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  • 1
    In: Neuro-Oncology, Oxford University Press (OUP), Vol. 21, No. Supplement_6 ( 2019-11-11), p. vi137-vi137
    Abstract: A major impediment to improving neuro-oncology outcomes is poor clinical trial accrual. METHODS We convened a multi-stakeholder group including Society for Neuro-Oncology, Response Assessment in Neuro-Oncology, patient advocacy groups, clinical trial cooperative groups, and other partners to determine how we can improve trial accrual. RESULTS We described selected factors contributing to poor trial accrual and possible solutions. We focused on patient and community factors, disparities, physician and provider factors, clinical trial factors, and site and organizational factors CONCLUSIONS We will implement strategies with the intent to double accrual to neuro-oncology trials over the next 5 years.
    Type of Medium: Online Resource
    ISSN: 1522-8517 , 1523-5866
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2019
    detail.hit.zdb_id: 2094060-9
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  • 2
    In: Neuro-Oncology, Oxford University Press (OUP), ( 2019-06-07)
    Abstract: Many factors contribute to the poor survival of malignant brain tumor patients, some of which are not easily remedied. However, one contributor to the lack of progress that may be modifiable is poor clinical trial accrual. Surveys of brain tumor patients and neuro-oncology providers suggest that clinicians do a poor job of discussing clinical trials with patients and referring patients for clinical trials. Yet, data from the Cancer Action Network of the American Cancer Society suggest that most eligible oncology patients asked to enroll on a clinical trial will agree to do so. To this end, the Society for Neuro-Oncology (SNO) in collaboration with the Response Assessment in Neuro-Oncology (RANO) Working Group, patient advocacy groups, clinical trial cooperative groups, including the Adult Brain Tumor Consortium (ABTC), and other partners are working together with the intent to double clinical trial accrual over the next 5 years. Here we describe the factors contributing to poor clinical trial accrual in neuro-oncology and offer possible solutions.
    Type of Medium: Online Resource
    ISSN: 1522-8517 , 1523-5866
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2019
    detail.hit.zdb_id: 2094060-9
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  • 3
    In: Alzheimer's & Dementia, Wiley, Vol. 19, No. S3 ( 2023-06)
    Abstract: Black individuals (BIs) are at an increased risk of Alzheimer’s disease (AD) than white individuals (WIs), which is partially explained by increased prevalence of vascular risk, in conjunction with structural inequities including healthcare. Studies suggest that neuroimaging and CSF AD biomarkers may differ across race. We previously identified disparate relationships between brain activity within the frontal and parietal lobes and CSF AD biomarkers. We include analysis of structural and functional neuroimaging in a racially diverse, middle‐aged cohort with an AD family history. We aimed to identify relevant neuroimaging correlates of vascular health and AD, and how relationships may vary according to race. Methods We analyzed data from 76 individuals (29 BIs, 47 WIs). Neuroimaging measures included functional connectivity from functional resting state magnetic resonance imaging (rs‐fMRI) between fronto‐striatal regions (putamen, middle frontal gyrus, superior frontal gyrus), regions of the default mode network (hippocampus, parrahippocampal gyrus (PHG), ventromedial prefrontal cortex, inferior parietal lobule, temporal pole), structural neuroimaging (hippocampal volumes), and regional white matter hyperintensity volumes (frontal, temporal, parietal, occipital, cerebellar volumes). AD biomarkers included CSF phospho‐tau, total tau, & AB42. We included a race X CSF biomarker interaction term in our linear models. Results We identified a race X tau and race X AB42 interaction term for connectivity measures between the middle frontal and superior frontal gyri and the putamen such that as biomarker burden increased, connectivity between these regions decreased within BIs. PHG to temporal pole connectivity also exhibited these same relationships to CSF tau and AB42. Hippocampal volumes did not exhibit relationships to AD biomarkers. We identified a significant race X CSF Ab42 interaction term such that increased AD CSF biomarker burden was related to increased WMH volume in the temporal and parietal lobe. Conclusion We extend previous work in rs‐fMRI of AD to a middle‐aged cohort, supporting neuroimaging and CSF biomarker relationships may differ by race. Front‐striatal connectivity may be a clinically relevant biomarker in mid‐life studies of AD, sensitive to CSF AD biomarker levels. Results support previous consensus that functional and WM measures are more sensitive to early AD pathology and extends this knowledge to BIs.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2201940-6
