TY - JOUR
T1 - Personalized risk prediction for event-free survival at 24 months in patients with diffuse large B-cell lymphoma
AU - Maurer, Matthew J.
AU - Jais, Jean Philippe
AU - Ghesquières, Hervé
AU - Witzig, Thomas E.
AU - Hong, Fangxin
AU - Haioun, Corinne
AU - Thompson, Carrie A.
AU - Thieblemont, Catherine
AU - Micallef, Ivana N.
AU - Porrata, Luis F.
AU - Ribrag, Vincent
AU - Nowakowski, Gregorz S.
AU - Casasnovas, Olivier
AU - Bologna, Serge
AU - Morschhauser, Franck
AU - Morrison, Vicki A.
AU - Peterson, Bruce A.
AU - Macon, William R.
AU - Copie-Bergman, Christiane
AU - Feldman, Andrew L.
AU - Syrbu, Sergei I.
AU - Kurtin, Paul J.
AU - Gascoyne, Randy D.
AU - Li, Hailun
AU - Allmer, Cristine
AU - Kahl, Brad S.
AU - Ansell, Stephen M.
AU - Slager, Susan L.
AU - Link, Brian K.
AU - Salles, Gilles
AU - Habermann, Thomas M.
AU - Tilly, Hervé
AU - Cerhan, James R.
N1 - Funding Information:
National Institutes of Health to the University of Iowa/Mayo Clinic Lymphoma Specialized Program of Research Excellence; The Henry J. Predolin Foundation.
Funding Information:
National Institutes of Health to the University of Iowa/Mayo Clinic Lymphoma Specialized Program of Research Excellence; The Henry J. Predolin Foundation.
Publisher Copyright:
© 2016 Wiley Periodicals, Inc.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - We recently defined event-free survival at 24 months (EFS24) as a clinically relevant outcome for patients with DLBCL. Patients who fail EFS24 have very poor overall survival, while those who achieve EFS24 have a subsequent overall survival equivalent to that of the age- and sex-matched general population. Here, we develop and validate a clinical risk calculator (IPI24) for EFS24. Model building was performed on a discovery dataset of 1,348 patients with DLBCL and treated with anthracycline-based immunochemotherapy. A multivariable model containing age, Ann Arbor stage, normalized serum LDH, ALC, ECOG performance status, bulky disease, and sex was identified. The model was then applied to an independent validation dataset of 1,177 DLBCL patients. The IPI24 score estimates the probability of failing to achieve the EFS24 endpoint for an individual patient. The IPI24 model showed superior discriminatory ability (c-statistic=0.671) in the validation dataset compared to the IPI (c-statistic=0.649) or the NCCN-IPI (c-statistic=0.657). After recalibration of the model on the combined dataset, the median predicted probability of failing to achieve EFS24 was 36% (range, 12-88%), and the IPI24 showed an EFS24 gradient in all IPI groups. The IPI24 also identified a significant percentage of patients with high risk disease, with over 20% of patients having a 50% or higher risk of failing to achieve EFS24. The IPI24 provides an individual patient level probability of achieving the clinically relevant EFS24 endpoint. It can be used via electronic apps.
AB - We recently defined event-free survival at 24 months (EFS24) as a clinically relevant outcome for patients with DLBCL. Patients who fail EFS24 have very poor overall survival, while those who achieve EFS24 have a subsequent overall survival equivalent to that of the age- and sex-matched general population. Here, we develop and validate a clinical risk calculator (IPI24) for EFS24. Model building was performed on a discovery dataset of 1,348 patients with DLBCL and treated with anthracycline-based immunochemotherapy. A multivariable model containing age, Ann Arbor stage, normalized serum LDH, ALC, ECOG performance status, bulky disease, and sex was identified. The model was then applied to an independent validation dataset of 1,177 DLBCL patients. The IPI24 score estimates the probability of failing to achieve the EFS24 endpoint for an individual patient. The IPI24 model showed superior discriminatory ability (c-statistic=0.671) in the validation dataset compared to the IPI (c-statistic=0.649) or the NCCN-IPI (c-statistic=0.657). After recalibration of the model on the combined dataset, the median predicted probability of failing to achieve EFS24 was 36% (range, 12-88%), and the IPI24 showed an EFS24 gradient in all IPI groups. The IPI24 also identified a significant percentage of patients with high risk disease, with over 20% of patients having a 50% or higher risk of failing to achieve EFS24. The IPI24 provides an individual patient level probability of achieving the clinically relevant EFS24 endpoint. It can be used via electronic apps.
UR - http://www.scopus.com/inward/record.url?scp=84956609481&partnerID=8YFLogxK
U2 - 10.1002/ajh.24223
DO - 10.1002/ajh.24223
M3 - Article
C2 - 26492520
AN - SCOPUS:84956609481
SN - 0361-8609
VL - 91
SP - 179
EP - 184
JO - American journal of hematology
JF - American journal of hematology
IS - 2
ER -