@article{discovery10087523,
          number = {1},
           title = {New directions in clinical trials for frontotemporal lobar degeneration: Methods and outcome measures},
            year = {2020},
          volume = {16},
            note = {This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.},
         journal = {Alzheimer's \& Dementia},
           pages = {131--143},
           month = {January},
        abstract = {INTRODUCTION: Frontotemporal lobar degeneration (FTLD) is the most common form of dementia for those under 60�years of age. Increasing numbers of therapeutics targeting FTLD syndromes are being developed. METHODS: In March 2018, the Association for Frontotemporal Degeneration convened the Frontotemporal Degeneration Study Group meeting in Washington, DC, to discuss advances in the clinical science of FTLD. RESULTS: Challenges exist for conducting clinical trials in FTLD. Two of the greatest challenges are (1) the heterogeneity of FTLD syndromes leading to difficulties in efficiently measuring treatment effects and (2) the rarity of FTLD disorders leading to recruitment challenges. DISCUSSION: New personalized endpoints that are clinically meaningful to individuals and their families should be developed. Personalized approaches to analyzing MRI data, development of new fluid biomarkers and wearable technologies will help to improve the power to detect treatment effects in FTLD clinical trials and enable new, clinical trial designs, possibly leveraged from the experience of oncology trials. A computational visualization and analysis platform that can support novel analyses of combined clinical, genetic, imaging, biomarker data with other novel modalities will be critical to the success of these endeavors.},
             url = {https://doi.org/10.1016/j.jalz.2019.06.4956},
          author = {Boxer, AL and Gold, M and Feldman, H and Boeve, BF and Dickinson, SL-J and Fillit, H and Ho, C and Paul, R and Pearlman, R and Sutherland, M and Verma, A and Arneric, SP and Alexander, BM and Dickerson, BC and Dorsey, ER and Grossman, M and Huey, ED and Irizarry, MC and Marks, WJ and Masellis, M and McFarland, F and Niehoff, D and Onyike, CU and Paganoni, S and Panzara, MA and Rockwood, K and Rohrer, JD and Rosen, H and Schuck, RN and Soares, HD and Tatton, N},
        keywords = {ARTFL, Biomarker, C9orf72, Clinical trial, FTD, FTLD, Frontotemporal dementia, Frontotemporal lobar degeneration, GRN, LEFFTDS, MAPT, Primary progressive aphasia, Progressive supranuclear palsy}
}