the head and neck region in relation to clinical outcome. Cancer Med 2014;3 (02):376–384 The most common LNs harboring metastasis in CUP usually reside at levels II (46.9%) and III (26.6%), with the majority having N2 (79%) and N3 (7%) disease. Previous studies have reported poor prognosis in the advanced nodal (N2b-N3) stage as compared to N1 and N2a combined.2121 Axelsson L, Nyman J, Haugen-Cange H, et al. Prognostic factors for head and neck cancer of unknown primary including the impact of human papillomavirus infection. J Otolaryngol Head Neck Surg 2017;46(01):45,2727 Hung YH, Liu SA, Wang CC, Wang CP, Jiang RS, Wu SH. Treatment outcomes of unknown primary squamous cell carcinoma of the head and neck. PLoS One 2018;13(10):e0205365 Our results have shown no significant survival difference between N1 and N2a and N2b and N3 disease (77.1% vs 61.8%, p = 0.887).

Distant metastasis in CUP has been reported in approximately 5 to 40% of patients within the first 2 years of treatment.2828 Adams JR, O’Brien CJ. Unknownprimarysquamouscellcarcinoma of the head and neck: a review of diagnosis, treatment and outcomes. Asian J Surg 2002;25(02):188–193 All the patients in our study who developed distant metastasis (7%) have depicted poor 5-year survival outcome (p = 0.005).

The detection of p16 or HPV in cervical LN metastasis helps in localizing the primary tumor site in the oropharyngeal region.2929 Begum S, Gillison ML, Ansari-Lari MA, Shah K, Westra WH. Detection of human papillomavirus in cervical lymph nodes: a highly effective strategy for localizing site of tumor origin. Clin Cancer Res 2003;9(17):6469–6475,3030 Zhang MQ, El-Mofty SK, Dávila RM. Detection of human papillomavirus-related squamous cell carcinoma cytologically and by in situ hybridization in fine-needle aspiration biopsies of cervical metastasis: a tool for identifying the site of an occult head and neck primary. Cancer 2008;114(02):118–123 Despite an extensive diagnostic work up, primary tumor remains undetected in 2 to 9% of patients.3131 Le NS, Janik S, Simmel H, Erovic BM. Bilateral vs ipsilateral adjuvant radiotherapy in patients with cancer of unknown primary of the head and neck: An analysis of the clinical outcome and radiation-induced side effects. Head Neck 2019;41(06): 1785–1794 Therefore, we decided to evaluate the prognostic value of p16 immuno-positivity in cervical LNs and other related clinicopathological factors in our cohort of CUP patients. Dixon et al. have reported a controversial association between LN positivity of p16 and survival outcome as predictor of OS. A recent study has demonstrated age and LN ratio as significant risk factors for survival and recurrence but failed to find a prognostic significance of p16 positivity in metastatic LNs. Human papilloma-virus or p16 positivity are documented as the most important prognostic determinants in oropharyngeal and other head and neck squamous cell carcinomas1313 O’Rorke MA, Ellison MV, Murray LJ, Moran M, James J, Anderson LA. Human papillomavirus related head and neck cancer survival: a systematic review and meta-analysis. Oral Oncol 2012;48(12): 1191–1201,3232 Ang KK, Harris J, Wheeler R, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med 2010;363(01):24–35,3333 Sedghizadeh PP, Billington WD, Paxton D, et al. Is p16-positive oropharyngeal squamous cell carcinoma associated with favorable prognosis? A systematic review and meta-analysis. Oral Oncol 2016;54:15–27]. Similarly, Cho et al. have failed to determine a significant role of p16 in OS and DFS.3434 Cho WK, Roh JL, Cho KJ, Choi SH, Nam SY, Kim SY. Predictors of survival and recurrence after primary surgery for cervical metastasis of unknown primary. J Cancer Res Clin Oncol 2020;146(04): 925–933 A recent analysis comprising 3 Radiation Therapy Oncology Group trials has shown p16 + rate of 19.2% in non-oropharyngeal primaries but could not find a convincing relationship between p16 and HPV.3535 Chung CH, Zhang Q, Kong CS, et al. p16 protein expression and human papillomavirus status as prognostic biomarkers of non-oropharyngeal head and neck squamous cell carcinoma. J Clin Oncol 2014;32(35):3930–3938 Similarly, McDowell et al. have found p16 + cervical LNs in 31% of cutaneous SCC but could not establish significant clinical outcome.3636 McDowell LJ, Young RJ, Johnston ML, et al. p16-positive lymph node metastases from cutaneous head and neck squamous cell carcinoma: No association with high-risk human papillomavirus or prognosis and implications for the workup of the unknown primary. Cancer 2016;122(08):1201–1208

