Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-x24gv Total loading time: 0 Render date: 2024-06-10T11:51:16.354Z Has data issue: false hasContentIssue false

29 - Symptom research: looking ahead

from Section 6 - Conclusion

Published online by Cambridge University Press:  05 August 2011

Charles S. Cleeland
Affiliation:
The University of Texas M. D. Anderson Cancer Center
Michael J. Fisch
Affiliation:
The University of Texas M. D. Anderson Cancer Center
Adrian J. Dunn
Affiliation:
University of Hawaii at Manoa
Charles S. Cleeland
Affiliation:
University of Texas, M. D. Anderson Cancer Center
Michael J. Fisch
Affiliation:
University of Texas, M. D. Anderson Cancer Center
Adrian J. Dunn
Affiliation:
University of Hawaii, Manoa
Get access

Summary

Both cancer and cancer treatment produce multiple, disabling symptoms, the most prominent and distressing of which are addressed in this book. Our aim in assembling this volume has been to balance information from clinical research in cancer-related symptoms, including pain, fatigue, appetite and weight loss, sleep disturbance, cognitive impairment, and cancer-related affective changes, with basic laboratory research that explores, often in animal models, the potential mechanisms responsible for these symptoms.

Several chapters have considered new approaches to studying symptoms, including developing more-pertinent animal models and approaching symptoms from molecular, genetic, and neuroimaging perspectives. Other chapters have focused on issues of symptom assessment by self-report, longitudinal modeling of the relationship between symptom report and biology, and novel clinical trial designs. Finally, several chapters have addressed such real-world issues as obtaining funding for symptom research, establishing the cost-benefit of symptom management, integrating symptom research into collaborative cancer research groups, understanding regulatory guidelines for stating that symptom-relieving drugs really are effective, and exploring pathways for the development of new symptom-management agents. Together, these chapters lend support to the real possibility of a multidisciplinary collaboration that could become a science of symptoms – at least, of symptoms related to cancer.

Type
Chapter
Information
Cancer Symptom Science
Measurement, Mechanisms, and Management
, pp. 341 - 348
Publisher: Cambridge University Press
Print publication year: 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

,US Food and Drug Administration, Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research, Center for Devices and Radiological Health. Guidance for industry. Patient-reported outcome measures: use in medical product development to support labeling claims. Available from: URL: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM071975.pdf. Accessed Dec 18, 2009.Google Scholar
Basch, E. The missing voice of patients in drug-safety reporting. N Engl J Med 362(10):865–869, 2010.CrossRefGoogle ScholarPubMed
Cleeland, CS, Bennett, GJ, Dantzer, R, et al. Are the symptoms of cancer and cancer treatment due to a shared biologic mechanism?Cancer 97(11):2919–2925, 2003.CrossRefGoogle ScholarPubMed
Kurzrock, R. The role of cytokines in cancer-related fatigue. Cancer 92(6 Suppl):1684–1688, 2001.3.0.CO;2-Z>CrossRefGoogle ScholarPubMed
Valentine, AD, Meyers, CA. Cognitive and mood disturbance as causes and symptoms of fatigue in cancer patients. Cancer 92(6 Suppl):1694–1698, 2001.3.0.CO;2-S>CrossRefGoogle ScholarPubMed
Bilbo, SD, Biedenkapp, JC, Der-Avakian, A, Watkins, LR, Rudy, JW, Maier, SF. Neonatal infection-induced memory impairment after lipopolysaccharide in adulthood is prevented via caspase-1 inhibition. J Neurosci 25(35):8000–8009, 2005.CrossRefGoogle ScholarPubMed
Ledeboer, A, Jekich, BM, Sloane, EM, et al. Intrathecal interleukin-10 gene therapy attenuates paclitaxel-induced mechanical allodynia and proinflammatory cytokine expression in dorsal root ganglia in rats. Brain Behav Immun 21(5):686–698, 2007.CrossRefGoogle ScholarPubMed
Cata, JP, Weng, HR, Dougherty, PM. The effects of thalidomide and minocycline on taxol-induced hyperalgesia in rats. Brain Res 1229:100–110, 2008.CrossRefGoogle ScholarPubMed
Xiao, WH, Bennett, GJ. Chemotherapy-evoked neuropathic pain: abnormal spontaneous discharge in A-fiber and C-fiber primary afferent neurons and its suppression by acetyl-L-carnitine. Pain 135(3):262–270, 2008.CrossRefGoogle ScholarPubMed
Kroenke, K, Harris, L. Symptoms research: a fertile field. Ann Intern Med 134(9 Pt 2):801–802, 2001.CrossRefGoogle ScholarPubMed
Craig, AD. How do you feel? Interoception: the sense of the physiological condition of the body. Nat Rev Neurosci 3(8):655–666, 2002.CrossRefGoogle Scholar
Dworkin, RH, Turk, DC, Peirce-Sandner, S, et al. Research design considerations for confirmatory chronic pain clinical trials: IMMPACT recommendations. Pain:e-pub ahead of print, 2010.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×