Evolving information needs among colon, breast, and prostate cancer survivors: Results from a longitudinal mixed-effects analysis

Cancer Epidemiology Biomarkers and Prevention

Volumn 24, Issue 7, 2015, Pages 1071-1078

  Tan, Andy S L ^a,b   Nagler, Rebekah H ^c   Hornik, Robert C ^d   DeMichele, Angela ^e  

^a DANA FARBER CANCER INSTITUTE   (United States)

^b HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^c UNIVERSITY OF MINNESOTA   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BREAST CANCER; CANCER DIAGNOSIS; CANCER RECURRENCE; CANCER RISK; CANCER SURVIVAL; CANCER SURVIVOR; CANCER THERAPY; COLON CANCER; COMPARATIVE STUDY; CONTROLLED STUDY; FEMALE; HEALTH SURVEY; HIGH RISK PATIENT; HUMAN; INFORMATION SEEKING; MAJOR CLINICAL STUDY; MALE; MANAGED CARE; MEDICAL INFORMATION; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PROSTATE CANCER; RISK ASSESSMENT; RISK FACTOR; TIME TO TREATMENT; BREAST TUMOR; COLON TUMOR; FOLLOW UP; MIDDLE AGED; PROSTATE TUMOR; PSYCHOLOGY; QUALITY OF LIFE; REGISTER; RETROSPECTIVE STUDY; STATISTICS AND NUMERICAL DATA; SURVIVOR; VERY ELDERLY; YOUNG ADULT;

ADULT; AGED; AGED, 80 AND OVER; BREAST NEOPLASMS; COLONIC NEOPLASMS; FEMALE; FOLLOW-UP STUDIES; HUMANS; INFORMATION SEEKING BEHAVIOR; MALE; MIDDLE AGED; PROSTATIC NEOPLASMS; QUALITY OF LIFE; REGISTRIES; RETROSPECTIVE STUDIES; SURVIVORS; YOUNG ADULT;

EID: 84941774158     PISSN: 10559965     EISSN: None     Source Type: Journal    
DOI: 10.1158/1055-9965.EPI-15-0041     Document Type: Article

References (37)

