PoD-BIN: A probability of decision Bayesian interval design for time-to-event dose-finding trials with multiple toxicity grades

We introduce a Bayesian framework centered on the “probability of decision” for designing dose-finding trials. The proposed PoD-BIN design evaluates the posterior predictive probabilities of up-and-down decisions. In PoD-BIN, multiple grades of toxicity, categorized as mild toxicity (MT) and dose-limiting toxicity (DLT), are simultaneously modeled, with the primary outcome being time-to-toxicity for both MT and DLT. This approach allows the enrollment of new patients while previously enrolled patients are still being monitored for toxicity, potentially reducing the trial duration. The Bayesian decision rules in PoD-BIN employ the probability of decisions to balance the trade-off between accelerating the trial and the risk of exposing patients to excessively toxic doses. Through numerical examples, we illustrate the trade-off between speed and safety of PoD-BIN and compare it with existing designs. PoD-BIN demonstrates the ability to control the frequency of risky decisions while simultaneously shortening trial duration in simulations.

Authors

Institutions

Publication Details

Journal
The Annals of Applied Statistics
Published
2025-03-01
DOI
https://doi.org/10.1214/24-aoas1946
Primary Topic
Statistical Methods in Clinical Trials
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

PoD-BIN: A probability of decision Bayesian interval design for time-to-event dose-finding trials with multiple toxicity grades

Meizi Liu, Christelle Lorenzato, Gu Mi, Ji Lin et al.
The Annals of Applied Statistics
Statistical Methods in Clinical Trials
article

PoD-BIN: A probability of decision Bayesian interval design for time-to-event dose-finding trials with multiple toxicity grades

Meizi Liu, Christelle Lorenzato, Gu Mi, Ji Lin, Yuan Ji, Xun Chen
article en

Abstract

We introduce a Bayesian framework centered on the “probability of decision” for designing dose-finding trials. The proposed PoD-BIN design evaluates the posterior predictive probabilities of up-and-down decisions. In PoD-BIN, multiple grades of toxicity, categorized as mild toxicity (MT) and dose-limiting toxicity (DLT), are simultaneously modeled, with the primary outcome being time-to-toxicity for both MT and DLT. This approach allows the enrollment of new patients while previously enrolled patients are still being monitored for toxicity, potentially reducing the trial duration. The Bayesian decision rules in PoD-BIN employ the probability of decisions to balance the trade-off between accelerating the trial and the risk of exposing patients to excessively toxic doses. Through numerical examples, we illustrate the trade-off between speed and safety of PoD-BIN and compare it with existing designs. PoD-BIN demonstrates the ability to control the frequency of risky decisions while simultaneously shortening trial duration in simulations.

The Annals of Applied StatisticsVol. 19(1)
Chicago Department of Public Health (US), Sanofi (France) (FR), University of Chicago (US), Takeda (France) (FR)
Openalex Percentile: Top 95%
Statistical Methods in Clinical Trials
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.