4.3 Article

Care Experience, by Site of Care, for Adolescents and Young Adults With Cancer

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JCO ONCOLOGY PRACTICE
卷 17, 期 6, 页码 355-E826

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1200/OP.20.00840

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  1. Patient-Centered Outcomes Research Institute (PCORI) [2909-MCHS]
  2. Agency for Healthcare Research and Quality (AHRQ)
  3. University of Washington [R25HS023 207]
  4. Hyundai Hope on Wheels Impact Fund
  5. Mary Bridge Children's Foundation

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The study found that AYAs treated at academic centers are more likely to be offered clinical trials and be aware of supportive services, while those treated at academic centers are more satisfied with support, communication, and overall treatment. Respondents treated at academic centers were more likely to receive information relevant to their age group and reported higher overall satisfaction with their healthcare team's knowledge of AYAs.
PURPOSE: Most of the 77,000 adolescents and young adults (AYAs) 15-39 years of age diagnosed with cancer annually in the United States are treated at community rather than academic centers. Little is known about their healthcare experience. METHODS: A cross-sectional, anonymous, online survey was conducted with a convenience sample of AYAs treated for cancer at US academic (n = 112) or community centers (n = 64). RESULTS: Clinical trials were offered more frequently to respondents treated at academic centers (26.8% v 7.8%; P = .005). Eighty percent of all those offered a clinical trial chose to enroll. Over three-fourths reported awareness of community-based or online AYA oncology support services; however, significantly more respondents from academic centers reported awareness of services provided by the institution itself (40.2% v 7.8%; P < .001). Significantly more respondents from academic centers reported receiving information relevant to their age group (41.1% v 15.6%; P < .001). Respondents treated at academic centers were significantly more satisfied with support, communication, and overall treatment. Odds of respondents treated at an academic center reporting that their healthcare team knew enough about AYAs were 3.12-fold higher than those treated at community centers (95% CI, 1.6 to 6.4; P = .002). Odds of overall satisfaction were significantly higher for respondents who reported that their healthcare team knew enough about AYAs (aOR, 9.7, 95% CI, 2.4 to 53.9; P = .003). CONCLUSION: Cancer treatment for AYAs at both academic and community centers can be optimized by improving healthcare providers' understanding of the key issues facing AYAs with cancer and by increasing AYA-specific institutional resources and support services.

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