Abstract
Oral Cavity Squamous Cell Carcinoma (OSCC), is a heterogenous disease with respect to risk factors, geographic predelictions, treatment response and outcome. Although non-surgical treatment is employed in other head and neck sub-sites, surgery is the primary treatment modality to treat oral cancers followed by adjuvant treatment either in the form of radiation or chemoradiation based on the risk features on final histopathology. It is utmost importance that all the patients before undergo treatment are discussed and treatment plan is formulated in a multidisciplinary tumor board. This chapter intent to elaborate the basic surgical principles involved in management of different sub-sites of oral cavity as well as reconstruction of the defects.
You have full access to this open access chapter, Download chapter PDF
Similar content being viewed by others
Keywords
1 Introduction
Management of oral cavity cancers in a curative intent setting mainly involves surgery. The other treatment modalities such as radiotherapy and chemotherapy are most commonly used as adjuvant treatment based on the histopathological features. However, it is to be noted that surgery alone is insufficient to treat oral cancer. Chemotherapy is either concurrent with radiotherapy or in very rare scenario used as induction therapy. The primary cancer treatment and risk factor reduction are of utmost importance to improve effectiveness of the primary treatment and to prevent development of second-primary cancers.
Ablative surgery has evolved over the years with the attempt to extirpate the tumor in its entirety with the understanding of the molecular tumor biology, pattern of tumor invasion of the tumors, as well as availability of better instrumentations.
With the advent of endoscopic assisted and robotic-assisted neck dissection, the branch of oral oncology has truly made progress, thus improving visualization and three-dimensional navigation; however it is still in its infancy and needs further research to understand the benefits over the conventional methods.
This chapter outlines details of ablative surgery and rationale for addressing neck (node positive/node negative) in patients with oral cavity cancers.
2 Initial Evaluation and Staging
Initial evaluation as for any other medical condition includes history, a clinical examination and investigations to form a diagnosis. The other two important aspects influencing management of oral cavity cancer (mainly squamous cell carcinoma) are habit history and performance status. Table 82.1 describes the performance status scales.
Staging of the disease is particularly important as it helps the clinicians in better communication in a scientific forum and forming a treatment plan for a patient. Various phases in management of oral cancer include accurate diagnosis, appropriate treatment plan, and execution of the advised treatment with relevant reconstruction, rehabilitation, and surveillance. So, to help clinicians in decision-making, there are several guidelines that exist. As these guidelines have a more generalized approach, it is the clinician’s knowledge and understanding and experience which will help in tailoring the treatment plan to each individual distinctly. This individualized approach cannot be implemented unless there are multidisciplinary tumor board meetings, which are crucial for clinicians practicing oncology and hence provides team-based practice keeping the patient in mind [2,3,4]. This is best done before initiating the treatment.
To be able to know the extent of disease and decide the intent and modality of treatment, imaging plays a very important role. Precise imaging information is needed to determine the locoregional extent, erosion, and involvement of underlying bone and marrow space, lymph node involvement and to rule out distant metastasis—especially to the lungs. However the dilemma that most clinicians face is which is the imaging modality of choice for different clinical scenarios. In the following section, we attempt to provide indications of each imaging type available, which probably will help the clinicians in deciding what suits their needs.
Plain radiography is restricted to evaluation of pathological fractures or initial benign lesions. Contrast-enhanced computed tomography (CECT) is considered as the most popular, easily available, and cost-effective diagnostic imaging. It is the imaging modality of choice to know the presence of bone erosion and lymph node characteristic. Bony expansion is usually a feature of slow-growing/benign disease process; however destruction of bone and replacement by the tumor depicts the aggressiveness and hence is a feature of malignant process (Figs. 82.1, 82.2, 82.3 and 82.4).
Magnetic resonance imaging (MRI) is usually indicated as an adjunct as it has better soft tissue delineation. It is also used for assessing dural invasion (linear or nodular), medullary bone involvement, and perineural invasion. Radiographic assessment of tumor extent is invaluable for treatment planning. In case of tongue cancers, MRI has gained popularity for assessment of tongue cancer especially as it is helpful in identifying tumor thickness, involvement of the contralateral side, and involvement of extrinsic muscles. With recent addition of depth of invasion in the AJCC classification for staging, MRI has proven its role. As for buccal mucosa tumors, assessment of masticatory muscles involvement is crucial because it has historically been considered unresectable. However, according to Liao, infra-notch lesions are still amenable for resection with favorable oncological outcome.
As oral cancers usually metastasize first to the lung, preoperative chest imaging is a part of initial pre-operative work-up. This can be in the form of either plain film or 3D imaging such as computed tomography (CT). Fluorodeoxyglucose positron emission tomography (FDG-PET) scan has emerged as the imaging modality of choice in patient with recurrence and high clinical suspicion for distant metastasis (Figs. 82.5, 82.6, 82.7 and 82.8).
