Literature DB >> 15548350

Chemotherapy-induced and/or radiation therapy-induced oral mucositis--complicating the treatment of cancer.

Maddireddy Umameshwar Rao Naidu1, Gogula Venkat Ramana, Pingali Usha Rani, Iyyapu Krishna Mohan, Avula Suman, Priyadarshni Roy.   

Abstract

The term mucositis is coined to describe the adverse effects of radiation and chemotherapy treatments. Mucositis is one of the most common adverse reactions encountered in radiation therapy for head and neck cancers, as well as in chemotherapy, in particular with drugs affecting DNA synthesis (S-phase-specific agents such as fluorouracil, methotrexate, and cytarabine). Mucositis may limit the patient's ability to tolerate chemotherapy or radiation therapy, and nutritional status is compromised. It may drastically affect cancer treatment as well as the patient's quality of life. The incidence and severity of mucositis will vary from patient to patient. It will also vary from treatment to treatment. It is estimated that there is 40% incidence of mucositis in patients treated with standard chemotherapy and this will not only increase with the number of treatment cycles but also with previous episodes. Similarly, patients who undergo bone marrow transplantation and who receive high doses of chemotherapy have a 76% chance of getting mucositis. Patients receiving radiation, in particular to head and neck cancers, have a 30% to 60% chance. The exact pathophysiology of development is not known, but it is thought to be divided into direct and indirect mucositis. Chemotherapy and/or radiation therapy will interfere with the normal turnover of epithelial, cells leading to mucosal injury; subsequently, it can also occur due to indirect invasion of Gram-negative bacteria and fungal species because most of the cancer drugs will cause changes in blood counts. With the advancement in cytology, a more precise mechanism has been established. With this understanding, we can select and target particular mediators responsible for the mucositis. Risk factors such as age, nutritional status, type of malignancy, and oral care during treatment will play important roles in the development of mucositis. Many treatment options are available to prevent and treat this condition, but none of them can completely prevent or treat mucositis. More and more pathological methods are being developed to understand this condition so that better therapeutic regimens can be selected. Emphasis also should be made in assessing the patient's psychologic condition, particular depressive disorders. This is important because treatment with antidepressants will not only contribute in lifting depression but also reduces pain somatization. Although mucositis is rarely life-threatening, it will interfere with treatment of cancer to a great extent.

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Year:  2004        PMID: 15548350      PMCID: PMC1531648          DOI: 10.1593/neo.04169

Source DB:  PubMed          Journal:  Neoplasia        ISSN: 1476-5586            Impact factor:   5.715


  43 in total

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Journal:  Cancer       Date:  1990-04-15       Impact factor: 6.860

Review 4.  Prevention and management of oral mucositis induced by antineoplastic therapy.

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Journal:  Oncology (Williston Park)       Date:  1991-12       Impact factor: 2.990

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Review 6.  Regulation of the immune response by prostaglandins.

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7.  Clinical evaluation of MGI 209, an anesthetic, film-forming agent for relief from painful oral ulcers associated with chemotherapy.

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8.  Effect of epidermal growth factor on ulcerative mucositis in hamsters that receive cancer chemotherapy.

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Journal:  Oral Surg Oral Med Oral Pathol       Date:  1992-12

9.  Studies of oral neutrophil levels in patients receiving G-CSF after autologous marrow transplantation.

Authors:  G J Lieschke; U Ramenghi; M P O'Connor; W Sheridan; J Szer; G Morstyn
Journal:  Br J Haematol       Date:  1992-11       Impact factor: 6.998

10.  Inhibition of fluorouracil-induced stomatitis by oral cryotherapy.

Authors:  D J Mahood; A M Dose; C L Loprinzi; M H Veeder; L M Athmann; T M Therneau; J M Sorensen; D K Gainey; J A Mailliard; N L Gusa
Journal:  J Clin Oncol       Date:  1991-03       Impact factor: 44.544

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  85 in total

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2.  Post hoc analysis of a randomized controlled trial comparing concurrent chemoradiation with cisplatin versus nimotuzumab-cisplatin, focusing on acute oral mucositis.

Authors:  Vanita Noronha; Vijay M Patil; Gunjesh Kumar Singh; Amit Joshi; Nandini Menon; Sarbani Ghosh Lashkar; Vijayalakshmi Mathrudev; Kavita Nawale Satam; Kumar Prabhash
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3.  The impact of dairy consumption on salivary inoculum.

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4.  A phase II study of HMB/Arg/Gln against oral mucositis induced by chemoradiotherapy for patients with head and neck cancer.

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Review 5.  The Therapeutic Potential of Mesenchymal Stromal Cells in the Treatment of Chemotherapy-Induced Tissue Damage.

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6.  Live and heat-killed Lactobacillus rhamnosus GG upregulate gene expression of pro-inflammatory cytokines in 5-fluorouracil-pretreated Caco-2 cells.

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7.  Interleukin-18 as a target for modulation of irinotecan-induced intestinal toxicity: a step towards a better therapeutic index?: Commentary on Lima-Junior et al., Br J Pharmacol 171: 2335-2350.

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8.  Low-level laser and antimicrobial photodynamic therapy on experimental periodontitis in rats submitted to chemotherapy by 5-fluorouracil.

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9.  The Mechanisms of the Anti-Inflammatory and Anti-Apoptotic Effects of Omega-3 Polyunsaturated Fatty Acids during Methotrexate-Induced Intestinal Damage in Cell Line and in a Rat Model.

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10.  Efficacy and safety of transdermal fentanyl for the treatment of oral mucositis pain caused by chemoradiotherapy in patients with esophageal squamous cell carcinoma.

Authors:  Shao-Zhi Xing; Ying Zhang
Journal:  Support Care Cancer       Date:  2014-09-02       Impact factor: 3.603

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