Open Journal of Stomatology, 2013, 3, 486-491 OJST http://dx.doi.org/10.4236/ojst.2013.39079 Published Online December 2013 (http://www.scirp.org/journal/ojst/) Dysphagia in head and neck cancer: A review Roxana Moayer, Uttam Sinha Department of Otolaryngology—Head & Neck Surgery, Keck School of Medicine, Los Angeles, USA Email: rmoayer@usc.edu Received 1 October 2013; revised 13 November 2013; accepted 26 November 2013 Copyright © 2013 Roxana Moayer, Uttam Sinha. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Head and neck cancers are frequently associated with dysphagia. Both pre-treatment and post-treatment etiologies have been described in the literature. The result of dysphagia has been well-documented as caus- ing reductions in both quality-of-life and physical well- being. The goal of this review is to consolidate the current understanding of the relationship between head and neck cancers and dysphagia. Keywords: Dysphagia; Deglutition; Otolaryngology 1. INTRODUCTION Dysphagia is a common, yet, understudied phenomenon. It has been well established that dysphagia has an enor- mous impact on both the overall quality-of-life and health of patients. Patients with head and neck cancers comprise a significant number of those affected by dys- phagia. According to the Nation al Cancer Institute’s Sur- veillance, Epidemiology, and End Results (SEER) pro- gram, the most recent age-adjusted incidences of oral/ oropharyngeal cancer, laryngeal cancer, esophageal can- cer, and thyroid cancer are 10.8, 3.3, 4.25, and 13.21 per 100,000, respectively [1]. These values reflect individu- als at risk of developing dysphagia. Furthermore, dys- phagia is not only a manifestation of head and neck can- cer, but also a complication of cancer treatment. This suggests that dysphagia is a salient issue for a much lar- ger population than previously recognized. The goal of this paper is to consolidate current understanding of the etiology and impact of dysphagia in head and neck can- cer patients. Ultimately, our goal is to provide a new baseline understanding from which further innovations in therapy can develop. In order to do this, it is necessary to begin by reviewing normal swallow function. 2. SWALLOW SEQUENCE Magendie is largely credited with the current, three- phase description of deglutitio n [2]. The phases represen t a necessary oversimplification of deglutition. In reality, deglutition is a flu id and con certed act with some ove rlap of the phases. The 3-phase description is, however, help- ful for at least two reasons. First, each delineation grossly reflects innervation patterns and the muscles which are predominantly active during a given phase. Second, the subdivisions provide a convenient nomenclature to dis- cuss sites of dysfunction or breakdown in the swallow apparatus. Various investigators have developed alternate deglutition descriptions with some authors preferring a two-phase scheme and still others pr eferring a four-phase scheme [2-4]. For simplicity’s sake, only the three-phase mechanism will be described below. 2.1. Oral Phase The oral phase marks the initiation of the swallow se- quence and is the only truly voluntary portion of the mechanism. The structures involved in this phase include the tongue, hard palate, soft palate, suprahyoid muscles, orbicularis oris muscle and buccinator muscle. The ton- gue, assisted by the suprahyoid muscles, is responsible for shaping and propelling the bolus posteriorly. The orbicularis oris and buccinator muscles provide closure of the oral orifice to prevent spillage. The soft palate is displaced inferiorly and anteriorly to provide closure of the posterior oral cavity and to widen the nasal airway. Increases in patient age and in bolus viscosity may lengthen the duration of this phase. In healthy individuals, the oral phase lasts 1 to 1.5 seconds at which point the pharyngeal reflex is triggered [2-4]. 2.2. Pharyngeal Phase The pharyngeal phase of swallowing is an involuntary reflex which is physiologically more complex than the oral phase. The pharyngeal phase is unique in that it is the only phase of deglutition during which respiration is momentarily halted to prevent aspiration. The phase is triggered by the glossopharyngeal nerve upon afferent OPEN ACCESS
R. Moayer, U. Sinha / Open Journal of Stomatology 3 (2013) 486-491 487 input from the oropharyngeal mucosa carried by cranial nerves IX and X. The pharyngeal phase it broken down further into a sequence of five events listed below [2-4]: 1) Velopharyngeal closure by the palate to prevent re- gurgitation of the bolus through the nasal cavity. 2) Retraction of the tongue base to further propel the bolus. 3) Pharyngeal retraction occurs as a peristaltic wave to clear residual contents left behind the bolus. 4) Elevation and closure of the larynx, mediated by the strap muscles, suprahyoid muscles, submental muscles, and laryngeal vocal fold muscles, is directly responsible for airway protection. 5) Opening of the upper esophageal sphincter (UES) allows passage of the bolus into the esophagus and oc- curs by relaxation of the cricopharyngeus muscle. The opening of th e UES marks the transition from the pharyngeal phase of deglution to the esophageal phase. The pharyngeal phase typically lasts 1 second in the healthy individual and is the least variable of all the phases [2-5]. 