Patient, Parent, and Oncologist Perspectives and Recommendations on the Right Way to Talk About Prognosis in Advanced Childhood Cancer

Author:

Kaye Erica C.1ORCID,Farner Harmony1,Mehler Shoshana1ORCID,Bien Kelly1,Mali Nidhi1,Brinkman Tara M.23ORCID,Baker Justin N.4,Hinds Pamela56ORCID,Mack Jennifer W.78ORCID

Affiliation:

1. Department of Oncology, St Jude Children's Research Hospital, Memphis, TN

2. Department of Psychology and Biobehavioral Sciences, St Jude Children's Research Hospital, Memphis, TN

3. Department of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN

4. Department of Pediatrics, Stanford University, Palo Alto, CA

5. Department of Nursing Science, Professional Practice & Quality, Children's National Hospital, Washington, DC

6. Department of Pediatrics, School of Medicine and Health Sciences, The George Washington University, Washington, DC

7. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA

8. Division of Population Sciences' Center for Outcomes and Policy Research, Dana-Farber Cancer Institute, Boston, MA

Abstract

PURPOSE Clear prognostic communication is associated with improvements in quality of life and suffering for children with advanced illness. Yet recent evidence demonstrates that pediatric oncologists often avoid, defer, or soften prognostic disclosure. We aimed to describe pediatric cancer shareholder perspectives on quality prognostic communication to inform design of an intervention to improve prognostic disclosure in advanced childhood cancer. METHODS Semi-structured interviews were conducted with a purposeful sample of pediatric patients with cancer (n = 20), parents (n = 20), and oncologists (n = 20) representing six institutions across five states. Rapid analysis was performed using the National Cancer Institute core communication functions to organize domains of inquiry. RESULTS Three main themes were endorsed by participants regarding the ideal timing of prognostic disclosure: early, ongoing, individualized. Although each group emphasized the need for an individualized approach, oncologists rarely elicited patient/parent preferences for prognostic communication and more commonly inferred what a patient/family wanted to hear. Participants described five key pillars for how to facilitate quality prognostic disclosure: conversation leadership, overall attendance, patient inclusion, location, and atmosphere. They also identified four themes around ideal prognostic content: range of information, use of numbers, population-level versus patient-specific information, and tone/delivery. Discordant recommendations between patients/parents and oncologists emerged for how much and what information to share. CONCLUSION Pediatric cancer shareholders advocated for diverse, and sometimes conflicting, approaches for prognostic disclosure. Although nearly all participants endorsed the importance of individualized prognostic disclosure, specific strategies to encourage or facilitate person-centered prognostic conversation are lacking. Future research will focus on collaboration with pediatric patients, parents, and oncologists to codesign a clinical intervention to improve prognostic communication for children with advanced cancer and their families.

Publisher

American Society of Clinical Oncology (ASCO)

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