Background: According to standard of care, adolescents and young adults (AYAs) should be introduced to palliative care concepts regardless of disease status.1 This does not consistently occur,2 with health-professionals reporting barriers to doing so.3
Objective: To explore health-professionals’ practices, and perspectives, regarding introduction of palliative care concepts with AYAs with cancer.
Method: Study 1 examined palliative care communication among AYA oncology health-professionals in Australia, New Zealand and the UK. Study 2 used a modified two-round global Delphi survey to establish when health-professionals felt palliative care concepts were appropriate to introduce according to (i) patient prognosis, and (ii) treatment time-points.
Results: Study 1 (148 health-professionals from Australia/NZ/UK) found palliative care concepts were introduced regardless of disease status ‘usually’ or ‘always’ in 55% of the Australian, 20% New Zealand, and 48% UK health-professionals. Study 2 (248 health-professionals across 8 countries) reached consensus that some palliative care concepts (e.g., emotional and existential issues) were appropriate at all prognoses and treatment/disease timepoints. End-of-life-related medical care topics were only considered appropriate for patients with prognoses <50%, or from a patient’s second relapse onwards. Prognosis and goals of care, and quality of life topics were considered appropriate for most patients (<75% prognosis, most of the treatment trajectory).
Conclusions: Some palliative care topics are considered appropriate for most AYAs, across most of the treatment trajectory. Our data indicate that health-professionals’ opinions differ regarding introducing palliative care concepts to AYAs during cancer treatment, including at their first relapse. Supports for health-professionals will ensure best-practice team-based AYA oncology care.