Introduction

Head and neck squamous cell cancer (HNSCC) is a heterogeneous group of tumours responsible for 5% of cancer cases diagnosed in Spain. It is estimated that each year, approximately 12,000 people develop HNSCC, of whom 1600 die [1]. Treatment modalities include surgery, radiation, chemotherapy, targeted therapies, and immune checkpoint inhibitors (ICIs). For many patients who are cured, the sequelae of treatment can affect their functioning, quality of life, and noncancer-related mortality [2,3,4]. In this context, indicators of biological behaviour and sensitivity to treatment can be enormously valuable for designing individualized therapies, which justifies the search for predictive biomarkers of response to treatment and prognosis in patients with HNSCC.

Although the human papillomavirus (HPV) prevalence varied from 0 to 85% worldwide, Spain is one of the countries with the lowest proportion of HPV-positive oropharyngeal cancer [5]. Numerous studies have demonstrated the usefulness of biomarkers associated with HPV in oropharyngeal cancer to predict outcomes and select therapies for these patients [6]. In randomized studies, immunotherapy with programmed cell death protein 1 (PD-1) inhibitors such as nivolumab and pembrolizumab has been shown to be effective in patients with advanced HNSCC; however, the percentage of positive tumour cells and the percentage of positive immune cells have been decisive for its indication for approval [7,8,9]. Promising results have also been published for targeted therapies, such as treatments for patients with fusion of the neurotrophic tyrosine receptor kinase (NTRK) gene or mutations in the HRas GTPase gene (HRAS) [10, 11]. Table 1 summarizes the main biomarkers currently in use in head and neck cancer.

Table 1 Biomarkers in use for different types of head and neck tumours
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This consensus of the Spanish Society of Pathology (Sociedad Española de Anatomía Patológica—SEAP) and the Spanish Society of Medical Oncology (Sociedad Española de Oncología Médica—SEOM) evaluates the available information on prognostic and predictive biomarkers that determine therapeutic choices in different tumours of the head and neck region. The existing information is analysed both for biomarkers currently used in clinical practice and for new biomarkers that are under investigation.

Squamous carcinoma

p16 and HPV

Squamous carcinomas of the oropharynx mediated by HPV represent a biologically distinct entity from the classical squamous carcinomas of the oropharynx related to tobacco and alcohol. They have very different epidemiological characteristics and [12], most importantly, they have a much better prognosis, both as localized disease and with regard to recurrence or metastasis [6, 13, 14]. The old TNM/AJCC classifications (TNM Classification of Malignant Tumours/American Joint Committee on Cancer) were not able to highlight prognostic differences by stage, especially for HPV-related tumours between stages I–III. However, the 8th edition of the TNM/AJCC classifies aetiological forms as clinical (cTNM) or pathological (pTNM) stage [15,16,17], and clearly differentiates the entity of HPV-related oropharyngeal cancer.

In 2018, the College of American Pathologists (CAP) published a consensus recommendation advising screening for high-risk HPV (HR-HPV) for all patients with squamous cell carcinoma of the oropharynx, regardless of morphology [18]. There are several techniques to identify HR-HPV [19]. Immunohistochemistry (IHC) detection of p16 is very sensitive for identifying infections by transcriptionally active HR-HPV. p16 expression is independent of virus subtype and, in the oropharynx, it has a strong correlation with HR-HPV infection. Therefore, the CAP and the American Society of Clinical Oncology (ASCO) recommend its use as an appropriate surrogate marker to identify HR-HPV infection [18, 20]. However, in other locations of the head and neck, p16 shows little correlation with HR-HPV infection [19]; therefore, outside the oropharynx, the use of p16 as a marker is not recommended [18, 20].

In biopsy material, a sample is considered p16 positive when 70–75% of the tumour cells exhibit moderate to strong diffuse and confluent nuclear and cytoplasmic staining [18, 20]. Samples for which 50–75% of cells exhibit staining require a more specific test. If less than 50% of cells exhibit staining, the result is considered negative. In cytology material, staining for p16 can generate false negatives; therefore, molecular analyses would be advised [21].

