tsdata: sample data for R package TreatmentSelection
In TreatmentSelection: Evaluate Treatment Selection Biomarkers
Description
Usage
Format
References
See Also
Description
Simulated data set consisting of two continuous markers, two discrete markers, treatment, and event status.
Usage
1
Format
A data frame with 1000 simulated observations reflecting the following clinical context. Markers Y1 and Y2 are candidates for identifying a subset of women with estrogen-receptor positive breast cancer who do not benefit from adjuvant chemotherapy over and above tamoxifen. The clinical outcome of interest, termed "event", is 5-year breast cancer recurrence or death. Data come from a hypothetical randomized trial where subjects are randomly assigned to tamoxifen alone or tamoxifen plus chemotherapy and followed to ascertain this outcome; markers Y1 and Y2 are measured at baseline.
trta numeric vector distinguishing chemotherapy-treated individuals (trt = 1) vs individuals treated with tamoxifen alone (trt = 0)
eventa numeric vector indicating event status (1 for recurrence or death within 5 years, 0 otherwise)
Y1a numeric vector of values for marker 1. This marker has relatively weak performance.
Y2a numeric vector of values for marker 2. This marker has strong performance.
Y1_disca discrete version of marker 1, coded 1 if Y1 > mean(Y1) and 0 otherwise.
Y2_disca discrete version of marker 2, coded 1 if Y2 > 0, and 0 otherwise.
References
Janes, Holly; Brown, Marshall D; Pepe, Margaret; Huang, Ying; "An Approach to Evaluating and Comparing Biomarkers for Patient Treatment Selection" The International Journal of Biostatistics. Volume 0, Issue 0, ISSN (Online) 1557-4679, ISSN (Print) 2194-573X, DOI: 10.1515/ijb-2012-0052, April 2014
See Also
trtsel for creating trtsel objects, plot.trtsel for plotting risk curves and more, evaluate.trtsel for evaluating marker performance, calibrate.trtsel for assessing model calibration, and compare.trtsel to compare two trtsel object.
TreatmentSelection documentation built on May 1, 2019, 6:32 p.m.
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Description Usage Format References See Also
Description
Simulated data set consisting of two continuous markers, two discrete markers, treatment, and event status.
Usage
1 |
Format
A data frame with 1000 simulated observations reflecting the following clinical context. Markers Y1 and Y2 are candidates for identifying a subset of women with estrogen-receptor positive breast cancer who do not benefit from adjuvant chemotherapy over and above tamoxifen. The clinical outcome of interest, termed "event", is 5-year breast cancer recurrence or death. Data come from a hypothetical randomized trial where subjects are randomly assigned to tamoxifen alone or tamoxifen plus chemotherapy and followed to ascertain this outcome; markers Y1 and Y2 are measured at baseline.
trta numeric vector distinguishing chemotherapy-treated individuals (trt = 1) vs individuals treated with tamoxifen alone (trt = 0)
eventa numeric vector indicating event status (1 for recurrence or death within 5 years, 0 otherwise)
Y1a numeric vector of values for marker 1. This marker has relatively weak performance.
Y2a numeric vector of values for marker 2. This marker has strong performance.
Y1_disca discrete version of marker 1, coded 1 if Y1 > mean(Y1) and 0 otherwise.
Y2_disca discrete version of marker 2, coded 1 if Y2 > 0, and 0 otherwise.
References
Janes, Holly; Brown, Marshall D; Pepe, Margaret; Huang, Ying; "An Approach to Evaluating and Comparing Biomarkers for Patient Treatment Selection" The International Journal of Biostatistics. Volume 0, Issue 0, ISSN (Online) 1557-4679, ISSN (Print) 2194-573X, DOI: 10.1515/ijb-2012-0052, April 2014
See Also
trtsel for creating trtsel objects, plot.trtsel for plotting risk curves and more, evaluate.trtsel for evaluating marker performance, calibrate.trtsel for assessing model calibration, and compare.trtsel to compare two trtsel object.
R Package Documentation
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We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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