TY - JOUR
T1 - Initial therapy for chronic graft-versus-host disease
T2 - analysis of practice variation and failure-free survival
AU - Pidala, Joseph
AU - Onstad, Lynn
AU - Martin, Paul J.
AU - Hamilton, Betty K.
AU - Cutler, Corey
AU - Kitko, Carrie L.
AU - Carpenter, Paul A.
AU - Chen, George L.
AU - Arora, Mukta
AU - Flowers, Mary E.D.
AU - Arai, Sally
AU - Alousi, Amin
AU - White, Jennifer
AU - Jacobsohn, David
AU - Pusic, Iskra
AU - Lee, Stephanie J.
N1 - Publisher Copyright:
ß 2021 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
PY - 2021/11/23
Y1 - 2021/11/23
N2 - Prior clinical trials largely considered prednisone 1 mg/kg per day with or without calcineurin inhibitor as standard initial therapy for chronic graft-versus-host disease (cGVHD), but uncertainty remains regarding the extent of practice variation and whether this affects subsequent outcomes. We assembled a cohort of 745 patients with cGVHD treated with initial systemic immune suppressive (IS) therapy from 3 prior cGVHD Consortium observational studies. Initial therapy was defined as first IS therapy started for cGVHD or prednisone increased to $0.4 mg/kg per day from lower doses within 30 days before cGVHD diagnosis to any time afterward. Initial therapies were nonprednisone IS therapies (n 5 137, 18%), prednisone alone (n 5 411, 55%), or prednisone plus other IS therapy (n 5 197, 26%). In multivariate analysis, initial therapy group was not associated with failure-free survival (FFS; a composite of death, relapse, and new IS therapy), overall survival (OS), or nonrelapse mortality (NRM). Among the prednisone-based approaches, steroid dose was,0.25 (9%), 0.25 to 0.74 (36%), 0.75 to 1.25 (42%), or .1.25 mg/kg per day (13%). Prednisone dose within the patients treated with steroids was not significantly associated with FFS, OS, or NRM. No significant interactions were detected between overall cGVHD severity and either initial therapy group or prednisone dose for the outcomes of FFS, OS, or NRM. These observational data document heterogeneity in more contemporary cGVHD initial treatment practices, including prednisone dose and use of nonsteroid approaches. This variation was not associated with FFS, OS, or NRM. Prospective trials are needed to verify efficacy of reduced-dose prednisone or prednisone-free initial therapy approaches.
AB - Prior clinical trials largely considered prednisone 1 mg/kg per day with or without calcineurin inhibitor as standard initial therapy for chronic graft-versus-host disease (cGVHD), but uncertainty remains regarding the extent of practice variation and whether this affects subsequent outcomes. We assembled a cohort of 745 patients with cGVHD treated with initial systemic immune suppressive (IS) therapy from 3 prior cGVHD Consortium observational studies. Initial therapy was defined as first IS therapy started for cGVHD or prednisone increased to $0.4 mg/kg per day from lower doses within 30 days before cGVHD diagnosis to any time afterward. Initial therapies were nonprednisone IS therapies (n 5 137, 18%), prednisone alone (n 5 411, 55%), or prednisone plus other IS therapy (n 5 197, 26%). In multivariate analysis, initial therapy group was not associated with failure-free survival (FFS; a composite of death, relapse, and new IS therapy), overall survival (OS), or nonrelapse mortality (NRM). Among the prednisone-based approaches, steroid dose was,0.25 (9%), 0.25 to 0.74 (36%), 0.75 to 1.25 (42%), or .1.25 mg/kg per day (13%). Prednisone dose within the patients treated with steroids was not significantly associated with FFS, OS, or NRM. No significant interactions were detected between overall cGVHD severity and either initial therapy group or prednisone dose for the outcomes of FFS, OS, or NRM. These observational data document heterogeneity in more contemporary cGVHD initial treatment practices, including prednisone dose and use of nonsteroid approaches. This variation was not associated with FFS, OS, or NRM. Prospective trials are needed to verify efficacy of reduced-dose prednisone or prednisone-free initial therapy approaches.
UR - http://www.scopus.com/inward/record.url?scp=85120422801&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2021005286
DO - 10.1182/bloodadvances.2021005286
M3 - Article
C2 - 34535015
AN - SCOPUS:85120422801
SN - 2473-9529
VL - 5
SP - 4549
EP - 4559
JO - Blood Advances
JF - Blood Advances
IS - 22
ER -