|Year : 2010 | Volume
| Issue : 2 | Page : 127-134
Prevention and management of antineoplastic therapy induced oral mucositis
Afshan Bey1, Syed S Ahmed2, Bilal Hussain3, Seema Devi3, Sarwat H Hashmi2
1 Department of Periodontics and Community Dentistry, Dr. Z.A. Dental College, Aligarh Muslim University, Aligarh, India
2 Department of Oral and Maxillofacial Surgery, Dr. Z.A. Dental College, Aligarh Muslim University, Aligarh, India
3 Department of Radiotherapy, J. N. Medical College, Aligarh Muslim University, Aligarh, India
|Date of Web Publication||9-Apr-2011|
Syed S Ahmed
Department of Oral and Maxillofacial Surgery, Dr. Z.A. Dental College, Aligarh Muslim University, Aligarh
Source of Support: None, Conflict of Interest: None
| Abstract|| |
With the scientific advancements in the management of malignant diseases, the treatment is expensive and bears high morbidity in term of oral mucositis. It is a debilitating condition and has been researched extensively for its pathogenesis and treatment. Various treatment options include barrier forming, mucosal protectants, mouth rinses, growth factors, lasers and midline-sparing procedures. Some agents are used locally while others are administered systemically. Despite the availability of a wide range of treatment options for mucositis, a cost-effective treatment is yet to be evolved.
Keywords: Antineoplastic therapy, mucosal protectants, oral mucositis
|How to cite this article:|
Bey A, Ahmed SS, Hussain B, Devi S, Hashmi SH. Prevention and management of antineoplastic therapy induced oral mucositis. Natl J Maxillofac Surg 2010;1:127-34
|How to cite this URL:|
Bey A, Ahmed SS, Hussain B, Devi S, Hashmi SH. Prevention and management of antineoplastic therapy induced oral mucositis. Natl J Maxillofac Surg [serial online] 2010 [cited 2020 Jul 12];1:127-34. Available from: http://www.njms.in/text.asp?2010/1/2/127/79214
| Introduction|| |
Treatment of cancer is increasingly more effective but is associated with short- and long-term side-effects. Oral side-effects remain a major source of illness despite the use of a variety of agents to prevent them. One of these side-effects is oral mucositis, which is a debilitating condition and results from the cytotoxic effects of chemotherapeutic drugs and radiation on the oral mucosa. Mucositis causes severe pain and distress and may limit the tolerability of chemo/radiotherapy and, hence, its effectiveness. It usually follows chemo and/or radiotherapy of the head and neck region and can be seen in 40-70% of the cases. It damages the epithelium of the oral cavity and manifests in the form of erythema, ulceration and swelling. This not only makes the swallowing and speech difficult but also affects the quality of life of the patient. Furthermore, patients with damaged oral mucosa and reduced immunity resulting from chemotherapy and radiotherapy are prone to opportunistic infections in the mouth. The mucositis may be so severe that patients' food and fluid intake and speech are reduced, further compromising the patients' response to treatment and/or palliative care. In addition, the damaged mucosal surface provides a safe site to harbor various microorganisms and provide a portal of entry allowing the microorganisms to flow into systemic circulation. Thus, the side-effects are local and systemic. While the local effects of severe mucositis may lead to reduction of the chemotherapeutic dose in subsequent cycles, the systemic effects may lead to infection, complication and interruption of therapy. At this stage, the hospitalization becomes unavoidable and parenteral nutritional therapy with analgesics is mandatory.
Currently, a large number of interventions are available. This paper reviews the pathogenesis, classification of mucositis and range of treatment available to manage this condition.
| Pathogenesis|| |
Oral mucositis secondary to the cancer therapy is the side-effect of treatment. Its pathogenesis was unclear until Sonis projected a hypothesis that involved four sequential events.  In the first phase (inflammatory/vascular phase), the chemotherapeutic insult causes the release of inflammatory cytokines (tumor necrosis factor-α, interleukins-1 and -6, C-reactive protein) that result in local tissue damage and increased vascularity. In the next phase (epithelial phase), the chemotherapeutic agent decreases the mitosis of the proliferating epithelial cells of the oral cavity, leading to reduced turn over of epithelial cells, atrophy and ulceration. In the third phase (ulcerative/infectious phase), discrete areas of full-thickness erosion develop due to trauma and cytokine-mediated damage. These areas are colonized by mixed microorganisms and lead to a portal of entry for infection. The fourth and final stage is healing, with epithelial proliferation and differentiation. The intermediate phases exhibit marked neutropenia and leucopenia. The healing phase is characterized by the recovery of white blood counts.
