Relapse and clonal disease in children with aplastic anemia (AA) after immunosuppressive therapy (IST): the SAA94 experience

被引:68
作者
Fuhrer, M
Burdach, S
Ebell, W
Gadner, H
Haas, R
Harbott, J
Janka-Schaub, G
Klingebiel, T
Kremens, B
Niemeyer, C
Rampf, U
Reiter, A
Ritter, J
Schulz, A
Walther, U
Zeidler, C
Bender-Gotze, C
机构
[1] LMU Munchen, Kinderpoliklin, D-80336 Munich, Germany
[2] Univ Dusseldorf, Kinderklin, D-4000 Dusseldorf, Germany
[3] Klinikum Rudolf Virchow, Kinderklin, Berlin, Germany
[4] St Anna Childrens Hosp, Vienna, Austria
[5] Univ Munich, Dr Von Haunerschen Kinderspital, D-80337 Munich, Germany
[6] Univ Giessen, Kinderklin, Giessen, Germany
[7] Univ Hamburg, Kinderklin, Hamburg, Germany
[8] Univ Tubingen, Kinderklin, D-7400 Tubingen, Germany
[9] Univ Essen Gesamthsch, Kinderklin, Essen, Germany
[10] Univ Freiburg, Kinderklin, Freiburg, Germany
[11] Hannover Med Sch, Kinderklin, Hannover, Germany
[12] Univ Munster, Kinderklin, D-4400 Munster, Germany
[13] Univ Ulm, Kinderklin, D-89069 Ulm, Germany
来源
KLINISCHE PADIATRIE | 1998年 / 210卷 / 04期
关键词
aplastic anemia; children; immunosuppressive therapy; relapse; clonal disease;
D O I
10.1055/s-2008-1043875
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Since the introduction of combined immunosuppressive therapy (IST) into management of aplastic anemia (AA) in childhood response and probability of survival improved. In contrast to bone marrow transplantation (BMT), however, patients after IST are not considered cured as high rates of relapse and development of clonal disease demonstrate. From 11/93 to 9/97 114 children (65 m, 49 f; median age 9.5 y.) from 37 centers in Germany and Austria were registered in the SAA 94 study. 86 patients lacking a matched sibling donor received IST. Most of the patients suffered from very severe (VSAA: PMN <200/mu l) or severe AA (SAA: PMN <500/mu l). All patients were treated with combined IST consisting of ALG and Cyclosporin A (CSA). VSAA and SAA patients were additionally treated with G-CSF. Therapy response was evaluated at day 112, after 6, 12 and 18 months. 8/86 patients died, the probability of survival being 87% after 4 years. At d 112 61% of evaluable patients became independent of transfusions (IST response: CR+PR), 13% with normal blood counts (CR). After 6 months 33% showed CR. At 12 and 18 months response improved to 74% resp. 80%,39% resp. 55% CR. The best response was achieved in the subgroup of VSAA with 90% (PR+CR) and 65% CR after 18 months. 4 patients developed AML 3-19 months after the beginning of IST. In 2/4 pts. an aberrant clone ( -7; 5q-) could be detected retrospectively in BM at diagnosis of AA. 3 nonresponders developed chromosomal aberrations (+19; -7, +12; +8) after 4, 12 and 16 months without morphological signs of AML or MDS. Overall 11 relapses occurred at a median time of 12 months (range 5-27 months) after the beginning of IST. 2 of them relapsed under CSA therapy, 2 under tapering of CSA and 7 after cessation of CSA. 7 patients responded again to CSA monotherapy. Overall response rate is 77% with a probability of event free survival (EFS) of 54% after 4 years regarding all complications mentioned as events.
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页码:173 / 179
页数:9
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