Despite the strong correlation of p16 with HR-HPV infection in the oropharynx, staining is very nonspecific and there is a certain percentage of false-positives. The EPIC study confirmed that overall, up to 11% of patients in whom only p16 was assessed had a positive result for p16, but a negative test result for HPV DNA [22]. This percentage increased to 29% in geographic regions where the prevalence of HR-HPV in oropharyngeal squamous cell carcinomas was lower, as in southern European countries. In addition, p16-positive/HPV-negative patients had a prognosis that was intermediate between those for patients with HPV-related and other unrelated tumours. Therefore, and according to what has already been proposed by other working groups [23], a sequential strategy is recommended: first, the use of IHC for the detection of p16 and, if positive, confirmation of the presence of HR-HPV using other molecular tests to avoid undertreatment of false-positives. Figure 1 shows the HPV diagnostic algorithm according to tumour type and location.

Fig. 1
figure 1

Algorithm of the diagnostic procedure of head and neck tumours according to their location and the presence of HPV. IHC immunohistochemistry, HPV human papillomavirus, HR-HPV high-risk human papillomavirus, DNA deoxyribonucleic acid, PCR polymerase chain reaction, ISH In situ hybridization

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The presence of HPV is also an independent predictor of response to any type of treatment [12]. However, the results of studies that evaluated the impact on the efficacy of less aggressive treatments, which aim to reduce acute and chronic toxicity in patients who will foreseeably have longer survival times, are not yet known [24]. From initial published results, treatment with radiotherapy and cetuximab is inferior to standard treatment with radiotherapy and high-dose cisplatin [25, 26].

PD-L1

Programmed death ligand 1 (PD-L1) is a transmembrane protein that is expressed in haematopoietic and nonhaematopoietic tumour cells. The expression of PD-L1 is one of the mechanisms by which tumour cells escape the antitumour response of the immune system. The interaction of PD-L1 molecules with the PD-1 receptor on T lymphocytes represses the intratumoural lymphocyte response.

The development of oncological therapies that block this pathway of lymphocyte regulation have revolutionized cancer treatment. The results of the Keynote-048 study represent a paradigm shift in the first-line treatment of platinum-sensitive recurrent or metastatic squamous head and neck carcinoma [7]. This study demonstrated that pembrolizumab in monotherapy or in combination with chemotherapy (with platinum and 5-fluorouracil) lengthened overall survival (OS) for patients who expressed PD-L1, with a combined positive score (CPS) ≥ 1, compared to OS for patients who received standard treatment based on cetuximab (EXTREME scheme), especially in patients with a CPS ≥ 20 [27]. However, this benefit was not clear for patients with a CPS < 1, although the combination of pembrolizumab and chemotherapy was considered superior to the EXTREME regimen in this group [28].

Therefore, PD-L1 CPS emerges as a predictive biomarker of response to treatment essential for decision-making in this stage of the disease [29, 30]. The Food and Drug Administration (FDA) has approved pembrolizumab as monotherapy for patients with a CPS ≥ 1 when evaluated with an FDA-approved test and has also approved the combination of pembrolizumab with chemotherapy regardless of the PD-L1 value. In 2020, the European Medicines Agency (EMA) approved the use of pembrolizumab in monotherapy or in combination with chemotherapy as first-line treatment in patients with a CPS ≥ 1 with platinum-refractory disease, without specifying a specific diagnostic test [7,8,9, 27,28,29,30,31,32].

In the Checkmate-141 study [9], nivolumab improved survival compared to standard treatment, regardless of PD-L1 positivity as measured by IHC, in platinum-resistant disease. Although the PD-L1 value in routine clinical practice is unknown [29, 30], PD-L1 positivity is a predictive marker of efficacy [32]. In a study with a similar design [8], pembrolizumab only resulted in slight improvement in survival for the entire population, with a greater survival for patients with a tumour proportion score (TPS) ≥ 50. Therefore, the EMA has only approved pembrolizumab for patients with platinum-refractory disease with a TPS ≥ 50.