However, the oral mucositis is associated with other factors also, of which the chemotherapeutic agent, field and dose of irradiation play an important role. It is seen in patients treated with antimetabolites like 5-fluorouracil, methotrexate and purine antagonists. It is also seen in patients receiving cytostatic antibiotics (e.g. Anthracycline) and cytotoxic agents (e.g. Taxanes) and patients receiving bone marrow transplant-conditioning therapies for hematological or solid tumors. ,
Now, there are evidences that suggest that radiation- or chemotherapy-induced mucositis is initiated by direct injury to the basal epithelial cells and cells in the underlying tissue. DNA-strand breaks can result in cell death or injury. Non-DNA injury is initiated through a variety of mechanisms, some of which are mediated by the generation of reactive oxygen species. Sonis characterized five phases of pathophysiologic progression of mucositis, viz. initiation, upregulation and message generation, signalling and amplification, ulceration and healing. Each phase offers a potential target for therapeutic interventions.  The complex pathogenesis of mucositis in fact involves dynamic interactions of all of the cell and tissue types that comprise the epithelium and the submucosa. Identification of the molecular events that lead to treatment-induced mucosal injury have given a hope for identifying the interventions that may prevent and treat mucositis.  However, the patient's mucosal response to antineoplastic treatment has been shown to be controlled by two factors: global factors that include gender, underlying systemic disease and race and tissue-specific factors like epithelial type, intrinsic endocrine system, local microbial environment and function. Interaction of these specific elements plus genetic influences probably govern the phases of mucosal injury. 
Prevention and pretreatment interventions of oral mucositis
The chances of mucositis are always associated cancer therapy. However, there are certain predisposing factors, which if considered properly, the mucositis may be prevented. These factors have been shown in [Table 1]. The patient and carers should always be told precisely these predisposing factors and to follow the advice given to help prevent/minimize the mucositis.
Because the mucositis is aggravated by dental factors and poor oral hygiene, it is in the best interest of the patient that the medical team should interact with dental specialists to discuss issues and possible complications that may develop in response to chemo-radiotherapy. In addition, the available time for onset of neutropenia should also be discussed. Considering the medical status of the cancer patient, the dental team should formulate a plan to manage the existing oral and dental disease before, during and after the chemotherapy. The overall goal should be, however, to eliminate orodental diseases and stabilize the oral health and other dental conditions that may produce complications during the phase of cancer therapy.
In patients with poor oral health, the benefits of dental treatment should be weighed against the potential disadvantages, such as incomplete healing. Simultaneously, in cases where oral disease poses an eminent danger, the cytotoxic therapy should be delayed. Intervals between the chemotherapy cycle can be utilized to complete the necessary dental treatment. For patients who received radiotherapy, the surgical treatment should be delayed by 3-6 months to lower the risk of osteoradionecrosis. Neutropenia and thrombocytopenia are the common side-effects of cancer chemotherapy. In patients with neutropenia <1,000/cubic mm, where the invasive procedure is direly needed, an aggressive broad-spectrum antibiotic therapy by the parenteral route should be given. Periodontal treatment and tooth/teeth extractions should be carried out as atraumatically as possible. Where tooth extraction is performed, primary closure of wound is recommended. 
| Assesment of Oral Mucositis|| |
Prior to institution of therapy to treat mucositis, the assessment of its extent is necessary. WHO oral mucositis index [Table 2] is an ideal means of assessing the severity of the condition. On this basis, the extent of mucositis should be graded and, accordingly, medications should be decided if there is no existing treatment administration protocol that may directly correlate with the index.
Patients and their attendants should be informed about the various complications of cancer therapy, significance of oral hygiene and avoiding oral trauma during brushing of teeth and eating, etc. A soft brush is more suitable in such situations and, every time before use, it should be rinsed properly and dried to avoid any bacterial overgrowth. If the patient is a denture wearer, the prosthesis should be withdrawn until the mucositis subsides. Continuation of use of denture may traumatize the mucosa, aggravate the inflammation and delay the healing. Further ulceration thus caused become areas of colonization for microorganisms, from where they can get an easy entry into the systemic circulation.
Interventions during cancer therapy
During the active phase of cancer therapy, the measures taken are aimed to prevent or to relieve the side-effects of chemo and/or radiotherapy. This involves maintenance of oral hygiene, prevention of infection and trauma, management of pain associated with mucositis, xerostomia, dysgeusia and control of spontaneous oral bleeding associated with thrombocytopenia. Various traetemnt options to treat mucositis have been shown in [Table 3].
|Table 3: Treatment options of chemo/radiotherapy-induced oral mucositis |
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It is not possible to discuss these methods in detail. Here, we will review the current measures involved in practice and research to treat oral mucositis.
During cancer therapy, strong oral hygiene measures should be adopted. The nursing team of the hospital should monitor the measures taken during hospitalization. The mouth should be examined daily to detect the complications of therapy as early as possible. In ambulant patients, where the patient condition does not allow the examination of the oral cavity, antimicrobial rinses should be given. Chlorhexidine is an effective, broad-spectrum antiseptic and bears antiplaque activity. In addition, it has got an antifungal action too. In place of chlorhexidine, povidine iodine rinse is a better alternative. , In herpes simplex seropositive patients, prophylactic oral administration of acyclovir reduces the incidence of clinical herpes simplex viral lesion. 
