TY - JOUR
T1 - Cognitive functioning in allogeneic hematopoietic stem cell transplantation recipients and its medical correlates
T2 - A prospective multicenter study
AU - Scherwath, Angela
AU - Schirmer, Lena
AU - Kruse, Margitta
AU - Ernst, Gundula
AU - Eder, Matthias
AU - Dinkel, Andreas
AU - Kunze, Sabine
AU - Balck, Friedrich
AU - Bornhäuser, Martin
AU - Ehninger, Gerhard
AU - Dolan, Karin
AU - Gramatzki, Martin
AU - Kolb, Hans Jochem
AU - Heußner, Pia
AU - Wilhelm, Hans
AU - Beelen, Dietrich W.
AU - Schulz-Kindermann, Frank
AU - Zander, Axel R.
AU - Koch, Uwe
AU - Mehnert, Anja
PY - 2013/7
Y1 - 2013/7
N2 - Background Owing to its neurotoxicity, allogeneic hematopoietic stem cell transplantation (HSCT) carries risks for cognitive impairment. In this multicenter study, we prospectively evaluated cognitive functioning and its medical and demographic correlates in patients undergoing allogeneic HSCT. Methods A total of 102 patients were consecutively assessed prior to (T 0), 100 ± 20 days (T1) after, and 12 ± 1 months (T2) after HSCT (61% men, 41% acute myeloid leukemia). A comprehensive neuropsychological test battery was applied to evaluate attention, memory, executive function, and fine motor function, summing up into 14 test scores. Results Before and after HSCT, patients performed below test norms in up to 50% of the test scores. Patients were mostly impaired on word fluency (24%, T0), fine motor function, and verbal delayed recall (19% each, T 2). Impairment on ≥1/5 cognitive domains occurred in 47% (T 0) and 41% (T2) of the patients. Performance (mean z-scores) partially improved over time (i.e., visual span forward, verbal learning, and word fluency). However, from baseline to T2, 16% of the patients showed reliable decline on ≥3/14 test scores (reliable change index method). For the majority of neuropsychological subtests, no associations with conditioning intensity, total body irradiation, graft-versus-host disease, cyclosporine treatment, and length of hospital stay were found. Age and premorbid intelligence level were consistently associated with cognition. Conclusions Below average cognitive performance is common in this patient group. In addition, a subgroup shows reliable cognitive decline after allogeneic HSCT. Healthcare professionals should be aware of these treatment-related cognitive side effects.
AB - Background Owing to its neurotoxicity, allogeneic hematopoietic stem cell transplantation (HSCT) carries risks for cognitive impairment. In this multicenter study, we prospectively evaluated cognitive functioning and its medical and demographic correlates in patients undergoing allogeneic HSCT. Methods A total of 102 patients were consecutively assessed prior to (T 0), 100 ± 20 days (T1) after, and 12 ± 1 months (T2) after HSCT (61% men, 41% acute myeloid leukemia). A comprehensive neuropsychological test battery was applied to evaluate attention, memory, executive function, and fine motor function, summing up into 14 test scores. Results Before and after HSCT, patients performed below test norms in up to 50% of the test scores. Patients were mostly impaired on word fluency (24%, T0), fine motor function, and verbal delayed recall (19% each, T 2). Impairment on ≥1/5 cognitive domains occurred in 47% (T 0) and 41% (T2) of the patients. Performance (mean z-scores) partially improved over time (i.e., visual span forward, verbal learning, and word fluency). However, from baseline to T2, 16% of the patients showed reliable decline on ≥3/14 test scores (reliable change index method). For the majority of neuropsychological subtests, no associations with conditioning intensity, total body irradiation, graft-versus-host disease, cyclosporine treatment, and length of hospital stay were found. Age and premorbid intelligence level were consistently associated with cognition. Conclusions Below average cognitive performance is common in this patient group. In addition, a subgroup shows reliable cognitive decline after allogeneic HSCT. Healthcare professionals should be aware of these treatment-related cognitive side effects.
KW - cancer
KW - cognitive function
KW - neuropsychology
KW - oncology
KW - stem cell transplantation
UR - http://www.scopus.com/inward/record.url?scp=84879906243&partnerID=8YFLogxK
U2 - 10.1002/pon.3159
DO - 10.1002/pon.3159
M3 - Article
C2 - 22945857
AN - SCOPUS:84879906243
SN - 1057-9249
VL - 22
SP - 1509
EP - 1516
JO - Psycho-Oncology
JF - Psycho-Oncology
IS - 7
ER -