Oral Mucositis Induced by Chemoradiotherapy: Comparison
Please note this is a comparison between Version 2 by Camila Xu and Version 1 by DANIELA Jicman STAN.

Oral mucositis, a severe non-hematological complication, can be induced by chemoradiotherapy. It is associated with severe local dysfunction, severely affecting the patient’s quality of life; it increases the risk of oral infections and interrupts oncological treatment, thus prolonging the duration and cost of hospitalization.

 

  • oral mucositis
  • honey
  • head and neck cancer
  • chemotherapy

1. Introduction

Currently epidemiological data support that head and neck tumors are a public health problem due to their increasing incidence, prevalence and high mortality. Head and neck cancer (HNC) accounts for more than 550,000 cases and 380,000 deaths annually, worldwide [1].
Head and neck oncology faces real challenges as these types of tumors have serious repercussions on the patient’s quality of life. They affect various areas that directly interfere with the patient’s everyday life, such as: speech, taste, ability to chew, swallow, breathe, facial bone changes, dental mobility, local or remote vascular-nerve functionality, physical appearance; these types of cancers can also have a profound, long-lasting psychological impact, sometimes with extensive recovery processes. Therefore the treatment of Ear, Nose & Throat (ENT) cancers is extremely complex, multimodal and requires, on one hand, the involvement of a multidisciplinary therapeutic team, which must include medical oncologists, radiation therapists, pathologists, dentists, nutritionists, and on the other hand, the availability of certain technologies and techniques for radiotherapy (3D conformal 3DCRT or intensity modulated, IMRT). In addition to surgery and radiotherapy, chemotherapy and immunotherapy have undergone major developments, based on new and effective clinical trials but with more or less manageable toxicities [2,3][2][3].
Of all chemoradiotherapeutic toxicities, OM seems to be difficult to manage and despite many studies, there is no unanimously accepted protocol by clinicians today [4].
Considered one of the most severe non-hematological complications, OM seriously affects the patient’s quality of life. It is associated with severe local dysfunctions, increases the risk of oral infections, may interfere with oncological treatment prolonging the duration and cost of hospitalization [5].
From a radiobiological point of view, the oral mucosa is one of the acute-response tissues whose lesions may be reversible and frequently occur during irradiation or after treatment completion [6].
However, radiotherapy has an adverse influence on other mucosae and the inflammatory and indurated cutaneous changes associated with mucositis (as an expression of the effects of radiotherapy) must be clinically dissociated from other dermatological manifestations, similar in clinical expression: atrophic lichen sclerosus, morphea or lichen planus [7].
In order to prevent and treat chemoradiotherapy-induced OM, a variety of natural and synthetic substances are currently used. In addition to the recognized and marketed recommendations, more and more emphasis is being placed on natural products in view of their minimal adverse effects [4].
One of the best known natural agents is honey, which can be defined as a heterogeneous mixture of substances such as proteins, sugars, which come from the nectar of flowers and glandular secretions produced by bees. Honey is an extremely complex product and can be considered both a plant and an animal product [8,9][8][9]. Honey contains more than 200 different natural compounds, grouped into macro and micronutrients, depending on the type of bees, natural floral source, environmental factors and processing methods. Among the compounds that make up honey are: sugar, proteins, enzymes, minerals, vitamins, amino acids and a wide range of polyphenols. These compounds give honey its color, taste, viscosity and various therapeutic properties. Various scientific studies have shown that honey has numerous benefits. Thanks to flavonides and phenolic acids, honey has important antimicrobial activity. Moreover, it has antiviral, antioxidant, anti-inflammatory and antineoplastic effects [10]. These properties can be attributed to physicochemical characteristics such as high osmolarity and low pH, due to the presence of organic acids; the concomitant effects of the antioxidant and antimicrobial properties of honey, together with the anti-inflammatory properties, produce a healing effect on lesions. Honey is a good preventive agent against bacterial effects because its physicochemical properties provide an environment that is not conducive to bacterial proliferation, thus inhibiting the inflammation process [11].
As it can be seen, honey, as a natural agent has a broad-spectrum activity comparable to other systemic anti-inflammatory agents, e.g., dexamethasone, which due to its anti-inflammatory and other effects can be used in dermatology, oncology, surgery, etc. [12]. Honey also stimulates the immune system by producing antibodies [13]. Research has established that honey has a strong impact on the proliferation of B and T lymphocytes, thereby activating macrophages.

