Head and Neck Cancer

The scope of this page is limited to malignant tumors in adults, located in and/or around the nose, paranasal sinuses, oral cavity, pharynx, larynx, and salivary glands. This resource does not discuss benign tumors of the head and neck region, skin cancers involving the head and neck, auditory nerve lesions, brain tumors, or cancer that has metastasized to this region from elsewhere in the body. This resource also does not address thyroid cancer. Thyroid cancer does not fall under the National Cancer Institute’s head and neck cancer (HNC) classification system, although some speech-language pathologists (SLPs) may consider it in this category given their evaluation and treatment approaches.

See the Head and Neck Cancer Evidence Map for summaries of available research on this topic.

HNC includes malignant tumors that most commonly arise from the moist squamous cell mucosa or lining of the head and neck regions. Although curative treatment may be different based on region and severity, some audiology and speech-language pathology interventions will be the same.

HNC is characterized according to the primary site of origin as malignancies of the

  • nasal cavity and paranasal sinuses;
  • oral cavity (lip, anterior two-thirds of the tongue, gums, oral mucosa, floor of mouth, hard palate, maxilla, and mandible);
  • pharynx, including the nasopharynx, oropharynx (soft palate, tongue base, tonsils, and adenoids), and hypopharynx;
  • larynx (supraglottic, glottic, and subglottic regions); and
  • salivary glands.

The most commonly used model for classifying HNC is the TNM staging model, which classifies the extent of cancer spread (Amin et al., 2017; Lydiatt et al., 2018). The TNM model assigns a numerical status (Stage 0, x, I, II, III, or IV) based on

  • tumor size and spread of cancer into nearby tissue (T),
  • degree of lymph node involvement (N), and
  • presence or absence of distant metastasis (M).

Lymph node involvement is typically defined as a late-stage (III or IV) malignancy regardless of the size or location of the primary tumor (Amin et al., 2017; Lydiatt et al., 2017, 2018). This rule does not apply to HNC from human papillomavirus (HPV), as HPV-related tumors have their own staging system (Economopoulou et al., 2020).

Tumor staging and location, physiologic impact, and patient/care partner goals often determine the course of cancer treatment. The following factors help determine overall prognosis:

  • Natural history of the specific tumor based on staging, histology, and other comorbidities.
  • Ability to control disease through treatment (surgery, radiation therapy, immunotherapy, chemotherapy—alone or in combination).
  • Etiology—for example, HPV-associated oropharyngeal cancers have a better prognosis than HPV-negative oropharyngeal cancers (National Cancer Institute, 2015; You et al., 2019).
  • Complexity, timing, and nature of treatment—for example, in advanced HNC, multimodal treatment (e.g., surgery, radiation therapy, chemotherapy, and immunotherapy) and reconstructive or salvage surgeries (surgery following curative-intent treatment failure) are more likely to result in short- and long-term side effects and may result in greater communication, swallowing, respiratory, and hearing needs (Bertolin et al., 2021; Nilsen et al., 2019).

Cancer treatment may involve surgery, radiation therapy, and/or systemic therapy (i.e., chemotherapy, hormone therapy, and/or immunotherapy). Different surgery types (e.g., laser, TransOral Robotic Surgery [TORS], open surgical resection with or without reconstruction) and chemoradiation therapy regimens have different side effects and rehabilitation timelines. Such differences may affect intervention approaches, quality of life, and functional outcomes (Aggarwal et al., 2021; Zebralla et al., 2021).

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