The mucositis causes severe soreness and pain in the oral cavity and makes swallowing and speech very difficult. Thus, pain management at this stage is essential. As the severity of mucositis increases, the typical pain management strategies become less effective. Their usefulness is limited to mild to moderate mucositis pain. In severe mucositis, non-steroidal antiinflammatory drugs (NSAIDs) with opioid can make the patient comfortable. However, analgesic treatment starts with NSAIDs and, as the pain increases, they are combined with opioid. NSAIDs are titrated to effective pain relief. Systemic analgesics are given by clock to achieve the maximum therapeutic effect. Adjuvant medication may be required to potentiate analgesia and manage the side-effects of NSAIDs and opioid.
Sucralfate, a complex of sucrosulfate and aluminum hydroxide, has been used as a mucosal protectant and its role has been thoroughly evaluated for the prevention of mucositis. Its suspension is another choice for managing mucositis. It provides significant pain relief and resolution of mucositis.  This agent stimulates the production of prostaglandin E2, resulting in increased mucosal blood flow, higher mitotic activity and migration of epithelial cells. Prostaglandin E2 possesses cytoprotective activity and thus its effect can be anticipated. Sucralfate may also prevent the colonization of microorganisms on the mucous membrane. However, the results of studies are conflicting and do not favor adoption of this medication as standard therapy.
Epstein et al., in their study, found that prophylactic oral rinsing with sucralfate did not prevent oral ulcerative mucositis. However, it may reduce the experience of pain during radiation therapy.  On the other hand, Cengiz et al. have shown that sucralfate decreases the intensity of radiation  -induced mucositis and oral discomfort. It is cheap, easy to administer with no serious side-effects and may be routinely used in patients receiving head and neck radiotherapy.  The beneficial effects of sucralfate have been established by histopathological demonstration. 
Gelclair is another mucosal protectant and it helps in the management of pain associated with oral mucositis. Chemically, it contains polyvinylpyrrolidone and sodium hyluronate in a liquid gel. It forms a bioprotective coating that provides almost instant comfort and effective pain relief.  Benzydamine is a non-steroidal drug that has shown to possess antiinflammatory, analgesic, anesthetic and antimicrobial activities. It is an effective inhibitor of TN-α production, which explains its antiinflammatory effect. A multicenter, randomized, double-blind study was performed to evaluate the role of benzydamine HCl as prophylaxis for radiation-induced oral mucositis in patients with head and neck cancer.  Benzydamine 0.15% oral rinse was found to be effective, safe and well tolerated for the prophylactic treatment of radiation-induced mucositis with head and neck carcinoma receiving a variety of radiotherapy regimen. ,
The oral rinse reduced the pain associated with mucositis also. Fewer patients using benzydamine rinse required systemic analgesics.  Corticosteroids - hydrocortisone and betamethasone - have also been reported to reduce the radiation-induced mucositis.
Prophylactic cryotherapy in the form of ice chips sucking has been found to be effective in patents on 5-fluorouracil chemotherapy to prevent mucositis. It has been proposed that if blood flow to the cheek mucosa is diminished, less drug will reach the oral mucosa, thereby reducing the ill effects. This can be achieved by sucking the ice chips (cryotherapy). Few studies have shown that oral cryotherapy is effective in preventing 5 FU-induced mucositis.  Cryotherapy has also been found to reduce mucositis in patients receiving combination chemotherapy.  It also reduces the requirement of narcotic analgesics to manage pain relief and parenteral nutrition. 
In a randomized study in 225 patients, Sorensen et al. found that the frequency and duration of oral mucositis may be significantly improved by either prophylactic chlorhexidine or by cryotherapy.  The latter is easy and inexpensive but is drug- and schedule-dependent as it cannot be used with infusional 5-FU or with chemotherapy with substantially longer half-lives than 5-FU.
The results of three randomized trials have also shown a significantly lower incidence and severity of oral mucositis compared with the controlled groups. , Cryotherapy is also effective in the prophylaxis of mucositis. , Libelly et al. reported that 6 h of exposure to oral ice chips significantly decreased the incidence of grade 3 and grade 4 mucositis in patients receiving melphalan.  Cryotherapy is an alternative method of preventing mucositis associated with chemotherapy agents that have a short life in blood.
In addition, low-level laser therapy (LLLT) may also be effective in preventing and suppressing mucositis in patients receiving high-dose chemotherapy. LLLT refers to the use of red-beam or near-infrared lasers with a wavelength between 600 and 1000 nm and power from 5 to 500 milliwatts. These lasers are non-thermal. Because of low absorption by human skin, the laser light can penetrate deeply into the tissues where it produces a photo-biostimulation effect. These types of lasers have been advocated for use in a range of medical conditions like delayed wound healing and tuberculosis and in a variety of musculoskeletal conditions like rheumatoid arthritis.
Nes and Posso investigated the effect of low-intensity lasers in chemotherapy-induced oral mucositis. They found that there was a statistically significant decrease in the daily average experience of pain felt before and after each treatment and confirmed that low-intensity laser therapy can relieve pain among patients who develop chemotherapy-induced mucositis. 
