Early detection of BCR-ABL transcripts by quantitative reverse transcriptase-polymerase chain reaction predicts outcome after allogeneic stem cell transplantation for chronic myeloid leukemia

被引:119
作者
Olavarria, E [1 ]
Kanfer, E [1 ]
Szydlo, R [1 ]
Kaeda, J [1 ]
Rezvani, K [1 ]
Cwynarski, K [1 ]
Pocock, C [1 ]
Dazzi, F [1 ]
Craddock, C [1 ]
Apperley, JF [1 ]
Cross, NCP [1 ]
Goldman, JM [1 ]
机构
[1] Hammersmith Hosp, Imperial Coll, Sch Med, Dept Haematol, London W12 0NN, England
关键词
D O I
10.1182/blood.V97.6.1560
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The reverse transcriptase-polymerase chain reaction (RT-PCR) has become widely used for monitoring minimal residual disease after allogeneic stem cell transplantation (SCT) for chronic myeloid leukemia (CML). However, most of these studies were performed using qualitative RT-PCR, and the interpretation of the results obtained has been conflicting. The correlation of a quantitative RT-PCR test performed early after SCT (at 3 to 5 months) and long-term outcome of CML patients surviving for more than 6 months was studied. Between January 1991 and Introduction June 1999, data from 138 CML patients who received allografts were evaluated. Early RT-PCR results were classified as (1) negative if there were no BCR-ABL transcripts detected (n = 61), (2) positive at low level if the total number of BCR-ABL transcripts was less than 100 per mug RNA and/or the BCR-ABL/ABL ratio was less than 0.02% (n = 14), or (3) positive at high level if transcript levels exceeded the thresholds defined above (n = 63), Three years after SCT the cumulative incidence of relapse was 16.7%, 42.9%, and 86.4%, respectively (P = .0001). The relationship between BCR-ABL transcript level and probability of relapse was apparent whether patients had received sibling or unrelated donor SCT and also whether or not the transplantation was T cell depleted. The results suggest that quantitative RT-PCR performed early after SCT is useful for predicting outcome and may help to define the need for further treatment. (Blood, 2001;97:1560-1565) (C) 2001 by The American Society of Hematology.
引用
收藏
页码:1560 / 1565
页数:6
相关论文
共 35 条
[1]  
ARCESE W, 1993, BLOOD, V82, P3211
[2]   Presenting white blood cell count and kinetics of molecular remission predict prognosis in acute promyelocytic leukemia treated with all-trans retinoic acid:: Result of the randomized MRC trial [J].
Burnett, AK ;
Grimwade, D ;
Solomon, E ;
Wheatley, K ;
Goldstone, AH .
BLOOD, 1999, 93 (12) :4131-4143
[3]   Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia [J].
Cavé, H ;
ten Bosch, JV ;
Suciu, S ;
Guidal, C ;
Waterkeyn, C ;
Otten, J ;
Bakkus, M ;
Thielemans, K ;
Grandchamp, B ;
Vilmer, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (09) :591-598
[4]  
Cross NCP, 1998, HEMATOL CELL THER, V40, P224
[5]  
CROSS NCP, 1994, LEUKEMIA, V8, P186
[6]  
CROSS NCP, 1993, BLOOD, V82, P1929
[7]  
CROSS NCP, 1996, METH MOLEC MED, P25
[8]   Comparison of single-dose and escalating-dose regimens of donor lymphocyte infusion for relapse after allografting for chronic myeloid leukemia [J].
Dazzi, F ;
Szydlo, RM ;
Craddock, C ;
Cross, NCP ;
Kaeda, J ;
Chase, A ;
Olavarria, E ;
van Rhee, F ;
Kanfer, E ;
Apperley, JF ;
Goldman, JM .
BLOOD, 2000, 95 (01) :67-71
[9]   Donor lymphocyte infusions for relapse of chronic myeloid leukemia after allogeneic stem cell transplant: Where we now stand [J].
Dazzi, F ;
Szydlo, RM ;
Goldman, JM .
EXPERIMENTAL HEMATOLOGY, 1999, 27 (10) :1477-1486
[10]  
Diverio D, 1998, BLOOD, V92, P784