AB.withoutDescalation: A + B Escalation Design without Dose De-escalation

In TrialSize: R Functions for Chapter 3,4,6,7,9,10,11,12,14,15 of Sample Size Calculation in Clinical Research

Description

The general A+B designs without dose de-escalation. There are A patients at dose level i.

(1) If less than C/A patients have dose limiting toxicity (DLTs), then the dose is escalated to the next dose level i+1.

(2)If more than D/A (D ≥ C) patients have DLTs, then the previous dose i-1 will be considered the maximum tolerable dose (MTD).

(3)If no less than C/A but no more than D/A patients have DLTs, B more patients are treated at this dose level i.

(4)If no more than E (where E ≥ D) of the total A+B patients have DLT, then the dose is escalated.

(5)If more than E of the total of A+B patients have DLT, then the previous dose i-1 will be considered the MTD.

Usage

AB.withoutDescalation(A, B, C, D, E, DLT)

Arguments

A	number of patients for the start A
B	number of patients for the continuous B
C	number of patients for the first cut off C
D	number of patients for the second cut off D, D ≥ C
E	number of patients for the third cut off D, E ≥ D
DLT	dose limiting toxicity rate for each dose level.

References

Chow SC, Shao J, Wang H. Sample Size Calculation in Clinical Research. New York: Marcel Dekker, 2003

Examples

DLT=c(0.01,0.014,0.025,0.056,0.177,0.594,0.963)
Example.11.6.1<-AB.withoutDescalation(A=3,B=3,C=1,D=1,E=1,DLT=DLT)
Example.11.6.1
# Example.11.6.1[1]=3.1

TrialSize documentation built on July 8, 2020, 7:19 p.m.