Currently, there are several staining methods for PD-L1 that use different primary antibodies and different platforms with variable cut-off scores. Some studies suggest that different tests can be interchangeable if the tests are administered with appropriate methodology and cut-off points, but more validation studies are necessary to allow a consensus regarding the determination of PD-L1 expression by IHC [33,34,35,36,37].

The certified diagnostic tests are DAKO (22C3) for pembrolizumab and Ventana (SP263) for durvalumab, with the former being the most widely used. The recommendations for the correct determination of the CPS are provided in Table 2.

Table 2 Recommendations and procedure for the calculation of PD-L1 CPS
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Nasopharyngeal carcinoma

Epstein–Barr virus

Nasopharyngeal carcinoma is a relatively infrequent neoplasm that has unique characteristics related to its aetiology, prognosis and treatment compared to those of other head and neck carcinomas [38].

The World Health Organization distinguishes 3 histological subtypes: keratinizing carcinoma, nonkeratinizing carcinoma and basaloid squamous carcinoma. The nonkeratinizing subtype is further subdivided into differentiated and undifferentiated carcinoma. The latter is the most common in East and Southeast Asian countries (> 95%) and is associated in practically all cases with Epstein–Barr virus (EBV) infection [39]. Its prognosis is better than that of keratinizing carcinoma.

This geographical distribution of undifferentiated nonkeratinizing carcinoma is due to the concurrence of several risk factors, such as EBV infection, genetic factors that increase susceptibility to developing carcinoma and environmental factors, such as the consumption of foods high in nitrosamines [38].

Practically all cells of undifferentiated nonkeratinizing carcinomas are infected by EBV. The primary infection by EBV in the epithelial cells of the nasopharynx is lytic, which does not induce cell proliferation or immortalization. For this to occur, evolution to latent EBV infection is facilitated by the presence in premalignant epithelial cells of somatic mutations and alterations in cellular signalling, which activate telomerase and inactivate the tumour suppression genes RASSF1A and p16. Type II latent EBV infection occurs in undifferentiated nonkeratinizing carcinomas, in which the expression of the EBNA1, LMP1, LMP2A, EBERs and BART gene products facilitates the clonal expansion of infected epithelial cells [40]. It is therefore necessary for all nasopharyngeal carcinomas, both for diagnostic and therapeutic purposes, to test for the presence of EBV in the tumour tissue; such tests include IHC for latent membrane protein 1 (LMP-1) and in situ hybridization (ISH) for EBV-encoded small mRNAs (EBERs).

Screening for the presence of EBV in populations who live in areas endemic for undifferentiated nonkeratinizing carcinoma allows the identification of the disease in the initial stages and improves the therapeutic and prognostic outcomes for patients. The serological assessment of the EA-IgA (early antigen), VCA-IgA (capsid antigen) and EBNA1-IgA (nuclear antigen 1) antibodies against EBV has been the most widely used test for this purpose; however, it has been found to have low sensitivity and specificity [41]. More recent studies have demonstrated greater sensitivity in the detection of DNA or RNA in the BamHI-WVEB and EBNA1 genome regions or in EBERs in plasma or serum [42].

Cervical metastasis of carcinoma of unknown origin

Squamous cell carcinoma of unknown origin of the head and neck is defined as cervical lymph node metastasis without evidence of a primary tumour, after examinations that should include fibroendoscopy and radiological evaluation, preferably positron emission tomography/computerized axial tomography (PET-CAT). These tumours represent between 3 and 10% of head and neck tumours [43, 44], with level II being the most common location, followed by level III.

The initial diagnostic test of choice is fine needle aspiration (FNA), which is a simple, minimally invasive and inexpensive technique that provides a posterior diagnostic biopsy. In addition, it allows immunohistochemical and molecular studies using cell blocks [45]. In cystic metastases, where FNA may not be diagnostic, core needle biopsy guided by ultrasound is recommended [46].