It is to be noted that any suspicious lesions in PET-CT scan needs to be corroborated with tissue diagnosis (direct or guided) as there are a subset of lesions with false-positive findings; however, PET-CT is considered to have the highest negative predictive value approaching 100%. Although as per the NCCN guidelines, PET-CT has to be advised for all stage III and IV disease, it is usually reserved for patients with recurrent or second primary disease in a resource-constrained setting [5, 6]. Tables 82.2 and 82.3 provide imaging considerations in oral cavity tumors.
Baseline follow-up imaging is usually done after 3 months, and CECT has established its role in ruling out recurrence/residual disease. To avoid misinterpretation, it is important that the concerned imaging radiologist is familiarized with postoperative sequelae of tissue changes or changes that occur following radiotherapy such as nonspecific tissue thickening, edema, or fibrosis and various bony and soft tissue reconstruction methods to facilitate interpretation.
Staging the disease is developed to provide ease of communication and helps in understanding the prognosis and planning the treatment. AJCC staging system has been followed for years and provides concise information on size characteristics and extent of primary tumor and involvement of lymph nodes. The recent eighth edition has features like tumor thickness, depth of invasion, and extranodal extension (clinical and pathological).
4 Principles of Surgical Management
In majority of oral cavity squamous cell cancers, surgery has been the mainstay of treatment, and hence, the need to know intricate surgical aspects has to be emphasized. As there has been improved understanding of disease pattern, biologic behavior of the disease at the molecular level, and the potential aggressive nature, the need has arisen for several technical modifications in this era. Hence as surgeons, we have to evolve and adapt to the required changes to improve outcomes of ablative surgery (oncological and functional) in patients with squamous cell carcinoma of oral cavity.
For early-stage oral cavity cancers, especially tongue, it has been proven that both surgery and radiotherapy/brachytherapy offer similar outcome (single modality). For advanced lesions with extensive disease, multimodality treatment is required; surgery being the primary modality and followed by adjuvant radiotherapy +/− chemotherapy (depending on the histopathological evaluation) has been the standard of care.
5 Treatment Decision Algorithm [14]
Critical decisions which have to be made are as follows:
-
1.
Intent of treatment—curative vs. palliative treatment.
-
2.
Primary modality—surgical vs. non-surgical treatment.
-
3.
Need for addressing neck in clinically node-negative patients.
-
4.
Type of neck dissection in patients with metastatic lymph nodes.
-
5.
Need for adjuvant treatment.
-
6.
Type of adjuvant treatment.
-
7.
Best supportive care.
Decision 1
Primary intent of treatment: This is the first and most critical decision-making point. All patients other than those with technically unresectable tumors, distant metastasis, poor performance status, and major comorbidities precluding surgery must be considered for treatment with curative intent. However, it is to be noted that surgical excision with positive margins portends poor prognosis. Palliative care is usually when patient has distant metastasis and given only to relieve symptoms and control spread. This is in the form of chemotherapy, radiotherapy or metronomics.
Decision 2
Curative modality of treatment: The primary treatment for patients with oral cavity cancers is surgery. However, in selected scenarios, non-surgical treatment may be considered. This includes primary radiotherapy for tumors of the commissure of mouth and lip tumors where surgery can cause significant esthetic and functional disability. In addition, significant comorbidities that preclude long anesthesia may necessitate the need for primary radiotherapy or chemoradiotherapy. However primary chemoradiotherapy has very limited role in treatment of oral cancers.
Decision 3
Management of neck in N0 stage: Even with no radiographic evidence of significant suspicious lymph-nodes, rate of occult metastasis reaches up to as high as 30% [15]. Presence of lymph node metastasis and the number of lymph nodes involved have a direct relation with the prognosis of the disease; decreasing the overall survival rate by 50%. Moreover, a significant subset of metastatic nodes of less than 1 cm can have extranodal extension [16]. This further worsens the prognosis. There is now level I evidence from a randomized control trial, that addressing the neck surgically irrespective of the lymph node status improves overall survival to about 84% when compared to 69% in patients who were selected for wait-and-watch policy [17]. Therefore, almost all the patients with oral cavity cancer should undergo elective neck dissection. A subset analysis of the same study did not show benefit for primary tumors of depth less than 3 mm. This may be considered in selected patients with cancers of lower nodal metastatic prevalence such as lip and buccal mucosa.
Decision 4
Extent of neck dissection in N+ve oral squamous cell carcinoma: Conventional teaching is that any patients with N+ve neck should undergo modified radical neck dissection covering levels 1–5. This has been questioned by several observational studies. Large cohort of patients who have undergone radical neck dissection for N+ve disease has showed less than 3% incidence of level V nodes [17]. This also was observed only when there were pathologically positive level IV nodes [18]. There are reports of oncologic safety for clearing level I–III lymph nodes for alveolus and buccal mucosal cancers and to clear level IV in addition to levels I, II, and III lymph nodes in patients with oral tongue cancers as they bore high risk of skip metastasis [19]. It is to be noted that when a patient is found to have pathological nodal metastasis, in general, it is recommended for adjuvant radiation that covers all levels of the neck with additional boost in the levels which are positive for metastasis.
