FIRST EXPERIENCE WITH PROGNOSTIC FACTORS IN UNSELECTED NEUROBLASTOMA PATIENTS - THE AUSTRIAN NEUROBLASTOMA-87 STUDY

被引:25
作者
LADENSTEIN, R
URBAN, C
GADNER, H
FINK, FM
ZOUBEK, A
EMMINGER, W
GRIENBERGER, H
SCHMITT, K
AMBROS, PF
AMBROS, IM
HORCHER, E
AMANN, G
HOFLER, G
KERBEL, R
MUTZ, I
机构
[1] GRAZ UNIV, DEPT PAEDIAT ONCOL, GRAZ, AUSTRIA
[2] UNIV INNSBRUCK, DEPT PAEDIAT ONCOL, INNSBRUCK, AUSTRIA
[3] LANDESKRANKENHAUS SALZBURG, SALZBURG, AUSTRIA
[4] UNIV VIENNA, DEPT PAEDIAT SURG, VIENNA, AUSTRIA
[5] UNIV VIENNA, DEPT PATHOL, VIENNA, AUSTRIA
[6] GRAZ UNIV, DEPT PATHOL, GRAZ, AUSTRIA
[7] LANDESKRANKENHAUS LEOBEN, LEOBEN, AUSTRIA
关键词
NEUROBLASTOMA; PROSPECTIVE STUDY; PROGNOSTIC FACTORS; NEURON SPECIFIC ENOLASE; FERRITIN; AGE; MYCN; DEL; 1P;
D O I
10.1016/0959-8049(95)00069-U
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Between January 1987 and December 1993, 117 patients were registered in the Austrian A-NB87 study. The male/female ratio was 1.18, with 50 patients below the age of 1 year at diagnosis. Patients were assigned to stage according to the result of primary surgery in localised disease. Age, ferritin and neuron specific enolase were used in addition in stage III disease for risk-adapted treatment. Adrenal or pelvic primary tumour sites were mainly associated (81%) with advanced disease. The median observation time of the study is 3.5 years. The overall survival at 3 years was excellent in low stage disease and IVs patients, i.e. 100% for stage I and IIA (20 patients), 92% in stage IVs (13 patients), 81% in stage IIIA (18 patients) and 69% in stage IIB (8 patients). Stage IV (38 patients) showed a survival rate of 51%, whereas stage IIIB (10 patients) had the worst outcome in this study, i.e. 20%, due to treatment-related toxicity. Significant unfavourable prognostic factors were neuron specific enolase (NSE)> 100 ng/ml, ferritin > 300 mu g/ml and amplified MYCN. This study achieved a better survival rate in stage IV patients and a subgroup of stage III in comparison to our previous study (Padiatrie und Padologie 1986, 21, 269) and gives the basis to further reduce treatment intensity in low-risk disease based on biological factors. However, prognosis for high-risk cases was still poor in spite of a very aggressive treatment concept.
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页码:637 / 641
页数:5
相关论文
共 30 条
[1]  
BERTHOLD F, 1992, AM J PEDIAT HEMATOL, V14, P207
[2]  
BERTHOLD F, 1994, AM J PEDIAT HEMATOL, V2, P107
[3]  
BRODEUR GM, 1992, CANCER-AM CANCER SOC, V70, P1685, DOI 10.1002/1097-0142(19920915)70:4+<1685::AID-CNCR2820701607>3.0.CO
[4]  
2-H
[5]   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
[6]   PROGNOSTIC VALUE OF DIFFERENT STAGING SYSTEMS IN NEUROBLASTOMAS AND COMPLETENESS OF TUMOR-EXCISION [J].
CARLSEN, NLT ;
CHRISTENSEN, IJ ;
SCHROEDER, H ;
BRO, PV ;
HESSELBJERG, U ;
JENSEN, KB ;
NIELSEN, OH .
ARCHIVES OF DISEASE IN CHILDHOOD, 1986, 61 (09) :832-842
[7]   RADIOTHERAPY IMPROVES THE OUTLOOK FOR PATIENTS OLDER THAN 1 YEAR WITH PEDIATRIC ONCOLOGY GROUP STAGE-C NEUROBLASTOMA [J].
CASTLEBERRY, RP ;
KUN, LE ;
SHUSTER, JJ ;
ALTSHULER, G ;
SMITH, IE ;
NITSCHKE, R ;
WHARAM, M ;
MCWILLIAMS, N ;
JOSHI, V ;
HAYES, FA .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (05) :789-795
[8]   TUMOR KARYOTYPE DISCRIMINATES BETWEEN GOOD AND BAD PROGNOSTIC OUTCOME IN NEURO-BLASTOMA [J].
CHRISTIANSEN, H ;
LAMPERT, F .
BRITISH JOURNAL OF CANCER, 1988, 57 (01) :121-126
[9]  
EMMINGER W, 1991, BONE MARROW TRANSPL, V8, P119
[10]  
EVANS AE, 1987, CANCER, V59, P1853, DOI 10.1002/1097-0142(19870601)59:11<1853::AID-CNCR2820591102>3.0.CO