A pragmatic dose-finding approach using short-term surrogate efficacy outcomes to evaluate binary efficacy and toxicity outcomes in phase I cancer clinical trials
Author:
Affiliation:
1. Clinical Research Planning Department; Chugai Pharmaceutical Co., Ltd.; Tokyo; Japan
2. Faculty of Engineering; Tokyo University of Science; Tokyo; Japan
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Reference17 articles.
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5. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1);Eisenhauer;European Journal of Cancer,2009
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