Sandoval et al. also noticed the beneficial effect of low-intensity lasers in chemotherapy- and/or radiotherapy-induced mucositis. They established that a low-energy laser was well tolerated by patients and produced beneficial effects on the management of oral mucositis, improving the quality of life during the oncologic treatment. 
Genot reviewed the role of LLLT in radiation- and chemotherapy-induced mucositis. On the basis of the literature data, he concluded that there is substantial evidence to suggest that LLLT may be used in decreasing the severity of chemotherapy-associated or radiotherapy-associated mucositis. 
The midline-sparing block technique is the method that has been used to protect the mucosa of the aerodigestive tract in the low-neck field during head and neck irradiation in treating oropharyngeal and nasopharyngeal cancers. The technique lacks wide acceptance and documentation of its efficacy. However, it has been shown to cause less weight loss and nutritional supplementation, leading to unplanned treatment interruption. 
Current trends in management of Oral Mucositis
Current trends in the management of oral mucositis are more toward the search of a suitable biological agent. Various agents have been tried and tested, but with varied results. Growth factors have attracted much attention. They are naturally occurring proteins capable of stimulating cellular proliferation, differentiation and maturation. They are important for a variety of cellular processes and, typically, act as signalling molecules between cells, binding to specific receptors on the surface of their target cells. The growth factors can be applied locally or administered systemically.
Epidermal growth factor (EGF) binds to specific high-affinity, low-capacity receptors on the surface of responsive cells. It exerts a proliferative effect on cells of ectodermal and mesodermal origin. It also exhibits negative growth effects on certain carcinoma. They have been proved to be helpful for the prevention of oral mucositis in autologous stem cell transplant recipients. The study performed by Stiff et al. concluded that patients receiving Kepivance (EGF) reported a significant improvement in the daily functioning activities of swallowing, drinking, eating, etc. compared with the control group. The same study also documents the effectiveness of Kepivance in preventing oral mucositis in stem cell transplanting.  Lee et al. performed their study on rat models using human recombinant epidermal growth factor (rhEGF). They found that the survival and oral intake was significantly increased and concluded that orally administered rhEGF decreased the radiation-induced oral mucositis in rats. 
Keratinocyte growth factor is a normal cytokine that is present in many tissues and is produced in response to tissue injury.  KGF stimulates growth epithelial cells in tissues that have receptors for this cytosine.  A clinical study was performed on randomly selected patients with colorectal cancer who were being treated with 5 FU and leucovorin to receive KGF or placebo. The KGF at a dose of 40 ΅g/kg/d for 3 days produced meaningful biological effects. There was a lower rate of mucositis in contrast to placebo. 
Plifermin, a recombinant human keratinocyte growth factor, is effective for treating mucositis resulting from chemotherapy or radiotherapy. This cytokine significantly reduced the duration of mucositis after extensive therapy. Speilberger et al. found that patients receiving palifermin used significantly lower cumulative doses of morphine equivalents and for fewer days than did placebo recipients and had minor adverse effects, such as rash. 
Palifermin has also produced a beneficial effect on mucositis in human recipients of hemopoietic stem cell transplantation who received etoposide, cytarabine and melanphan. In these patients, pre-treatment with keratinocyte growth factor reduced the mucosal atrophy and weight loss, accelerated mucosal regeneration, decreased ulceration and improved survival through gene-mediated effects on growth and differentiation. 
Granulocyte macrophage colony stimulating factor (GM-CSF) has been used topically to prevent chemo/radiotherapy-induced mucositis; however, the results are not encouraging. Sprinzle et al. demonstrated that its topical use as such cannot be recommended as its superiority could not be statistically proved over the conventional mouth washes and due to its tremendous cost.  The studies performed by Dazzi et al. reveal that it neither reduces the frequency nor duration of severe oral mucositis induced by high-dose chemotherapy given to recipients of an autologous peripheral blood hemopoietic stem cell transplant to treat solid tumors. 
Results of studies performed by Lieschke et al. indicate that patients receiving granulocyte-colony stimulating factor (G-CSF) suffered less-severe mucositis than patients who did not receive this cytokine. 
Interleukin-11 is believed to increase the proliferation and suppress the apoptosis of mucosal cells. However, the safety and efficacy of this cytokine in the oral mucositis has yet to be thoroughly evaluated. 
L-glutamine is an essential amino acid involved in cellular repair and has also been used as a supplement in parenteral nutrition preparation, with some evidence that it prevents infection in debilitated patients. It is combined with a vehicle that enhances its availability to cells of the mucous membrane. This combination favorably affects the course of the chemotherapy-induced mucositis. In a double-blind study, the control group had severe mucositis in comparison with the L-glutamine group. 
Kuhrer et al. reported the pain relief and healing of the oral lesion using prostaglandin PGE2. Some other studies have also indicated a cytoprotective activity of PGE2. However, others disapprove this effect. ,
Wadleigh et al. have shown that Vit. E, an antioxidant, ameliorates oral mucositis. Beta carotene also has been proved to prevent the development of several mucosal lesions. 