2.3. Esophageal Phase The esophageal phase is the final and most variable phase of deglutition, lasting from 8 to 20 seconds in healthy individuals. The primary function of the eso- phageal phase is to propel the bolus through the lower esophageal sphincter (LES) and into the stomach. This occurs by peristaltic contraction under mixed autonomic and somatic control in the upper one third of the eso- phagus. Purely autonomic control occurs in the lower two thirds of the esophagus. The esophageal phase is complete once the bolus has passed through the LES [2-4]. 3. MEASUREMENT OF DYSPHAGIA The complexity of the swallow function is what makes its study so difficult. It has been noted that dysphagia has been studied far less than other basic survival functions such as respiration or ambulation [3]. For these reasons, no single measurement modality has provided th e variety of data needed to fully characterize dysphagia. Instead, several modalities have been developed to quantify various aspects of swallow function in clinical settings. 3.1. Videoflu or oscopy Videofluoroscopic swallow study (VFSS) has been the gold standard for evaluation of dysphagia since the 1980s [6]. VFSS is performed by radiographically re- cording the anatomic structures and real-time function of the mouth, pharynx, and esophagus. This occurs while the patient it asked to take a liquid bolus of known vis- cosity. Radiographic evaluation with a jog-wheel is nec- essary to identify the site of dysfunction through frame- by-frame analysis of the swallow mechanism [6]. Ad- vances in imaging resolution through the last two dec- ades have significantly enhanced the sensitivity and specificity of VFSS. Image intensifiers in digital imaging systems improve image resolution and thus interpretation accuracy of VFSS data [6]. Interpretation is one drawback of VFSS. Several scales have been developed to objectify the interpretation of VFSS. Reference [7] evaluated the inter-rater reliability of Videofluoroscopic Dsyphagia Scale (VDS). The scale consists of 14 items each of which can be classified as a measure of oral, pharyngeal, or esophageal function. Reference [7] found low reliability of all oral phase pa- rameters. Pharyngeal and esophageal parameters demon- strated respectively higher inter-rater reliability, however total score reliability according to intra-class correlation coefficient was only 0.556. To maximize utility, it is im- perative that videofluoroscopic data be interpreted under the supervision of a high ly experienced provider. 3.2. Manometry Manometry is the gold standard for the assessment of esophageal muscular contraction. Manometry was de- veloped in the 1950s to record esophageal muscle con- traction in patients with dysphagia. Manometry has pri- marily been used to evaluate patients with gastroeso- phageal reflux disease, achalasia, and dysphagia follow- ing gastric band placement. Concurrent use of video- fluoroscopy enhances the ability to detect functional success of bolus transport [8]. The original manometric studies recorded pressures via esophageal electrodes spaced 5 centimeters apart to generate a graph of pressures over time. Over the course of several decades, manometry has progressed from fluid-state transducers, to solid-state transducers, to the most recent, high-resolution manometry. High-resolution manometry uses electrodes spaced only 1 centimeter apart to provide fewer pressure reading gaps between electrodes and thus more accurate pressure readings [8]. Recent literature is controversial regarding the true benefit high-resolution manometry over conventional manometry. Most authors site the lack of a well-estab- lished tool for interpreting the sheer volume of pressure signals generated by high-resolution manometry as the greatest drawback in utility [9]. As data interpretation catches up to the advance in technology, manometry will provide even more useful evaluation of dysfunctional esophageal motor segments. 3.3. Endoscopy Endoscopy provides direct observation of the pharyngeal phase of deglutition as the flexible scope bypasses the Copyright © 2013 SciRes. OPEN ACCESS
R. Moayer, U. Sinha / Open Journal of Stomatology 3 (2013) 486-491 488 oral cavity. It was developed in the nineteenth century, but has made several recent advances in technology. Endoscopy can now be used to evaluate sensory func- tion. This technique is known as, flexible endoscopic evaluation of swallowing with sensory testing (FEESST). Its suggested use is as a non-radio active altern ativ e to the modified barium swallow study. Reference [10] used FEESST to assess laryngopharyngeal sensory threshold (LPST) which refers to the intensity of an air pulse stimulus required to trigger laryngeal adductor reflex. Their study showed a significant correlation between LPST impairment and functional impairment. Most recently, endoscopy has been developed as a 3D modality. Reference [11] demonstrated that 3D endo- scopy provided superior visualization over conventional 2D endoscopy in a case series. While this technology is primarily geared toward surgical use, as familiarity in- creases and cost decreases, it has the poten tial to become a diagnostic tool. 4. HEAD & NECK CANCER CAUSES OF DYSPHAGIA 4.1. Oral Cancer