Long-Term Health-Related Quality of Life of Autologous Hematopoietic Cell Transplantation Patients and Nontransplant Patients With Aggressive Lymphoma: A Prospective Cohort Analysis.

Strouse, Christopher S; Larson, Melissa C; Ehlers, Shawna L; Yost, Kathleen J; Maurer, Matthew J; Ansell, Stephen M; Inwards, David J; Johnston, Patrick B et al. · JCO Oncol Pract · 2022

prospective_cohort · Level II

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Abstract

This study assessed the long-term quality of life (QOL) of patients with aggressive lymphoma subtypes treated with autologous hematopoietic cell transplant (autoHCT) compared with those without history of transplant. Patient-reported QOL measures were prospectively gathered from patients enrolled in the Iowa/Mayo Specialized Program of Research Excellence Molecular Epidemiology Resource cohort with aggressive lymphoma subtypes. QOL was measured using the Functional Assessment of Cancer Therapy-General (FACT-G), Functional Assessment of Chronic Illness Therapy-Fatigue Scale, State-Trait Anxiety Inventory (STAI), and Profile of Mood States instruments and with a numeric rating scale for overall QOL and spiritual QOL. The autoHCT group and no HCT groups were compared at 3 years (FU3) and 6 years (FU6) after lymphoma diagnosis. In total, 980 patients with lymphoma (106 autoHCT and 874 no HCT) diagnosed between 2002 and 2013 were included for analysis. The mean FACT-G total score was similar in the autoHCT and no HCT groups at FU3 (89.9 <i>v</i> 90.1, <i>P</i> = .64) and also at FU6 (91.5 <i>v</i> 89.6, <i>P</i> = .44). No differences between the autoHCT and no HCT groups were identified in the FACT subscales. The STAI identified lower anxiety in the autoHCT group by mean STAI1 (state) at FU3 (30.1 <i>v</i> 33.4, <i>P</i> < .01) and by mean STAI2 (trait) at FU6 (30.1 <i>v</i> 33.5, <i>P</i> = .02). No other clinically meaningful differences were identified between the two groups using the other QOL instruments. Patients remaining in remission at 3 and 6 years after diagnosis had a high level of QOL with no significant differences associated with history of treatment with autoHCT.

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