Learn R Programming

dtpcrm (version 0.1.1)

Dose Transition Pathways for Continual Reassessment Method

Description

Provides the dose transition pathways (DTP) to project in advance the doses recommended by a model-based design for subsequent patients (stay, escalate, deescalate or stop early) using all the accumulated toxicity information; See Yap et al (2017) . DTP can be used as a design and an operational tool and can be displayed as a table or flow diagram. The 'dtpcrm' package also provides the modified continual reassessment method (CRM) and time-to-event CRM (TITE-CRM) with added practical considerations to allow stopping early when there is sufficient evidence that the lowest dose is too toxic and/or there is a sufficient number of patients dosed at the maximum tolerated dose.

Copy Link

Version

Install

install.packages('dtpcrm')

Monthly Downloads

196

Version

0.1.1

License

GPL (>= 2)

Maintainer

Christina Yap

Last Published

August 20th, 2019

Functions in dtpcrm (0.1.1)

stop_for_excess_toxicity_empiric

Stopping for excess toxicity - Empiric method
applied_titecrmts_sim

Simulate TITE-CRM trials using specified design options
applied_crm

Execute the CRM
calculate_dtps

Produce the Dose Transition Pathways
stop_for_consensus_reached

Stopping for consensus
applied_crm_sim

Simulate CRM trials using specified design options
dtpflow

Produce DTP flow diagram
summary_crm

Provide a summary of applied_crm output
plot_crm

Plot of posterior estimates from the CRM
stop_for_excess_toxicity_logistic

Stopping for excess toxicity - Logistic method
applied_titecrm

Execute the TITE-CRM
stop_for_sample_size

Stopping for sample size reached
applied_titecrm_sim

Simulate TITE-CRM trials using specified design options