For a metastasis of a carcinoma of unknown origin, an HPV assessment is recommended and, if negative, an EBV assessment should be performed.

HPV

The presence of HR-HPV should be assessed routinely for levels II and III lymphadenopathies, for which it is common to identify hidden oropharyngeal tumours, especially of the palatine tonsil and base of the tongue. The determination of HPV has prognostic and therapeutic value [46, 47]. Initially, an immunohistochemical assessment of p16 is recommended. p16 is a surrogate marker of the presence of HR-HPV, with high sensitivity and specificity. ASCO recommends confirming positive results with a specific assessment of HR-HPV using DNA-based techniques [20, 46].

Epstein–Barr virus

Carcinomas of unknown origin associated with EBV are much less frequent. The determination of EBV by the ISH of EBERs is recommended for HPV-negative cases. The presence of EBV usually indicates a nasopharyngeal origin, although it may occasionally be present in tumours that originate in other locations [46].

Salivary gland tumours

The treatment of choice for salivary gland carcinomas is surgery with adjuvant radiotherapy. However, there are subtypes with rapid progression that complicate surgery and that, until recently, could only be treated with palliative chemotherapy [48]. Currently, androgen receptors, HER-2 and NTRK are recommended as possible therapeutic targets.

Androgen receptors

Salivary ductal carcinoma is a rare tumour that account for 5–10% of all salivary malignancies. It is an aggressive subtype that microscopically resemble high-grade breast duct carcinoma. In salivary glands, 64–98% of ductal carcinomas are positive for androgen receptors [49]. Androgen receptors can be assessed by IHC. Samples are considered positive when ≥ 10% of the nuclei are strongly stained [50]. For ductal carcinomas, positivity is intense and diffuse and correlates with the response to anti-androgenic treatment. There are other subtypes of salivary gland carcinomas that can be positive for androgen receptors, but for these carcinomas, focal and heterogeneous positivity does not correlate with oncogenic development [51].

The AR-V7 androgen receptor variant described in prostate adenocarcinoma causes resistance to anti-androgenic treatment. AR-V7 in ductal carcinoma of the salivary glands also seems indicative of resistance to treatment, although more studies are needed [50]. This variant can be assessed by IHC.

From the therapeutic point of view, complete androgen blockade has shown activity in a single-arm phase II clinical trial evaluating the combination of leuprorelin and bicalutamide in patients with malignant tumours of the salivary gland with androgen receptor positivity, with a response rate of 42% (complete response 11% and partial response 31%) [52]. In this study, there was no restriction due to histological type, although 94% of patients had ductal carcinoma, and only 2 patients (6%) had NOS adenocarcinoma (not otherwise specified) [52]. In a retrospective multicentre study, treatment with adjuvant complete androgen blockade in patients with ductal carcinoma resulted in an improvement in progression-free survival (PFS) [HR 0.138 (95% CI 0.025–0.751, p = 0.022)] [53]. Currently, there are no data from randomized studies. The EORTC 1206 (NCT01969578) study is underway. This trial is comparing the activity of complete androgen blockade (bicalutamide and triptorelin) with that of chemotherapy in patients with salivary gland tumours with androgen receptor positivity.

Therefore, in patients with ductal carcinoma or NOS metastatic adenocarcinoma with androgen receptor expression ≥ 10%, treatment should include complete androgen blockade. In addition, for patients with ductal carcinoma and androgen receptor positivity, adjuvant treatment with complete androgen blockade can be considered.

HER-2

HER-2 is overexpressed in several subtypes of salivary gland carcinomas (ductal carcinoma: 43%; ex pleomorphic adenoma carcinoma: 39%; NOS adenocarcinoma: 13%; and mucoepidermoid carcinoma: 5%) [54]. Its positivity is related to more aggressive tumour behaviour. HER-2 overexpression is measured semiquantitatively by IHC or ISH (fluorescent, chromogenic or silver). Although an attempt has been made to establish a scale to assess IHC results specific for salivary glands, no studies have been validated. Therefore, currently, the same criteria are applied for salivary gland carcinomas as for breast carcinomas [55] (Table 3).

