TY - JOUR
T1 - Salivary Gland Hypofunction and Xerostomia in Head and Neck Radiation Patients
AU - Jensen, Siri Beier
AU - Vissink, Arjan
AU - Limesand, Kirsten H.
AU - Reyland, Mary E.
N1 - Funding Information:
Although for some studies, such as those aimed at selecting the most effective method to alleviate the problems of radiation damage to salivary glands, a sufficiently large patient cohort often can be selected within the researcher’s own institution, a multidisciplinary and often multi-institutional approach is needed for studies aimed at either the prevention of radiation injury to salivary gland tissue or the restoration of radiation-damaged salivary gland tissue. The development and testing of strategies for gene transfer and stem cell research to restore radiation-induced functional loss of the salivary glands may also require collaboration of researchers from diverse research backgrounds. Furthermore, a lot of work, including transfer of a preclinical protocol to good medical practice, has to be done to bring gene transfer and stem cell therapy from a laboratory bench to the clinic (174). Such research efforts are very costly and need the involvement of researchers that have access to national and international scientific societies (eg, European Organisation for Research and Treatment of Cancer Head and Neck Cancer Group, European Society for Therapeutic Radiation Oncology, International Society for Stem Cell Research, Stem Cells in Development and Disease, and Multinational Association of Supportive Care in Cancer and International Society of Oral Oncology). Such researchers have access to a network that will allow them to successfully compete for multinational translational grants from, for instance, the NIH and the European Framework Programs. Moreover, the interest of governmental, public, and private funding organizations and among researchers with an interest in healthy aging is growing, and research aimed at prevention and reduction of the morbidity of cancer treatment well fits within these programs.
Publisher Copyright:
© 2019 The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Background: The most manifest long-term consequences of radiation therapy in the head and neck cancer patient are salivary gland hypofunction and a sensation of oral dryness (xerostomia). Methods: This critical review addresses the consequences of radiation injury to salivary gland tissue, the clinical management of salivary gland hypofunction and xerostomia, and current and potential strategies to prevent or reduce radiation injury to salivary gland tissue or restore the function of radiation-injured salivary gland tissue. Results: Salivary gland hypofunction and xerostomia have severe implications for oral functioning, maintenance of oral and general health, and quality of life. Significant progress has been made to spare salivary gland function chiefly due to advances in radiation techniques. Other strategies have also been developed, e.g., radioprotectors, identification and preservation/expansion of salivary stem cells by stimulation with cholinergic muscarinic agonists, and application of new lubricating or stimulatory agents, surgical transfer of submandibular glands, and acupuncture. Conclusion: Many advances to manage salivary gland hypofunction and xerostomia induced by radiation therapy still only offer partial protection since they are often of short duration, lack the protective effects of saliva, or potentially have significant adverse effects. Intensity-modulated radiation therapy (IMRT), and its next step, proton therapy, have the greatest potential as a management strategy for permanently preserving salivary gland function in head and neck cancer patients. Presently, gene transfer to supplement fluid formation and stem cell transfer to increase the regenerative potential in radiation-damaged salivary glands are promising approaches for regaining function and/or regeneration of radiation-damaged salivary gland tissue.
AB - Background: The most manifest long-term consequences of radiation therapy in the head and neck cancer patient are salivary gland hypofunction and a sensation of oral dryness (xerostomia). Methods: This critical review addresses the consequences of radiation injury to salivary gland tissue, the clinical management of salivary gland hypofunction and xerostomia, and current and potential strategies to prevent or reduce radiation injury to salivary gland tissue or restore the function of radiation-injured salivary gland tissue. Results: Salivary gland hypofunction and xerostomia have severe implications for oral functioning, maintenance of oral and general health, and quality of life. Significant progress has been made to spare salivary gland function chiefly due to advances in radiation techniques. Other strategies have also been developed, e.g., radioprotectors, identification and preservation/expansion of salivary stem cells by stimulation with cholinergic muscarinic agonists, and application of new lubricating or stimulatory agents, surgical transfer of submandibular glands, and acupuncture. Conclusion: Many advances to manage salivary gland hypofunction and xerostomia induced by radiation therapy still only offer partial protection since they are often of short duration, lack the protective effects of saliva, or potentially have significant adverse effects. Intensity-modulated radiation therapy (IMRT), and its next step, proton therapy, have the greatest potential as a management strategy for permanently preserving salivary gland function in head and neck cancer patients. Presently, gene transfer to supplement fluid formation and stem cell transfer to increase the regenerative potential in radiation-damaged salivary glands are promising approaches for regaining function and/or regeneration of radiation-damaged salivary gland tissue.
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U2 - 10.1093/jncimonographs/lgz016
DO - 10.1093/jncimonographs/lgz016
M3 - Review article
C2 - 31425600
AN - SCOPUS:85071532333
SN - 1052-6773
VL - 2019
JO - NCI Monographs
JF - NCI Monographs
IS - 53
M1 - lgz016
ER -