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儿童癌症患者参与合作组癌症项目的情况:一项基于人群的研究。

Childhood cancer patients' access to cooperative group cancer programs: a population-based study.

作者信息

Liu Lihua, Krailo Mark, Reaman Gregory H, Bernstein Leslie

机构信息

Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles 90033, USA.

出版信息

Cancer. 2003 Mar 1;97(5):1339-45. doi: 10.1002/cncr.11192.

Abstract

BACKGROUND

The Children's Oncology Group (COG), a merger of the Children's Cancer Group (CCG) and the Pediatric Oncology Group (POG), conducts clinical trials for the treatment of childhood cancer. To assess the feasibility of developing a nationwide childhood cancer registry, the authors attempted to determine whether COG could serve as a resource for identifying all children with cancer.

METHODS

A consolidated file of children age < 20 years who were diagnosed with cancer between 1992-1997 and registered with either CCG or POG was linked with records from the National Cancer Institute's Surveillance, Epidemiology and End Results (SEER) Program. Age-specific registration rates and age-adjusted registration rates (AARR) were calculated overall and by year of diagnosis, gender, race/ethnicity, stage of disease at diagnosis, and type of cancer.

RESULTS

Of 10,108 children age < 20 years with cancer who were identified by the 11 SEER registries between 1992-1997, 5796 were registered with CCG or POG. The AARR was 71% for children age < 15 years, 24% for adolescents ages 15-19 years, and 57% for children age < 20 years. Registration rates were stable over the years studied, varied by geographic region, and were found to be higher among children with more advanced disease. Registration rates were highest for children with leukemia, hepatic tumors, and renal tumors, and were lowest for carcinoma and retinoblastoma.

CONCLUSIONS

The results of the current study demonstrate that not all children with cancer are registered by the cooperative groups; however, a national registry program can be achieved by supplementing cases identified through COG with data collected by statewide population-based cancer registries. Such a partnership would be mutually beneficial, allowing COG to achieve 100% registration of children with cancer and, for the statewide cancer registries, improving the timeliness of case-finding and follow-up information for cancer outcomes.

摘要

背景

儿童肿瘤学组(COG)由儿童癌症组(CCG)和儿科肿瘤学组(POG)合并而成,开展儿童癌症治疗的临床试验。为评估建立全国性儿童癌症登记处的可行性,作者试图确定COG是否可作为识别所有患癌儿童的资源。

方法

将1992年至1997年间诊断为癌症且在CCG或POG登记的年龄小于20岁儿童的合并档案与美国国立癌症研究所的监测、流行病学和最终结果(SEER)计划的记录相链接。总体上以及按诊断年份、性别、种族/族裔、诊断时疾病分期和癌症类型计算特定年龄登记率和年龄调整登记率(AARR)。

结果

1992年至1997年间,11个SEER登记处识别出10108名年龄小于20岁的患癌儿童,其中5796名在CCG或POG登记。15岁以下儿童的AARR为71%,15至19岁青少年为24%,20岁以下儿童为57%。在研究的年份中登记率稳定,因地理区域而异,且在疾病更晚期的儿童中登记率更高。白血病、肝肿瘤和肾肿瘤儿童的登记率最高,癌和视网膜母细胞瘤儿童的登记率最低。

结论

当前研究结果表明,并非所有患癌儿童都在合作组登记;然而,通过用基于全州人口的癌症登记处收集的数据补充通过COG识别的病例,可实现全国登记计划。这样的合作将互利共赢,使COG能够实现患癌儿童100%登记,对全州癌症登记处而言,则可提高病例发现的及时性以及癌症结局随访信息。

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