TY - JOUR
T1 - Statistical considerations on prognostic models for glioma
AU - Molinaro, Annette M.
AU - Wrensch, Margaret R.
AU - Jenkins, Robert B.
AU - Eckel-Passow, Jeanette E.
N1 - Publisher Copyright:
© 2015 The Author(s). Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Given the lack of beneficial treatments in glioma, there is a need for prognostic models for therapeutic decision making and life planning. Recently several studies defining subtypes of glioma have been published. Here, we review the statistical considerations of how to build and validate prognostic models, explain the models presented in the current glioma literature, and discuss advantages and disadvantages of each model. The 3 statistical considerations to establishing clinically useful prognostic models are: study design, model building, and validation. Careful study design helps to ensure that the model is unbiased and generalizable to the population of interest. During model building, a discovery cohort of patients can be used to choose variables, construct models, and estimate prediction performance via internal validation. Via external validation, an independent dataset can assess how well the model performs. It is imperative that published models properly detail the study design and methods for both model building and validation. This provides readers the information necessary to assess the bias in a study, compare other published models, and determine the model's clinical usefulness. As editors, reviewers, and readers of the relevant literature, we should be cognizant of the needed statistical considerations and insist on their use.
AB - Given the lack of beneficial treatments in glioma, there is a need for prognostic models for therapeutic decision making and life planning. Recently several studies defining subtypes of glioma have been published. Here, we review the statistical considerations of how to build and validate prognostic models, explain the models presented in the current glioma literature, and discuss advantages and disadvantages of each model. The 3 statistical considerations to establishing clinically useful prognostic models are: study design, model building, and validation. Careful study design helps to ensure that the model is unbiased and generalizable to the population of interest. During model building, a discovery cohort of patients can be used to choose variables, construct models, and estimate prediction performance via internal validation. Via external validation, an independent dataset can assess how well the model performs. It is imperative that published models properly detail the study design and methods for both model building and validation. This provides readers the information necessary to assess the bias in a study, compare other published models, and determine the model's clinical usefulness. As editors, reviewers, and readers of the relevant literature, we should be cognizant of the needed statistical considerations and insist on their use.
KW - glioma
KW - model building
KW - prognostic models
KW - statistics
KW - validation
UR - http://www.scopus.com/inward/record.url?scp=84965157590&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84965157590&partnerID=8YFLogxK
U2 - 10.1093/neuonc/nov255
DO - 10.1093/neuonc/nov255
M3 - Review article
C2 - 26657835
AN - SCOPUS:84965157590
SN - 1522-8517
VL - 18
SP - 609
EP - 623
JO - Neuro-oncology
JF - Neuro-oncology
IS - 5
ER -