Age and LNR have been identified as potential factors impacting survival outcome in head and neck cancer patients with high LNR adversely affecting survival in oral cavity tumors.3737 Ebrahimi A, Clark JR, Zhang WJ, et al. Lymph node ratio as an independent prognostic factor in oral squamous cell carcinoma. Head Neck 2011;33(09):1245–1251 In our study population, age has not seemed to be a significant factor in terms of survival (p > 0.05). On that the contrary, LNR < 0.05 has resulted in significantly improved OS (58% vs 43%, p = 0.001) and RFS (63% vs 49%, p = 0.008). In recent years, LNR has been attributed as an integral component of risk stratification in breast, colon, and gastric cancers. Similarly, an attempt has been made to incorporate LNR in head and neck cancers as a predictor of survival. Rudra et al. have emphasized the importance of LNR using a cutoff value of 0.20 in HNSCC. Sano et al. have also revealed a LNR > 0.068 as an independent prognostic factor for OS and PFS.3838 Patel SG, Amit M, Yen TC, et al; International Consortium for Outcome Research (ICOR) in Head and Neck Cancer. Lymph node density in oral cavity cancer: results of the International Consortium for Outcomes Research. Br J Cancer 2013;109(08):2087–2095,3939 Wang YL, Feng SH, Zhu J, et al. Impact of lymph node ratio on the survival of patients with hypopharyngeal squamous cell carcinoma: a population-based analysis. PLoS One 2013;8(02):e56613,4040 Rudra S, Spiotto MT, Witt ME, Blair EA, Stenson K, Haraf DJ. Lymph node density–prognostic value in head and neck cancer. Head Neck 2014;36(02):266–272,4141 Ong W, Zhao R, Lui B, et al. Prognostic significance of lymph node density in squamous cell carcinoma of the tongue. Head Neck 2016;38(Suppl 1):E859–E866,4242 Prabhu RS, Hanasoge S, Magliocca KR, et al. Lymph node ratio influence on risk of head and neck cancer locoregional recurrence after initial surgical resection: implications for adjuvant therapy. Head Neck 2015;37(06):777–782,4343 Sano D, Yabuki K, Takahashi H, et al. Lymph node ratio as a prognostic factor for survival in patients with head and neck squamous cell carcinoma. Auris Nasus Larynx 2018;45(04): 846–853 [published correction appears in Auris Nasus Larynx. 2019 Oct;46(5):818–819]

Our cohort had more than 50% of patients who were positive for p16 overexpression in LNs without true primary. This seems to be an interesting subset of patients having p16 positivity with no identifiable primary or HPV association. The results have shown improved 5-year OS and RFS in patients who were tested positive for p16 (p = 0.008). When subjected to Cox regression analysis, p16 + patients in our series without an identifiable primary tumor have depicted significantly improved RFS (p = 0.021). This finding may unfold avenues regarding this small group of p16+ and unidentifiable primary tumors depicting improved survival-related outcomes.

There is a dire need to stratify the subset of LN metastatic p16+ cases with unidentified primary. Furthermore, large scale studies may be required to prove our study results and provide an evidential statement about the prognostic significance of p16 overexpression in LNs of CUP.

Conclusions

Our study has suggested the prognostic significance of p16 overexpression in metastatic cervical LNs for true CUP. The presence has resulted in significantly improved RFS. Future large-scale studies are required for validation of our results.

  • Funding
    This study was funded by the Medical University of Vienna.
  • Ethics Approval and Consent to Participate
    Ethical exemption was granted by the ethics committee of the Medical University of Vienna.
  • Availability of Data and Materials
    All data generated or analyzed during this study are included in this published article.

