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Treatment of locoregionally advanced (stage III and IV) head and neck cancer: The oral cavity

Treatment of locoregionally advanced (stage III and IV) head and neck cancer: The oral cavity
Authors:
Nancy Y Lee, MD
Neil D Gross, MD, FACS
Scott Okuno, MD
Shyam SD Rao, MD, PhD
Section Editors:
Bruce E Brockstein, MD
David M Brizel, MD
Marshall R Posner, MD
Deputy Editor:
Sonali Shah, MD
Literature review current through: Feb 2022. | This topic last updated: Oct 30, 2020.

INTRODUCTION — The treatment of locoregionally advanced (stage III and IV (table 1)) squamous cell carcinoma of the oral cavity is discussed here.

An overview of the approach to oral cavity cancer and the treatment of early stage disease are presented separately, as is the management of patients with metastatic and recurrent disease:

(See "Treatment of stage I and II (early) head and neck cancer: The oral cavity".)

(See "Treatment of metastatic and recurrent head and neck cancer".)

(See "Overview of treatment for head and neck cancer".)

ANATOMY AND STAGING — The oral cavity extends from the skin-vermilion junction of the lips to the junction of the hard and soft palate above and to the line of circumvallate papilla of the tongue below (figure 1). The anterior tonsillar pillars and glossotonsillar folds serve as the lateral boundaries between the oral cavity and oropharynx.

Specific sites of oral cavity cancer include the lip, floor of the mouth, oral tongue (anterior two-thirds of the tongue), lower alveolar ridge, upper alveolar ridge, retromolar trigone (retromolar gingiva), hard palate, and buccal mucosa.

The tumor, node, metastases (TNM) staging system of the American Joint Committee on Cancer (AJCC) and the Union for International Cancer Control (UICC) is used to classify lip and oral cavity carcinoma (table 1) [1]. (See "Overview of the diagnosis and staging of head and neck cancer".)

By definition, patients with stage III and IV disease have tumors greater than 4 cm in greatest dimension, invasion of adjacent structures, and/or evidence of lymph node involvement.

MANAGEMENT

General principles — Locoregionally advanced oral cavity cancers are aggressive malignancies with high rates of recurrence following definitive treatment with either surgery or radiation therapy (RT) alone [2]. Thus, a combined modality approach is generally indicated when permitted by the patient's overall condition.

Decisions about the optimal integration of surgery, RT, and chemotherapy for each patient should be made with multidisciplinary input. The management plan should take into account the likely functional consequences of treatment as well as the expertise of the treatment team.

There are inadequate data from randomized clinical trials to define an optimal strategy for patients with stage III and IV oral cavity cancers. Recommendations and treatment planning are based upon trials that included large numbers of patients with primary tumors at other head and neck sites, observational data from series of patients with oral cavity cancer, and an analysis of individual patient circumstances.

Surgery is generally recommended as the initial therapy for locally advanced oral cavity cancers [3]. In most cases, simultaneous resection and reconstruction is feasible with acceptable functional outcomes. RT and/or chemoradiotherapy are alternatives for patients who refuse surgery, have a technically unresectable tumor (eg, due to carotid artery encasement, vertebral or brain invasion), would have an unacceptable functional outcome with surgery, or are medically inoperable.

Although there is a rationale for induction chemotherapy for locally advanced oral cavity cancer, the best available data show no survival advantage. As such, the use of induction chemotherapy in this setting should be restricted to highly selected cases and/or clinical trials.

Pretreatment evaluation — Delineation of the tumor size and extent of invasion, as well as potential involvement of regional lymph nodes, is essential prior to treatment in patients with oral cavity cancer. (See "Overview of the diagnosis and staging of head and neck cancer" and "Treatment of stage I and II (early) head and neck cancer: The oral cavity", section on 'Pretreatment evaluation'.)

In addition, patients with locoregionally advanced disease should be evaluated for the presence of distant metastases. CT of the chest is a screen for lung metastases, and a PET/CT can be considered to rule out distant metastatic disease and potentially better characterize the primary tumor or neck nodes. Small, clinically indeterminate pulmonary nodules are often identified and should be followed.

