Cargando…
Bayesian Design for Identifying Cohort-Specific Optimal Dose Combinations Based on Multiple Endpoints: Application to a Phase I Trial in Non-Small Cell Lung Cancer
Immunotherapy and chemotherapy combinations have proven to be a safe and efficacious treatment approach in multiple settings. However, it is not clear whether approved doses of chemotherapy developed to achieve a maximum tolerated dose are the ideal dose when combining cytotoxic chemotherapy with im...
Autores principales: | Horton, Bethany Jablonski, Wages, Nolan A., Gentzler, Ryan D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582706/ https://www.ncbi.nlm.nih.gov/pubmed/34769970 http://dx.doi.org/10.3390/ijerph182111452 |
Ejemplares similares
-
Impact of dose feasibility on the conduct of phase I trials of adoptive cell therapy
por: Bagley, Evan M., et al.
Publicado: (2021) -
A web tool for designing and conducting phase I trials using the continual reassessment method
por: Wages, Nolan A., et al.
Publicado: (2018) -
Optimal experimental designs for dose–response studies with continuous endpoints
por: Holland-Letz, Tim, et al.
Publicado: (2014) -
Obtaining the Optimal Dose in Alcohol Dependence Studies
por: Wages, Nolan A., et al.
Publicado: (2012) -
Bayesian optimization for estimating the maximum tolerated dose in Phase I clinical trials
por: Takahashi, Ami, et al.
Publicado: (2021)