Neurocognitive Impairment After Hematopoietic Stem Cell Transplant for Hematologic Malignancies: Phenotype and Mechanisms

Author:

Harrison Rebecca A.1ORCID,Sharafeldin Noha2,Rexer Jennie L.1,Streck Brennan3,Petersen Melissa4,Henneghan Ashley M.56,Kesler Shelli R.57

Affiliation:

1. Department of Neuro-Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA

2. Department of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, Alabama, USA

3. Milken Institute School of Public Health, The George Washington University, Washington, DC, USA

4. Department of Family Medicine, University of North Texas Health Science Center, Fort Worth, Texas, USA

5. School of Nursing, Dell School of Medicine, University of Texas at Austin, Austin, Texas, USA

6. Department of Oncology, Dell School of Medicine, University of Texas at Austin, Austin, Texas, USA

7. Department of Diagnostic Medicine, Dell School of Medicine, University of Texas at Austin, Austin, Texas, USA

Abstract

Abstract Hematopoietic stem cell transplant (HSCT) plays a central role in the treatment of hematologic cancers. With the increasing survival of patients after HSCT, survivorship issues experienced by this population have become an important outcome. Cognitive impairment is an established sequela of HSCT, with studies to date establishing its presence, associated risk factors, and clinical phenotype. There are multiple potential contributors to cognitive impairment after HSCT. Efforts are ongoing to further characterize its clinical phenotype, associated biomarkers, and biologic underpinnings. A fundamental knowledge of post-HSCT cognitive impairment is of value for all clinicians who interface with this population, and further academic efforts are needed to more fully understand the impact of this cancer treatment on brain health. Implications for Practice As survival outcomes after hematopoietic stem cell transplant (HSCT) improve, an awareness of the post-treatment challenges faced by this population has become central to its care. HSCT can have a sustained and broad impact on brain health, causing cognitive dysfunction, fatigue, disturbed mood, and sleep. In affected patients, autonomy, return to work, relationships, and quality of life may all be affected. A fundamental fluency in this area is important for clinicians interfacing with HSCT survivors, facilitating the identification and management of cognitive dysfunction and concurrent symptom clusters, and stimulating interest in these sequelae as areas for future clinical research.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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