Decision 5
Indication for adjuvant radiotherapy: Any patients with more than one of the high risk features should be considered for adjuvant radiotherapy.
This includes (1) nodal metastasis without extracapsular extension, (2) perineural invasion, (3) lymphovascular invasion, (4) poor differentiation, (5) close margin (1–5 mm), and (6) depth of invasion over 1 cm.
But the absolute indication for radiotherapy is stage III and IV disease.
Decision 6
Indication for adjuvant chemoradiotherapy: Meta-analysis of two randomized trials has suggested that in patients with positive surgical margin (<1 mm) and neck nodes with extranodal extension would benefit from adjuvant chemoradiotherapy.
Decision 7
Best supportive care options: This is an important and critical decision. Once the decision for treatment with palliative intent is arrived at, the goal should be made clear with the treating team of doctors and the patient/patient attenders. Ambiguity at this stage may result in loss of trust between the treating team and the patient, causing delay in treatment and possible increase in morbidity. Although this decision is made in the multidisciplinary tumor board, it requires series of meetings with the family to convey the treatment goals. It is also essential to appreciate by treatment group that lack of active treatment does not mean stoppage of care, which needs to be provided by the same team till the end. The quality of death is equally important as quality of life.
The role of best supportive care is to palliate the symptoms the patients may have. In this situation, it is essential to balance the morbidity of treatment versus potential benefit the patient may receive. Often one may have ethical dilemma when faced with young patients with locoregionally advanced tumors. In this situation, temptation of surgery should be tempered. One should consider surgery as palliation to alleviate fungating ulcers or to close a cutaneous fistula. The goal of this surgery must be made very clear to the family. It is essential not to give false hope to the family, which will have deleterious consequence in the patient-physician relationship. In patients with good performance status, especially those who have not received previous radiotherapy, one may consider chemoradiotherapy with curative dose, with the goal to obtain durable palliation. In doubtful situations, induction chemotherapy followed by chemoradiotherapy could also be considered. Local radiation or re-radiation to a limited field may be considered for fungating ulcers. The dose, fractionation, and volume of radiation field need to be tailored for palliative purpose.
In patients with advanced metastatic disease, one needs to be very selective in recommending systemic therapy as the benefit is doubtful. Chemotherapy with targeted anti-EGFr treatment has shown improved survival up to 4 months, with significant morbidity associated with the regimen [20]. An alternate approach is chemotherapy at metronomic dosing regimen, especially the use of methotrexate and celecoxib [21]. Recent evidence of nivolumab, a checkpoint inhibitor, showing improved survival of about 3 months, and acceptable morbidity, is to be considered. However the cost of the treatment is a major deterrent for its wider application. Table 82.5 provides the indications for adjuvant RT and adjuvant CT + RT.
6 Indications for Adjuvant RT and Adjuvant CT + RT
After various comparative studies, it has been concluded that in adjuvant setting, postoperative IMRT has to be given at dose of 60 Gy in 30 fractions to surgical bed and first echelon nodal stations and the high-risk regions receive a total dose of 66 Gy. It has to be remembered that for salvage surgery cases, concept of re-irradiation should be explained to the patient. A minimum of 12-month duration gap is required prior to re-irradiation to allow for the spinal cord recovery.
In cases with postoperative histopathological features like extranodal extension or positive surgical margins, patients are treated with concurrent chemoradiation (usually 100 mg/m2 of cisplatin for a maximum of 6 cycles in India). Indication of chemotherapy as described is usually in adjuvant setting in oral cavity cancers.
However role of chemotherapy as induction therapy is evolving. Chemotherapy usually exerts its cytotoxic effects systemically and hence associated with side effects. The major drawbacks of chemotherapeutic agents used commonly are the adverse toxicities and cellular resistance. In an induction setting, most commonly taxanes, platinum, and 5FU are used as 3 cycle regimen (also refer Chap. 84 of this book on Adjunctive therapy in Oral Cancer).
Tumors of oral cavity which are considered technically unresectable are as follows:
-
Erosion of skull base, sphenoid bone, and widening of foramen ovale.
-
Encasement of internal carotid artery, >270 degree.
-
Involvement of mediastinal structures.
-
Involvement of prevertebral fascia or cervical vertebrae.
These are considered unresectable not due to surgical technicality but because of the inability to get negative margins and to achieve R0 resection. However, with the superior skills such as endoscopic-assisted surgeries which are associated with less morbidity, and better adjuvant treatment including chemotherapy, an attempt has been made to consider resection of tumors involving muscles of mastication and pterygoid plates especially with the anterior infratemporal fossa involved. Recent studies have shown that surgical resection of these tumors along with adjuvant treatment has shown survival benefit. Also studies from Tata Memorial Hospital, India have shown better outcome in patients who have undergone surgical resection following neoadjuvant chemotherapy.