Transforming Growth Factor β3
Transforming Growth Factor β3 (TGF β3) is an inhibitor of a variety of normal epithelial cell proliferation and hemopoietic stem cells and preventing the cell cycle progression and accumulating cells during the phase of chemotherapy. It protects the stem cells from radiation-induced cytotoxic damage and initiates the regeneration of clonogenic stem cells thus causing the reduction of mucositis. ,
The tumor cells are less responsive to inhibiting the effects of TGF β3. The ability of TGF β3 to reversibly inhibit cycling of normal epithelial and hemopoietic stem cells allows it to be used as a chemoprotectant of normal tissue during cytotoxic chemotherapy. It is preferably administered topically; however, the administration may be systemic also. 
Azelastine is a mast cell inhibitor and is known to suppress the neutrophil-reactive oxygen production and cytokine release from the lymphocyte. Osaki et al. established the role of prophylactic azelastine hydrochloride, with other antioxidants reducing oral mucositis in patients receiving concomitant chemo/radiotherapy. However, a thorough study is still needed to understand its potential role. 
Effect of the antifibrotic protein serum amyloid-P
Murray et al. studied the effect of of the antifibrotic protein Serum Amyloid-P (SAP) on radiation-induced oral mucositis and fibrosis in a hamster cheek-pouch model. They found that its administration, in general, significantly attenuated the radiation-induced injury and, in particular, attenuated the severity of oral mucositis and inhibited the pathogenic remodelling. They concluded that SAP may be a useful therapy for the palliation of the side-effects observed during the treatment for head and neck cancer.
Associated problems: Xerostomia, candidiasis and degeusia
Besides mucositis, the radiation patients suffer from poor salivary flow lead to xerostomia and taste disorders. The use of sialogogues, such as pilocarpine, has been proposed. But, the results of studies are inconsistent. In a study, 214 patients undergoing radiation therapy for head and neck cancer were allocated to receive placebo and pilocarpine. Patients in the placebo arm felt greater pain and swallowing difficulty, but the salivary function was preserved statistically significant in the pilocarpine receiving group. There was no apparent effect on mucositis.  Similar effects were observed in another study in which the parotid salivary floe was compared with the placebo.  Amifostine is another option for use with ionizing radiation for maintaining salivary floe, but it has some significant side-effects and its effect on salivation are moderate. However, if used subcutaneously, the side-effects are minimum. 
Candidiasis is the most common infection seen clinically in the oral cavity in the irradiated patients and studies have demonstrated in quantitative counts and rates for clinical infection of Candida. It may exacerbate the symptoms of mucositis. In such cases of mucositis, typical antifungals such as nystatin and clotrimazole are primarily helpful. Compliance can be compromised secondary to oral mucositis, nausea, pain and difficulty in dissolving nystatin pastilles and clotrimazole troches. Systemic antifungals - ketoconazole and fluconazole - have proved to be effective and are advantageous over topical agents. 
As the oral and pharyngeal mucosa are exposed to radiation, taste receptors become damaged and taste discrimination becomes increasingly compromised. , After several weeks of radiation, it is common for patients to complain of no sense of taste. It will generally take upwards of 6-8 weeks after the end of radiation therapy for the taste receptors to recover and become functional. Zinc sulfate supplements have been reported to help with the recovery of the sense of taste. ,,
| Discussion|| |
Chemotherapy, radiotherapy and a combination of the two are the methods of treating malignant neoplastic diseases. Although these approaches have lead to a significant improvement in the survival, it has come at the cost of severe complications of which oral complications are extremely debilitating in that they affect swallowing, speech, taste and interruption of antineoplastic therapy as well. The literatures are in abundance to address these problems in general and oral mucositis in particular. But, most of the studies are performed in the experimental phase and inconsistency exists in the interventional options employed. The overall results are, however, inconclusive. Sonis'  findings on radiation- or chemotherapy-induced mucositis help us to think of different agents at different phases for relief of the patient. The management of oral mucositis should involve a three-point approach - prevention, enhancement of healing and emotional and psychological support, which should be administered in a stage-wise manner. There is need to perform a series of multicenter, prospective, randomized trials on this aspect. Until studies give identical results, probably, it would be difficult to arrive at an acceptable solution. However, a gold standard rule has not yet been formulated to deal with such common side-effects of chemo/radiotherapy.
