Long-term patient-reported neurocognitive outcomes in adult survivors of hematopoietic cell transplant

Author:

Wu Natalie L.1ORCID,Phipps Amanda I.23,Krull Kevin R.4,Syrjala Karen L.35,Carpenter Paul A.56,Connelly-Smith Laura S.57,Flowers Mary E.58,Krakow Elizabeth F.58ORCID,Ueda Oshima Masumi58ORCID,Lee Stephanie J.58ORCID,Chow Eric J.356

Affiliation:

1. 1Division of Hematology/Oncology, Department of Pediatrics, University of California San Francisco Benioff Children’s Hospital, Oakland, CA;

2. 2Department of Epidemiology, University of Washington, Seattle, WA;

3. 3Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

4. 4Department of Epidemiology and Cancer Control, Department of Psychology, St. Jude Children’s Research Hospital, Memphis, TN;

5. 5Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA; and

6. 6Division of Hematology/Oncology and Bone Marrow Transplant, Department of Pediatrics,

7. 7Division of Hematology, Department of Medicine, and

8. 8Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA

Abstract

Abstract Survivors of hematopoietic cell transplant (HCT) are at risk for neurocognitive impairments, which can negatively affect quality of life. Given limited studies, we aimed to describe the neurocognitive outcomes in a cohort of long-term adult HCT survivors. Eligible survivors (age ≥21 years at HCT and alive ≥2 years following HCT) completed a 60-question survey of neurocognitive function and quality of life, which included the Neuro-Quality of Life Cognitive Function Short Form (Neuro-QoL) and the Childhood Cancer Survivor Study Neurocognitive Questionnaire (NCQ). Analyses of risk factors included univariate comparisons and multivariable logistic regression. Survivors (n = 1861, 47.7% female, 65.6% allogeneic HCT) were surveyed at a median age of 64.2 years (interquartile range [IQR], 56.8-70.5) and a median 12.0 years (IQR, 6.0-21.0) from HCT. Survivors reported average Neuro-QoL scores (50.0 allogeneic; 49.2 autologous survivors) compared with an expected mean of 50 in the general population. On the NCQ, 17.4% to 31.2% of survivors reported impairments (Z-score >1.28) in task efficiency, memory, emotional regulation, or organization, compared with an expected 10% in the general population (all P < .01). In multivariable regression analyses, impaired Neuro-QoL (T-score <40) was independently associated with hearing issues (odds ratio [OR], 2.13; 95% confidence interval [CI], 1.46-3.10) and sleep impairment (OR, 4.41; 95% CI, 2.80-6.94) among allogeneic survivors, with comparable associations in autologous survivors. Overall, long-term adult HCT survivors reported average cognitive quality of life compared with the general population. Subsets of survivors with hearing issues and sleep impairments were more likely to report lower quality of life and impaired neurocognitive function, which may facilitate targeted monitoring or interventions following HCT.

Publisher

American Society of Hematology

Subject

Hematology

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