7 Principles of Ablative Surgery
-
1.
Adequate access to the tumor.
-
2.
To achieve negative surgical margins.
-
3.
Utilization of intraoperative frozen section for margin assessment.
-
4.
Wide excision versus compartment resection.
The surgical approaches for tumors of oral cavity depends primarily on the site of tumor (anterior versus posterior), its size, and its proximity to bone (maxilla or mandible). The various approaches frequently used for oral cavity cancers are shown in Figs. 82.9, 82.10, 82.11, 82.12, 82.13, and 82.14 (Also refer Chap. 85 of this book on Access Surgeries and Osteotomies of the Maxillofacial Region).
Types of mandibulotomy is shown in (Figs. 82.15, 82.16a, b) shows marginal mandibulectomy and segmental mandibulectomy.
8 Sub-Site-Wise Surgical Management
8.1 Tongue and Floor of Mouth
The tongue is a muscular organ which is composed of intrinsic and extrinsic muscles and divided anatomically into the oral tongue (falls in oral cavity cancers) and base of tongue (BOT, sub-site of oropharynx). The tongue is innervated by the hypoglossal nerve, and vascularity is by lingual artery (branch of external carotid artery). Pathway of tumor spread from the oral tongue can be into the floor of mouth, mandible, or/and base of tongue via local extension, the lingual septum being the barrier to tumor spread. For tumors abutting the mandible, marginal mandibulectomy is indicated for negative surgical margin encompassing the tumor and at the same time preserving the mandibular continuity. Segmental mandibulectomy is usually done when there is mandibular erosion or paramandibular spread. Anterior segmental mandibulectomy is more commonly indicated in floor of the mouth cancers.
Lingual artery is an end artery, and hence clinicians have to be careful in resections involving more than two-thirds of tongue mass as this may jeopardize the vascularity and utmost care to be taken to preserve the neurovascular bundle.
There is a recent concept of compartment resection in patients with infiltrative disease where the adjacent extrinsic musculature and neurovascular bundle is excised in continuity to ensure negative margins. This was proposed by Calabrese [23], and all cases underwent access mandibulotomy; hence it is not commonly followed. Tumors of floor of the mouth are usually infiltrative and lymph node metastasis is seen bilaterally. According to Byers, the rate of lymph node skip metastasis at level IV is observed in about 10–15% cases. According to the study by Kowalski [24], tumors of floor of the mouth, tongue cancers crossing the midline, and advanced stage of the disease have a propensity of developing contralateral lymph node metastasis.
8.1.1 Surgery
Wide local excision (WLE)/adequate glossectomy procedure with adequate surgical margins has been the procedure of choice for early tongue cancers, and this is amenable with per-oral approach. Before planning resection, thorough knowledge about the extent of lesion is important, and palpation of induration provides a guide for the same. Ideal margin for resection of tumour is all 1–1.5 cm all around. Usually it is the deep soft tissue margin which is prone for being close or positive, and this can be avoided by palpation method. In many institutions, it is a useful practice to ligate the lingual artery in the neck before performing WLE for adequate bleeding control and clean surgical field. The resulting defects of adequate glossectomy for early lesions are usually closed primarily avoiding tethering of the tongue. Excisional biopsy for suspicious lesions is highly discouraged even if the lesion is about 1 cm.
Moderately advanced cancers of the tongue and floor of the mouth (T2–T3) warrant classical hemiglossectomy which sacrifices the tip jeopardizing the tongue mobility resulting in compromised speech and swallowing. Majority of these tumors are excised by combinations of per-oral and pull-through approaches, without the actual need for lip-split or access mandibulotomy. The pull through technique helps in avoiding positive posterior margins as the resection is done under direct vision. All these patients require reconstructive surgery (lining or bulk), along with long-term tracheostomy and feeding tube (ryles tube/PEG) dependence. Free-flap reconstructions have become inevitable following resection of tongue cancers. Locally advanced (T4a) cancers (tumor depth > 20 mm, restricted mobility and hypoglossal palsy) of tongue warrant total glossectomy or near-total glossectomy. Standard total glossectomy procedure involves complete removal of anatomical tongue from mandible to hyoid and from the tip of the tongue upto the vallecula.
The following a is brief outlay of surgical steps: anterior belly of digastric muscle is first divided through the cervical neck incision followed by intra-oral crevicular incision. Then the genioglossus, geniohyoid is divided from the genial tubercle and mylohyoid muscle from the mylohyoid line from the mandible. At the contralateral retromolar region come the division of buccopharyngeal fascia, styloglossus muscle, and the palatoglossus muscle and incision at the vallecula. The same steps are repeated on the other side for total glossectomy. However in near-total/subtotal glossectomy, base of the tongue of uninvolved side is preserved. It is the extent of excision of the base of tongue which determines the postoperative swallowing function.
