Prognostic value of pretransplantation positron emission tomography using fluorine 18-fluorodeoxyglucose in patients with aggressive lymphoma treated with high-dose chemotherapy and stem cell transplantation

被引:167
作者
Spaepen, K
Stroobants, S
Dupont, P
Vandenberghe, P
Maertens, J
Bormans, G
Thomas, J
Balzarini, J
De Wolf-Peeters, C
Mortelmans, L
Verhoef, G
机构
[1] Univ Hosp Gasthuisberg, Dept Nucl Med, B-3000 Louvain, Belgium
[2] Univ Hosp Gasthuisberg, Dept Oncol, B-3000 Louvain, Belgium
[3] Univ Hosp Gasthuisberg, Dept Hematol, B-3000 Louvain, Belgium
[4] Univ Hosp Gasthuisberg, Dept Pathol, B-3000 Louvain, Belgium
[5] Katholieke Univ Leuven, Rega Inst, Louvain, Belgium
关键词
D O I
10.1182/blood-2002-12-3842
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The study assessed the prognostic value of fluorine 18-fluorodeoxyglucose positron emission tomography ([F-18]FDG-PET) after salvage chemotherapy before high-dose chemotherapy with stem cell transplantation (HDT/SCT) in patients with induction failure or relapsing chemosensitive lymphoma. Retrospective analysis of the clinical and conventional imaging data of 60 patients scheduled for HDT/SCT was performed in parallel with the analysis of the [F-18]FDG-PET results. To determine the ability of [F-18]FDG-PET to predict clinical outcome, PET images were reread without knowledge of conventional imaging and clinical history. Presence or absence of abnormal [F-18]FDG uptake was related to progression-free survival (PFS) and overall survival (OS) using Kaplan-Meier survival analysis. Thirty patients showed a negative [F-18]FDG-PET scan before HDT/SCT, 25 of those remained in complete remission, with a median follow-up of 1510 days. Two patients died due to a treatment-related mortality but without evidence of recurrent disease at that time (228-462 days). Only 3 patients had a relapse (median PFS, 1083 days) after a negative [F-18]FDG-PET scan. Persistent abnormal [F-18]FDG uptake was seen in 30 patients and 26 progressed (median PFS, 402 days); of these 26, 16 died from progressive disease (median OS, 408 days). Four patients are still in complete remission after a positive scan. Comparison between groups indicated a statistically significant association between [F-18]FDG-PET findings and PFS (P < .000001) and OS (P < .00002). [F-18]FDG-PET has an important prognostic role in the pretransplantation evaluation of patients with lymphoma and enlarges the concept of chemosensitivity used to select patients for HDT/SCT. (C) 2003 by The American Society of Hematology.
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页码:53 / 59
页数:7
相关论文
共 30 条
[1]  
ARMITAGE JO, 1993, NEW ENGL J MED, V328, P1023
[2]   Positron emission tomography with [18F]2-fluoro-D-2-deoxyglucose (FDG-PET) predicts relapse of malignant lymphoma after high-dose therapy with stem cell transplantation [J].
Becherer, A ;
Mitterbauer, M ;
Jaeger, U ;
Kalhs, P ;
Greinix, HT ;
Karanikas, G ;
Pötzi, C ;
Raderer, M ;
Dudczak, R ;
Kletter, K .
LEUKEMIA, 2002, 16 (02) :260-267
[3]   CHEMOTHERAPY OF ADVANCED HODGKINS-DISEASE WITH MOPP, ABVD, OR MOPP ALTERNATING WITH ABVD [J].
CANELLOS, GP ;
ANDERSON, JR ;
PROPERT, KJ ;
NISSEN, N ;
COOPER, MR ;
HENDERSON, ES ;
GREEN, MR ;
GOTTLIEB, A ;
PETERSON, BA .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (21) :1478-1484
[4]   RESIDUAL MASS IN LYMPHOMA MAY NOT BE RESIDUAL DISEASE [J].
CANELLOS, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (06) :931-933
[5]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[6]   Non-Hodgkin's lymphoma - Pre-transplant positron emission tomography (PET) using fluorine-18-fluoro-deoxyglucose (FDG) predicts outcome in patients treated with high-dose chemotherapy and autologous stem cell transplantation for non-Hodgkin's lymphoma [J].
Cremerius, U ;
Fabry, U ;
Wildberger, JE ;
Zimny, M ;
Reinartz, P ;
Nowak, B ;
Schaefer, W ;
Buell, U ;
Osieka, R .
BONE MARROW TRANSPLANTATION, 2002, 30 (02) :103-111
[7]   18FDG-PET following treatment as valid predictor for disease-free survival in Hodgkin's lymphoma [J].
de Wit, M ;
Bohuslavizki, KH ;
Buchert, R ;
Bumann, D ;
Clausen, M ;
Hossfeld, DK .
ANNALS OF ONCOLOGY, 2001, 12 (01) :29-37
[8]   Intensive salvage therapy with high-dose chemotherapy for patients with advanced Hodgkin's disease in relapse or failure after initial chemotherapy:: Results of the Groupe d'Etudes des Lymphomes de l'Adulte H89 trial [J].
Fermé, C ;
Mounier, N ;
Diviné, M ;
Brice, P ;
Stamatoullas, A ;
Reman, O ;
Voillat, L ;
Jaubert, J ;
Lederlin, P ;
Colin, P ;
Berger, F ;
Salles, G .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (02) :467-475
[9]   COMPARISON OF A STANDARD REGIMEN (CHOP) WITH 3 INTENSIVE CHEMOTHERAPY REGIMENS FOR ADVANCED NON-HODGKINS-LYMPHOMA [J].
FISHER, RI ;
GAYNOR, ER ;
DAHLBERG, S ;
OKEN, MM ;
GROGAN, TM ;
MIZE, EM ;
GLICK, JH ;
COLTMAN, CA ;
MILLER, TP .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (14) :1002-1006
[10]  
HARRIS NL, 1994, BLOOD, V84, P1361