๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Optimal three-stage designs for phase II cancer clinical trials

โœ Scribed by T. Timothy Chen


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
136 KB
Volume
16
Category
Article
ISSN
0277-6715

No coin nor oath required. For personal study only.

โœฆ Synopsis


The objective of a phase II cancer clinical trial is to screen a treatment that can produce a similar or better response rate compared to the current treatment results. This screening is usually carried out in two stages as proposed by Simon. For ineffective treatment, the trial should terminate at the first stage. Ensign et al. extended two-stage optimal designs to three stages; however, they restricted the rejection region in the first stage to be zero response, and the sample size to at least 5. This paper extends Simon's two-stage to a three-stage design without these restrictions, and provides tables for both optimal and minimax designs. One can use the three-stage design to reduce the expected sample size when the treatment is not promising a priori and when the accrual rate is slow. The average reduction in size from a two-stage to three-stage design is 10 per cent.


๐Ÿ“œ SIMILAR VOLUMES


Optimal flexible designs in phase II cli
โœ T. Timothy Chen; Tie-Hua Ng ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 107 KB ๐Ÿ‘ 1 views

In the conduct of a phase II cancer clinical trial, patients usually enter in two stages. If the response rate from the first stage is low, then the study terminates. Within various two-stage designs, Simon proposed the optimal and minimax criteria. In the co-operative group setting, practical consi

Optimal multi-stage designs for a phase
โœ John J. Hanfelt ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 133 KB ๐Ÿ‘ 1 views

Simon's optimal two-stage design is widely used to conduct single-dose phase II clinical trials. We extend this basic methodology to the situation where the researcher desires to test an experimental drug for activity at a low dose level, but is willing to increase the dose part-way through the tria