TY - JOUR
T1 - High-dose chemotherapy for relapsed and refractory diffuse large B-cell lymphoma
T2 - Mediastinal localization predicts for a favorable outcome
AU - Popat, Uday
AU - Przepiork, Donna
AU - Champlin, Richard
AU - Pugh, William
AU - Amin, Kamal
AU - Mehra, Rakesh
AU - Rodriguez, Jose
AU - Giralt, Sergio
AU - Romaguera, Jorge
AU - Rodriguez, Alma
AU - Preti, Alex
AU - Andersson, Borje
AU - Khouri, Issa
AU - Claxton, David
AU - de Lima, Marcos
AU - Donato, Michele
AU - Anderlini, Paolo
AU - Gajewski, James
AU - Cabanillas, Fernando
AU - van Besien, K.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1998/1
Y1 - 1998/1
N2 - Purpose: This study was performed to evaluate the outcome of high-dose chemotherapy and autologous transplantation in patients with diffuse B-cell large-cell lymphoma, and, specifically, to evaluate the impact of primary mediastinal localization on the outcome of high-dose chemotherapy. Patients and Methods: A retrospective review was performed of all patients with diffuse large B-cell lymphoma who underwent autologous marrow or peripheral- blood stem-cell transplantation at our institution between January 1986 and December 1995. Results: Ninety patients were identified, of whom 31 (34%) o primary mediastinal B-cell large-cell lymphoma (PML). Cumulative probabilities of disease-free survival, overall survival, and disease progression are 40% (95% confidence interval [CI], 29 to 51), 42% (95% CI, 31 to 53), and 52% (95% CI, 40 to 64), respectively. By univariate analysis, low lactate dehydrogenase (LDH) level and low Ann Arbor stage at transplant were associated with improved survival and disease-free survival. There was a trend far improved disease-free survival and survival far patients with PMI. Multivariate stepwise Cox regression analysis showed that LDH level, Ann Arbor stage, and primary mediastinal localization were independent favorable prognostic factors far disease-free survival and survival. LDH level and Ann Arbor stage were also predictive for the risk of disease progression. Conclusion: Our results indicate that patients with PML may display an increased susceptibility to high-dose chemotherapy compared with other types of B-cell large-cell lymphoma. These findings, if confirmed, may have implications far the initial management of patients with PML.
AB - Purpose: This study was performed to evaluate the outcome of high-dose chemotherapy and autologous transplantation in patients with diffuse B-cell large-cell lymphoma, and, specifically, to evaluate the impact of primary mediastinal localization on the outcome of high-dose chemotherapy. Patients and Methods: A retrospective review was performed of all patients with diffuse large B-cell lymphoma who underwent autologous marrow or peripheral- blood stem-cell transplantation at our institution between January 1986 and December 1995. Results: Ninety patients were identified, of whom 31 (34%) o primary mediastinal B-cell large-cell lymphoma (PML). Cumulative probabilities of disease-free survival, overall survival, and disease progression are 40% (95% confidence interval [CI], 29 to 51), 42% (95% CI, 31 to 53), and 52% (95% CI, 40 to 64), respectively. By univariate analysis, low lactate dehydrogenase (LDH) level and low Ann Arbor stage at transplant were associated with improved survival and disease-free survival. There was a trend far improved disease-free survival and survival far patients with PMI. Multivariate stepwise Cox regression analysis showed that LDH level, Ann Arbor stage, and primary mediastinal localization were independent favorable prognostic factors far disease-free survival and survival. LDH level and Ann Arbor stage were also predictive for the risk of disease progression. Conclusion: Our results indicate that patients with PML may display an increased susceptibility to high-dose chemotherapy compared with other types of B-cell large-cell lymphoma. These findings, if confirmed, may have implications far the initial management of patients with PML.
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U2 - 10.1200/JCO.1998.16.1.63
DO - 10.1200/JCO.1998.16.1.63
M3 - Article
C2 - 9440724
AN - SCOPUS:0031972560
SN - 0732-183X
VL - 16
SP - 63
EP - 69
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 1
ER -