Proportional odds model for dose-finding clinical trial designs with ordinal toxicity grading

Emily M Van Meter, Elizabeth Garrett-Mayer, Dipankar Bandyopadhyay

Research output: Contribution to journalArticlepeer-review

32 Scopus citations


Currently many dose-finding clinical trial designs, including the continual reassessment method (CRM) and the standard ' 3 + 3' design, dichotomize toxicity outcomes based on the pre-specified dose-limiting toxicity (DLT) criteria. This loss of information is particularly inefficient due to the small sample sizes in phase I trials. Common Toxicity Criteria (CTCAEv3.0) classify adverse events into grades 1-5, which range from 1 as a mild adverse event to 5 as death related to an adverse event. In this paper, we extend the CRM to include ordinal toxicity outcomes as specified by CTCAEv3.0 using the proportional odds model (POM) and compare results with the dichotomous CRM. A sensitivity analysis of the new design compares various target DLT rates, sample sizes, and cohort sizes. This design is also assessed under various dose-toxicity relationship models including POMs as well as those that violate the proportional odds assumption. A simulation study shows that the proportional odds CRM performs as well as the dichotomous CRM on all criteria compared (including safety criteria such as percentage of patients treated at highly toxic or suboptimal dose levels) and with improved estimation of the maximum tolerated dose when the PO assumption is not violated. These findings suggest that it is beneficial to incorporate ordinal toxicity endpoints into phase I trial designs.

Original languageEnglish (US)
Pages (from-to)2070-2080
Number of pages11
JournalStatistics in Medicine
Issue number17
StatePublished - Jul 30 2011


  • Continual reassessment method
  • Dose finding
  • Ordinal
  • Proportional odds


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