Increasing mixed chimerism defines a high-risk group of childhood acute myelogenous leukemia patients after allogeneic stem cell transplantation where pre-emptive immunotherapy may be effective

被引:77
作者
Bader, P
Kreyenberg, H
Hoelle, W
Dueckers, G
Kremens, B
Dilloo, D
Sykora, KW
Niemeyer, C
Reinhardt, D
Vormoor, J
Gruhn, B
Lang, P
Greil, J
Handgretinger, R
Niethammer, D
Klingebiel, T
Beck, JF
机构
[1] Univ Childrens Hosp, Dept Pediat Hematol & Oncol, D-72076 Tubingen, Germany
[2] Univ Childrens Hosp, Essen, Germany
[3] Univ Childrens Hosp, Dusseldorf, Germany
[4] Childrens Hosp, Hannover Med Sch, Hannover, Germany
[5] Univ Childrens Hosp, Freiburg, Germany
[6] Univ Childrens Hosp, Munster, Germany
[7] Univ Childrens Hosp, Jena, Germany
[8] St Jude Childrens Res Hosp, Memphis, TN 38105 USA
[9] Univ Childrens Hosp, Frankfurt, Germany
[10] Univ Childrens Hosp, Greifswald, Germany
关键词
allogeneic stem cell transplantation; AML; childhood; chimerism; adjuvant immunotherapy;
D O I
10.1038/sj.bmt.1704444
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Children with leukemias and increasing mixed chimerism ( increasing MC) after allogeneic stem cell transplantation have the highest risk to relapse. Early immunological intervention was found to be effective in these cases. To substantiate this on a defined group of pediatric acute myelogenous leukemia (AML) patients, we performed serial analysis of post transplant chimerism and preemptive immunotherapy in patients with increasing MC. In total, 81 children were monitored, 62 patients revealed complete chimerism (CC), low-level MC or decreasing MC. Increasing MC was detected in 19 cases. Despite early immunological intervention relapse was still significantly more frequent in patients with increasing MC (9/19) than in patients with CC, low-level or decreasing MC (8/62, P<0.005). The probability of 3-year event-free survival (EFS) was 52% for all patients ( n = 81), 59% for patients with CC, low-level MC, 60% for patients with decreasing MC ( n = 62), and 28% for patients with increasing MC ( n = 19, P<0.005). Patients with increasing MC who received early immunological intervention showed a significantly enhanced probability for event-free survival (pEFS 36%, n = 15) compared to patients with increasing MC without intervention ( pEFS 0%, n = 4, P<0.05). These results prove that pediatric AML patients with increasing MC are at highest risk for relapse and that early immunological intervention can prevent relapse in these patients.
引用
收藏
页码:815 / 821
页数:7
相关论文
共 44 条
[11]   Second allogeneic bone marrow transplantation in acute leukemia: Results of a survey by the European Cooperative Group for Blood and Marrow Transplantation [J].
Bosi, A ;
Laszlo, D ;
Labopin, M ;
Reffeirs, J ;
Michallet, M ;
Gluckman, E ;
Alessandrino, PE ;
Locatelli, F ;
Vernant, JP ;
Sierra, J ;
Jouet, JP ;
Frassoni, F .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3675-3684
[12]   TREATMENT OF CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA - PRESENT ISSUES AND FUTURE-PROSPECTS [J].
CHESSELLS, JM .
BLOOD REVIEWS, 1992, 6 (04) :193-203
[13]   Donor leukocyte infusions in 140 patients with relapsed malignancy after allogeneic bone marrow transplantation [J].
Collins, RH ;
Shpilberg, O ;
Drobyski, WR ;
Porter, DL ;
Giralt, S ;
Champlin, R ;
Goodman, SA ;
Wolff, SN ;
Hu, W ;
Verfaillie, C ;
List, A ;
Dalton, W ;
Ognoskie, N ;
Chetrit, A ;
Antin, JH ;
Nemunaitis, J .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) :433-444
[14]  
COLLINS RH, 1992, BONE MARROW TRANSPL, V10, P391
[15]   Monitoring of lineage-specific chimaerism allows early prediction of response following donor lymphocyte infusions for relapsed chronic myeloid leukaemia [J].
Gardiner, N ;
Lawler, M ;
O'Riordan, JM ;
Duggan, C ;
De Arce, M ;
McCann, SR .
BONE MARROW TRANSPLANTATION, 1998, 21 (07) :711-719
[16]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[17]   Graft-versus-leukemia effect and its clinical implications [J].
Imamura, M ;
Hashino, S ;
Tanaka, J .
LEUKEMIA & LYMPHOMA, 1996, 23 (5-6) :477-492
[18]   Chimerism and tolerance: From freemartin cattle to neonatal mice to humans [J].
Jankowski, RA ;
Ildstad, ST .
HUMAN IMMUNOLOGY, 1997, 52 (02) :155-161
[20]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481