Clinical Trials for Personalized Medicine: Design and Data Analysis
Author:
Affiliation:
1. Department of Biostatistics, Nagoya University Graduate School of Medicine
Publisher
The Biometric Society of Japan
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjb/43/1/43_97/_pdf
Reference107 articles.
1. Amann, J., Blasimme, A., Vayena, E., Frey, D., and Madai, V. I.; Precise4Q consortium (2020). Explainability for artificial intelligence in healthcare: a multidisciplinary perspective. BMC Medical Informatics and Decision Making 20, 310.
2. Bauer, P. and Posch, M. (2004). Letter to the editor: Modification of the sample size and the schedule of interim analyses in survival trials based on data inspections, by H. Schäfer and H.-H. Müller, Statistics in Medicine 2001; 20: 3741-3751. Statistics in Medicine 2004; 23: 1333-1334.
3. Beam, A. L., Manrai, A. K., and Ghassemi, M. (2020). Challenges to the reproducibility of machine learning models in health care. Journal of American Medical Association, 323, 305-306.
4. Berry, D. A. (2015). The brave new world of clinical cancer research: adaptive biomarker-driven trials integrating clinical practice with clinical research. Molecular Oncology 9, 951-959.
5. Bhattacharyya, A. and Rai, S. N. (2019). Adaptive signature design- review of the biomarker guided adaptive phase-III controlled design. Contemporary Clinical Trials Communications 15, 100378.
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