All patients should be seen preoperatively by the surgeon, radiation oncologist, and medical oncologist for preoperative treatment planning. Assessment of comorbidity, speech and swallowing function, nutritional status, and dental and psychosocial evaluations are also important steps in treatment planning.

Treatment of primary tumor — Surgery is generally preferred as the initial step in the treatment of locoregionally advanced oral cavity cancer, although data comparing surgery with RT are limited [4,5].

Surgical technique — Oral cavity cancers can be accessed through a transoral approach or a combined transoral and transcervical approach. Traditional surgical techniques are generally used for locally advanced cancers. For these tumors, there is no advantage to minimally invasive approaches, such as transoral laser resection or robotic-assisted surgery, particularly given the complexity of the reconstruction that is often required.

Every attempt should be made to ensure negative resection margins, since there is an increased risk of treatment failure in patients with positive surgical margins, even when postoperative RT or chemoradiotherapy is used [6]. If positive margins are identified, reresection is indicated when feasible. Postoperative RT or chemoradiotherapy is indicated when positive surgical margins are identified.

Surgical procedures (eg, glossectomy, maxillectomy, mandibulectomy) can result in severe functional defects in speech and swallowing. The functional loss associated with these procedures may be mitigated by reconstruction and intense speech and swallowing rehabilitation. (See "Mandibular and palatal reconstruction in patients with head and neck cancer".)

Postoperative RT and chemoradiotherapy — Postoperative radiation therapy (RT) with or without concurrent chemotherapy is the standard of care for patients with resected locoregionally advanced oral cavity cancer since these patients are at significant risk for local recurrence after surgery [3]. The exception would be patients with a negative-margin resection of a thin primary lesion and a single metastatic lymph node without extranodal extension (ENE). (See "Treatment of stage I and II (early) head and neck cancer: The oral cavity".)

Observation may be appropriate in such cases, particularly for patients with a marginal performance status. Randomized trials that included patients with oral cavity cancers have confirmed the benefit of postoperative concurrent chemoradiation compared with postoperative RT alone for high-risk patients with locally advanced head and neck cancer. (See "Postoperative radiation therapy in the management of head and neck cancer", section on 'Chemoradiation versus radiation therapy alone'.)

Risk factors associated with a particularly increased risk of recurrence include ENE, positive resection margins, N2 or N3 nodal disease, nodal disease in levels IV or V, perineural invasion, or vascular invasion. Positive margins and ENE are indications for chemoradiotherapy, and advanced nodal disease or perineural or vascular invasion may be a consideration for adding chemotherapy to RT. The presence of T3 or T4 disease, without any other high-risk features, is an indication for RT alone. (See "Postoperative radiation therapy in the management of head and neck cancer", section on 'Chemoradiation versus radiation therapy alone'.)

The largest trial to attempt to determine the optimal postoperative RT specifically in advanced oral cavity cancer was a phase III trial in patients with locally advanced oral cavity cancer conducted in India [7]. In that trial, 900 patients with predominantly gingival or buccal carcinoma were randomly assigned following surgery to RT alone (60 Gy in 30 fractions over six weeks), accelerated RT (60 Gy in 30 fractions over five weeks), or RT (60 Gy in 30 fractions over six weeks) in conjunction with chemotherapy (cisplatin 30 mg/m2 weekly). For the entire study population, there was no difference in locoregional tumor control, disease-free survival, or overall survival. However, in an unplanned post hoc analysis, there was a statistically significant improvement in all three outcome parameters, particularly overall survival, for high-risk patients (T3-T4, N2/N3, ENE) and for patients treated with either concurrent chemotherapy or standard fractionation versus the accelerated RT course. Treatment compliance was equivalent in all groups. In a preliminary analysis, toxicity rates were equivalent in all three groups, although they trended towards more mucositis and dermatitis with six-days-per-week radiation.