Oral cancer is the most common site of head and neck cancers, accounting for approximately 30% of all cases [1]. According to NCI data collected through the SEER program, the age-adjusted incidence of oral cancer is 10.8 per 100,000 people [1]. Half of these cases are di- agnosed in individuals between the age of 35 and 64. The median age at diagnosis was 62 years-old. The vast ma- jority of oral cancer is squamous cell (greater than 80%). Other causes include adenocarcinoma, verrucous carci- noma, lymphoma, and Kaposi’s sarcoma [1]. Dysphagia related to oral cancer is more commonly a post-treatment than pre-treatment phenomenon, espe- cially when compared to laryngeal and hypopharyngeal cancer sites [12]. Reference [12] showed that among patients with stage III-IV oral and oropharyngeal cancer, 6% suffered pre-treatment dysphagia compared with 68% who suffered post-treatment dysphagia. A similar study [13] reported significantly different rates of pre- treatment swallow dysfunction between tumor sites. Pa- tients with oral and oropharyngeal cancer had aspiration rates of 14% and 30% respectively, while 67% of pa- tients with laryngeal cancer and 80% with hypopharyn- geal cancer had problems with aspiration [13]. Pre-treatment mechanisms of dysphagia in oral cancer include mechanical obstruction, muscle weakness, and neural invasion. Reference [14] found dysphagia to be present in 28.2% of patients with at least stage T2 oral cancer. Adenoid cystic carcinoma of the base of the tongue has been reported as a rare cause of dysphagia [15]. The paucity of literature regarding pre-treatment dysphagia makes it difficult to ascertain the most com- mon mechanis m responsible for pre-treatm ent dysphagia. Post-treatment dysphagia in oral cancer is being stud- ied extensively. Causes can be broadly categorized as post-surgical effects or chemoradiation effects. Surgical mechanisms include large resection defects and nerve damage. Reference [16] recognized a need to quantify functional outcomes following glossectomy. In an effort to achieve this, they found that patients with tongue strength greater than 30 kPa post-glossectomy had sig- nificantly better functional outcomes. Chemoradiation mechanisms include tissue fibrosis, sensory and motor denervation, and xerostomia [16]. Post-treatment dys- phagia related to chemoradiation will be discussed later as a phenomenon common to treatment of all types of head and neck cancer. 4.2. Esophageal Cancer The age-adjusted incidence of esophageal cancers was most recently estimated to be 4.4 per 100,000 men and women per year. The median age at diagnosis was re- ported to be 67 years of age [1]. Rates of esophageal cancer vary greatly by international region, likely re- flecting significant differences in known risk factors. Worldwide, the rate of esophageal cancer is increasing [17]. In the United States, a reduction in tobacco smoking has been followed by a reduction in the rate of squamous cell carcinoma (SCC), while increased rates of obesity and reflux disease have been associated with a rise in adenocarcinoma [18]. Together, SCC and adenocarci- noma account for more than 90% of all esophageal can- cer cases [19]. The remaining cases have been reported to be lymphoma, more commonly non-Hodgkin’s type, MALT, melanoma, carcinoid, and leiomyosarcoma [20]. Dysphagia is a common pre-treatment manifestation of esophageal cancers. Many cases are not diagnosed until the tumor burden is large enough to cause lumen obstruction [21]. Late stage disease requires treatment by esophagectomy with the use of neoadjuvant therapy be- ing decided on individual case basis. The surgical man- agement of esophageal cancer has seen a shift toward minimally invasive techniques [22]. Reference [23] foun d no difference in survival between open versus minimally invasive esophagectomy. These findings were consistent with those of other investigators [24]. Unfortunately, prog- nosis remains poor despite advances in surgical tech- nique and adjuvant therapies. Such poor survival has re- sulted in little conclusion regarding how to improve dys- phagia associated with esophageal cancer. 4.3. Laryngeal Cancer The age-adjusted incidence of laryngeal cancer is 3.4 per Copyright © 2013 SciRes. OPEN ACCESS
R. Moayer, U. Sinha / Open Journal of Stomatology 3 (2013) 486-491 489 100,000 men and women per year with a median age at diagnosis of 67 years [1]. Laryngeal cancer has garnered more attention as Human Papilloma Virus (HPV) has emerged as a significant risk factor [25]. Laryngeal cancer may arise in the supraglottis, the glottis, or the sub-g lottis. The g lottis is the most common site and is more commonly associated with vocal chang- es than with dysphagia. When dysphagia does occur, it usually manifests itself as an increase in aspiration due to vocal cord or epiglottic dysfunction during the pharyn- geal phase of deglutition. In a prospective study of pa- tients with SCC of head and neck, patients whose pri- mary cancer site was located in the larynx suffered the highest rate of aspiration [2 6] . Patients with HPV develop later stage cancer at an ear- lier age than their non-HPV counterparts [27]. Recent studies show that the basaloid subtype of laryngeal SCC does confer worse prognosis, and likely greater risk of dysphagia, even after accounting for stage and site [27]. 