Tongue and the FOM lesions involving or abutting mandible pose a unique challenge. Resecting the segment of mandible increases morbidity and reconstructive challenge by many times. In such situations an attempt should be made to preserve the mandible whenever possible.
Removal of the level V lymph node is reserved in situations when level IV or V is involved or in N3 nodal disease. According to Kowalski et al., the indications for addressing contralateral lymph nodes are lesions of the tongue crossing the midline, floor of the mouth tumors, and locally advanced T3 and T4 tumors [24].
Reconstruction of the tongue requires a soft tissue flap with large volume to provide the adequate bulk which in turn is believed to aid in swallowing. The drawback of a reconstructed tongue is the impaired mobility resulting in compromised speech. The most commonly used flap is radial forearm free flap and anterolateral thigh free flap. The other uncommon examples for free tissue transfer are lateral arm flap, gracilis flap, and local flap such as FAMM flap and submental flap.
Reconstruction of tongue defect using radial forearm free flap (Figs. 82.17, 82.18, 82.19, 82.20 and 82.21).
Reconstruction of tongue defect with local flap: facial artery myomucosal flap (Figs. 82.22, 82.23, 82.24 and 82.25).
8.2 Buccal Mucosa
8.2.1 T1/T2 Lesions
Surgical Steps: For Early Buccal Cancer
Per-oral approach is adequate. It is important to ensure oncologic completeness and appreciate depth. Inadvertent injury to the buccal branch of facial nerve and to the parotid duct should be avoided. Facial artery, facial vein, and parotid duct (if encountered or injured) should be ligated. Mucosal incision around the lesion, with adequate margin, taking the buccinator muscle in specimen forms the deep soft tissue margin. These defects can be reconstructed with split thickness skin grafts/buccal pad of fat/local flaps such as nasolabial flap.
Advanced T3/T4 Lesions (Lesions with Skin Involvement/Bone Involvement/Involvement of Muscles of Mastication)
Pre-operative clinical examination revealing a subtle skin puckering and imaging studies shows stranding of subcutaneous fat that is the early sign of skin involvement. If buccal space involvement is suspected, then buccal fat pad should be included in the specimen.
These advanced lesions require full-thickness cheek resection. The planning of incision may be a midline lip split or angle split, both of which will help in raising a lower cheek flap or when overlying skin is involved, an incision around the skin involved in continuity with the neck dissection incision. The muscle of mastication involvement warrants infratemporal fossa clearance (Figs. 82.26, 82.27 and 82.28).
8.3 Gingivobuccal Sulcus
Gingivobuccal sulcus (GBS) tumors are tumors occurring in the upper or lower GBS, usually seen to abut the bone adjacent (Fig. 82.29). These occur almost exclusively in Southeast Asia due to high incidence of chewing tobacco use. Due to the high propensity for local invasion and close proximity of bone, skin, and masticator space, presentation is often advanced, and outcomes are poor. If there is superficial erosion of bone or if the lesion is abutting the mandible, then the resection should include marginal mandibulectomy. Superficial cortical erosion in alveolar tumors is not considered as T4 lesion, and marginal mandibulectomy may still suffice. Although MRI is considered most sensitive imaging modality to determine extent of bony involvement, periosteal stripping is by far the best method to determine extent of bony erosion and helps in decision-making regarding extent of mandibulectomy. GBS tumors usually present at an advanced stage with gross mandibular erosion, paramandibular spread, or overlying skin involvement (skin involvement is never seen in the masseter region as it is a tumor barrier). These findings preclude the use of marginal mandibulectomy, and hence patients often require segmental mandibulectomy and bony reconstruction.
8.4 Retromolar Trigone Carcinoma
Retromolar trigone tumors are rare but more aggressive malignancies with poorer outcome. Higher incidence of local recurrence has been reported in squamous cell carcinoma of the retromolar trigone (RMT) and posterior GBS carcinomas. This is attributed to to its higher propensity of infratemporal fossa (ITF) and pterygomandibular fissure involvement. Due to restricted mouth opening at the time of presentation, thorough clinical examination is hindered. For both oncologic and anatomic reasons, tumors with mandibular invasion are best managed surgically by segmental mandibulectomy including coronoid process of the mandible.
The reason to preserve condyle is as follows: (a) it may be used for secondary reconstruction, and (b) as the condyle lacks medullary bone, it does not act as a pathway of spread and hence can be oncologically safe to preserve it.
As a large proportion of the RMT tumors involve both the upper and lower jaw (Fig. 82.30), excision of ramus of mandible in the form of subsigmoid marginal mandibulectomy with at least an upper alveolectomy and ITF clearance (anterior ITF comprising masseter and medial pterygoid with or without pterygoid plates) is required. Selective neck dissection comprising of level I–V lymph nodes is usually performed electively for all stage cancers for purpose of staging.
