All functions |
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A sample of patients that experience correlated events in simulations. |
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A sample of patients to use in simulations. |
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Cast |
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Cast |
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Convert a simulations_collection to a tibble |
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Calculate dose-path probabilities |
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Check the consistency of a dose_selector instance |
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Cohort numbers of evaluated patients. |
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Sample times between patient arrivals using the exponential distribution. |
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Should this dose-finding experiment continue? |
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Plot the convergence processes from a collection of simulations. |
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Dose-paths with probabilities attached. |
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Demand there are n patients at a dose before condisdering stopping. |
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Prevent skipping of doses. |
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Is each dose admissible? |
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Dose indices |
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Dose pathways |
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Get function for calculating dose pathways. |
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Doses given to patients. |
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Binary efficacy outcomes. |
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Number of toxicities seen at each dose. |
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Efficacy rate limit |
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Observed efficacy rate at each dose. |
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Observed toxicity rate at each dose. |
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Enforce that a trial path has followed the 3+3 method. |
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The 'escalation' package. |
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Fit a dose-finding model. |
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Follow a pre-determined dose administration path. |
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Get an object to fit the BOIN model using the BOIN package. |
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Get an object to fit the BOIN12 model for phase I/II dose-finding. |
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Get an object to fit the CRM model using the dfcrm package. |
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Get an object to fit the TITE-CRM model using the dfcrm package. |
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Calculate future dose paths. |
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Get posterior model weights for several empiric CRM skeletons. |
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Get an object to fit the mTPI dose-finding model. |
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Get an object to fit the mTPI-2 dose-finding model. |
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Get potential outcomes from a list of PatientSamples |
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Get an object to fit a dose-selector that randomly selects doses. |
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Get an object to fit the 3+3 model. |
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Get an object to fit the TPI dose-finding model. |
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Get an object to fit the CRM model using the trialr package. |
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Get an object to fit the TITE-CRM model using the trialr package. |
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Get an object to fit the EffTox model using the trialr package. |
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Get an object to fit the NBG dose-finding model using the trialr package. |
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Get an object to fit a TITE version of the NBG dose-finding model using trialr |
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Get an object to fit Wages & Tait's model for phase I/II dose-finding. |
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Visualise dose-paths as a graph |
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Is this selector currently randomly allocating doses? |
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Weights for tolerance and toxicity events using linear function of time |
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Mean efficacy rate at each dose. |
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Mean toxicity rate at each dose. |
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Median efficacy rate at each dose. |
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Median toxicity rate at each dose. |
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Model data-frame. |
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Number of patients treated at each dose. |
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Number of patients treated at the recommended dose. |
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Number of different possible outcomes for a cohort of patients |
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Number of nodes in dose-paths analysis |
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Number of doses. |
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Total number of efficacies seen. |
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Number of patients evaluated. |
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Total number of toxicities seen. |
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Parse a string of phase I/II dose-finding outcomes to vector notation. |
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Parse a string of phase I dose-finding outcomes to vector notation. |
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Break a phase I/II outcome string into a list of cohort parts. |
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Break a phase I outcome string into a list of cohort parts. |
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Percentage of patients treated at each dose. |
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Quantile of the efficacy rate at each dose. |
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Probability of recommendation |
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Probability that the toxicity rate exceeds some threshold. |
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Quantile of the toxicity rate at each dose. |
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Get samples of the probability of toxicity. |
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Recommended dose for next patient or cohort. |
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Select dose by BOIN12's OBD-choosing algorithm. |
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Select dose by BOIN's MTD-choosing algorithm. |
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Select dose by the CIBP selection criterion. |
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Select dose by mTPI2's MTD-choosing algorithm. |
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Select dose by mTPI's MTD-choosing algorithm. |
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Select dose by TPI's MTD-choosing algorithm. |
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Dose selector. |
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Dose selector factory. |
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Simulate clinical trials for several designs using common patients. |
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Simulate clinical trials. |
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Get function for simulating trials. |
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Simulated trials. |
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Make an instance of type |
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Spread the information in dose_finding_paths object to a wide data.frame format. |
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Stack |
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Stop when there are n patients in total. |
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Stop when there are n patients at a dose. |
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Stop trial and recommend no dose when a dose is too toxic. |
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Stop when uncertainty interval of prob tox is covered. |
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Does this selector support sampling of outcomes? |
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Fit the 3+3 model to some outcomes. |
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Binary toxicity outcomes. |
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Number of toxicities seen at each dose. |
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Toxicity rate limit |
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Target toxicity rate |
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Duration of trials. |
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Demand that a rescue dose is tried before stopping is permitted. |
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Utility score of each dose. |
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Outcome weights. |