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<h5 class="section-title" id="d3190652e143">Context</h5>
<p id="P1">Symptom researchers have proposed a model of inflammatory cytokine activity
and dysregulation
in cancer to explain co-occurring symptoms including pain, fatigue, and sleep disturbance.
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<h5 class="section-title" id="d3190652e148">Objectives</h5>
<p id="P2">We tested the hypothesis that psychological stress accentuates inflammation,
and that
stress and inflammation contribute to one's experience of the pain, fatigue, sleep
disturbance symptom cluster (symptom cluster severity, symptom cluster distress) and
its impact (symptom cluster interference with daily life, quality of life).
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<h5 class="section-title" id="d3190652e153">Methods</h5>
<p id="P3">We used baseline data from a symptom cluster management trial. Adult participants
(N=158) receiving chemotherapy for advanced cancer reported pain, fatigue and sleep
disturbance upon enrollment. Prior to intervention, participants completed measures
of demographics, perceived stress, symptom cluster severity, symptom cluster distress,
symptom cluster interference with daily life, and quality of life (QoL), and provided
a blood sample for 4 inflammatory biomarkers (IL-1β, IL-6, TNF-α, CRP).
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<h5 class="section-title" id="d3190652e158">Results</h5>
<p id="P4">Stress was not directly related to any inflammatory biomarker. Stress and
TNF-α were
positively related to symptom cluster distress, although not symptom cluster severity.
TNF-α was indirectly related to symptom cluster interference with daily life, through
its effect on symptom cluster distress. Stress was positively associated with symptom
cluster interference with daily life, and inversely with QoL. Stress also had indirect
effects on symptom cluster interference with daily life, through its effect on symptom
cluster distress.
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<h5 class="section-title" id="d3190652e163">Conclusion</h5>
<p id="P5">The proposed inflammatory model of symptoms was partially supported. Investigators
should test interventions that target stress as a contributing factor in co-occurring
pain, fatigue, and sleep disturbance, and explore other factors that may influence
inflammatory biomarker levels within the context of an advanced cancer diagnosis and
treatment.
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