8.5 Hard Palate
Tumors of the hard palate are less common when compared to tumors of the mandible, tongue, or buccal mucosa and are often of minor salivary gland etiology. Premaxilla provides support for the nose and midface; lesions involving anterior alveolus and hard palate will require bony reconstruction to prevent midface deformity. Lesions of the posterior alveolus and hard palate have a higher tendency to locally invade the orbital floor and skull base or through various neurovascular bundles (greater palatine foramen, sphenopalatine foramen, palatovaginal canal).
Lymph node involvement is very rare for salivary neoplasm of the palate, and neck dissection is reserved only for node-positive disease. However, maxillary alveolar carcinoma has a high propensity for occult lymph node metastasis (15–20%), and also in patients where neck is not addressed, they tend to present with nodal recurrences which are not salvageable in two-thirds of the cases; hence it is wise to consider elective neck dissection. The other point worthwhile and to be noted is that perifacial group of lymph nodes have to be cleared for effective disease control for the upper alveolus (Figs. 82.31, 82.32, 82.33 and 82.34).
8.5.1 Brown’s Classification System for Maxillary Defects [25] (Fig. 82.35)
Vertical Component
-
Class I, maxillectomy with no oroantral fistula.
-
Class II, low maxillectomy.
-
Class III, high maxillectomy.
-
Class IV, radical maxillectomy.
Horizontal Component
I, unilateral alveolar maxilla and resection of the hard palate;
(a) resection of less than or equal to half of the alveolar and hard palate, not involving the nasal septum or crossing the midline;
(b) resection of the bilateral alveolar maxilla and hard palate, including a smaller resection that crosses the midline of the alveolar bone, including the nasal septum; and
(c) removal of the entire alveolar maxilla and hard palate.
8.6 Lip Carcinoma
Squamous cell carcinoma of the lip is most frequently associated with sun exposure as the risk factor. Lower lip is more commonly involved than the upper lip. Submental and submandibular nodal basins are the primary echelon drainage pathways; regional nodal metastasis occurs in only 10% of patients. Full-thickness excision with up to 1 cm margin is necessary. Lesions that involve less than one-third of the lip are managed with simple wedge excision and primary closure and hence offer acceptable oncologic and reconstructive results. For lesions larger than one-third but less than two-thirds, Abbe-Estlander or Karapandzic flap can be utilized (refer Chap. 86 on Soft tissue reconstruction of the Maxillofacial Region). For defects more than two-thirds, free tissue transfer is preferred to achieve better cosmetic result and avoid microstomia and oral incompetence. To ensure oral competence, adjunctive procedures such as fascial sling, palmaris longus sling, or temporalis muscle sling can be used along with the adynamic soft tissue flap.
Table 82.6 describes the treatment modalities of use in oral cancer.
8.6.1 Management of the Neck in Oral Cavity
8.6.1.1 Introduction
Although skip metastasis can occur, lymph node metastasis usually follows a predictable fashion from the first echelon nodes to the second echelon nodes. Tumors of the oral cavity most commonly drain to levels I (submental and submandibular group) and level II (upper jugular group) in the neck. Level IA is between the two anterior belly of digastric muscle, and level IB is between anterior and posterior belly of digastric muscle on either side. The submental triangle drains the anterior portion of the oral cavity and hence can get involved in the tumors of the incisor region, the anterior floor of mouth, or anterior mandibular gingival/alveolar cancers. The level II nodes are found between the level of the hyoid bone inferiorly and anteriorly, the posterior belly of the digastric muscle superiorly, and the posterior border of the sternocleidomastoid muscle (SCM) posteriorly. In the jugular chain, the level III lymph node station is demarcated inferiorly by the omohyoid muscle as it crosses the internal jugular vein (IJV) and contains the mid-jugular lymph nodes particularly the prominent omohyoid node lying in close relationship to the muscle. Level IV (between the omohyoid muscle and the transverse cervical vessels, medially bound by the IJV) and V (between the posterior border of SCM and anterior border of trapezius muscle, further divided into levels A and B by the spinal accessory nerve) nodes are very rarely directly involved by early initial spread of oral SCC. In addition to these classical patterns of spread, buccal cancers may present with parotid nodes, and the posterior maxillary alveolus/hard palate may spread initially to retropharyngeal nodes. Tumors involving/crossing midline and tumors of the floor of the mouth generally require bilateral neck dissection.
9 Evaluation and Diagnosis
Evaluation of neck disease for the purpose of staging is best done by USG-guided FNAC, it being both highly sensitive and specific, simple, and cost-effective but observer dependent. Although palpation is most commonly employed, it has a very low accuracy ranging between 50 and 65%. The limitations of palpation method are obese patients or patients with previously treated necks; examination is more difficult. Imaging with CT scan or MR has been said to improve accuracy for metastatic neck disease to approximately 90%. Chaukar et al. found contrast-enhanced CT to give better concordance with histology in the N0 neck than either US or PET/CT.