D2. Oral Mucositiscussio Induced by Chemoradiotherapy in Head and Neck Cancer

Currently, chemoradiotherapy-induced OM benefits from a multitude of pharmacological and non-pharmacological therapeutic options. Although numerous agents exposed in the present studyarcher's research are available, researchers have not yet reached a consensus regarding the prevention and treatment of this toxicity [50][14]. There are many studies in the literature on the usefulness of honey in the prevention and treatment of OM based on the biological properties of this agent. As an anti-inflammatory and antimicrobial agent and immunomodulator, this natural product has a great impact on OM [8,9,10,11,13,51,52][8][9][10][11][13][15][16]. For example, Pradip Kumar Maiti et al. conducted a study on 50 patients diagnosed with head and neck cancer who were radiotreated and divided into two study groups. The study arm was given 20 mL of honey 15 min before, 15 min after treatment, and a similar amount at bedtime. After evaluation, there was a significant reduction in grade 3 or 4 OM in the honey arm from 18% to 41% in the control arm [53][17]. The working method is similar to Howdler et al.’s, mentioned in this paper. Both Pradip Kumar Maiti et al. and Howdler conclude that honey is an inexpensive, readily available, effective agent for treating OM. The difference between these studies is in the oncological treatment applied to the patients, i.e., radiotherapy alone versus radiochemotherapy in combination with cisplatin-based chemotherapy. Not all studies specify the type of honey used. Howdler et al. used 20 mg of fresh, organic, unprocessed honey and in the study by Pradip Kumar Maiti et al. honey of unspecified origin was used but the recommendations of the studies are similar [39,53][17][18]. On the other hand, Motallebnejad M et al. conducted a double-blind randomized clinical trial in which 40 patients randomly assigned to two groups are examined. The study protocol is similar to the studies described above. However, the type of honey used is specified, this being pure natural honey obtained mainly from Thymus and Astragale in the Alborz Mountains, northern Iran. It is assumed that the beneficial effect of honey is based not only on its antibacterial properties but also on its geographical location, pollen source, season, type of bee, or other factors influencing its quality [10,11,54][10][11][19]. In contrast in the subspecialty review of Tharakan, T et al. [43][20], in which oncology patients are administered thyme honey, polyfloral honey, Ziziphus honey, pure or diluted honey oral rinse with satisfactory results, Karsten Münstedt [19][21] evaluated the efficacy of conventional bee honey and Manuka honey on radiochemotherapy-induced OM. Conventional honey has been shown to be more beneficial than Manuka honey, which requires caution when administered [11] for example due to adverse effects (severe nausea, vomiting, and severe burning sensations in the mouth) it was necessary to change the protocol in a study conducted by Parsonset et al. [11,54,55][11][19][22]. On the other hand, Hunter et al.’s study also found adverse effects of Manuka honey in a group treated with this type of honey [11] compared to Bardy et al., who conducted a double-blind, placebo-controlled, randomized trial with 131 patients. Consequently, a different form of honey presentation is recommended using a more liquid formula with active ingredients [11,56][11][23]. In other respects in the systematic reviews and meta-analyses [37,42,44,45][24][25][26][27] introduced in the present study, reference is made to honey combined locally and systemically, “natural” honey, royal jelly, honey extracted from Camellia sinensis, Thymus, and Astragale, from the Western Ghats forests, from Trifolium alexandrenum, pure natural honey, manuka, local honey, or unspecified honey applied locally or administered systemically. The results of studies are positive, honey administered either in dilution or in pure form has beneficial effects on OM [43,46,47][20][28][29]. Although the literature, as wresearchers have extensively exposed in this studyby researchers, supports the benefits of bee honey in preventing and treating OM in patients with head and neck cancer, this topic is still controversial. Effective management of this toxicity is needed, but in neoplastic patients who are given different types of treatments such as pain relievers and anti-inflammatory drugs, which may influence the results of the research, these studies sometimes seem inconsistent [44][26]. On the other hand, it is very difficult to control the purity of honey, as it differs depending on a multitude of factors. In order to avoid inconsistent results in future research, it is necessary to specify and recognize the differences between different types of honey or to identify the active substances of this agent responsible for its beneficial effect on OM [19][21]. Despite these pros and cons, there is sufficient evidence and scientific studies conducted by researchers recommending bee honey to be included in the guidelines responsible for the management of this post-radiochemotherapy toxicity [34,36,37,38,42][24][25][30][31][32]. Despite its many benefits, honey consumption is still limited. Many researchers also warn patients about potential health problems caused by the excessive consumption of honey. Although honey has extraordinary anti-inflammatory, antibacterial, antiviral, anticancer, and tissue-repairing properties, caution is still required in its consumption [52][16]. Moreover, honey is a food subject to adulteration. In its composition there must not be any other ingredient, flavor, or foreign substance. Honey must not be overheated in order not to lose its properties. Pure honey can be altered either directly by adding adulterants, indirectly by feeding bees, or by mixing honey with other low-quality products [57][33]. Apart from the nutrients and compounds that give it these beneficial physicochemical properties, there may be contaminants in the composition of honey, such as pesticides, antibiotics, heavy metals, or other toxic agents, caused by exposure to the environment, faulty handling by beekeepers, or even the presence of numerous bee diseases that can ultimately affect the quality of honey. Honey can be contaminated by various chemicals or pathogens, which is why it is recommended that before consumption honey should be sterilized in order to remove contaminated agents without losing the therapeutic properties of honey. The use of honey should not be recommended for cancer patients with associated diabetes. Another important problem is the presence of allergens that can cause severe anaphylactic reactions. Honey can also be a factor in the development of dental caries, therefore careful care of the oral cavity is recommended, especially during antineoplastic treatment. Given the benefits but also the contraindications, manufacturers are encouraged to label each beekeeping product appropriately, especially honey [52][16].