Postoperative RT is generally preferred over preoperative RT for patients with locoregionally advanced oral cavity cancer. The administration of preoperative RT can delay surgery and increases the risk of postoperative complications.

Preoperative (neoadjuvant) chemotherapy or immunotherapy

Preoperative chemotherapy — Two trials in patients with oral cavity squamous cell carcinoma (OCSCC) have failed to demonstrate an improvement in overall survival with preoperative (neoadjuvant) chemotherapy. However, both trials have shown a possible impact on minimizing surgery or postoperative radiation. Observational data also suggest that neoadjuvant chemotherapy does not increase overall perioperative complication rates [8]. Additionally, it is not known if a longer course of induction docetaxel, cisplatin, and fluorouracil would have improved survival.

In one trial from the 1990s, 195 patients with resectable oral cavity disease were randomly assigned to either three cycles of preoperative cisplatin plus fluorouracil followed by surgery or immediate surgery. Postoperative RT was used for high-risk patients in both arms of the trial [9]. There was no significant difference in overall survival (five-year survival 55 percent in both arms), although the use of chemotherapy prior to surgery resulted in a decreased requirement for mandibulectomy (31 versus 52 percent) and postoperative radiation (33 versus 46 percent). However, advances in patient selection and surgical techniques since this study was performed may result in lower rates of mandibulectomy and postoperative radiation without preoperative treatment. A later report from this trial, based upon 11.5 years median follow-up, confirmed the lack of a statistically significant difference in local disease control, rate of distant metastasis, or overall survival [10].

In a second trial, 256 patients were randomly assigned to two cycles of docetaxel, cisplatin, and fluorouracil followed by surgery and postoperative RT versus immediate surgery and postoperative RT [11]. Planned treatment was completed in 222 cases. After a median follow-up of 30 months, there was no significant difference in either overall or disease-free survival (HRs 0.98 and 0.97, respectively).

Preoperative immunotherapy — Preoperative immunotherapy is not indicated for advanced OCSCC outside of a clinical trial. The use of preoperative immunotherapy warrants further investigation, and randomized trials are ongoing.

The following studies have evaluated the feasibility of preoperative immunotherapy in OCSCC:

In a single institution open label phase II trial, 29 patients with ≥T2 OCSCC were randomly assigned to a very brief course of preoperative nivolumab with or without ipilimumab [12]. A minority of patients (24 percent) experienced grade 3 or greater toxicity, and none required delay of surgery. Despite the short time to surgery, pathologic downstaging was noted in approximately half, with complete or near complete responses in four patients (14 percent). The extent of surgery was not modified by neoadjuvant treatment and progression-free and overall survival data have not been reported.

Another open label phase II trial included 36 patients with advanced stage HPV-negative HNSCC, most with advanced stage OCSCC (22 patients, 61 percent) [13]. Using a single dose of pembrolizumab prior to surgery, no grade 3 or greater toxicity or surgical delays were observed. Some degree of pathologic tumor response was noted in 44 percent of patients and pathologic downstaging was observed in seven patients (19 percent).

Nonsurgical candidates — Functional organ preservation approaches are widely used for patients with locoregionally advanced oropharyngeal, hypopharyngeal, and laryngeal cancers. However, this approach has not been widely applied to patients with oral cavity cancer. Data are more limited, there are concerns about increased toxicity [14], and no survival advantage has been demonstrated for patients with stage III or IV primary tumors of the oral cavity [9,11,15]. A randomized trial of surgery with postoperative RT compared with definitive chemoradiation for locally advanced head and neck cancer found that while survival rates were similar overall between the groups, a subset analysis for oral cavity cancers specifically demonstrated a survival advantage with surgery [5].

Initial RT and/or definitive chemotherapy is an alternative for patients who refuse surgery, have a technically unresectable tumor (carotid artery encasement, vertebral or brain invasion), would have an unacceptable functional outcome with surgery, or are medically inoperable.