Of all the agents reviewed, palifermin and low-level laser appear to be most promising. However, for administration of palifermin, a scientific approach should be developed and administration of low-level laser would need very costly equipment and well-trained professionals. Both the options are very costly. Thus, a cost-effective prophylactic and therapeutic treatment with high-dose chemotherapy are the need of the time to base the research.
| Conclusion|| |
Oral complications of cancer therapy are varied and bear a high morbidity. The mouth not only acts as a mirror of the oral manifestation of antineoplastic therapy, but it is the portal of entry of life-threatening infections too. The oncologist should involve the dental team in different stages of treatment to assess the mucosal damage and to render specific oral hygiene measures. A cost-effective, perfect treatment of antineoplastic therapy-induced mucositis is yet to be evolved that could be administered and matched with different stages of the WHO oral mucositis scale.
| References|| |
|1.||Sonis ST. Mucositis as a biological process: A new hypothesis for the development of chemotherapy-induced stomatotoxicity. Oral Oncol 1998;34:39-43. |
|2.||Knox JJ, Puodziunas AL, Feld R. Chemotherapy-induced oral mucositis: Prevention and management. Drugs Aging 2000;17:257-67. |
|3.||Woo SB, Sonis ST, Monopoli MM, Sonis AL. A longitudinal study of oral ulcerative mucositis in bone marrow transplant recipients. Cancer 1993;72:1612-7. |
|4.||Sonis ST. A biological approach to mucositis. J Support Oncol 2004;2:21-36. |
|5.||Sonis ST. The Pathobiology of Mucositis. Nat Rev Cancer 2004;4:277-84. |
|6.||Anthony L, Bowen J, Garden A, Hewson I, Sonis S. New thoughts on the pathobiology of regimen-related mucosal injury. Support Care Cancer 2006;214:516-8. |
|7.||Wong JK, Wood RE, Mc Lean M. Conservative management of Osteoradionecrosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997;84:16-22. |
|8.||Raber-DurlacherJE, Epstein JB, Raber J, van Dissel JT, van Winkelhofff AJ, Guiot HF, et al. Periodontal infection in cancer patients treated with high dose chemotherapy. Support Care Cancer 2002;10:466-73. |
|9.||Epstein JB, Vickars L, Spinelli J, Reece D. Efficay of chlorhexidine and nystatin rinses in prevention of oral complications in leukaemia and bone marrow transplantation. Oral surg Oral Med Oral Pathol 1992;73:682-9. |
|10.||Burgmann OJ. Alterations in oral microflora and pathogenesis of acute oral infections during remission-induction therapy in patients with acute myeloid leukemia. Scand J Infect Dis 1991;23:355-66. |
|11.||Comeau TB, Epsrein JB, Christo M. Taste and smell dysfunction in patients receiving chemotherapy: A review of current knowledge. Support Care Cancer 2001;9:575-80. |
|12.||Epstein JB, Wong FL. The efficacy of sucralfate suspension in the prevention of mucositis due to radiation therapy. Int J Radia Oncol Biol Phys 1994;28:693-8. |
|13.||Cengiz M, Ozyar E, Oztürk D, Akyol F, Atahan IL, Hayran M. Sucralfate in the prevention of radiation induced mucositis. J Clin Gasteroenterol 1999;28:40-3. |
|14.||Etiz D, Erkal HS, Serin M, Küçük B, Hepari A, Elhan AH, et al. Clinical histopatholoical evaluation of sucralfate in prevention of of oral mucositis induced radiotherapy in patients with head and neck malignancies. Oral Oncol 2000;36:116-20. |
|15.||Innocenti M, Moscatelli G, Lopez S. Efficacy of Gelclair in Reducing Pain in Patients with Oral Lesions: Preliminary Findings from an Open Pilot Study. J Pain Symptom Manage 2002;24:456-7. |
|16.||Sroni MK, Pozzi P, Pollentarutti N, Benigni F, Colleta I, Gugliemotti A, et al. Inhibition of inflammatory cytokine production and protection against endotoxin toxicity by Benzydamine. Cytokine 1996;8:710-6. |
|17.||Epstein JB, Silverman S Jr, Paggiarino DA, Crockett S, Schubert MM, Senzer NN, et al. Benzydamine HCl for prophylaxis of radiation-induced oral mucositis: Results from a multicenter, randomized, double-blind, placebo-controlled clinical trial. Cancer 2001;92:875-85. |
|18.||Epstein JB, Stevenson-More P, Jackson S, Mohamed JH, Spnelli JJ. Prevenion of oral mucostis in radiotherapy: A controlled study with benzydamine hydrochloride rinse. Int J Radiat Oncol Biol Phys 1989;16:1571-5. |
|19.||Epstein JB, Stevenson-More P. Benzydamine hydrochloride in prevention and management of pain in oral mucositis associated with radiotherapy. Oral surg Oral Med Oral Pathol 1986;62:145-8. |
