Biologic factors determine prognosis in infants with stage IV neuroblastoma: A prospective Children's Cancer Group study

被引:161
作者
Schmidt, ML
Lukens, JN
Seeger, RC
Brodeur, GM
Shimada, H
Gerbing, RB
Stram, DO
Perez, C
Haase, GM
Matthay, KK
机构
[1] Childrens Canc Grp, Arcadia, CA 91066 USA
[2] Univ Illinois, Coll Med, Dept Pediat, Chicago, IL USA
[3] Univ So Calif, Sch Med, Dept Pediat, San Francisco, CA USA
[4] Univ So Calif, Sch Med, Dept Pediat, San Francisco, CA USA
[5] Univ So Calif, Sch Med, Dept Pathol, San Francisco, CA USA
[6] Univ So Calif, Sch Med, Dept Prevent Med, San Francisco, CA USA
[7] Childrens Hosp, San Francisco, CA USA
[8] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA
[9] Univ Penn, Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
[10] Vanderbilt Univ, Dept Pediat, Nashville, TN USA
[11] Denver Pediat Surg, Denver, CO USA
关键词
D O I
10.1200/JCO.2000.18.6.1260
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: A prospective Children's Cancer Group study, CCG-3881, has been completed to determine if a more accurate prediction of prognosis by biologic features can identify subgroups of infants with stage IV neuroblastoma (NBL) who require differing intensities of treatment. Patients and Methods: One hundred thirty-four infants were registered from June 1989 to August 1995, with a median follow-up of 47.1 months (range, 0 to 88 months). The biologic factors examined were tumor MYCN copy number, Shimada histopathologic classification, serum ferritin, and bone marrow immunocytology (sensitivity, one tumor cell per 10(5) bone marrow cells). patients treated on CCG-3881 (n = 116) received four-drug chemotherapy for 9 months (cisplatin, cyclophosphamide, doxorubicin, and etoposide), with surgery and local radiation to residual disease. After January 1991, all subsequent infants with tumor MYCN amplification (9 = 18) were transferred after one cycle of therapy to the high-risk CCG-3891 protocol (open January 1991 to April 1996) for more intensive treatment, Results: The 3-year event-free survival (EFS) and overall survival (mean +/- SD) for the 134 infants were 63% +/- 5% and 71% +/- 5%, respectively. patients whose tumors were without MYCN amplification had a 93% +/- 4% 3-year EFS, whereas those with amplified MYCN had a 10% +/- 7% 3-year EFS (P < .0001). Each of the other biologic features studied had prognostic significance in univariate analysis but not after stratifying by MYCN copy number. Conclusion: infants less: than 1 year of age at diagnosis with stage IV NBL have a much improved outcome compared with children greater than or equal to 1 year of age. Nonamplified MYCN tumors identify ct group of infants with a 93% +/- 4% EFS, whereas amplified MYCN copy number clearly identifies patients who are unlikely to survive despite intensive chemotherapy, (C) 2000 by American Society of Clinical Oncology.
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收藏
页码:1260 / 1268
页数:9
相关论文
共 26 条
[1]   IMPACT OF INTENSIFIED THERAPY ON CLINICAL OUTCOME IN INFANTS AND CHILDREN WITH NEUROBLASTOMA - THE ST-JUDE-CHILDRENS-RESEARCH-HOSPITAL EXPERIENCE, 1962 TO 1988 [J].
BOWMAN, LC ;
HANCOCK, ML ;
SANTANA, VM ;
HAYES, FA ;
KUN, L ;
PARHAM, DM ;
FURMAN, WL ;
RAO, BN ;
GREEN, AA ;
CRIST, WM .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (09) :1599-1608
[2]   Genetic staging of unresectable or metastatic neuroblastoma in infants: A Pediatric Oncology Group Study [J].
Bowman, LC ;
Castleberry, RP ;
Cantor, A ;
Joshi, V ;
Cohn, SL ;
Smith, EI ;
Yu, A ;
Brodeur, GM ;
Hayes, FA ;
Look, AT .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (05) :373-380
[3]   AMPLIFICATION OF N-MYC IN UNTREATED HUMAN NEUROBLASTOMAS CORRELATES WITH ADVANCED DISEASE STAGE [J].
BRODEUR, GM ;
SEEGER, RC ;
SCHWAB, M ;
VARMUS, HE ;
BISHOP, JM .
SCIENCE, 1984, 224 (4653) :1121-1124
[4]   PROGNOSTIC VALUE OF HISTOPATHOLOGY IN ADVANCED NEURO-BLASTOMA - A REPORT FROM THE CHILDRENS CANCER STUDY-GROUP [J].
CHATTEN, J ;
SHIMADA, H ;
SATHER, HN ;
WONG, KY ;
SIEGEL, SE ;
HAMMOND, GD .
HUMAN PATHOLOGY, 1988, 19 (10) :1187-1198
[5]  
COX DR, 1972, J R STAT SOC B, V34, P187
[6]  
Crabbe D C, 1992, Diagn Mol Pathol, V1, P229, DOI 10.1097/00019606-199203000-00034
[7]  
DEBERNARDI B, 1992, CANCER-AM CANCER SOC, V70, P1625, DOI 10.1002/1097-0142(19920915)70:6<1625::AID-CNCR2820700631>3.0.CO
[8]  
2-6
[9]   INFANTS WITH METASTATIC NEUROBLASTOMA HAVE IMPROVED SURVIVAL WITH RESECTION OF THE PRIMARY TUMOR [J].
DECOU, JM ;
BOWMAN, LC ;
RAO, BN ;
SANTANA, VM ;
FURMAN, WL ;
LUO, XL ;
LOBE, TE ;
KUMAR, M .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (07) :937-941
[10]  
HANN HWL, 1985, CANCER RES, V45, P2843