4.4. Thyr oid Cancer The NCI reported age-adjusted incidence of thyroid can- cers to be 12.2 per 100,000 women and men. The most common thyroid cancer, by far, is papillary carcinoma, which represents 70% - 85% of cases [1]. Follicular cell carcinoma is the next most common. Medullary thyroid, poorly differentiated, and anaplastic thyroid are far less common. Rare forms of thyroid cancers include squa- mous cell carcinoma, lymphoma, and sarcoma of the thyroid. Insular thyroid carcinoma is the most recently described form, only being recognized as a unique entity since 1983 [28]. Thyroid disease is a common cause of dysphagia. In a study of patients undergoing thyroidectomy, dysphagia was the most common pre-operative complaint. Thyroid disease causes compressive forces on the swallow appa- ratus resulting in a progression of worsening symptoms from globus sensation to overt dyspagia [29]. The sever- ity of compressive symptoms directly relates to gland size, owing to direct force by the thyroid gland. The most common causes of thyroid related compressive symp- toms are benign goiter, followed by papillary thyroid carcinoma, follicular thyroid carcinoma, and thyroiditis [29]. The presence of more severe compressive symptoms found in patients with smaller gland sizes may be due to underlying disease processes. This suggests that factors in addition to gland size contribute to the development of dysphagia. In particular, invasion and inflammation have been implicated in the development of dysphagia. This notion is supported by disproportionately higher rates of dysphagia reported in patients with lymphocytic thyroid- itis than in patients with thyroid carcinoma despite com- parable gland size [29]. While anaplastic thyroid carcinoma comprises only 1% - 2% of thyroid carcinomas [1], patients commonly present with dysphagia due to rapid growth and distor- tion of normal anatomy. For this reason, patients pre- senting with dysphagia as a primary complaint should receive aggressive work-up to rule out malignant etiolo- gies. 5. POST-TREATMENT DYSPHAGIA Chemoradiation has been an empirically supported main- stay in the treatment of head and neck cancer for over two decades. This practice, combined with earlier age at diagnosis and longer survival has led to a rise in the de- velopment of post-treatment dysphagia [30]. Postchemo- radiation mechanisms of dysphagia include tissue fibro- sis, sensory and motor denervation, and xerostomia [16]. Reference [31] followed 112 patients at 3, 6, and 12 months post-CRT. They found that most patients suffered the greatest functional decline between pre-treatment to 3 months post-treatment. Despite some patient’s showing an improveme nt on objective measures of dysphagi a most, patients did not report subjective improvement within th e year following CRT [31]. Several modalities to prevent dysphagia and improve functional outcomes following chemoradiation are cur- rently under extensive study. These include use of pro- phylactic, pre-treatment swallow therapy, use of NG-tube in place of G-tube for feeding during treatment, and use of intensity-modulated radiation therapy (IMRT). In a meta-analysis, reference [32] found that 5 out of the 6 studies examining prophylactic swallow therapy proved the modality to be beneficial. They noted, how- ever, that neither the cost-benefit ratio nor long term outcomes have been studied. In general it has been shown that use of NG tube in place of G-tube decreases dysphagia. Maintenance of nutrition through chemoradiation treatment is a difficult task achieved by a diligent multi-disciplinary team. It is thought that use of an NG-tube helps to maintain the strength of motion of muscles involved in the swallow mechanism. Evaluation of patients’ appropriateness for NG-tube placement should be done on an individual and multi-discipline basis [32]. Organ-sparing CRT does not spare the structures in- volved in successful swallow. IMRT is being investigated as a possible alternative to conventional CRT to spare structures critical to successful swallow. Reference [33] demonstrated that IMRT could successfully spare dys- phagia/aspiration related structures (DARS), especially the pharyngeal constrictors and th e glottic and supraglo t- tic larynx. This resulted in significantly improved post- treatment swallow function [32,33]. Copyright © 2013 SciRes. OPEN ACCESS
R. Moayer, U. Sinha / Open Journal of Stomatology 3 (2013) 486-491 490 6. CONCLUSION Dysphagia is an important phenomenon in head and neck cancer presentation and outcome. There are several fac- tors that make study of this phenomenon difficult. First, the swallow apparatus is a complex structure. There are several etiologies responsible for dysphagia which may occur at any point during the mechanism. Second, no standard measurement exists to quantify dysphagia across studies. Even within a given measure, there is a lack of consensus regarding the interpretation of data. Third, because head and neck cancers comprise such a wide variety of neoplasms, it is difficult to generalize findings between cancer groups. Finally, head and neck cancers, especially once classified by region and histol- ogy, are relatively rare. 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