References

  1. Jicman (Stan), D.; Niculet, E.; Lungu, M.; Onisor, C.; Rebegea, L.; Vesa, D.; Bezman, L.; Bujoreanu, F.C.; Sarbu, M.I.; Mihailov, R.; et al. Nasopharyngeal carcinoma: A new synthesis of literature data (Review). Exp. Ther. Med. 2022, 23, 136.
  2. Rebegea, L.F.; Firescu, D.; Anghel, R.M.; Gales, L.; Ilie, A.M.; Dumitru, M.E.; Craescu, M.; Niculet, E.; Tatu, A.L.; Cretu, M.S.; et al. Clinical, histological and therapeutical aspects in the management of uterine and extrauterine stromal sarcomas: Case reports. Exp. Ther. Med. 2021, 22, 1456.
  3. Koyfman, S.A.; Ismaila, N.; Crook, D.; D’Cruz, A.; Rodriguez, C.P.; Sher, D.J.; Silbermins, D.; Sturgis, E.M.; Tsue, T.T.; Weiss, J.; et al. Management of the Neck in Squamous Cell Carcinoma of the Oral Cavity and Oropharynx: ASCO Clinical Practice Guideline. J. Clin. Oncol. 2019, 37, 1753–1774.
  4. Ferreira, A.S.; Macedo, C.; Silva, A.M.; Delerue-Matos, C.; Costa, P.; Rodrigues, F. Natural Products for the Prevention and Treatment of Oral Mucositis—A Review. Int. J. Mol. Sci. 2022, 23, 4385.
  5. Isozaki, A.B.; Brant, J.M. Clinical Updates in Mucositis-Related Symptom Management. Semin. Oncol. Nurs. 2022, 38, 151252.
  6. Rebegea, L.; Firescu, D.; Dumitru, M.; Dumitrache, M.; Diaconu, C. Linear-quadratic model applied in reirradiation of brain meastases. Rom. J. Phys. 2015, 60, 1095–1102.
  7. Tatu, A.L.; Nwabudike, L.C. The treatment options of male genital lichen sclerosus et atrophicus: Treatments of genital lichen sclerosus. In Proceedings of the 14th National Congress of Urogynecology and the National Conference of the Romanian Association for the Study of Pain, Eforie, Romania, 26–27 October 2017; pp. 262–264.
  8. Amanat, A.; Ahmed, A.; Kazmi, A.; Aziz, B. The effect of honey on radiation-induced oral mucositis in head and neck cancer patients. Indian J. Palliat. Care 2017, 23, 317–320.
  9. Hbibi, A.; Sikkou, K.; Khedid, K.; El Hamzaoui, S.; Bouziane, A.; Benazza, D. Antimicrobial activity of honey in periodontal disease: A systematic review. J. Antimicrob. Chemother. 2020, 75, 807–826.
  10. Jibril, F.I.; Hilmi, A.B.M.; Manivannan, L. Isolation and characterization of polyphenols in natural honey for the treatment of human diseases. Bull. Natl. Res. Cent. 2019, 43, 4.
  11. Hunter, M.; Kellett, J.; D’Cunha, N.M.; Toohey, K.; McKune, A.; Naumovski, N. The Effect of Honey as a Treatment for Oral Ulcerative Lesions: A Systematic Review. Explor. Res. Hypothesis Med. 2020, 5, 27–37.
