English

On the Interval-Based Dose-Finding Designs

Methodology 2017-06-15 v2

Abstract

The landscape of dose-finding designs for phase I clinical trials is rapidly shifting in the recent years, noticeably marked by the emergence of interval-based designs. We categorize them as the iDesigns and the IB-Designs. The iDesigns are originated by the toxicity probability inter- val (TPI) designs and its two modifications, the mTPI and mTPI-2 designs. The IB-Designs started as the cumulative cohort design (CCD) and is recently extended by the BOIN design. We discuss the differences and similarities between these two classes of interval-based designs, and compare their simulation performance with popular non-interval designs, such as the CRM and 3+3 designs. We also show that in addition to the population-level operating characteristics from simulated trials, investigators should also assess the dose-finding decision tables from the implemented designs to better understand the per-trial and per-patient behavior. This is particularly important for nonstatisticians to assess the designs with transparency. We pro- vide, to our knowledge, the most comprehensive simulation-based comparative study on various interval-based dose-finding designs.

Keywords

Cite

@article{arxiv.1706.03277,
  title  = {On the Interval-Based Dose-Finding Designs},
  author = {Yuan Ji and Shengjie Yang},
  journal= {arXiv preprint arXiv:1706.03277},
  year   = {2017}
}

Comments

This is the second version with typos corrected and an incorrect reference removed

R2 v1 2026-06-22T20:15:04.224Z