|20.||Rocke LK, Loprinzi CL, Lee JK, Kunselman SJ, Iverson RK, Finck G, et al. A randomized clinical trial of two different durations of oral cryotherapy for prevention of oral stomatitis. Cancer 1993;72:2234-8. |
|21.||Karagozugulu S, Filiz S, Ulusoy M, Chemotherapy: The effect of cryotherapy on the development of mucositis. J Clin Nurs 2005;14:754-65. |
|22.||Mori T, Yamazaki R, Aisa Y, Nakazato T, Kudo M, Yashima T, et al. Brief oral Cryotheray for prevention of high dose melphalan induced mucositis in allogenic hemopoietic stem cell transplant recipients. Support Care Cancer 2006;14:392-5. |
|23.||Sorensen JB, Skovsgaard T, Damstrup L, Ingeberg S. Prophylaxis of chemotherapy-induced oral mucositis: Double blind, placebo-controlled randomized study of chlorhexidine versus placebo and with non-blinded randomized comparison to oral cooling (cryotherapy). Washington: UICC World Cancer Congress; 2006. p. 8-12. |
|24.||Rocke LK, Loprinzi CL, Lee JK, Kunselman SJ, Iverson RK, Finck G, et al. A randomized clinical trial of two different durations of oral cryotherapy for prevention of oral stomatitis. Cancer 1993;72:2234-8. |
|25.||Cascinus S, Fedeli A, Fedeli SL, Catalano G. Oral cooloing (cryotherapy) an alternative treatment for the prevention of 5 fluorouracil induced stomatitis. Eur J Canc Oral Oncol 1994;30B:234-6. |
|26.||Mahood DJ, Dose AM, Loprinzi CL, Veeder MH, Athmann LM, Therneau TM, et al. Inhibition of fluorouracil induced stomatitis by oral cryotherapy. J Clin Oncol 1991;9:449-52. |
|27.||Scully C, Epstein J, Sonis S. Oral mucositis: A challenging complication of radiotherapy, chemotherapy and radiochemotherapy. 1. Pathogenesis and prophylaxis of mucositis. Head Neck 2003;25:1057-70. |
|28.||Lilleby K, Garcia P, Gooley T, McDonnnell P, Taber R, Holmberg L, et al. A prospective randomized study of cryotherapy during administration of high dose melphalan to decrease the severity and duration of oral mucositis in patients with multiple myeloma undergoing autologous blood stem cell transplantation. Bone Marrow Transplant 2006;37:1031-5. |
|29.||Nes AG, Posso MB. Patients with moderate chemotherapy-induced mucositis: Pain therapy using low intensity lasers. Int Nurs Rev 2005;52:68-72. |
|30.||Sandoval RL, Koga DH, Buloto LS, Suzuki R, Dib LL. Management of chemo and radiotherapy induced oral mucositis with low-energy laser: Initial results of A.C. Camargo Hospital. Appl oral Sci 2003;11:337-41. |
|31.||Genot M, Klastersky J. Low level laser for prevention and therapy for oral mucositis induced by chemotherapy or radiotherapy. Curr Opin Oncol 2005;17:236-40. |
|32.||Madenhall WM, Parson JT, Million RR, Unnecessary radiation of the normal larynx. Int J Radiat Oncol Biol Phys 1990;18:1531-3. |
|33.||Stiff PJ, Emmanouilides C, Bensinger WI, Gentile T, Blazar B, Shea TC, et al. Pifermin reduces patient reported mouth and throat soarness and improves patient functioning in the hemopoietic stem cell transplant setting. J Clin Oncol 2006;24:5186-93. |
|34.||Perch SJ, Machtay M, Markiewiz DA, Kingermann MM. Decreased acute toxicity by using midline mucosa-sparing block during radiation therapy for carcinoma of the oral cavity, oropharynx and nasopharynx. Radiology 1995;197:863-6. |
|35.||Lee S, Jung K, Kim Y, Jung H, Kim H, Hong J. Effect of epidermal growth factor against radiotherapy-induced oral mucositis in rats. Int J Radiat Oncol Biol Phys 2007;67:1172-8. |
|36.||Meropol NJ, Soer RA, Guthial J. Randomized phase I trial of recombinant human keratinocyte growth factor plus chemotherapy: Potential role as mucosal protectant. J Clin Oncol 2003;21:1452-8. |
|37.||Spielberger R, Stiff P, Bensinger W, Gentile T, Weisdorf D, Kewalramani T, et al. Palifermin for oral mucositis after intensive therapy for hematologic cancer. N Engl J Med 2004;351:2590-8. |
|38.||Sonis ST, Elting LS, Keefe D, Peterson DE, Schubert M, Hauer-Jensen M, et al. Perspective on cancer therapy-induced mucosal injury: Pathogenesis, measurements, epidemiology and consequences for patients. Cancer 2004;100:1995-2025. |
|39.||Sprinzl GM, Galvan O, de Vries A, Ulmer H, Gunkel AR, Lukas P, et al. Local application of granulocyte-macrophage colony stimulating factor (GM-CSF) for the treatment of oral mucositis. Eur J Cancer 2001;37:2003-9 . |
