Oxana Palesh PhD, MPH, Sarah E. Braun PhD, LCP, Tina Truong BS, MS, Susan Hong MD, Masato Mitsuhashi MD, PhD, Ruth Nyagaka BA, Susanne Lee MPH, Adithi Gandhi BA, Alexa De La Torre Schutz BS, Shelli R. Kesler PhD
{"title":"失眠的乳腺癌患者认知障碍的自然轨迹亚类","authors":"Oxana Palesh PhD, MPH, Sarah E. Braun PhD, LCP, Tina Truong BS, MS, Susan Hong MD, Masato Mitsuhashi MD, PhD, Ruth Nyagaka BA, Susanne Lee MPH, Adithi Gandhi BA, Alexa De La Torre Schutz BS, Shelli R. Kesler PhD","doi":"10.1002/cncr.35816","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Cancer-related cognitive impairment (CRCI) has traditionally been assessed in a dichotomous manner. Identifying subclasses of CRCI and novel biomarkers can improve the accuracy of identifying patients most at risk for CRCI.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A total of 139 breast cancer patients undergoing chemotherapy completed neurocognitive batteries over 12 months. Growth mixture modeling (GMM) was used to determine latent subgroups based on different trajectories of cognitive test performance across the four time points. Additionally, the authors collected peripheral blood to measure neuron-derived exosomes (NDE).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Mean cognitive performance improved significantly over time (<i>p</i> < .001). However, GMM identified three distinct latent subgroups: patients with stable, high performance (class 1, <i>N</i> = 45), patients with variable low performance (class 2, <i>N</i> = 15), and patients with average performance who improved over time (class 3, <i>N</i> = 79). Cognitive subclass 2 was characterized by significantly lower education levels than the other two classes (<i>p</i> = .001). Cognitive subclass 1 had fewer racial/ethnic minority patients than the other two classes (<i>p</i> = .015). Cognitive subclasses did not differ significantly in any other demographic or clinical characteristic. There were no significant differences observed by NDE.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>There are multiple distinct longitudinal trajectories of CRCI and these may be influenced by social determinants of health such as education and race/ethnicity. Future research can focus on ways to administer interventions earlier to those at most risk for CRCI and continue to explore novel biomarkers of CRCI.</p>\n </section>\n </div>","PeriodicalId":138,"journal":{"name":"Cancer","volume":"131 8","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cncr.35816","citationCount":"0","resultStr":"{\"title\":\"Natural trajectory subclasses of cognitive impairment in breast cancer patients experiencing insomnia\",\"authors\":\"Oxana Palesh PhD, MPH, Sarah E. Braun PhD, LCP, Tina Truong BS, MS, Susan Hong MD, Masato Mitsuhashi MD, PhD, Ruth Nyagaka BA, Susanne Lee MPH, Adithi Gandhi BA, Alexa De La Torre Schutz BS, Shelli R. Kesler PhD\",\"doi\":\"10.1002/cncr.35816\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Cancer-related cognitive impairment (CRCI) has traditionally been assessed in a dichotomous manner. Identifying subclasses of CRCI and novel biomarkers can improve the accuracy of identifying patients most at risk for CRCI.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>A total of 139 breast cancer patients undergoing chemotherapy completed neurocognitive batteries over 12 months. Growth mixture modeling (GMM) was used to determine latent subgroups based on different trajectories of cognitive test performance across the four time points. Additionally, the authors collected peripheral blood to measure neuron-derived exosomes (NDE).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Mean cognitive performance improved significantly over time (<i>p</i> < .001). However, GMM identified three distinct latent subgroups: patients with stable, high performance (class 1, <i>N</i> = 45), patients with variable low performance (class 2, <i>N</i> = 15), and patients with average performance who improved over time (class 3, <i>N</i> = 79). Cognitive subclass 2 was characterized by significantly lower education levels than the other two classes (<i>p</i> = .001). Cognitive subclass 1 had fewer racial/ethnic minority patients than the other two classes (<i>p</i> = .015). Cognitive subclasses did not differ significantly in any other demographic or clinical characteristic. There were no significant differences observed by NDE.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>There are multiple distinct longitudinal trajectories of CRCI and these may be influenced by social determinants of health such as education and race/ethnicity. Future research can focus on ways to administer interventions earlier to those at most risk for CRCI and continue to explore novel biomarkers of CRCI.</p>\\n </section>\\n </div>\",\"PeriodicalId\":138,\"journal\":{\"name\":\"Cancer\",\"volume\":\"131 8\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-04-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cncr.35816\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/cncr.35816\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer","FirstCategoryId":"3","ListUrlMain":"https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/cncr.35816","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
Natural trajectory subclasses of cognitive impairment in breast cancer patients experiencing insomnia
Background
Cancer-related cognitive impairment (CRCI) has traditionally been assessed in a dichotomous manner. Identifying subclasses of CRCI and novel biomarkers can improve the accuracy of identifying patients most at risk for CRCI.
Methods
A total of 139 breast cancer patients undergoing chemotherapy completed neurocognitive batteries over 12 months. Growth mixture modeling (GMM) was used to determine latent subgroups based on different trajectories of cognitive test performance across the four time points. Additionally, the authors collected peripheral blood to measure neuron-derived exosomes (NDE).
Results
Mean cognitive performance improved significantly over time (p < .001). However, GMM identified three distinct latent subgroups: patients with stable, high performance (class 1, N = 45), patients with variable low performance (class 2, N = 15), and patients with average performance who improved over time (class 3, N = 79). Cognitive subclass 2 was characterized by significantly lower education levels than the other two classes (p = .001). Cognitive subclass 1 had fewer racial/ethnic minority patients than the other two classes (p = .015). Cognitive subclasses did not differ significantly in any other demographic or clinical characteristic. There were no significant differences observed by NDE.
Conclusions
There are multiple distinct longitudinal trajectories of CRCI and these may be influenced by social determinants of health such as education and race/ethnicity. Future research can focus on ways to administer interventions earlier to those at most risk for CRCI and continue to explore novel biomarkers of CRCI.
期刊介绍:
The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society.
CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research