dtpcrm: Dose Transition Pathways for Continual Reassessment Method
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) <doi:10.1158/1078-0432.CCR-17-0582>. 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.
| Version: | 
0.1.1 | 
| Imports: | 
diagram, dfcrm | 
| Suggests: | 
knitr, rmarkdown, testthat | 
| Published: | 
2019-08-20 | 
| Author: | 
Christina Yap [aut, cre],
  Daniel Slade [aut],
  Kristian Brock [aut],
  Yi Pan [aut] | 
| Maintainer: | 
Christina Yap  <yapchristina17 at gmail.com> | 
| License: | 
GPL-2 | GPL-3 [expanded from: GPL (≥ 2)] | 
| NeedsCompilation: | 
no | 
| CRAN checks: | 
dtpcrm results | 
Documentation:
Downloads:
Linking:
Please use the canonical form
https://CRAN.R-project.org/package=dtpcrm
to link to this page.