A combined modality approach utilizing both chemotherapy and RT is appropriate for patients who are not surgical candidates but whose overall condition will tolerate the potential increase in toxicity. Approaches that may be used include induction chemotherapy followed by definitive concurrent chemoradiotherapy or RT and immediate concurrent chemoradiotherapy. (See "Locally advanced squamous cell carcinoma of the head and neck: Approaches combining chemotherapy and radiation therapy".)

RT without chemotherapy is appropriate for patients who are not surgical candidates and whose medical condition will not tolerate the increased toxicity associated with chemotherapy or concurrent chemoradiotherapy.

For patients where a nonsurgical approach was originally undertaken because of either the low probability of surgical cure or the morbidity associated with resection, complete resection or neck dissection may be indicated as a salvage procedure for residual disease. However, the risks of salvage surgery are substantial, and the oncologic outcomes are generally poor.

Oral cavity subsites

Lip — Although squamous cell carcinomas are the most frequent histologic type of lip cancer, these tumors generally are more related to skin cancers than to other oral cavity cancers. Because they are readily visible, most lip cancers are diagnosed at early stages, with T3 and T4 tumors representing a very small proportion of cases [16,17]. (See "Treatment of stage I and II (early) head and neck cancer: The oral cavity", section on 'Lip (squamous cell carcinoma)'.)

Occasionally, definitive RT may be functionally and cosmetically preferable to surgical resection. In cases with bone or nerve invasion, resection with postoperative RT is indicated [18].

Floor of mouth — Locally advanced cancer of the floor of mouth is typically treated with surgical resection to achieve negative margins, followed by postoperative RT with or without concurrent chemotherapy. The combination of surgery and postoperative RT has been associated with better local control than either modality alone, as surgical resection alone (with 1 to 2 cm margins) for stage III and IV disease (table 1) results in five-year overall survival of only 46 and 26 percent [19,20].

Cancer of the floor of mouth has a high rate of mandibular invasion and cervical lymph node metastases. Furthermore, anterior floor of mouth cancers often involve the geniohyoid tubercle and genioglossus muscle anteriorly. Thus, surgery will frequently require segmental mandibulectomy as a marginal resection of bone is generally not possible in the coronal plane.

Oral tongue — The oral tongue is the most common subsite for oral cavity cancer. Cancer of the oral tongue has been associated with a worse prognosis compared with other oral cavity subsites in some but not all series [21,22]. Typically, five-year disease-specific survival rates of 39 and 27 percent have been achieved for stage III and IV disease, respectively [23].

Partial glossectomy is commonly required for locoregionally advanced disease. Total glossectomy is occasionally required in cases where bilateral lingual arteries are involved by cancer. In those cases, total laryngectomy may also be required to prevent aspiration. The addition of postoperative RT or chemoradiotherapy, appears to improve disease control compared with surgery alone [24].

Primary treatment with concurrent chemoradiotherapy or sequential therapy may be preferred when total glossectomy is indicated, given the overall poor prognosis and functional loss associated with surgery. Patients considering this option should be aware of the potential trade-off between oncologic and functional outcome. (See 'Nonsurgical candidates' above.)

Lower alveolar ridge and retromolar trigone — The surgical approach to resection of locoregionally advanced oral cavity cancer involving the lower alveolar ridge depends upon the status of the teeth. Patients with good dentition are often candidates for marginal resection of the mandible, which can be performed transorally. In contrast, edentulous patients and those with loose teeth involved by cancer require segmental resection of the mandible to ensure adequate clearance of disease.

Similarly, locally advanced retromolar trigone lesions typically require segmental mandibulectomy followed by postoperative RT [25,26]. Resection of the ascending ramus of the mandible including the pterygoid muscles is important to ensure eradication of disease. Microvascular reconstruction with a fibular free tissue transfer provides optimal functional and cosmetic rehabilitation. (See "Treatment of stage I and II (early) head and neck cancer: The oral cavity", section on 'Lower alveolar ridge and retromolar trigone'.)

Upper alveolar ridge and hard palate — Hard palate cancers are rare. Locally advanced lesions typically involve the underlying bone, and primary surgery is used more commonly than definitive RT [27]. Resection is generally well tolerated. These patients can be reconstructed with either an immediate surgical obturator or microvascular-free tissue transfer.

