Emerging evidence on the pathobiology of mucositis
Background Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely. Methods Panel members reviewed the...
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Published in | Supportive care in cancer Vol. 21; no. 11; pp. 3233 - 3241 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.11.2013
Springer Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0941-4355 1433-7339 1433-7339 |
DOI | 10.1007/s00520-013-1900-x |
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Abstract | Background
Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely.
Methods
Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011.
Results
Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology.
Conclusion
The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity. |
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AbstractList | Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely. Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011. Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology. The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity.[PUBLICATION ABSTRACT] Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely. Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011. Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology. The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity. Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely.BACKGROUNDConsiderable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely.Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011.METHODSPanel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011.Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology.RESULTSRecent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology.The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity.CONCLUSIONThe ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity. Background Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely. Methods Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011. Results Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology. Conclusion The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity. Keywords Mucosal injury * Cancer therapy * Targeted drugs * Toxicity* Alimentary tract * Pharmacogenetics Background Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely. Methods Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011. Results Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology. Conclusion The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity. |
Audience | Academic |
Author | Al-Dasooqi, Noor Bowen, Joanne M. Gibson, Rachel J. Elad, Sharon Bateman, Emma Blijlevens, Nicole Logan, Richard M. Stringer, Andrea M. Lalla, Rajesh V. Sonis, Stephen T. Nair, Raj G. Yazbeck, Roger |
Author_xml | – sequence: 1 givenname: Noor surname: Al-Dasooqi fullname: Al-Dasooqi, Noor email: noor.al-dasooqi@adelaide.edu.au organization: Discipline of Medicine, University of Adelaide – sequence: 2 givenname: Stephen T. surname: Sonis fullname: Sonis, Stephen T. organization: Brigham and Women’s Hospital, Dana-Farber Cancer Institute – sequence: 3 givenname: Joanne M. surname: Bowen fullname: Bowen, Joanne M. organization: Discipline of Physiology, University of Adelaide – sequence: 4 givenname: Emma surname: Bateman fullname: Bateman, Emma organization: Discipline of Medicine, University of Adelaide – sequence: 5 givenname: Nicole surname: Blijlevens fullname: Blijlevens, Nicole organization: Department of Haematology, University Medical Center Nijmegen – sequence: 6 givenname: Rachel J. surname: Gibson fullname: Gibson, Rachel J. organization: Discipline of Anatomy and Pathology, University of Adelaide – sequence: 7 givenname: Richard M. surname: Logan fullname: Logan, Richard M. organization: School of Dentistry, University of Adelaide – sequence: 8 givenname: Raj G. surname: Nair fullname: Nair, Raj G. organization: Discipline of Oral Medicine, Griffith University and Department of Haematology and Oncology, Queensland Health – sequence: 9 givenname: Andrea M. surname: Stringer fullname: Stringer, Andrea M. organization: School of Pharmacy and Medical Sciences, University of South Australia – sequence: 10 givenname: Roger surname: Yazbeck fullname: Yazbeck, Roger organization: School of Pharmacy and Medical Sciences, University of South Australia – sequence: 11 givenname: Sharon surname: Elad fullname: Elad, Sharon organization: Division of Oral Medicine, Eastman Institute for Oral Health, University of Rochester Medical Center – sequence: 12 givenname: Rajesh V. surname: Lalla fullname: Lalla, Rajesh V. organization: Section of Oral Medicine and Neag Comprehensive Cancer Center, University of Connecticut Health Center |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23842598$$D View this record in MEDLINE/PubMed |
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Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The... Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal... Background Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The... |
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SubjectTerms | Antineoplastic Agents - adverse effects Biology Cancer therapies Chemoradiotherapy - adverse effects Evidence-Based Medicine Head and Neck Neoplasms - complications Head and Neck Neoplasms - genetics Head and Neck Neoplasms - therapy Humans Medicine Medicine & Public Health Mucous membrane Nursing Nursing Research Oncology Pain Medicine Pathology Pharmacogenetics Rehabilitation Medicine Review Article Stomatitis - chemically induced Stomatitis - genetics Stomatitis - microbiology Toxicity |
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Title | Emerging evidence on the pathobiology of mucositis |
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