10 Management
Evolution of neck dissection [26, 27]:
-
1906—George Crile described the classic radical neck dissection (RND).
-
1933 and 1941—Blair and Martin popularized the RND.
-
1967—Bocca and Pignataro described the “functional neck dissection” (FND).
-
1975—Bocca established oncologic safety of the FND compared to the RND.
Technique:
-
The incision is made through the skin and deepened to divide subcutaneous tissues. Thus exposing the platysma (Thin pink muscle layer) which is incised in a single stroke.
-
This is followed by raising of the subplatysmal flaps with the superior limit being the lower border of the mandible; anteriorly it is extends to the midline, posterior border of sternocleidomastoid (SCM) muscle posteriorly, and inferiorly till the clavicle [26].
-
Neck dissection can be done either as an antero-posterior fashion or as a postero-anterior approach.
-
Firstly the anterior belly of digastric muscle is identified, and mobilization of the fibrofatty tissue begins between the two anterior belly of digastric muscle and hyoid bone.
-
In level IB dissection, marginal mandibular nerve is identified and preserved. The next step is to divide the fascia below the submandibular salivary gland, and the gland per se is retracted cephalad. This maneuver exposes the posterior belly of digastric muscle and helps in the identification of the facial artery. It is ligated close to the entry point at the posterior belly of digastric muscle and lower border of mandible. However full length of the facial artery may be preserved in case of full flap reconstruction [27, 28].
-
The Sub mandibular gland (SMG), fibrofatty tissue, lymphatics and the prefacial LNs are mobilized off the mylohyoid and hence retracted it anteriorly.
-
For the level II–IV lymph node dissection, the fascia over the SCM is raised till the posterior belly of digastric muscle superiorly. Level IIA dissection begins with identification of the Spinal accessory nerve (SAN) and Internal Jugular Vein (IJV) and removal of the LNs, lymphatics, and fibrofatty tissue between these structures, the deep limit of dissection being the prepectoral fascia. At any given point on time tractional injury to the SAN has to be avoided.
-
This is followed by release of the fascia and tissue along the posterior border of SCM till the clavicle inferiorly; mylohyoid muscle retracted inferiorly and lateral border of IJV identified. Care is taken to preserve deep cervical plexus. Now the level II–IV tissue is retracted anteriorly and peeled off the IJV and continued in the anterior triangle of the neck till the midline, preserved the superior thyroid vessels and tributary of IJV.
-
Level IIB is dissected between the posterior belly of digastric and postero-superior to the SAN, posterior limit being SCM.
This completes the selective neck dissection (Figs. 82.36, 82.37, 82.38, 82.39, 82.40, 82.41, 82.42, 82.43, 82.44 and 82.45).
References
West H, Jin JO. Performance status in patients with Cancer. JAMA Oncol. 2015;1(7):998.
Chen AM, Chen LM, Vaughan A. Tobacco smoking during radiation therapy for head-and-neck cancer is associated with unfavorable outcome. Int J Radiat Oncol Biol Phys. 2011;79:414–9.
Hoff CM, Grau C, Overgaard J. Effect of smoking on oxygen delivery and outcome in patients treated with radiotherapy for head and neck squamous cell carcinoma–a prospective study. Radiother Oncol. 2012;103:38–44.
Deleyiannis FW, Thomas DB, Vaughan TL, Davis S. Alcoholism: independent predictor of survival in patients with head and neck cancer. J Natl Cancer Inst. 1996;88:542–9.
National Comprehensive Cancer Network. Oral cavity cancer (version 2.2014). http://www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf. Accessed 19 Dec 2014.
Edge SP, Byrd DR, Compton CC, et al., editors. AJCC cancer staging manual. 7th ed. New York: Springer; 2010.
Henrot P, Blum A, Toussaint B. Dynamic maneuvers in local staging of head and neck malignancies with current imaging techniques: principles and clinical applications. Radiographics. 2003;23:1201–13.
Pentenero M, Gandolfo S, Carrozzo M. Importance of tumor thickness and depth of invasion in nodal involvement and prognosis of oral squamous cell carcinoma: a review of the literature. Head Neck. 2005;27(12):1080–91.
Erkan M, Tolu I, Aslan T, Guney E. Ultrasonography in laryngeal cancers. J Laryngol Otol. 1993;17:293–7.
Curtin HD, Ishwaran H, Mancuso AA, Dalley RW, Caudry DJ, McNeil BJ. Comparison of CT and MR imaging in staging of neck metastases. Radiology. 1998;207:123–30.