|40.||Dazzi C, Cariello A, Giovanis P, Monti M, Vertogen B, Leoni M, et al. Prophylaxis with GM-CSF mouthwashes does not reduce frequency and duration of severe oral mucositis in patients with solid tumours undergoing highdose chemotherapy with autologous peripheral blood hemopoietic stem cell transplantation rescue: A double blind, randomized, placebo controlled study. Ann Oncol 2003;14:559-63. |
|41.||Lieschke GJ, Ramenghi U, O′ Conner MP, Sheridan W, Sner J, Morstyn G. Studies on neutrophil levels in patients receiving GpCSF after autologous bone marrow transplantation. Br J Haematol 1992;82:589-95. |
|42.||Orazi A, Du X, Yang Z, Kashai M, Williams DA. Interleukin-11 prevents apoptosis and accelerates recovery of small intestinal mucosa in mice treated with combined chemotherapy and radiation. Lab Invest 1996;75:33-42. |
|43.||Cerchietti LC, Navigante AH, Lutteral MA, Castro MA, Kirchuk R, Bonomi M, et al. Double blind, placebo-controlled trial on intravenous L-alanyl-L glutamine in the incidence of oral mucositis following chemotherapy in patients with head and neck cancer. Int J Radiat Oncol Biol Phys 2006;65:1330-7. |
|44.||Kuhrer I, Kuzmits R, Linkesch W, Ludwig H. Topical PGE 2 enhances healing of chemotherapy associated mucosal lesions. Lancet 1986;1:623. |
|45.||Labar B, Mrsiæ M, Pavletiæ Z, Bogdaniæ V, Nemet D, Aurer I, et al . Prostaglandin E2 for prophylaxis of oral mucositis following BMP. Bone Marrow Transplant 1993;11:379-82. |
|46.||Wadleigh RG, Redman RS, Graham ML, Krasnow SH, Anderson A, Cohen MH. Vitamin E in the treatment of chemotherapy induced mucositis. Am J Med 1992;92:481-4. |
|47.||Kurokowa M, Lynch K, Podolsky DK. Effects of growth factor on an intestinal epithelial cell line: Transforming growth factor inhibits proliferation and stimulates differentiation. Biochem Biophys Res Comm 1987;142:775-82. |
|48.||Booth D, Potten CS. Protection against mucosal injury by growth factors and cytokines. J Natl Cancer Inst Monogra 2001;29:17-20. |
|49.||Foncuberta MC, Cagnoni PJ, Brandts CH, Mandanas R, Fields K, Derigs HG, et al. Topical transforming growth factor-â3 in the prevention or alleviation of chemotherapy-induced oral mucositis in patients with lymphomas or solid tumors. J Immunother 2001;24:384-8 |
|50.||Osaki T, Ueta E, Yoneda K, Hirota J, Yamamoto T. Prophylaxis of oral mucositis associated with chemotherapy for oral carcinoma by azelastine hydrochloride(Azelastine) with other antioxidants. Head Neck 1995;16:331-9. |
|51.||Murray LA, Kramer MS, Hesson DP, Watkins BA, Edward G, Fey EG, et al. Serum amyloid P ameliorates radiation-induced oral mucositis and fibrosis. Fibrogenesis Tissue Repair 2010;3:11. Available from: http://www.fibrogenesis.com/content/3/1/11 )[ Last accessed on 2010 Sep 10]. |
|52.||Fisher J, Scott C, Scarantino CW, Leveque FG, White RL, Rotman M, et al. Phase III quality-of-life study results: Impact on patient′s quality of life to reducing xerostomia after radiotherapy for head-and -neck cancer-RTOG 97-09. Int J Radiat Oncol Biol Phys 2003;56:832-6. |
|53.||LeVeque FG, Montgomery M, Potter D, Zimmer MB, Rieke JW, Steiger BW, et al. A multicentre, randomized, double-blind placebo controlled, dose titration study of oral pilocarpine for treatment of radiation induced xerostomia in head and neck cancer patients. J Clin Oncol 1993;11:1124-31. |
|54.||Wong JK, Wood RE, Mc Lean M. Conservative management of osteoradionecrosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997;84:16-21. |
|55.||Epstein JB, Freilich MM, Le ND. Risk factors for oropharyngeal candidiasis in patients who receive radiation therapy for malignant conditions of the head and neck. Oral Surg Oral Med Oral Pathol 1993;76:169-74. |
|56.||Nelson GM. Biology of taste buds and the clinical problem of taste loss. Anat Rec 1998;253:70-8. |
|57.||Zheng WK, Inokuchi A, Yamamoto T, Komiyama S. Taste dysfunction in irradiated patients with head and neck cancer. Fukuoka Igaku Zasshi 2002;93:64-76. |
|58.||Silverman S Jr. Complications of treatment. In: Silverman S Jr, editor. Oral Cancer. 5th ed. Hamilton, Canada: BC Decker Inc; 2003. p. 113-28. |
|59.||Silverman JE, Weber CW, Silverman S Jr, Coulthard SL, Manning MR. Zinc supplementation and taste in head and neck cancer patients undergoing radiation therapy. J Oral Med 1983;38:14-6. |
|60.||Method of preventing oral mucositis with transforming growth factor beta. Available from: http://www.patentstorm.us/patents/5817625-description.html .Foncuberta [ Last accessed on 2010 Sep 10]. |
[Table 1], [Table 2], [Table 3]
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