Cognitive function after the initiation of adjuvant endocrine therapy in early-stage breast cancer: an observational cohort study.

TitleCognitive function after the initiation of adjuvant endocrine therapy in early-stage breast cancer: an observational cohort study.
Publication TypeJournal Article
Year of Publication2014
AuthorsGanz PA, Petersen L, Castellon SA, Bower JE, Silverman DHS, Cole SW, Irwin MR, Belin TR
JournalJ Clin Oncol
Volume32
Issue31
Pagination3559-67
Date Published2014 Nov 1
ISSN1527-7755
KeywordsAdult, Aged, Antineoplastic Agents, Hormonal, Aromatase Inhibitors, Breast Neoplasms, Chemotherapy, Adjuvant, Cognition Disorders, Cohort Studies, Female, Humans, Middle Aged, Neoplasm Staging, Neuropsychological Tests, Quality of Life, Risk Factors, Tamoxifen
Abstract

PURPOSE: This report examines cognitive complaints and neuropsychological (NP) testing outcomes in patients with early-stage breast cancer after the initiation of endocrine therapy (ET) to determine whether this therapy plays any role in post-treatment cognitive complaints.

PATIENTS AND METHODS: One hundred seventy-three participants from the Mind Body Study (MBS) observational cohort provided data from self-report questionnaires and NP testing obtained at enrollment (T1, before initiation of ET), and 6 months later (T2). Bivariate analyses compared demographic and treatment variables, cognitive complaints, depressive symptoms, quality of life, and NP functioning between those who received ET versus not. Multivariable linear regression models examined predictors of cognitive complaints at T2, including selected demographic variables, depressive symptoms, ET use, and other medical variables, along with NP domains that were identified in bivariate analyses.

RESULTS: Seventy percent of the 173 MBS participants initiated ET, evenly distributed between tamoxifen or aromatase inhibitors. ET-treated participants reported significantly increased language and communication (LC) cognitive complaints at T2 (P = .003), but no significant differences in NP test performance. Multivariable regression on LC at T2 found higher LC complaints significantly associated with T1 LC score (P < .001), ET at T2 (P = .004), interaction between ET and past hormone therapy (HT) (P < .001), and diminished improvement in NP psychomotor function (P = .05). Depressive symptoms were not significant (P = .10).

CONCLUSION: Higher LC complaints are significantly associated with ET 6 months after starting treatment and reflect diminished improvements in some NP tests. Past HT is a significant predictor of higher LC complaints after initiation of ET.

DOI10.1200/JCO.2014.56.1662
Alternate JournalJ. Clin. Oncol.
PubMed ID25267747
PubMed Central IDPMC4209106
Grant ListP30 AG028748 / AG / NIA NIH HHS / United States
P30 CA016042 / CA / NCI NIH HHS / United States
P30-AG028748 / AG / NIA NIH HHS / United States
R01-AG026364 / AG / NIA NIH HHS / United States
R01-AG034588 / AG / NIA NIH HHS / United States
R01-CA109650 / CA / NCI NIH HHS / United States
R01-CA119159 / CA / NCI NIH HHS / United States
R01-HL079955 / HL / NHLBI NIH HHS / United States
R01-HL095799 / HL / NHLBI NIH HHS / United States
UL RR033176 / RR / NCRR NIH HHS / United States