Cargando…
Using Patient-Reported Outcomes in Dose-Finding Oncology Trials: Surveys of Key Stakeholders and the National Cancer Research Institute Consumer Forum
BACKGROUND: Patient-reported adverse events may be a useful adjunct for assessing a drug’s tolerability in dose-finding oncology trials (DFOT). We conducted surveys of international stakeholders and the National Cancer Research Institute (NCRI) Consumer Forum to understand attitudes about patient-re...
Autores principales: | Lai-Kwon, Julia, Vanderbeek, Alyssa M, Minchom, Anna, Lee Aiyegbusi, Olalekan, Ogunleye, Della, Stephens, Richard, Calvert, Melanie, Yap, Christina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438918/ https://www.ncbi.nlm.nih.gov/pubmed/35762393 http://dx.doi.org/10.1093/oncolo/oyac117 |
Ejemplares similares
-
The Value of Pharmaceutical Industry-Sponsored Patient Registries in Oncology Clinical Research
por: Flick, E Dawn, et al.
Publicado: (2023) -
Rationale, Strengths, and Limitations of Real-World Evidence in Oncology: A Canadian Review and Perspective
por: Azoulay, Laurent
Publicado: (2022) -
Analysis of Female Participant Representation in Registered Oncology Clinical Trials in the United States from 2008 to 2020
por: Perera, Nirosha D, et al.
Publicado: (2023) -
Temporal Trends in Inpatient Oncology Census Before and During the COVID‐19 Pandemic and Rates of Nosocomial COVID‐19 Among Patients with Cancer at a Large Academic Center
por: Zubiri, Leyre, et al.
Publicado: (2021) -
Statistical methods and data visualisation of patient-reported outcomes in early phase dose-finding oncology trials: a methodological review
por: Alger, Emily, et al.
Publicado: (2023)