  12. Ciobotaru, O.R.; Lupu, M.-N.; Rebegea, L.; Ciobotaru, O.C.; Duca, O.M.; Tatu, A.L.; Voinescu, C.D.; Stoleriu, G.; Earar, K.; Miulescu, M. Dexamethasone-Chemical Structure and Mechanisms of Action in Prophylaxis of Postoperative Side Effects. Rev. Chim. 2019, 70, 843–847.
  13. Kudva, A.K.; Rao, S.; Rao, P.; Pais, M.L.; Adnan, M.; Pai, K.S.R.; Baliga, M.S. Evidence for anticancer properties of honey with emphasis on mechanistic overview. Funct. Foods Cancer Prev. Ther. 2020, 7, 121–135.
  14. Bulut, H.K.; Tüfekci, F.G. Honey prevents oral mocositis in children undergoing chemotherapy: A quasi-experimental study with a control group. Complement. Ther. Med. 2016, 29, 132–140.
  15. Ullah, S.; Khan, S.U.; Saleh, T.A.; Fahad, S. Mad honey: Uses, intoxicating/poisoning effects, diagnosis, and treatment. RSC Adv. 2018, 8, 18635–18646.
  16. Ranneh, Y.; Akim, A.M.; Hamid, H.A.; Khazaai, H.; Fadel, A.; Zakaria, Z.A.; Albujja, M.; Bakar, M. Honey and its nutritional and anti-inflammatory value. BMC Complement. Med. Ther. 2021, 21, 30.
  17. Maiti, P.K.; Ray, A.; Mitra, T.N.; Jana, U.; Bhattacharya, J.; Ganguly, S. The effect of honey on mucositis induced by chemoradiation in head and neck cancer. J. Indian Med. Assoc. 2012, 110, 453–456.
  18. Howlader, D.; Singh, V.; Mohammad, S.; Gupta, S.; Pal, U.S.; Pal, M. Effect of Topical Application of Pure Honey in Chemo-radiation-Induced Mucositis and Its Clinical Benefits in Improving Quality of Life in Patients of Oral Squamous Cell Carcinoma. J. Maxillofac. Oral Surg. 2018, 18, 73–79.
  19. Motallebnejad, M.; Akram, S.; Moghadamnia, A.A.; Moulana, Z.; Omidi, S. The Effect of Topical Application of Pure Honey on Radiation-induced Mucositis: A Randomized Clinical Trial. J. Contemp. Dent. Pract. 2008, 9, 40–47.
  20. Tharakan, T.; Bent, J.; Tavaluc, R. Honey as a Treatment in Otorhinolaryngology: A Review by Subspecialty. Ann. Otol. Rhinol. Laryngol. 2019, 128, 193–207.
  21. Münstedt, K.; Momm, F.; Hübner, J. Honey in the management of side effects of radiotherapy- or radio/chemotherapy-induced oral mucositis. A systematic review. Complement. Ther. Clin. Pract. 2018, 34, 145–152.
  22. Parsons, E.; Begley, A.; Herst, P. Manuka honey mouthwash does not affect oral mucositis in head and neck cancer patients in New Zealand. J. Radiother. Pract. 2011, 11, 249–256.
  23. Bardy, J.; Molassiotis, A.; Ryder, W.D.; Mais, K.; Sykes, A.; Yap, B.; Lee, L.; Kaczmarski, E.; Slevin, N. A double-blind, placebo-controlled, randomised trial of active manuka honey and standard oral care for radiation-induced oral mucositis. Br. J. Oral Maxillofac. Surg. 2012, 50, 221–226.
