Neuroimaging based biotypes for precision diagnosis and prognosis in cancer-related cognitive impairment

被引:1
作者
Kesler, Shelli R. [1 ,2 ,3 ]
Henneghan, Ashley M. [1 ,3 ]
Prinsloo, Sarah [4 ]
Palesh, Oxana [5 ]
Wintermark, Max [6 ]
机构
[1] Univ Texas Austin, Div Adult Hlth, Sch Nursing, Austin, TX 78712 USA
[2] Univ Texas Austin, Dell Sch Med, Dept Diagnost Med, Austin, TX 78712 USA
[3] Univ Texas Austin, Dell Sch Med, Dept Oncol, Austin, TX 78712 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Neurosurg, Houston, TX USA
[5] Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Neuroradiol, Houston, TX USA
基金
美国国家卫生研究院;
关键词
cancer; cognition; neuroimaging; biotypes; precision medicine; DEFAULT MODE NETWORK; QUALITY-OF-LIFE; BIPOLAR-SCHIZOPHRENIA NETWORK; HIGH-DOSE CHEMOTHERAPY; CEREBRAL WHITE-MATTER; BREAST-CANCER; FUNCTIONAL CONNECTIVITY; LONGITUDINAL ASSESSMENT; ADJUVANT CHEMOTHERAPY; SYSTEMIC CHEMOTHERAPY;
D O I
10.3389/fmed.2023.1199605
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cancer related cognitive impairment (CRCI) is commonly associated with cancer and its treatments, yet the present binary diagnostic approach fails to capture the full spectrum of this syndrome. Cognitive function is highly complex and exists on a continuum that is poorly characterized by dichotomous categories. Advanced statistical methodologies applied to symptom assessments have demonstrated that there are multiple subclasses of CRCI. However, studies suggest that relying on symptom assessments alone may fail to account for significant differences in the neural mechanisms that underlie a specific cognitive phenotype. Treatment plans that address the specific physiologic mechanisms involved in an individual patient's condition is the heart of precision medicine. In this narrative review, we discuss how biotyping, a precision medicine framework being utilized in other mental disorders, could be applied to CRCI. Specifically, we discuss how neuroimaging can be used to determine biotypes of CRCI, which allow for increased precision in prediction and diagnosis of CRCI via biologic mechanistic data. Biotypes may also provide more precise clinical endpoints for intervention trials. Biotyping could be made more feasible with proxy imaging technologies or liquid biomarkers. Large cross-sectional phenotyping studies are needed in addition to evaluation of longitudinal trajectories, and data sharing/pooling is highly feasible with currently available digital infrastructures.
引用
收藏
页数:14
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