1. American Cancer Society. Cancer facts & figures 2014 [Internet]. Atlanta, GA: American Cancer Society; 2014. Available from: http://www.cancer.org/acs/groups/content/@research/documents/webcontent/acspc-042151.pdf.
2. American Cancer Society. Cancer facts & figures 2013 [Internet]. Atlanta, GA: American Cancer Society; 2013. Available from: http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-036845.pdf.
3. Jacobs LA, Palmer SC, Schwartz LA, DeMichele A, Mao JJ, Carver J, et al. Adult cancer survivorship: Evolution, research, and planning care. CA Cancer J Clin 2009;59:391-410.
4. , Hewitt M, Greenfield S, Stovall E. From cancer patient to cancer survivor: lost in transition [Internet]. Washington, DC: National Academies Press; 2006. Available from: http://iom.edu/Reports/2005/From-Cancer-Patient-to-Cancer-Survivor-Lost-in-Transition.aspx.
5. Institute of Medicine. Delivering high-quality cancer care: charting a new course for a system in crisis [Internet]. Washington, D.C.: The National Academies Press; 2013. Available from: http://www.iom.edu/Reports/2013/Delivering-High-Quality-Cancer-Care-Charting-a-New-Course-fora-System-in-Crisis.aspx.
6. Finney Rutten LJ, Arora NK, Bakos AD, Aziz N, Rowland J. Information needs and sources of information among cancer patients: A systematic review of research (1980-2003). Patient Educ Couns 2005;57:250-61.
7. Ness S, Kokal J, Fee-Schroeder K, Novotny P, Satele D, Barton D. Concerns across the survivorship trajectory: results from a survey of cancer survivors. Oncol Nurs Forum 2013;40:35-42.
8. Nagler RH, Gray SW, Romantan A, Kelly BJ, DeMichele A, Armstrong K, et al. Differences in information seeking among breast, prostate, and colorectal cancer patients: results from a population-based survey. Patient Educ Couns 2010;81 Suppl:S54-S62.
9. Lee-Jones C, Humphris G, Dixon R, Bebbington Hatcher M. Fear of cancer recurrence - A literature review and proposed cognitive formulation to explain exacerbation of recurrence fears. Psychooncology 1997;6:95-105.
10. Lebel S, Rosberger Z, Edgar L, Devins GM. Emotional distress impacts fear of the future among breast cancer survivors not the reverse. J Cancer Surviv 2009;3:117-27.
11. Beckjord EB, Arora NK, McLaughlin W, Oakley-Girvan I, Hamilton AS, Hesse BW. Health-related information needs in a large and diverse sample of adult cancer survivors: implications for cancer care. J Cancer Surviv 2008;2:179-89.
12. Kent EE, Arora NK, Rowland JH, Bellizzi KM, Forsythe LP, Hamilton AS, et al. Health information needs and health-related quality of life in a diverse population of long-term cancer survivors. Patient Educ Couns 2012;89:345-52.
13. Bellizzi KM, Latini DM, Cowan JE, DuChane J, Carroll PR. Fear of recurrence, symptom burden, and health-related quality of life in men with prostate cancer. Urology 2008;72:1269-73.
14. Hodgkinson K, Butow P, Hunt GE, Pendlebury S, Hobbs KM, Wain G. Breast cancer survivors' supportive care needs 2-10 years after diagnosis. Support Care Cancer 2007;15:515-23.
15. Baker F, Denniston M, Smith T, West MM. Adult cancer survivors: How are they faring? Cancer 2005;104:2565-76.
16. Hart SL, Latini DM, Cowan JE, Carroll PR. Fear of recurrence, treatment satisfaction, and quality of life after radical prostatectomy for prostate cancer. Support Care Cancer 2008;16:161-9.
17. Hodges LJ, Humphris GM. Fear of recurrence and psychological distress in head and neck cancer patients and their carers. Psychooncology 2009; 18:841-8.
18. Costanzo ES, Lutgendorf SK, Mattes ML, Trehan S, Robinson CB, Tewfik F, et al. Adjusting to life after treatment: distress and quality of life following treatment for breast cancer. Br J Cancer 2007;97:1625-31.
19. Husson O, Mols F, van de Poll-Franse LV. The relation between information provision and health-related quality of life, anxiety and depression among cancer survivors: A systematic review. Ann Oncol 2011;22: 761-72.
20. Wei EK, Wolin KY, Colditz GA. Time course of risk factors in cancer etiology and progression. J Clin Oncol 2010;28:4052-7.
21. American Cancer Society. Cancer treatment & survivorship facts & figures (2012-2013) [Internet]. Atlanta, GA: American Cancer Society; 2012. Available from: http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-033876.pdf.
22. Luker KA, Beaver K, Leinster SJ, Owens RG. Information needs and sources of information for womenwith breast cancer: A follow-up study. J Adv Nurs 1996;23:487-95.
23. Dillman DA, Dillman DA. Mail and internet surveys: The tailored design method. 2nd ed. New York, NY: J. Wiley; 2000.
24. Nagler R, Romantan A, Kelly B, Stevens R, Gray S, Hull S, et al. How do cancer patients navigate the public information environment? Understanding patterns and motivations for movement among information sources. J Cancer Educ 2010;25:360-70.
25. Donald H, Robert D. G. mixed-effects regression models for binary outcomes. longitud data anal [Internet]. Hoboken, NJ: John Wiley & Sons, Inc.; 2006. Available from: http://onlinelibrary.wiley.com/doi/10.1002/0470036486.ch9/summary.
26. Earle C. Failing to plan is planning to fail: improving the quality of care with survivorship care plans. J Clin Oncol 2006;24:5112-6.
27. Demark-Wahnefried W, Aziz NM, Rowland JH, Pinto BM. Riding the crest of the teachable moment: promoting long-term health after the diagnosis of cancer. J Clin Oncol 2005;23:5814-30.
28. Demark-Wahnefried W, Pinto BM, Gritz ER. Promoting health and physical function among cancer survivors: potential for prevention and questions that remain. J Clin Oncol 2006;24:5125-31.
29. Bellizzi KM, Rowland JH, Jeffery DD, McNeel T. Health behaviors of cancer survivors: Examining opportunities for cancer control intervention. J Clin Oncol 2005;23:8884-93.
30. Aronowitz RA. Unnatural history: Breast Cancer and American Society. New York: Cambridge University Press; 2007.
31. Viswanath K, Nagler RH, Bigman-Galimore CA, McCauley MP, Jung M, Ramanadhan S. The communications revolution and health inequalities in the 21st century: implications for cancer control. Cancer Epidemiol Biomarkers Prev 2012;21:1701-8.
32. Niederdeppe J, Levy AG. Fatalistic beliefs about cancer prevention and three prevention behaviors. Cancer Epidemiol Biomarkers Prev 2007; 16:998-1003.
33. Jensen JD, Carcioppolo N, King AJ, Scherr CL, Jones CL, Niederdeppe J. The cancer information overload (CIO) scale: Establishing predictive and discriminant validity. Patient Educ Couns 2014;94:90-6.
34. Ramanadhan S, Viswanath K. Health and the information nonseeker: A profile. Health Commun 2006;20:131-9.
35. Cotten SR, Gupta SS. Characteristics of online and offline health information seekers and factors that discriminate between them. Soc Sci Med 2004;59:1795-806.
36. Salz T, Oeffinger KC, McCabe MS, Layne TM, Bach PB. Survivorship care plans in research and practice. CA Cancer J Clin 2012; 62:101-17.
37. Galarce EM, Ramanadhan S, Weeks J, Schneider EC, Gray SW, Viswanath K. Class, race, ethnicity and information needs in post-treatment cancer patients. Patient Educ Couns 2011;85:432-9.