Using Teamwork to Bridge the Adolescent and Young Adult Gap

Author:

Wolfson Julie A.12ORCID,Bhatia Smita12ORCID,Bhatia Ravi3,Smith Mark W.1,Dai Chen1,Campbell Sukhkamal B.4,Gunn Deidre D.4ORCID,Mahoney Anne Byrd5,Croney Christina M.1ORCID,Hageman Lindsey1,Francisco Liton1ORCID,Kenzik Kelly M.13ORCID

Affiliation:

1. Institute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham, Birmingham, AL

2. Division of Pediatric Hematology-Oncology, University of Alabama at Birmingham, Birmingham, AL

3. Division of Hematology-Oncology, University of Alabama at Birmingham, Birmingham, AL

4. Division of Reproductive Endocrinology and Infertility, University of Alabama at Birmingham, Birmingham, AL

5. Division of Pediatric Hematology-Oncology, Vanderbilt University, Birmingham, AL

Abstract

PURPOSE: Individuals diagnosed with cancer age between 15 and 39 years (adolescents and young adults [AYAs]) have not seen improvement in survival compared with children or older adults; clinical trial accrual correlates with survival. Unique unmet needs among AYAs related to psychosocial support and fertility preservation (FP) are associated with health-related quality of life. METHODS: We enhanced existing structures and leveraged faculty/staff across pediatric/adult oncology to create novel teams focused on AYA (age 15-39 years) care at a single center, with minimal dedicated staff and no change to revenue streams. We aimed to influence domains shown to drive survival and health-related quality of life: clinical trial enrollment, physician/staff collaboration, psychosocial support, and FP. We captured metrics 3 months after patients presented to the institution and compared them before/after Program implementation using descriptive statistics. RESULTS: Among 139 AYAs (age 15-39 years) from the pre-Program era (January 2016-February 2019: adult, n = 79; pediatric, n = 60), and 279 from the post-Program era (February 2019-March 2022: adult, n = 215; pediatric, n = 64), there was no change in clinical trial enrollment( P ≥ .3), whereas there was an increase in the proportion of AYAs referred for supportive care and psychology (pediatric: P ≤ .02; adult: P ≤ .001); whose oncologists discussed FP (pediatric: 15% v 52%, P < .0001; adult: 37% v 50%, P = .0004); and undergoing FP consults (pediatric: 8% v39%, P < .0001; adult 23% v 38%, P = .02). CONCLUSION: This team-based framework has effected change in most targeted domains. To affect all domains and design optimal interventions, it is crucial to understand patient-level and facility-level barriers/facilitators to FP and clinical trial enrollment.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Oncology (nursing),Health Policy,Oncology

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