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Two‐stage design for phase I–II cancer clinical trials using continuous dose combinations of cytotoxic agents

We present a two-stage phase I/II design of a combination of two drugs in cancer clinical trials. The goal is to estimate safe dose combination regions with a desired level of efficacy. In stage I, conditional escalation with overdose control is used to allocate dose combinations to successive cohor...

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Detalhes bibliográficos
Publicado no:J R Stat Soc Ser C Appl Stat
Autor principal: Tighiouart, Mourad
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6368405/
https://ncbi.nlm.nih.gov/pubmed/30745708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/rssc.12294
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