References

  • 1
    Miller FR, Karnad AB, Eng T, Hussey DH, Stan McGuff H, Otto RA. Management of the unknown primary carcinoma: long-term follow-up on a negative PET scan and negative panendoscopy. Head Neck 2008;30(01):28–34
  • 2
    Galloway TJ, Ridge JA. Management of Squamous Cancer Metastatic to Cervical Nodes With an Unknown Primary Site. J Clin Oncol 2015;33(29):3328–3337
  • 3
    Pavlidis N, Khaled H, Gaafar R. A mini review on cancer of unknown primary site: A clinical puzzle for the oncologists. J Adv Res 2015;6(03):375–382
  • 4
    Pavlidis N, Pentheroudakis G, Plataniotis G. Cervical lymph node metastases of squamous cell carcinoma from an unknown primary site: a favourable prognosis subset of patients with CUP. Clin Transl Oncol 2009;11(06):340–348
  • 5
    Guntinas-Lichius O, Peter Klussmann J, Dinh S, et al. Diagnostic work-up and outcome of cervical metastases from an unknown primary. Acta Otolaryngol 2006;126(05):536–544
  • 6
    Challis GB, Stam HJ. The spontaneous regression of cancer. A review of cases from 1900 to 1987. Acta Oncol 1990;29(05):545–550
  • 7
    van de Wouw AJ, Jansen RL, Speel EJ, Hillen HF. The unknown biology of the unknown primary tumour: a literature review. Ann Oncol 2003;14(02):191–196
  • 8
    Boscolo-Rizzo P, Da Mosto MC, Gava A, Marchiori C. Cervical lymph node metastases from occult squamous cell carcinoma: analysis of 82 cases. ORL J Otorhinolaryngol Relat Spec 2006;68 (04):189–194
  • 9
    Koivunen P, Laranne J, Virtaniemi J, et al. Cervical metastasis of unknown origin: a series of 72 patients. Acta Otolaryngol 2002; 122(05):569–574
  • 10
    Villeneuve H, Després P, Fortin B, et al. Cervical lymph node metastases from unknown primary cancer: a single-institution experience with intensity-modulated radiotherapy. Int J Radiat Oncol Biol Phys 2012;82(05):1866–1871
  • 11
    Haas I, Hoffmann TK, Engers R, Ganzer U. Diagnostic strategies in cervical carcinoma of an unknown primary (CUP). Eur Arch Otorhinolaryngol 2002;259(06):325–333
  • 12
    Müller von der Grün J, Bon D, Rödel C, Balermpas P. Patterns of care analysis for head & neck cancer of unknown primary site: a survey inside the German society of radiation oncology (DEGRO). Strahlenther Onkol 2018;194(08):750–758
  • 13
    O’Rorke MA, Ellison MV, Murray LJ, Moran M, James J, Anderson LA. Human papillomavirus related head and neck cancer survival: a systematic review and meta-analysis. Oral Oncol 2012;48(12): 1191–1201
  • 14
    Dixon PR, Au M, Hosni A, et al. Impact of p16 expression, nodal status, and smoking on oncologic outcomes of patients with head and neck unknown primarysquamous cellcarcinoma. Head Neck 2016;38(09):1347–1353
  • 15
    Rassy E, Nicolai P, Pavlidis N. Comprehensive management of HPV-related squamous cell carcinoma of the head and neck of unknown primary. Head Neck 2019;41(10):3700–3711
  • 16
    Deng Z, Hasegawa M, Aoki K, et al. A comprehensive evaluation of human papillomavirus positive status and p16INK4a overexpression as a prognostic biomarker in head and neck squamous cell carcinoma. Int J Oncol 2014;45(01):67–76
  • 17
    Mork J, Lie AK, Glattre E, et al. Human papillomavirus infection as a risk factor for squamous-cell carcinoma of the head and neck. N Engl J Med 2001;344(15):1125–1131
  • 18
    D’Souza G, Kreimer AR, Viscidi R, et al. Case-control study of human papillomavirus and oropharyngeal cancer. N Engl J Med 2007;356(19):1944–1956
  • 19
    Lydiatt WM, Patel SG, O’Sullivan B, et al. Head and Neck cancers-major changes in the American Joint Committee on cancer eighth edition cancer staging manual. CA Cancer J Clin 2017;67(02): 122–137
  • 20
    Keller LM, Galloway TJ, Holdbrook T, et al. p16 status, pathologic and clinical characteristics, biomolecular signature, and longterm outcomes in head and neck squamous cell carcinomas of unknown primary. Head Neck 2014;36(12):1677–1684
  • 21
    Axelsson L, Nyman J, Haugen-Cange H, et al. Prognostic factors for head and neck cancer of unknown primary including the impact of human papillomavirus infection. J Otolaryngol Head Neck Surg 2017;46(01):45
  • 22
    Jensen DH, Hedback N, Specht L, et al. Human papillomavirus in head and necksquamous cell carcinoma of unknownprimary is a common event and a strong predictor of survival. PLoS One 2014; 9(11):e110456
  • 23
    Schroeder L, Wichmann G, Willner M, et al. Antibodies against human papillomaviruses as diagnostic and prognostic biomarker in patients with neck squamous cell carcinoma from unknown primary tumor. Int J Cancer 2018;142(07):1361–1368
  • 24
