Abstract
Purpose
We described unmet information and service needs of adolescent and young adult (AYA) cancer survivors (15–39 years of age) and identified sociodemographic and health-related factors associated with these unmet needs.
Methods
We studied 523 AYAs recruited from seven population-based cancer registries, diagnosed with acute lymphocytic leukemia, Hodgkin’s lymphoma, non-Hodgkin’s lymphoma, germ cell cancer, or sarcoma in 2007–2008. Participants completed surveys a median of 11 months from diagnosis. Multivariable logistic regression analyses were used to estimate associations between unmet (information and service) needs and sociodemographic and health-related factors.
Results
More than half of AYAs had unmet information needs relating to their cancer returning and cancer treatments. AYAs needing services, but not receiving them, ranged from 29 % for in-home nursing to 75 % for a support group. The majority of AYAs who needed a pain management expert, physical/occupational therapist, mental health worker, or financial advice on paying for health care did not receive services. In multivariable analyses, older participants, men, participants of non-white race/ethnicity, and participants who reported less than excellent general health or fair/poor quality of care were more likely to report unmet information needs. Factors associated with both unmet service and information needs included physical health or emotional problems interfering with social activities or having ≥3 physical treatment-related symptoms.
Conclusions
Recently diagnosed AYA cancer survivors have substantial unmet information needs varying by demographic and health-related factors.
Implications for cancer survivors
We identified subgroups of AYA cancer survivors with high unmet needs that can be targeted for interventions and referrals.
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Acknowledgments
This study is supported by contract numbers N01-PC-54402, N01-PC-54404, N01-PC-35136, N01-PC-35139, N01-PC-35142, N01-PC-35143, and N01-PC-35145.
AYA HOPE Study Collaborative Group:
California Cancer Registry/Public Health Institute (Sacramento, CA, USA): Rosemary Cress, DrPH (P.I.); Gretchen Agha; and Mark Cruz.
Fred Hutchinson Cancer Research Center (Seattle, WA, USA): Stephen M. Schwartz, Ph.D. (P.I.); Martha Shellenberger; and Tiffany Janes.
Karmanos Cancer Center (Detroit, MI, USA): Ikuko Kato, Ph.D. (P.I.); Ann Bankowski; and Marjorie Stock.
Louisiana State University (New Orleans, LA, USA): Xiao-Cheng Wu, M.D., MPH (P.I.); Vivien Chen; Bradley Tompkins
Cancer Prevention Institute of California (Fremont, CA, USA): Theresa Keegan, Ph.D., M.S. (P.I.); Laura Allen; Zinnia Loya; and Karen Hussain.
University of Iowa (Iowa City, IA, USA): Charles F. Lynch M.D., Ph.D. (P.I.); Michele M. West, Ph.D.; and Lori A. Odle, R.N.
University of Southern California (Los Angeles, CA, USA): Ann Hamilton, Ph.D. (P.I.); Jennifer Zelaya; Mary Lo; and Urduja Trinidad.
National Cancer Institute (Bethesda, MD, USA): Linda C. Harlan, BSN, MPH, Ph.D. (investigator); Ashley Wilder Smith, Ph.D., MPH (co-investigator); Sonja M. Stringer, MPH; and Gretchen Keel, BS, BA.
Consultants: Arnold Potosky, PhD.; Keith Bellizzi, Ph.D.; Karen Albritton, MD, Michael Link, MD; and Brad Zebrack, Ph.D., MSW.
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Keegan, T.H.M., Lichtensztajn, D.Y., Kato, I. et al. Unmet adolescent and young adult cancer survivors information and service needs: a population-based cancer registry study. J Cancer Surviv 6, 239–250 (2012). https://doi.org/10.1007/s11764-012-0219-9
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DOI: https://doi.org/10.1007/s11764-012-0219-9