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Significance of Clinical and Biologic Features in Stage 3 Neuroblastoma: A Report from the International Neuroblastoma Risk Group Project
被引:30
|作者:
Meany, Holly J.
[1
]
London, Wendy B.
[2
]
Ambros, Peter F.
[3
]
Matthay, Katherine K.
[4
,5
]
Monclair, Tom
[6
]
Simon, Thorsten
[7
]
Garaventa, Alberto
[8
]
Berthold, Frank
[7
]
Nakagawara, Akira
[9
,10
]
Cohn, Susan L.
[11
]
Pearson, Andrew D. J.
[12
,13
]
Park, Julie R.
[14
]
机构:
[1] Childrens Natl Med Ctr, Dept Hematol Oncol, Washington, DC 20010 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston Childrens Hosp, Boston, MA 02115 USA
[3] St Anna Kinderkrebsforsch, Childrens Canc Res Inst, Vienna, Austria
[4] Univ Calif San Francisco, Sch Med, Dept Pediat, San Francisco, CA 94143 USA
[5] Benioff Childrens Hosp, San Francisco, CA USA
[6] Univ Oslo, Rikshosp, Univ Hosp, Div Surg,Sect Paediat Surg, N-0027 Oslo, Norway
[7] Univ Cologne, Dept Pediat Oncol & Hematol, D-50931 Cologne, Germany
[8] Giannina Gaslini Inst, Dept Paediat Hematol Oncol, Genoa, Italy
[9] Chiba Canc Ctr, Japan Neuroblastoma Study Grp JNBSG, Chiba 2608717, Japan
[10] Chiba Canc Ctr, Div Biochem & Innovat Canc Therapeut, Chiba 2608717, Japan
[11] Univ Chicago, Hematol Oncol Sect, Chicago, IL 60637 USA
[12] Royal Marsden NHS Fdn Trust, Inst Canc Res, Div Canc Therapeut & Clin Studies, Sutton, Surrey, England
[13] Royal Marsden NHS Fdn Trust, Children & Young Peoples Unit, Sutton, Surrey, England
[14] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle Childrens Hosp, Dept Hematol Oncol, Seattle, WA 98195 USA
关键词:
biologic factor;
neuroblastoma;
treatment outcome;
CHILDRENS ONCOLOGY GROUP;
PATHOLOGY CLASSIFICATION;
MYCN AMPLIFICATION;
N-MYC;
13-CIS-RETINOIC ACID;
PROGNOSTIC IMPACT;
CHROMOSOME;
1P;
CANCER GROUP;
TUMORS;
AGE;
D O I:
10.1002/pbc.25134
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BackgroundInternational Neuroblastoma Staging System (INSS) Stage 3 neuroblastoma is a heterogeneous disease. Data from the International Neuroblastoma Risk Group (INRG) database were analyzed to define patient and tumor characteristics predictive of outcome. ProcedureOf 8,800 patients in the INRG database, 1,483 with INSS Stage 3 neuroblastoma and complete follow-up data were analyzed. Secondary analysis was performed in 1,013 patients (68%) with MYCN-non-amplified (NA) tumors. Significant prognostic factors were identified via log-rank test comparisons of survival curves. Multivariable Cox proportional hazards regression model was used to identify factors independently predictive of event-free survival (EFS). ResultsAge at diagnosis (P<0.0001), tumor MYCN status (P<0.0001), and poorly differentiating/undifferentiated histology (P=0.03) were independent predictors of EFS. Compared to other Stage 3 subgroups, outcome was inferior for patients 547 days with MYCN-NA neuroblastoma (P<0.0001), and within this cohort, serum ferritin 96ng/ml was associated with inferior EFS (P=0.02). For patients <547 days of age with MYCN-NA tumors, serum ferritin levels were prognostic of overall survival (OS) (P=0.04) and chromosome 11q aberration was prognostic of EFS (P=0.03). ConclusionsAmong patients with INSS Stage 3 neuroblastoma patients, age at diagnosis, MYCN status and histology predict outcome. Patients <547 days of age with MYCN-NA tumors that lack chromosome 11q aberrations or those with serum ferritin <96ng/ml have excellent prognosis and should be considered for therapy reduction. Prospective clinical trials are needed to identify optimal therapy for those patients 547 days of age with undifferentiated histology or elevated serum ferritin. Pediatr Blood Cancer 2014;61:1932-1939. (c) 2014 Wiley Periodicals, Inc.
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页码:1932 / 1939
页数:8
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