Table 3 Criteria for the evaluation of HER-2 immunohistochemistry results for the salivary gland
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Several phase II studies support treatment with anti-HER-2 therapy in patients with salivary gland tumours and HER-2 overexpression. One of these nonrandomized single-centre phase II studies evaluated the combination of docetaxel and trastuzumab for patients with metastatic or unresectable ductal carcinoma with HER-2 overexpression, with a response rate of 70% [56]. Two basket trials that evaluated trastuzumab emtansine (T-DM1) and the combination of trastuzumab with pertuzumab have demonstrated the activity of these treatments in patients with salivary gland tumours and HER-2 amplification or overexpression [57, 58]. In a study that evaluated T-DM1 (NCT02675829), 10 patients were treated, of whom only 2 had received anti-HER-2 therapy. The response rate was 90%, and after 12 months of follow-up, the median PFS had not been reached [58]. In the multicentre study MyPathway, a cohort of 18 patients with salivary gland tumours with HER-2 amplification or overexpression was analysed, regardless of histology. The response rate in this group was 63%, the highest of all tumour cohorts classified by location [57].

Therefore, patients with salivary gland tumours with HER-2 overexpression or amplification should be treated with anti-HER-2 therapy, which has response rates like the following regimens: docetaxel-trastuzumab, T-DM1 and trastuzumab-pertuzumab.

NTRK

The identification of rearrangements in the NTRK gene and the development of tyrosine kinase inhibitors have opened a new horizon in the treatment of patients with a neoplasia who present this alteration. NTRK plays an important role in the development of secretory carcinomas of the salivary glands (ETV6-NTRK3 fusion in 90–100% of cases). The Canadian guide on tumours with potential NTRK fusions recommends testing for androgen receptors and HER-2 in ductal carcinomas and NOS adenocarcinomas and, if negative, testing for NTRK (Table 4) [59]. The fusion of this gene can be determined by IHC, fluorescence ISH (FISH) or next-generation sequencing (NGS) [60].

Table 4 Advantages and disadvantages of the diagnostic techniques for NTRK rearrangement
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The European Society for Medical Oncology (ESMO) recommends IHC as a screening tool to determine cases potentially susceptible to fusion. It is advisable to use a Pan-TRK antibody that allows the identification of the three gene products, NTRK1-3. The signal can be cytoplasmic, nuclear or mixed, and a result is considered positive if ≥ 1% of cells are stained. The sensitivity of IHC to detect NTRK fusions is 96.2% for NTRK1, 100% for NTRK2 and 79.4% for NTRK3. In salivary glands, the sensitivity is 88.9%, and the specificity is 52% [61]. It is very important to take care of the pre-analytical sample and include positive controls (such as neural structures which give a positive signal).

For FISH, three probes are necessary for NTRK1, NTRK2 and NTRK3, and it is advisable to use break-apart probes. Although the interpretation of the results is not standardized, it is recommended to count a minimum of 50 cells with a cut-off point for positive nuclei of 15–20% (separate red and green signals or isolated red signals). The FISH technique allows the confirmation of fusion in cases deemed positive by IHC, nuclear positivity for NTRK3 by IHC, and the fusion of NTRK in a neoplasm whose histology predicts the type of fusion.

Finally, in NGS, it is important to consider that NTRK fusions are exclusive and that not all the sequencing panels include the three gene products. In addition, RNA panels have a higher sensitivity than do DNA panels.