    Graboyes EM, Sinha P, Thorstad WL, Rich JT, Haughey BH. Management of human papillomavirus-related unknown primaries of the head and neck with a transoral surgical approach. Head Neck 2015;37(11):1603–1611
  • 25
    Bersani C, Sivars L, Haeggblom L, et al. Targeted sequencing of tonsillar and base of tongue cancer and human papillomavirus positive unknown primary of the head and neck reveals prognostic effects of mutated FGFR3. Oncotarget 2017;8(21): 35339–35350
  • 26
    Sivars L, Näsman A, Tertipis N, et al. Human papillomavirus and p53 expression in cancer of unknown primary in the head and neck region in relation to clinical outcome. Cancer Med 2014;3 (02):376–384
  • 27
    Hung YH, Liu SA, Wang CC, Wang CP, Jiang RS, Wu SH. Treatment outcomes of unknown primary squamous cell carcinoma of the head and neck. PLoS One 2018;13(10):e0205365
  • 28
    Adams JR, O’Brien CJ. Unknownprimarysquamouscellcarcinoma of the head and neck: a review of diagnosis, treatment and outcomes. Asian J Surg 2002;25(02):188–193
  • 29
    Begum S, Gillison ML, Ansari-Lari MA, Shah K, Westra WH. Detection of human papillomavirus in cervical lymph nodes: a highly effective strategy for localizing site of tumor origin. Clin Cancer Res 2003;9(17):6469–6475
  • 30
    Zhang MQ, El-Mofty SK, Dávila RM. Detection of human papillomavirus-related squamous cell carcinoma cytologically and by in situ hybridization in fine-needle aspiration biopsies of cervical metastasis: a tool for identifying the site of an occult head and neck primary. Cancer 2008;114(02):118–123
  • 31
    Le NS, Janik S, Simmel H, Erovic BM. Bilateral vs ipsilateral adjuvant radiotherapy in patients with cancer of unknown primary of the head and neck: An analysis of the clinical outcome and radiation-induced side effects. Head Neck 2019;41(06): 1785–1794
  • 32
    Ang KK, Harris J, Wheeler R, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med 2010;363(01):24–35
  • 33
    Sedghizadeh PP, Billington WD, Paxton D, et al. Is p16-positive oropharyngeal squamous cell carcinoma associated with favorable prognosis? A systematic review and meta-analysis. Oral Oncol 2016;54:15–27
  • 34
    Cho WK, Roh JL, Cho KJ, Choi SH, Nam SY, Kim SY. Predictors of survival and recurrence after primary surgery for cervical metastasis of unknown primary. J Cancer Res Clin Oncol 2020;146(04): 925–933
  • 35
    Chung CH, Zhang Q, Kong CS, et al. p16 protein expression and human papillomavirus status as prognostic biomarkers of non-oropharyngeal head and neck squamous cell carcinoma. J Clin Oncol 2014;32(35):3930–3938
  • 36
    McDowell LJ, Young RJ, Johnston ML, et al. p16-positive lymph node metastases from cutaneous head and neck squamous cell carcinoma: No association with high-risk human papillomavirus or prognosis and implications for the workup of the unknown primary. Cancer 2016;122(08):1201–1208
  • 37
    Ebrahimi A, Clark JR, Zhang WJ, et al. Lymph node ratio as an independent prognostic factor in oral squamous cell carcinoma. Head Neck 2011;33(09):1245–1251
  • 38
    Patel SG, Amit M, Yen TC, et al; International Consortium for Outcome Research (ICOR) in Head and Neck Cancer. Lymph node density in oral cavity cancer: results of the International Consortium for Outcomes Research. Br J Cancer 2013;109(08):2087–2095
  • 39
    Wang YL, Feng SH, Zhu J, et al. Impact of lymph node ratio on the survival of patients with hypopharyngeal squamous cell carcinoma: a population-based analysis. PLoS One 2013;8(02):e56613
  • 40
    Rudra S, Spiotto MT, Witt ME, Blair EA, Stenson K, Haraf DJ. Lymph node density–prognostic value in head and neck cancer. Head Neck 2014;36(02):266–272
  • 41
    Ong W, Zhao R, Lui B, et al. Prognostic significance of lymph node density in squamous cell carcinoma of the tongue. Head Neck 2016;38(Suppl 1):E859–E866
  • 42
    Prabhu RS, Hanasoge S, Magliocca KR, et al. Lymph node ratio influence on risk of head and neck cancer locoregional recurrence after initial surgical resection: implications for adjuvant therapy. Head Neck 2015;37(06):777–782
  • 43
    Sano D, Yabuki K, Takahashi H, et al. Lymph node ratio as a prognostic factor for survival in patients with head and neck squamous cell carcinoma. Auris Nasus Larynx 2018;45(04): 846–853 [published correction appears in Auris Nasus Larynx. 2019 Oct;46(5):818–819]

Publication Dates

  • Publication in this collection
    04 Dec 2023
  • Date of issue
    June 2023

History

  • Received
    18 Sept 2021
  • Accepted
    22 Aug 2022
Fundação Otorrinolaringologia R. Teodoro Sampaio, 483, 05405-000 São Paulo/SP Brasil, Tel.: (55 11) 3068-9855, Fax: (55 11) 3079-6769 - São Paulo - SP - Brazil
E-mail: iaorl@iaorl.org