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An Adaptive Multi-Stage Phase I Dose-finding Design Incorporating Continuous Efficacy and Toxicity Data from Multiple Treatment Cycles

Phase I designs traditionally use the dose-limiting toxicity (DLT), a binary endpoint from the first treatment cycle, to identify the maximum-tolerated dose (MTD) assuming a monotonically increasing relationship between dose and efficacy. In this article, we establish a general framework for a multi...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Biopharm Stat
Egile Nagusiak: Du, Yu, Yin, Jun, Sargent, Daniel J., Mandrekar, Sumithra J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2018
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6379115/
https://ncbi.nlm.nih.gov/pubmed/30403559
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/10543406.2018.1535497
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