“…34 They also indicated a significant improvement in symptom distress 38 especially for pain, fatigue, well-being, and insomnia 36 and in issues that were important for the patients such as pain, other symptoms, anxiety, and patient-perceived family anxiety. 37 Differences in changes in QoL within groups were statistically significant for symptoms, function, and overall QoL, 32 and for two psychological constructs: feeling of frustration and worry about pain. 35 It was not the purpose of this systematic review to examine palliative treatments delivered to patients as a consequence of QoL assessment; however, our results reinforce the need to incorporate patient's perspective to PC teams' discussions both to inform their work and to plan and deliver interventions according to patient's priorities, preferences, and values.…”