Document Detail

A Partitioning Deletion/Substitution/Addition Algorithm for Creating Survival Risk Groups.
MedLine Citation:
PMID:  22519965     Owner:  NLM     Status:  Publisher    
Accurately assessing a patient's risk of a given event is essential in making informed treatment decisions. One approach is to stratify patients into two or more distinct risk groups with respect to a specific outcome using both clinical and demographic variables. Outcomes may be categorical or continuous in nature; important examples in cancer studies might include level of toxicity or time to recurrence. Recursive partitioning methods are ideal for building such risk groups. Two such methods are Classification and Regression Trees (CART) and a more recent competitor known as the partitioning Deletion/Substitution/Addition (partDSA) algorithm, both of which also utilize loss functions (e.g., squared error for a continuous outcome) as the basis for building, selecting, and assessing predictors but differ in the manner by which regression trees are constructed. Recently, we have shown that partDSA often outperforms CART in so-called "full data" settings (e.g., uncensored outcomes). However, when confronted with censored outcome data, the loss functions used by both procedures must be modified. There have been several attempts to adapt CART for right-censored data. This article describes two such extensions for partDSA that make use of observed data loss functions constructed using inverse probability of censoring weights. Such loss functions are consistent estimates of their uncensored counterparts provided that the corresponding censoring model is correctly specified. The relative performance of these new methods is evaluated via simulation studies and illustrated through an analysis of clinical trial data on brain cancer patients. The implementation of partDSA for uncensored and right-censored outcomes is publicly available in the R package, partDSA.
Karen Lostritto; Robert L Strawderman; Annette M Molinaro
Related Documents :
22275195 - In the spotlight: biomedical signal processing.
21866315 - Quantum chemical modeling of the kinetic isotope effect of the carboxylation step in ru...
22665145 - Generalizability: the trees, the forest, and the low-hanging fruit.
21959365 - Thoracic respiratory motion estimation from mri using a statistical model and a 2-d ima...
23004555 - Improvement and extension of the generalized hard-sphere reaction probability model.
12899965 - An analysis of the sfstp guide on validation of chromatographic bioanalytical methods: ...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-4-22
Journal Detail:
Title:  Biometrics     Volume:  -     ISSN:  1541-0420     ISO Abbreviation:  -     Publication Date:  2012 Apr 
Date Detail:
Created Date:  2012-4-23     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0370625     Medline TA:  Biometrics     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
© 2012, International Biometric Society.
Division of Biostatistics, Yale University Schools of Public Health and Medicine, 60 College Street, New Haven, Connecticut 06519, U.S.A. Department of Biological Statistics and Computational Biology and Department of Statistical Science, Cornell University, Ithaca, New York, U.S.A. Departments of Neurological Surgery and Epidemiology and Biostatistics, University of California San Francisco, 505 Parnassus Avenue, San Francisco, California 94117, U.S.A. email:
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Is there a link between diabetic glomerular injury and crescent formation? A case report and literat...
Next Document:  Asthma treatment outcome in children is associated with vascular endothelial growth factor A (VEGFA)...