Buccal mucosa — Buccal mucosa cancers have a high tendency to recur locoregionally. Consequently, patients with buccal mucosa cancers have a worse survival rate compared with patients with cancer in other oral cavity subsites [28].

Exposure of a buccal mucosa cancer can be difficult via a transoral approach, which makes it difficult to obtain clear radial margins in an en bloc fashion. Furthermore, the thin distance between the buccal mucosa and the buccal space permits early invasion to deep structures or to anterior cheek skin. Exenteration of the buccal space, parotid, and skin may be needed to maximize oncologic outcome for deeply invasive tumors, although this is achieved with a considerable cost to cosmesis.

Cancer of the buccal mucosa can be treated with definitive RT. However, deeply invasive cancers should be managed with surgery and postoperative RT. Regardless of the method of treatment, there is a high risk of severe, irreversible trismus. Aggressive reconstruction and rehabilitation is required to optimize functional outcomes. (See "Management of late complications of head and neck cancer and its treatment", section on 'Trismus'.)

Supportive care measures — Prophylactic tracheostomy is often required for locoregionally advanced oral cavity cancers undergoing surgery, except for cancers of the upper alveolar ridge and hard palate. The tracheostomy can usually be removed within a couple of weeks of surgery and prior to adjuvant therapy. In some cases, tracheostomy is maintained during adjuvant RT or chemoradiotherapy.

A feeding tube is usually required after surgery. A nasogastric feeding tube is feasible if the impact on swallowing is expected to be minimal and of relatively short duration. A gastrostomy tube is advised for patients in whom swallowing will be severely compromised.

MANAGEMENT OF THE NECK — Patients with stage III and IV oral cavity cancer either have clinically involved lymph node(s) in the neck or are at significant risk of subclinical nodal involvement due to the size and extent of the primary tumor. Thus, treatment of the neck is indicated [3]; this usually includes unilateral or bilateral neck dissection with postoperative radiation therapy (RT).

Although there is disagreement regarding some details, our approach is generally consistent with guidelines from the American Society of Clinical Oncology (ASCO) and the National Comprehensive Cancer Network (NCCN) [29,30]. An important difference is that we recommend adjuvant neck RT to patients with a single pathologically positive lymph node. While the NCCN allows for RT in this population, ASCO limits RT in this scenario to patients with high-risk features such as perineural invasion, lymphovascular space invasion, or a T3/4 primary.

The extent of neck dissection remains controversial. Elective lymph node dissection for clinically N0 tumors should include at least 18 lymph nodes. Limiting the extent of dissection reduces surgical morbidity, particularly if level V is excluded (figure 2). A selective dissection including levels I to III, a supraomohyoid neck dissection, is typically sufficient for clinically N0 oral cavity cancer, as level IV and V nodes are rarely involved without clinical disease at other levels [31-35]. This dissection includes the submandibular gland but preserves the spinal accessory nerve, the internal jugular vein, and the sternocleidomastoid muscle. Some cancers of the oral tongue, however, involve level IV lymph nodes without disease being present in levels I to III, a phenomenon known as "skip metastases" [32]. Level IV lymph nodes are included for therapeutic dissection of clinically positive nodes.

While patients with clinically involved regional lymph nodes may benefit from a complete modified neck dissection, selective neck dissection has been demonstrated to be oncologically sound in patients with advanced oral cavity cancer.

Contralateral metastases, and hence the need for bilateral neck treatment, are more likely for tumors that approach or cross the midline [36]. In addition, ventral oral tongue and floor of mouth cancers are at very high risk for bilateral nodal involvement. If postoperative RT is planned for the ipsilateral neck, some groups advocate RT to the contralateral N0 neck rather than neck dissection. Bilateral neck dissection combined with bilateral neck RT has a high risk of significant lymphedema, although surgical sparing of the jugular vein is the most important aspect of preventing edema in patients undergoing a bilateral neck dissection [37].

For patients receiving definitive RT, irradiation of the neck should follow the same indications as for neck dissection.

