Statistics in Medicine

A practical design for a dual‐agent dose‐escalation trial that incorporates pharmacokinetic data

Journal Article

Traditionally, model‐based dose‐escalation trial designs recommend a dose for escalation based on an assumed dose‐toxicity relationship. Pharmacokinetic data are often available but are currently only utilised by clinical teams in a subjective manner to aid decision making if the dose‐toxicity model recommendation is felt to be too high. Formal incorporation of pharmacokinetic data in dose‐escalation could therefore make the decision process more efficient and lead to an increase in the precision of the resulting recommended dose, as well as decreasing the subjectivity of its use. Such an approach is investigated in the dual‐agent setting using a Bayesian design, where historical single‐agent data are available to advise the use of pharmacokinetic data in the dual‐agent setting. The dose‐toxicity and dose‐exposure relationships are modelled independently and the outputs combined in the escalation rules. Implementation of stopping rules highlight the practicality of the design. This is demonstrated through an example which is evaluated using simulation. Copyright © 2015 John Wiley & Sons, Ltd.

Related Topics

Related Publications

Related Content

Site Footer

Address:

This website is provided by John Wiley & Sons Limited, The Atrium, Southern Gate, Chichester, West Sussex PO19 8SQ (Company No: 00641132, VAT No: 376766987)

Published features on StatisticsViews.com are checked for statistical accuracy by a panel from the European Network for Business and Industrial Statistics (ENBIS)   to whom Wiley and StatisticsViews.com express their gratitude. This panel are: Ron Kenett, David Steinberg, Shirley Coleman, Irena Ograjenšek, Fabrizio Ruggeri, Rainer Göb, Philippe Castagliola, Xavier Tort-Martorell, Bart De Ketelaere, Antonio Pievatolo, Martina Vandebroek, Lance Mitchell, Gilbert Saporta, Helmut Waldl and Stelios Psarakis.