Persistence of transcriptionally silent BCR-ABL rearrangements in chronic myeloid leukemia patients in sustained complete cytogenetic remission

被引:13
作者
Kitzis, A
Brizard, F
Dascalescu, C
Chomel, JC
Guilhot, F
Brizard, A
机构
[1] CHU Poitiers, Lab Genet Cellulaire & Mol, UPRES EA 2622, F-86021 Poitiers, France
[2] CHU Poitiers, UPRES EA 2622, Dept Hematol & Oncol Med, F-86021 Poitiers, France
[3] CHU Poitiers, Hematol Lab, CNRS FRE 2224, F-86021 Poitiers, France
[4] Hop St Antoine, Hematol Serv, F-75571 Paris, France
关键词
chronic myeloid leukemia; complete cytogenetic remission; BCR-ABL rearrangement; fluorescence in situ hybridization; polymerase chain reaction;
D O I
10.3109/10428190109097712
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Persistence of BCR-ABL rearrangements was demonstrated by D-FISH technique in chronic myeloid leukemia (CML) patients in complete cytogenetic response (CCR) after allogeneic bone marrow transplantation (BMT) or interferon-alpha therapy (IFN-alpha). Samples from bone marrow aspirate or peripheral blood or both were analyzed by conventional cytogenetics, Southern blot, fluorescent interphase in situ hybridization (FISH), and quantitative reverse transcription polymerase chain reaction (Q-RT-PCR). In all patients, FISH detected 1% to 12% nuclei with a BCR-ABL fusion gene, whereas Q-RT-PCR were negative or weakly positive. Based on these results, we hypothesize that the BCR-ABL genomic rearrangement remains unexpressed in a small percentage of cells whatever the treatment (IFN-alpha or BMT), and this in spite of the negativity of the RT-PCR-based classical molecular remission criterion. These data corroborate those obtained by other investigators and point to the need for follow-up of CML patients in CCR over an extensive period, at the DNA level to evaluate the residual disease and at the RNA level (Q-RT-PCR) to estimate the risk of relapse and guide the therapeutic decision. Experimental models suggesting the persistence of positive BCR-ABL cells are discussed and tentative explanations of tumor "dormancy" are proposed.
引用
收藏
页码:933 / +
页数:13
相关论文
共 76 条
[51]   Evidence for specific immune response against P210 BCR-ABL in long-term remission CML patients treated with interferon [J].
Oka, T ;
Sastry, KJ ;
Nehete, P ;
Schapiro, SJ ;
Guo, JQ ;
Talpaz, M ;
Arlinghaus, RB .
LEUKEMIA, 1998, 12 (02) :155-163
[52]  
Patri S, 1996, BONE MARROW TRANSPL, V17, P625
[53]  
PICHERT G, 1994, BLOOD, V84, P2109
[54]   Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using a 'real time' quantitative RT-PCR assay [J].
Preudhomme, C ;
Révillion, F ;
Merlat, A ;
Hornez, L ;
Roumier, C ;
Duflos-Grardel, N ;
Jouet, JP ;
Cosson, A ;
Peyrat, JP ;
Fenaux, P .
LEUKEMIA, 1999, 13 (06) :957-964
[55]   POLYMERASE CHAIN-REACTION DETECTION OF THE BCR-ABL FUSION TRANSCRIPT AFTER ALLOGENEIC MARROW TRANSPLANTATION FOR CHRONIC MYELOID-LEUKEMIA - RESULTS AND IMPLICATIONS IN 346 PATIENTS [J].
RADICH, JP ;
GEHLY, G ;
GOOLEY, T ;
BRYANT, E ;
CLIFT, RA ;
COLLINS, S ;
EDMANDS, S ;
KIRK, J ;
LEE, A ;
KESSLER, P ;
SCHOCH, G ;
BUCKNER, CD ;
SULLIVAN, KM ;
APPELBAUM, FR ;
THOMAS, ED .
BLOOD, 1995, 85 (09) :2632-2638
[56]   BCR-ABL-positive progenitors in chronic myeloid leukaemia patients in complete cytogenetic remission after treatment with interferon-α [J].
Reiter, A ;
Marley, SB ;
Hochhaus, A ;
Sohal, J ;
Raanani, P ;
Hehlmann, R ;
Gordon, MY ;
Goldman, JM ;
Cross, NCP .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 102 (05) :1271-1278
[57]  
ROTH MS, 1992, BLOOD, V79, P276
[58]   IMMUNE-MEDIATED AND UNUSUAL COMPLICATIONS DURING INTERFERON-ALFA THERAPY IN CHRONIC MYELOGENOUS LEUKEMIA [J].
SACCHI, S ;
KANTARJIAN, H ;
OBRIEN, S ;
COHEN, PR ;
PIERCE, S ;
TALPAZ, M .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (09) :2401-2407
[59]  
Schulze E, 1995, EXP HEMATOL, V23, P1649
[60]  
Seong D, 1998, CLIN CANCER RES, V4, P861