Marginal decrease in mortality and marked increase in incidence as a result of neuroblastoma screening at 6 months of age: Cohort study in seven prefectures in Japan

被引:31
作者
Yamamoto, K
Ohta, S
Ito, E
Hayashi, Y
Asami, T
Mabuchi, O
Higashigawa, M
Tanimura, M
机构
[1] Saitama Childrens Med Ctr, Div Hematol Oncol, Iwatsuki, Saitama 3398551, Japan
[2] Shiga Univ Med Sci, Dept Pediat, Shiga, Japan
[3] Natl Childrens Med Res Ctr, Dept Child Ecol, Tokyo 154, Japan
[4] Mie Univ, Dept Pediat, Tsu, Mie, Japan
[5] Hyogo Childrens Hosp, Div Hematol Oncol, Kobe, Hyogo, Japan
[6] Tohoku Univ, Dept Pediat Surg Oncol, Sendai, Miyagi 980, Japan
[7] Hirosaki Univ, Dept Pediat, Hirosaki, Aomori, Japan
关键词
D O I
10.1200/JCO.2002.20.5.1209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : To determine the usefulness of 6-month screening for neuroblastoma. Patients and Methods: The cumulative incidence rates (IRs) and cumulative mortality rates (MRs) of neuroblastoma in children younger than 60 months of age were analyzed for control (n = 713,025), qualitative screening (Qual Screen, n = 1,142,519), and quantitative screening (Quan Screen, n = 550,33 1) cohorts, and for Screened and Unscreened subgroups within screening cohorts. Results: IRs (per 100,000) for infants aged 6 to 11 months were 1.12 in Control, 5.69 in Qual Screen (P < .0001), and 17.81 in Quan Screen (P < .0001); IRs for children aged 12 to 59 months were 7.29 in Control, 5.86 in Qual Screen (P = .28), and 6.36 in Quan Screen (P = .60). IRs for children aged 12 to 59 months in Unscreened or Screened subgroups remained at the same level. When patients diagnosed at younger than 6 months of age were excluded, the MR (per 100,000) under 60 months for Control was 4.21; those in Unscreened and Screened subgroups were 3.84 and 2.53 in Qual Screen (P = .30), and 3.20 and 1.97 in Quan Screen (P = .73), respectively; MRs between Control and Unscreened subgroups revealed no significant differences (P = .89 in Qual Screen, P = .85 in Quan Screen). Conclusion: Six-month screening resulted in a marked increase in incidence for infants with no significant decrease in incidence for children older than I year of age. A decrease in mortality was observed, but it was not significant. The usefulness of screening is questionable, because the decrease of mortality should be balanced against the adverse effect of overdiagnosis and the psychological burden on parents and children. (C) 2002 by American Society of Clinical Oncology.
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页码:1209 / 1214
页数:6
相关论文
共 28 条
[1]   SCREENING FOR NEUROBLASTOMA - A 9-YEAR BIRTH COHORT-BASED STUDY IN NIIGATA, JAPAN [J].
ASAMI, T ;
OTABE, N ;
WAKABAYASHI, M ;
KAKIHARA, T ;
UCHIYAMA, M ;
ASAMI, K .
ACTA PAEDIATRICA, 1995, 84 (10) :1173-1176
[2]  
Bergeron C, 1998, MED PEDIATR ONCOL, V31, P442
[3]   Which cases are found and missed by neuroblastoma screening at 1 year? Results from the 1992 to 1995 study in three federal states of Germany [J].
Berthold, F ;
Baillot, A ;
Hero, B ;
Schurr, P ;
Nerenz, A ;
Hunneman, DH ;
Sander, J .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1200-1207
[4]  
Bessho F, 1996, INT J CANCER, V67, P520, DOI 10.1002/(SICI)1097-0215(19960807)67:4<520::AID-IJC10>3.0.CO
[5]  
2-B
[6]  
Esteve J, 1998, MED PEDIATR ONCOL, V31, P401
[7]  
EVANS AE, 1971, CANCER, V27, P374, DOI 10.1002/1097-0142(197102)27:2<374::AID-CNCR2820270221>3.0.CO
[8]  
2-G
[9]  
HAYASHI Y, 1989, CANCER, V63, P126, DOI 10.1002/1097-0142(19890101)63:1<126::AID-CNCR2820630120>3.0.CO
[10]  
2-Z