Oral mucositis: the hidden side of cancer therapy

Claudio Pulito1, Antonio Cristaudo2, Caterina La Porta3,4, Stefano Zapperi5,6, Giovanni Blandino1, Aldo Morrone7, Sabrina Strano8
1Oncogenomic and Epigenetic Unit, IRCCS, Regina Elena National Cancer Institute, Rome, Italy
2STI/HIV Unit, San Gallicano Dermatological Institute IRCCS, Rome, Italy
3Center for Complexity and Biosystems, Department of Environmental Science and Policy, University of Milan, Milano, Italy
4CNR - Consiglio Nazionale Delle Ricerche, Istituto Di Biofisica, Milano, Italy
5Center for Complexity and Biosystems, Department of Physics, University of Milan, Milano, Italy
6CNR - Consiglio Nazionale delle Ricerche, Istituto di Chimica della Materia Condensata e di Tecnologie per l’Energia, Milano, Italy
7Scientific Director Office, San Gallicano Institute, Rome, Italy
8SAFU Laboratory, Department of Research, Advanced Diagnostic, and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome, Italy

Tóm tắt

Inflammation response of epithelial mucosa to chemo- radiotherapy cytotoxic effects leads to mucositis, a painful side effect of antineoplastic treatments. About 40% of the patients treated with chemotherapy develop mucositis; this percentage rises to about 90% for head and neck cancer patients (HNC) treated with both chemo- and radiotherapy. 19% of the latter will be hospitalized and will experience a delay in antineoplastic treatment for high-grade mucositis management, resulting in a reduction of the quality of life, a worse prognosis and an increase in patient management costs. Currently, several interventions and prevention guidelines are available, but their effectiveness is uncertain. This review comprehensively describes mucositis, debating the impact of standard chemo-radiotherapy and targeted therapy on mucositis development and pointing out the limits and the benefits of current mucositis treatment strategies and assessment guidelines. Moreover, the review critically examines the feasibility of the existing biomarkers to predict patient risk of developing oral mucositis and their role in early diagnosis. Despite the expression levels of some proteins involved in the inflammation response, such as TNF-α or IL-1β, partially correlate with mucositis process, their presence does not exclude others mucositis-independent inflammation events. This strongly suggests the need to discover biomarkers that specifically feature mucositis process development. Non-coding RNAs might hold this potential.

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