Van den Brekel MW, Castelijns JA, Stel HV, Golding RP, Meyer CJ, Snow GB. Modern imaging techniques and ultrasound- guided aspiration cytology for the assessment of neck node metastases: a prospective comparative study. Eur Arch Otorhinolaryngol. 1993;250:11–7.
Okura M, Iida S, Aikawa T, Adachi T, Yoshimura N, Yamada T, et al. Tumor thickness and paralingual distance of coronal MR imaging predicts cervical node metastases in oral tongue carcinoma. AJNR Am J Neuroradiol. 2008;29:45–50.
Arya S, Chaukar D, Pai P. Imaging in oral cancers. Indian J Radiol Imaging. 2012;22:195–208.
Weiss MH, Harrison LB, Isaacs RS. Use of decision tree analysis in planning a management strategy for the stage N0 neck. Arch Otolaryngol Head Neck Surg. 1994;120(7):699–702.
Kuriakose MA. Contemporary oral oncology. Cham: Springer Nature; 2017.
Huang SH, Hwang D, Lockwood G, Goldstein DP, O’Sullivan B. Predictive value of tumor thickness for cervical lymph-node involvement in squamous cell carcinoma of the oral cavity: a meta-analysis of reported studies. Cancer. 2009;115(7):1489–97.
Shah JP. Patterns of cervical lymph node metastasis from squamous carcinomas of the upper aerodigestive tract. Am J Surg. 1990;160:405–9.
Pantvaidya GH, Pal P, Vaidya AD, Pai PS, D'Cruz AK. Prospective study of 583 neck dissections in oral cancers: implications for clinical practice. Head Neck. 2014;36(10):1503–7.
D’Cruz AK. Elective versus therapeutic neck dissection in node-negative oral cancer. N Engl J Med. 2015 Aug 6;373(6):521–9.
Mehanna H, Robinson M, Hartley A, Kong A, Foran B, Lieuw TF, et al. Radiotherapy plus cisplatin or cetuximab in low-risk human papillomavirus-positive oropharyngeal cancer (De-ESCALaTE HPV): an open-label randomised controlled phase 3 trial. Lancet. 2018;393:51–60.
Parikh PM, Hingmire SS, Deshmukh CD. Selected current data on metronomic therapy (and its promise) from India. South Asian J Cancer. 2016 Apr–Jun;5(2):37–47.
Bernier J, Cooper JS, Pajak TF, van Glabbeke M, Bourhis J, Forastiere A, et al. Defining risk levels in locally advanced head and neck cancers: a comparative analysis of concurrent postoperative radiation plus chemotherapy trials of the EORTC (#22931) and RTOG (# 9501). Head Neck. 2005 Oct;27(10):843–50. https://doi.org/10.1002/hed.20279.
Calabrese L. Compartmental surgery in tongue tumours: description of a new surgical technique. Acta Otorhinolaryngol Ital. 2009;29:259–64.
Kowalski LP, Bagietto R, Lara JR, Santos RL, Tagawa EK, Santos IR. Factors influencing contralateral lymph node metastasis from oral carcinoma. Head Neck. 1999;21:104–10.
Brown JS, Rogers SN, McNally DN, Boyle M. A modified classification for the maxillectomy defect. Head Neck. 2000;22(1):17–26. https://doi.org/10.1002/(sici)1097-0347(200001)22:1<17::aid-hed4>3.0.co;2-2.
Robbins KT, Medina JE, Wolfe GT, Levine PA, Sessions RB, Pruet CW. Standardizing neck dissection terminology. Official report of the Academy’s committee for head and neck surgery and oncology. Arch Otolaryngol Head Neck Surg. 1991;117:601–5.
Medina JE. A rational classification of neck dissections. Otolaryngol Head Neck Surg. 1989;100:169–76.
Spiro RH, Strong EW, Shah JP. Classification of neck dissection: variations on a new theme. Am J Surg. 1994;168:415–8.
Parnell FW. Complications of radical neck dissection. Arch Otolaryngol. 1968;88(2):180–3.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Ethics declarations
Authors have no conflicts of interest to disclose.
1 Electronic Supplementary Material
Modified radical neck dissection(MRND) (MP4 342063 kb)
Rights and permissions
Open Access This chapter is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made.
The images or other third party material in this chapter are included in the chapter's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the chapter's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
Copyright information
© 2021 The Author(s)
About this chapter
Cite this chapter
Mehta, S., Kuriakose, M.A. (2021). Principles of Surgical Management of Oral Cancer. In: Bonanthaya, K., Panneerselvam, E., Manuel, S., Kumar, V.V., Rai, A. (eds) Oral and Maxillofacial Surgery for the Clinician. Springer, Singapore. https://doi.org/10.1007/978-981-15-1346-6_82
Download citation
DOI: https://doi.org/10.1007/978-981-15-1346-6_82
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-15-1345-9
Online ISBN: 978-981-15-1346-6
eBook Packages: MedicineMedicine (R0)