For patients initially treated with RT or chemoradiotherapy, management of the neck can be complex. A general discussion of the management of the neck in this situation is presented separately. (See "Management of the neck following definitive radiotherapy with or without chemoradiotherapy in head and neck squamous cell carcinoma".)

COMPLICATIONS — Both surgery and RT can have a profound effect on the quality of life, given the role of the oral cavity in speech, mastication, and swallowing. Thus, careful patient selection and surgical planning is required for all locoregionally advanced oral cavity cancer patients. The use of a multimodality approach in locally advanced oral cavity cancers increases the risk of serious complications.

Potential direct surgical complications include infection, bleeding, aspiration, wound breakdown, flap loss, and fistula [38].

Irradiation of the oral cavity and neck may result in mucositis, skin reaction, xerostomia, loss of taste, and dysphagia. Late toxicities may include skin and soft tissue atrophy and fibrosis, osteoradionecrosis, xerostomia, and trismus. (See "Management and prevention of complications during initial treatment of head and neck cancer" and "Management of late complications of head and neck cancer and its treatment".)

Recovery from xerostomia after irradiation of the oral cavity, even with modern conformal techniques, is more limited than with other head and neck sites because of higher doses of irradiation to the submandibular glands and larger volumes of oral mucosa and the minor salivary glands in the treatment fields [39]. Xerostomia also exacerbates other late complications, such as difficulty swallowing, impaired speech, and dental caries [40].

Osteoradionecrosis of the mandible is a particularly feared consequence of high-dose radiation to the oral cavity, and one of the primary reasons that surgery is often preferred to definitive RT [41].

The adoption of newer reconstructive techniques may decrease functional deficits from radical surgery involving the oral cavity [42,43]. However, these reconstructive techniques do not restore motor or sensory function. This is acceptable for smaller defects (eg, hemiglossectomy reconstructed with radial forearm free flap) where the remaining normal tissue can compensate well. On the other hand, larger defects (eg, total glossectomy reconstructed with rectus free flap) may result in permanent debilitating functional loss. (See "Mandibular and palatal reconstruction in patients with head and neck cancer".)

PROGNOSIS — The Surveillance, Epidemiology and End Results (SEER) Cancer Statistics review for the years 1975 to 2007 reports a five-year relative survival for locally advanced oral cavity and oropharyngeal cancer of 54.7 percent, in contrast to 82.5 percent for early-stage disease [44]. Although stage IVA patients have worse outcomes than stage III patients, it has been suggested that the subset of stage IVA patients with pT4N0 disease may have similar outcomes to stage III patients [45].

Lymph node involvement is the single most important prognostic factor for outcome in oral cavity cancer [46]. In addition to the presence or absence of lymph node metastasis, other factors include the number and size of positive lymph nodes, the presence of extranodal extension, and the ratio of positive lymph nodes to total number of excised lymph nodes [47-49]. With regard to the primary lesion, higher histologic grade, the presence of perineural invasion and increasing size have been correlated with worse outcomes [50,51].

POSTTREATMENT EVALUATION AND SURVEILLANCE — Regular posttreatment follow-up is an essential part of the care of patients after potentially curative treatment of oral cavity cancer, both to detect recurrent disease and to diagnose second malignancies that may develop, as well as to treat or prevent the consequences of functional issues. Patients should be educated about possible signs and symptoms of tumor recurrence, including hoarseness, pain, dysphagia, bleeding, and enlarged lymph nodes. (See "Second primary malignancies in patients with head and neck cancers".)

In general, the intensity of follow-up is greatest in the first two to four years, since approximately 80 to 90 percent of all recurrences will occur within this timeframe. Because of the higher risk of recurrence and second primary malignancy in those who continue tobacco use, many schedule more frequent surveillance visits for these patients and also continue surveillance beyond five years.

All patients treated for advanced stage oral cavity cancer will require intensive functional rehabilitation in addition to cancer surveillance. Patients should be counseled in smoking cessation and referred for dental, speech, hearing, and swallowing evaluation. (See "Overview of treatment for head and neck cancer" and "Speech and swallowing rehabilitation of the patient with head and neck cancer".)