There are two drugs directed against NTRK fusions authorized by the FDA and the EMA: larotrectinib (selective inhibitor of NTRK1, 2 and 3) and entrectinib (inhibitor of NTRK1, 2 and 3, ALK and ROS1). Both drugs have been approved based on basket trials with patients with molecular alterations of interest, regardless of histology. In the aggregate analysis of three phase I/II studies that evaluated larotrectinib, 20 patients with assessable salivary gland tumours were included. In this cohort, the response rate was 90%, with a median duration of response of 35.2 months [62]. In the aggregate analysis of patients with NTRK fusions in basket phase I and II studies that evaluated entrectinib, 54 patients evaluable for response were included, of whom 7 had salivary gland tumours (all had secretory carcinomas). No individual data have been reported for patients with salivary gland tumours, but the response rate of the overall population was 57%, with a median duration of response of 10.4 months [63].

Therefore, this committee of experts recommends that for patients with NTRK fusions, as determined by NGS, TRK inhibitors (larotrectinib, entrectinib) should be the treatment of choice.

Other biomarkers in development

HRAS

The appearance of mutations in RAS proto-oncogenes (K, N, H) is involved in oncogenic events; however, the development of targeted therapies against RAS has historically been a challenge [64]. HRAS mutations affect farnesylation, and tumours with HRAS mutations are particularly susceptible to treatment with farnesyl-transferase inhibitors [11]. In HNSCC, HRAS is mutated in approximately 4–8% of patients; among these patients, there is a subset of HPV-negative patients without p53 or caspase-8 mutations and with alterations in DNA copy number (low chromosomal instability) [65]. Tipifarnib is a farnesyl-transferase inhibitor that has been shown to be effective in the KO-TIP-001 phase II trial with patients with incurable solid HNSCC and HRAS mutations (mHRAS) with a high variant allele frequency (VAF) (mHRAS VAF > 20%) [66]. Of the 22 patients evaluated, responses were observed in 55%, with a median PFS of 5.6 months and OS of 15.4 months. The most frequent adverse events related to treatment were anaemia (37%) and lymphopenia (13%). These data support the efficacy of tipifarnib in patients with recurrent or metastatic HNSCC with HRAS mutations. HRAS mutations can be detected by polymerase chain reaction (PCR, Sanger), but NGS panels (based on RNA or DNA) using tissue, through sequence analysis of the entire coding region, is more suitable because it allows the detection of alterations in multiple genes simultaneously.

NOTCH1

Sequencing of the HNSCC genome revealed that NOTCH1 acts as a tumour suppressor gene and that it is the second most frequently mutated gene in this cancer, with an incidence of 15–19% [67]. A structural analysis of NOTCH1 mutations in HNSCC indicated that the majority are loss-of-function mutations [68]. NOTCH1 controls the genes involved in early differentiation, having different phenotypic consequences depending on the genetic background of the cancer, including the acquisition of properties like those of progenitor cells. In addition, NOTCH1 signalling can drive HNSCC tumourigenesis and clinical aggressiveness. The presence of NOTCH1 mutations detected by NGS can predict the response to treatment with ICIs or phosphatidylinositol-3-kinase (PI3K) inhibitors [69]. The latter are being tested in a clinical trial and, if validated, may lead to the development of the first biomarker associated with targeted therapy in HNSCC.

PI3K

The PI3K/AKT/mTOR signalling pathway is active in more than 90% of HNSCC cases as a result of EGFR activation (47%), mutations in the catalytic alpha subunit of PIK3CA (8.6%), PIK3CA amplifications (14.2%), PI3K overexpression (27.2%) and PTEN mutations (10–15%) [70]. The presence of alterations in this pathway is related to a poor prognosis and resistance to radiotherapy and cytostatic drugs. Preclinical and phase II trials of PI3K/AKT/mTOR inhibitors (buparlisib and alpelisib) have demonstrated efficacy in monotherapy and in combination with chemotherapy [71, 72] and radiotherapy [73,74,75]. In general, ongoing clinical trials are trying to elucidate the role of AKT and mTOR inhibitors in combination with chemotherapy and radiotherapy and in patients with resistance to them.