  24. Elad, S.; Rn, K.K.F.C.; Lalla, R.V.; Yarom, N.; Hong, C.; Logan, R.M.; Bowen, J.; Gibson, R.; Dds, D.P.S.; Zadik, Y.; et al. MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy. Cancer 2020, 126, 4423–4431.
  25. Yarom, N.; Hovan, A.; Bossi, P.; Ariyawardana, A.; Jensen, S.B.; Gobbo, M.; Saca-Hazboun, H.; Kandwal, A.; Majorana, A.; Ottaviani, G.; et al. Mucositis Study Group of the Multinational Association of Supportive Care in Cancer/International Society of Oral Oncology (MASCC/ISOO). Systematic review of natural and miscellaneous agents, for the management of oral mucositis in cancer patients and clinical practice guidelines-part 2: Honey, herbal compounds, saliva stimulants, probiotics, and miscellaneous agents. Support. Care Cancer 2020, 28, 2457–2472.
  26. Yang, C.; Gong, G.; Jin, E.; Han, X.; Zhuo, Y.; Yang, S.; Song, B.; Zhang, Y.; Piao, C. Topical application of honey in the management of chemo/radiotherapy-induced oral mucositis: A systematic review and network meta-analysis. Int. J. Nurs. Stud. 2018, 89, 80–87.
  27. Liu, T.-M.; Luo, Y.-W.; Tam, K.-W.; Lin, C.-C.; Huang, T.-W. Prophylactic and therapeutic effects of honey on radiochemotherapy-induced mucositis: A meta-analysis of randomized controlled trials. Support. Care Cancer 2019, 27, 2361–2370.
  28. Yu, Y.T.; Deng, J.L.; Jin, X.R.; Zhang, Z.Z.; Zhang, X.H.; Zhou, X. Effects of 9 oral care solutions on the prevention of oral mucositis:A network meta-analysis of randomized controlled trials. Medicine 2020, 99, 19661.
  29. Zhang, X.; Sun, D.; Qin, N.; Liu, M.; Zhang, J.; Li, X. Comparative prevention potential of 10 mouthwashes on intolerable oral mucositis in cancer patients: A Bayesian network analysis. Oral Oncol. 2020, 107, 104751.
  30. Peterson, D.E.; Boers-Doets, C.B.; Bensadoun, R.J.; Herrstedt, J.; ESMO Guidelines Committee. Management of oral and gastrointestinal mucosal injury: ESMO Clinical Practice Guidelines for diagnosis, treatment, and follow-up. Ann. Oncol. 2015, 26, v139–v151.
  31. Lalla, R.V.; Bowen, J.; Barasch, A.; Elting, L.; Epstein, J.; Keefe, D.M.; McGuire, D.B.; Migliorati, C.; Nicolatou-Galitis, O.; Dmd, D.E.P.; et al. MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy. Cancer 2014, 120, 1453–1461.
  32. Sener, D.K.; Aydin, M.; Cangur, S.; Guven, E. The Effect of Oral Care with Chlorhexidine, Vitamin E and Honey on Mucositis in Pediatric Intensive Care Patients: A Randomized Controlled Trial. J. Pediatr. Nurs. 2019, 45, e95–e101.
  33. Fakhlaei, R.; Selamat, J.; Khatib, A.; Razis, A.F.A.; Sukor, R.; Ahmad, S.; Babadi, A.A. The Toxic Impact of Honey Adulteration: A Review. Foods 2020, 9, 1538.
More
Video Production Service