Treatment of high-risk neuroblastoma with triple-tandem high-dose therapy and stem-cell rescue: Results of the Chicago Pilot II study

被引:89
作者
Kletzel, M
Katzenstein, HM
Haut, PR
Yu, AL
Morgan, E
Reynolds, M
Geissler, G
Marymount, MH
Liu, DC
Kalopurakal, JA
Shore, RM
Bardo, DK
Schmoldt, J
Rademaker, AW
Cohn, SL
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Surg, Chicago, IL 60611 USA
[3] Northwestern Univ, Feinberg Sch Med, Dept Radiotherapy, Chicago, IL 60611 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Radiol, Chicago, IL 60611 USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Biostat Core Facil, Chicago, IL 60611 USA
[6] Robert H Lurie Comprehens Canc Ctr, Chicago, IL USA
[7] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
关键词
D O I
10.1200/JCO.2002.06.060
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To investigate whether intensive induction therapy followed by triple-tandem cycles of high-dose therapy with peripheral-blood stem-cell rescue and local irradiation will improve event-free survival for patients with high-risk neuroblastoma. Patients and Methods: From August 1995 to January 2000, 25 consecutive newly diagnosed high-risk neuroblastoma patients and one child with recurrent MYCN-amplified disease were enrolled onto the Chicago Pilot 11 Protocol. After induction therapy and surgery, peripheral-blood stem cells were mobilixed with three cycles of high-dose cyclophosphamide and granulocyte colony-stimulating factor. Patients then underwent triple-tandem cycles of high-dose therapy with peripheral-blood stem-cell rescue followed by radiation to the primary site. Results: Twenty-two of the 26 patients successfully completed induction therapy and were eligible for the triple-tandem consolidation high-dose therapy. Sufficient numbers of peripheral-blood stem cells were collected in all but one patient. Seventeen patients were able to complete all three cycles of high-dose therapy and peripheral-blood stem-cell rescue two patients completed two cycles, and three patients completed one cycle. There was one toxic death, and one patient died from complications of treatment for graft failure. With a median follow-up of 38 months, the 3-year event-free survival and survival rates are 57% +/- 11% and 79% +/- 10%, respectively. Conclusion: The results of this pilot study demonstrate that it is feasible to intensify consolidation with triple-tandem high-dose chemotherapy and peripheral-blood stem-cell rescue and local irradiation, and suggest that this treatment strategy may lead to improved survival for patients with high-risk neuroblastoma. (C) 2002 by American Society of Clinical Oncology.
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页码:2284 / 2292
页数:9
相关论文
共 33 条
[1]   REVISIONS OF THE INTERNATIONAL CRITERIA FOR NEUROBLASTOMA DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT [J].
BRODEUR, GM ;
PRITCHARD, J ;
BERTHOLD, F ;
CARLSEN, NLT ;
CASTEL, V ;
CASTLEBERRY, RP ;
DEBERNARDI, B ;
EVANS, AE ;
FAVROT, M ;
HEDBORG, F ;
KANEKO, M ;
KEMSHEAD, J ;
LAMPERT, F ;
LEE, REJ ;
LOOK, AT ;
PEARSON, ADJ ;
PHILIP, T ;
ROALD, B ;
SAWADA, T ;
SEEGER, RC ;
TSUCHIDA, Y ;
VOUTE, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (08) :1466-1477
[2]   INTERNATIONAL CRITERIA FOR DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT IN PATIENTS WITH NEURO-BLASTOMA [J].
BRODEUR, GM ;
SEEGER, RC ;
BARRETT, A ;
BERTHOLD, F ;
CASTLEBERRY, RP ;
DANGIO, G ;
DEBERNARDI, B ;
EVANS, AE ;
FAVROT, M ;
FREEMAN, AI ;
HAASE, G ;
HARTMANN, O ;
HAYES, FA ;
HELSON, L ;
KEMSHEAD, J ;
LAMPERT, F ;
NINANE, J ;
OHKAWA, H ;
PHILIP, T ;
PINKERTON, CR ;
PRITCHARD, J ;
SAWADA, T ;
SIEGEL, S ;
SMITH, EI ;
TSUCHIDA, Y ;
VOUTE, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (12) :1874-1881
[3]   Circulating neuroblastoma cells detected by reverse transcriptase polymerase chain reaction for tyrosine hydroxylase mRNA are an independent poor prognostic indicator in stage 4 neuroblastoma in children over 1 year [J].
Burchill, SA ;
Lewis, IJ ;
Abrams, KR ;
Riley, R ;
Imeson, J ;
Pearson, ADJ ;
Pinkerton, R ;
Selby, P .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) :1795-1801
[4]   CHEMOTHERAPY DOSE INTENSITY CORRELATES STRONGLY WITH RESPONSE, MEDIAN SURVIVAL, AND MEDIAN PROGRESSION-FREE SURVIVAL IN METASTATIC NEUROBLASTOMA [J].
CHEUNG, NKV ;
HELLER, G .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (06) :1050-1058
[5]   Anti-GD2 antibody treatment of minimal residual stage 4 neuroblastoma diagnosed at more than 1 year of age [J].
Cheung, NKV ;
Kushner, BH ;
Cheung, IY ;
Kramer, K ;
Canete, A ;
Gerald, W ;
Bonilla, MA ;
Finn, R ;
Yeh, SJ ;
Larson, SM .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (09) :3053-3060
[6]  
Cheung NKV, 2000, NEUROBLASTOMA, P541
[7]   Treatment of poor-risk neuroblastoma patients with high-dose chemotherapy and autologous peripheral stem cell rescue [J].
Cohn, SL ;
Moss, TJ ;
Hoover, M ;
Katzenstein, HM ;
Haut, PR ;
Morgan, ER ;
Green, AA ;
Kletzel, M .
BONE MARROW TRANSPLANTATION, 1997, 20 (07) :543-551
[8]  
DICARO A, 1994, AM J PEDIAT HEMATOL, V16, P200
[9]   Analysis of parameters affecting engraftment in children undergoing autologous peripheral blood stem cell transplants [J].
Figuerres, E ;
Haut, PR ;
Olzewski, M ;
Kletzel, M .
BONE MARROW TRANSPLANTATION, 2000, 25 (06) :583-588
[10]   LMCE3 treatment strategy: Results in 99 consecutively diagnosed stage 4 neuroblastomas in children older than 1 year at diagnosis [J].
Frappaz, D ;
Michon, J ;
Coze, C ;
Berger, C ;
Plouvier, E ;
Lasset, C ;
Bernard, JL ;
Stephan, JL ;
Bouffet, E ;
Buclon, M ;
Combaret, V ;
Fourquet, A ;
Philip, T ;
Zucker, JM .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (03) :468-476