Total mutational load and microsatellite instability

Recently, numerous studies have established the role of neoepitopes as a result of nonsynonymous mutations in tumour cells in the immunological recognition of cancer and in the specific activation of T cells [76]. To determine the total tumour mutational burden (TMB), many studies use NGS based on the complete exome [77]. In HNSCC, TMB has been evaluated in the KEYNOTE-012 trial, with a cut-off of ≥ 102 mutations per exome, and a positive correlation with response to immunotherapy has been observed [78]. Additional data from a cohort of 126 patients who received anti-PD-1/L1 therapy revealed a higher TMB among responders; this was a positive predictor among patients negative for HPV/EBV in the same group. Additionally, microsatellite instability (MSI) was higher among responders [79]. Despite these observations, currently, the subcommittee of the Society of ImmunoTherapy for Cancer (SITC) does not recommend TMB or MSI as biomarkers of response to immunotherapy because they are present in only 1–3% of patients with HNSCC [31].

Interferon gamma signatures

These signatures were analysed in the KEYNOTE-012 trial, in which the interferon gamma (IFN-γ) signature of 6 genes (gene expression of IDO1, CXCL10, CXCL9, HLA-DRA, STAT1 and IFN-γ) was evaluated in biopsies prior to treatment. The results showed that this signature is significantly associated with the response rate and PFS and, due to its high negative predictive value, is a potential biomarker for the exclusion of patients from immunotherapy [78]. The determination of IFN-γ signatures is performed using the RNA of paraffin-embedded tissue, and analysis using a NanoString nCounter system allows the direct multiplex analysis of gene expression [80].

The role of NGS

In the last decade, massively parallel sequencing of genes by NGS has allowed the sequencing of the cancer genome on an unprecedented scale. NGS has allowed the development of new biomarkers and, more importantly, the identification of patients who are sensitive or resistant to certain therapies [81]. In head and neck carcinomas, the presence of genome alterations has been confirmed, such as mutations in TP53, HER-2, CDKN2A, PIK3CA, PTEN, HRAS and NOTCH1 [67, 82]. NOTCH1 is an important oncosuppressive gene and the second most commonly mutated gene in HNSCC [83]. In salivary gland neoplasms, NGS has allowed a new diagnostic characterization, decreasing the number of cases classified as NOS adenocarcinoma and describing actionable alterations in neoplasms with NTRK fusions [84, 85]. In addition, through NGS platforms, the state of tumour hypermutation can be determined, which improves the efficacy of immunotherapy for HNSCC.

The genomic alterations collected by the International Cancer Genome Consortium (ICGC), The Cancer Genome Atlas (TCGA), and the Catalogue of Somatic Mutations in Cancer (COSMIC) database provide the most complete source of somatic mutations in cancer to date. Currently, for HNSCC, NGS does not have a clear indication for routine use; however, multigenic sequencing with large panels in clinical research centres that allows the entry of patients into clinical trials is of great interest [86]. There are multiple NGS platforms on the market, all capable of producing precision data, but it is essential to apply guidelines and protocols that guarantee quality control and analytical validity [87]. This would allow, for example, to assess whether the results obtained from fixed and paraffin-embedded tissue samples are consistent with those obtained from frozen samples [88].

In the near future, it is expected that the molecular alterations identified by NGS in HNSCC will result in new therapeutic options, as options have already been identified for some salivary gland neoplasms with clinically treatable mutations, such as NTRK.

Conclusions

The treatment of head and neck and salivary gland tumours is complex and continuously evolving. This consensus describes the most relevant predictive biomarkers and proposes a guide for their determination and interpretation. Some biomarkers, such as p16, EBV, PD-L1, androgen receptors and HER-2, are already applied routinely, and others, such as NTRK fusions, have been identified more recently (Table 5). These biomarkers, together with the massively parallel sequencing of genes by NGS, open a hopeful future in the understanding and treatment of these neoplasms. To achieve this objective, the multidisciplinary assessment of these patients and close collaboration between pathologists and oncologists is essential.

Table 5 Summary of recommendations
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