Posttreatment surveillance of patients with head and neck cancer, including screening for treatment-related complications, is reviewed separately. (See "Posttreatment surveillance of squamous cell carcinoma of the head and neck".)

SOCIETY GUIDELINE LINKS — Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Head and neck cancer".)

INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5th to 6th grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10th to 12th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword(s) of interest.)

Basics topic (see "Patient education: Tongue cancer (The Basics)" and "Patient education: Mouth sores (The Basics)")

SUMMARY AND RECOMMENDATIONS

Oral cavity squamous cell carcinomas include tumors originating in the lip, floor of mouth, oral tongue, lower alveolar ridge, upper alveolar ridge, retromolar trigone, hard palate, and buccal mucosa.

Locally advanced oral cavity cancer typically requires multimodality treatment due to the relatively high risk of locoregional recurrence and disease-related mortality. All patients should be seen preoperatively by the surgeon, radiation oncologist, and medical oncologist for preoperative treatment planning. (See 'General principles' above.)

For most patients with locoregionally advanced oral cavity cancer, we suggest surgical resection of the primary tumor and neck dissection, followed by postoperative radiation therapy (RT) or chemoradiotherapy, as the initial treatment, rather than RT or chemotherapy (Grade 2B). (See 'Treatment of primary tumor' above.)

The optimal extent of the neck dissection is partially influenced by the extent of the primary tumor. Tumors that approach or cross the midline, and oral tongue and floor of mouth cancers are treated with bilateral neck treatment. For patients receiving definitive RT, irradiation of the neck should follow the same indications as for neck dissection. (See 'Management of the neck' above.)

Most patients with locoregionally advanced oral cavity cancer remain at significant risk for local recurrence after surgery. We recommend postoperative RT with or without concurrent chemotherapy (Grade 1B). We recommend postoperative chemoradiotherapy over postoperative RT alone for patients with positive surgical margins and extranodal extension (Grade 1B). (See 'Postoperative RT and chemoradiotherapy' above.)

Definitive RT or chemotherapy plus RT are options for patients who are medically inoperable, who have unresectable disease, or who have resectable disease where surgical resection cannot be accomplished with acceptable long-term functional consequences. (See 'Nonsurgical candidates' above.)

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  32. Byers RM, Weber RS, Andrews T, et al. Frequency and therapeutic implications of "skip metastases" in the neck from squamous carcinoma of the oral tongue. Head Neck 1997; 19:14.
  33. Dias FL, Lima RA, Kligerman J, et al. Relevance of skip metastases for squamous cell carcinoma of the oral tongue and the floor of the mouth. Otolaryngol Head Neck Surg 2006; 134:460.
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  40. Pauloski BR, Rademaker AW, Logemann JA, Colangelo LA. Speech and swallowing in irradiated and nonirradiated postsurgical oral cancer patients. Otolaryngol Head Neck Surg 1998; 118:616.
  41. Oh HK, Chambers MS, Martin JW, et al. Osteoradionecrosis of the mandible: treatment outcomes and factors influencing the progress of osteoradionecrosis. J Oral Maxillofac Surg 2009; 67:1378.
  42. Curtis DA, Plesh O, Miller AJ, et al. A comparison of masticatory function in patients with or without reconstruction of the mandible. Head Neck 1997; 19:287.
  43. Urken ML, Buchbinder D, Weinberg H, et al. Functional evaluation following microvascular oromandibular reconstruction of the oral cancer patient: a comparative study of reconstructed and nonreconstructed patients. Laryngoscope 1991; 101:935.
  44. http://seer.cancer.gov/csr/1975_2007/ (Accessed on March 14, 2011).
  45. Liao CT, Chang JT, Wang HM, et al. Survival in squamous cell carcinoma of the oral cavity: differences between pT4 N0 and other stage IVA categories. Cancer 2007; 110:564.
  46. Shah JP, Cendon RA, Farr HW, Strong EW. Carcinoma of the oral cavity. factors affecting treatment failure at the primary site and neck. Am J Surg 1976; 132:504.
  47. Gil Z, Carlson DL, Boyle JO, et al. Lymph node density is a significant predictor of outcome in patients with oral cancer. Cancer 2009; 115:5700.
  48. Gross ND, Patel SG, Carvalho AL, et al. Nomogram for deciding adjuvant treatment after surgery for oral cavity squamous cell carcinoma. Head Neck 2008; 30:1352.
  49. Myers JN, Greenberg JS, Mo V, Roberts D. Extracapsular spread. A significant predictor of treatment failure in patients with squamous cell carcinoma of the tongue. Cancer 2001; 92:3030.
  50. Fagan JJ, Collins B, Barnes L, et al. Perineural invasion in squamous cell carcinoma of the head and neck. Arch Otolaryngol Head Neck Surg 1998; 124:637.
  51. Arduino PG, Carrozzo M, Chiecchio A, et al. Clinical and histopathologic independent prognostic factors in oral squamous cell carcinoma: a retrospective study of 334 cases. J Oral Maxillofac Surg 2008; 66:1570.
Topic 3389 Version 36.0

