Observational studyBMC cancer2026
Trajectory and predictors of cancer- and treatment-related fatigue (CRF) in adolescent and young adult cancer patients: a prospective, longitudinal study.
Observational study in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03476070 (Adolescent and Young Adult Cancer Patients), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Adolescent and Young Adult Cancer Patients: Cognitive Toxicity on Survivorship (ACTS)
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Authors and funding
8 authors.
Funding
Abstract
backgroundAlthough cancer- and treatment-related fatigue (CRF) is well recognized as a clinically important and distressing symptom among adolescent and young adult cancer (AYAC) patients, the understanding of the underlying mechanisms behind CRF in AYAC remains limited. We evaluated the trajectory and associated predictors of CRF among AYAC patients (Clinicaltrials.gov: NCT03476070, registered 03/23/2018).
methodsNewly diagnosed AYAC (15-39 years old) and non-cancer controls (NC) recruited from National Cancer Centre Singapore completed clinical assessments and provided blood draws for inflammatory cytokine measurements every 3 months up to 12 months. Mixed-effects models were used to evaluate significant factors associated with fatigue (MFSI-SF Total score), with AYAC stratified by chemotherapy status (active chemotherapy vs. >30 days post-chemotherapy).
resultsFifty AYAC and 105 NC participants were included, with nearly 1 in 3 AYAC participants reported clinically important CRF at some point. Measurements collected during active chemotherapy had a higher rate of clinically important CRF symptoms relative to samples collected post-chemotherapy and from non-cancer controls. Regression analyses evaluating significant influencers of fatigue scores demonstrated that active chemotherapy, female sex, worsened psychological distress scores, and increased IL-10 levels were associated with worse self-reported fatigue symptoms (all p < 0.05).
conclusionGiven the observed prevalence of clinically important CRF amongst AYAC within our study, our results further demonstrate that these patients are vulnerable to fatigue challenges. Identifying factors associated with these debilitating symptoms enables clinicians to better recognize at-risk patients and proactively address symptom burden.
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