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  • 4
    Online Resource
    Online Resource
    SAGE Publications ; 2002
    In:  Progress in Transplantation Vol. 12, No. 3 ( 2002-09), p. 185-190
    In: Progress in Transplantation, SAGE Publications, Vol. 12, No. 3 ( 2002-09), p. 185-190
    Abstract: This study builds on previous research that identified fears and concerns heard by procurement coordinators during the donation discussion and that classified those concerns according to the ease with which they can be addressed. In this study, 53 coordinators working for 4 procurement agencies provided data on 323 donation discussions, including fears and concerns expressed by families. The fears and concerns were analyzed by outcome (consent or refusal), race and ethnicity of the family, frequency of reports, and difficulty in addressing. This research confirms many of the findings of the earlier study. The results also indicate that the types of concerns expressed by donor and non–donor families vary somewhat by the family's race and ethnicity. The results can be used to provide training targeted at raising consent rates and to train minority requestors.
    Type of Medium: Online Resource
    ISSN: 1526-9248 , 2164-6708
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2002
    detail.hit.zdb_id: 2864264-8
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2002
    In:  Progress in Transplantation Vol. 12, No. 3 ( 2002-09), p. 185-190
    In: Progress in Transplantation, SAGE Publications, Vol. 12, No. 3 ( 2002-09), p. 185-190
    Type of Medium: Online Resource
    ISSN: 1526-9248 , 2164-6708
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2002
    detail.hit.zdb_id: 2864264-8
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  • 6
    In: Alzheimer's & Dementia, Wiley, Vol. 17, No. S5 ( 2021-12)
    Abstract: White matter hyperintensities (WMH) are regions that appear very bright on Fluid‐Attenuated Inversion Recovery (FLAIR) magnetic resonance images (MRI). They are generally attributed to cerebrovascular disease (CVD) and confer a greater risk for Alzheimer’s Disease (AD). Black individuals (BIs) typically have greater WMH burden than their white counterparts and have a two‐fold greater risk of developing AD in their lifetimes. For this project, we wanted to determine whether WMH were related to diagnostic category, and if this relationship differed according to race. Method Cohort 1 included middle‐aged cognitively normal black and white individuals (N=50). Cohort 2 included older black and white individuals on the dementia continuum (NC=47, MCI=10, AD=3). Data collection included a neuropsychological battery and magnetic resonance imaging (MRI). Fluid attenuated inversion recovery (FLAIR) MRI data were analyzed to obtain lobe specific WMH volumes (frontal, temporal, occipital, parietal, cerebellar). Because of age and diagnostic differences, we analyzed each cohort separately. We constructed multivariate linear models for each cohort with WMH volumes as the outcome variable, age, race, gender, and diagnostic category (Cohort 2 only) as independent variables. We included age X race, and race X diagnosis (Cohort 2 only) interaction terms. Result There were no racial or diagnostic differences in regional WMH volume. However, in Cohort 1, there was a significant race X age interaction in the parietal lobe such that in BIs, as age increased, WMH volume also increased (B=, t(3,46)=2.07, p =0.04). In Cohort 2, this relationship extended to the temporal (B=0.09, t(3,55)=2.95, p=0.04), and occipital lobes (B=0.09, t(3,55)=2.99, p=0.04). There was no such relationship observed in WIs. Conclusion Age conferred greater WMH volume in BIs than in WIs in cognitively normal individuals and individuals on the dementia spectrum. The relationship we observed between WMH and AD could be seen as additive rather than causative, as we observed only a relationship between age and WMH volume, not diagnostic category. The differential findings across race suggest that age has a greater effect on BIs on CVD and brain health. These findings, although not causal, should encourage AD researchers to collect more diverse samples, and consider underlying CVD in data analyses.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2201940-6
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