References

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2 : Interventions for the treatment of oral and oropharyngeal cancers: surgical treatment.

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27 : Carcinoma of the hard palate treated with radiotherapy: a retrospective review of 31 cases.

28 : Squamous cell carcinoma of the buccal mucosa: one institution's experience with 119 previously untreated patients.

29 : Management of the Neck in Squamous Cell Carcinoma of the Oral Cavity and Oropharynx: ASCO Clinical Practice Guideline.

30 : Management of the Neck in Squamous Cell Carcinoma of the Oral Cavity and Oropharynx: ASCO Clinical Practice Guideline.

31 : Results of selective neck dissection in management of the node-positive neck.

32 : Frequency and therapeutic implications of "skip metastases" in the neck from squamous carcinoma of the oral tongue.

33 : Relevance of skip metastases for squamous cell carcinoma of the oral tongue and the floor of the mouth.

34 : Elective management of the neck in oral cavity squamous carcinoma: current concepts supported by prospective studies.

35 : Lymphatic mapping to tailor selective lymphadenectomy in cN0 tongue carcinoma: beyond the sentinel node concept.

36 : Prognostic factors influencing contralateral neck lymph node metastases in oral and oropharyngeal carcinoma.

37 : Prognostic factors influencing contralateral neck lymph node metastases in oral and oropharyngeal carcinoma.

38 : Prognostic factors influencing contralateral neck lymph node metastases in oral and oropharyngeal carcinoma.

39 : Intensity-modulated radiotherapy in postoperative treatment of oral cavity cancers.

40 : Speech and swallowing in irradiated and nonirradiated postsurgical oral cancer patients.

41 : Osteoradionecrosis of the mandible: treatment outcomes and factors influencing the progress of osteoradionecrosis.

42 : A comparison of masticatory function in patients with or without reconstruction of the mandible.

43 : Functional evaluation following microvascular oromandibular reconstruction of the oral cancer patient: a comparative study of reconstructed and nonreconstructed patients.

44 : Functional evaluation following microvascular oromandibular reconstruction of the oral cancer patient: a comparative study of reconstructed and nonreconstructed patients.

45 : Survival in squamous cell carcinoma of the oral cavity: differences between pT4 N0 and other stage IVA categories.

46 : Carcinoma of the oral cavity. factors affecting treatment failure at the primary site and neck.

47 : Lymph node density is a significant predictor of outcome in patients with oral cancer.

48 : Nomogram for deciding adjuvant treatment after surgery for oral cavity squamous cell carcinoma.

49 : Extracapsular spread. A significant predictor of treatment failure in patients with squamous cell carcinoma of the tongue.

50 : Perineural invasion in squamous cell carcinoma of the head and neck.

51 : Clinical and histopathologic independent prognostic factors in oral squamous cell carcinoma: a retrospective study of 334 cases.