意大利皮埃蒙特1970-1994年间诊断出的儿童癌症的生存趋势:来自儿童癌症登记处的报告。

G. Pastore, M. Mosso, F. Carnevale, L. C. Montezemolo, M. Forni, E. Madon, U. Ricardi, B. Terracini, C. Magnani
{"title":"意大利皮埃蒙特1970-1994年间诊断出的儿童癌症的生存趋势:来自儿童癌症登记处的报告。","authors":"G. Pastore, M. Mosso, F. Carnevale, L. C. Montezemolo, M. Forni, E. Madon, U. Ricardi, B. Terracini, C. Magnani","doi":"10.1002/MPO.1113","DOIUrl":null,"url":null,"abstract":"BACKGROUND\nThe Childhood Cancer Registry of Piedmont (CCRP) started its activity in 1967. It is population based and covers the Piedmont Region (population 4,500,000; NW Italy). This article reports on time trends in survival after a childhood cancer diagnosed during 1970-1994.\n\n\nPROCEDURE\nDuring 1970-1994, 2,329 incident cases were registered at CCRP on the basis of histological and/or clinical information, excluding 30 cases reported only by death certificate. Histological or hematological diagnosis was available for 2,067 cases. Vital status was assessed through the offices of the town of residence. At the end of follow-up, 1,202 cases were alive, 1,084 dead and 43 were not traceable. Survival was measured for the major diagnostic groups using both univariate and multivariate statistics.\n\n\nRESULTS\nThe 5-yr survival rate for acute lymphoblastic leukemia (ALL) improved regularly from 24.7% in 1970-1974 to 81.1% in 1990-1994, for acute nonlymphoblastic leukemia (ANLL) from 0% to 38.1%, for non-Hodgkin lymphoma (NHL) from 25.2% to 67.7%, for tumors of the central nervous system (CNS) (all types) from 33.4% to 75.9% and for Ewing tumor from 0% to 90%. Focusing on survival by period of diagnosis, the highest 5-year survival rate was observed for children diagnosed during 1985-1989 for medulloblastoma, neuroblastoma (NB), retinoblastoma, Wilms tumor, osteosarcoma, and rhabdomyosarcoma and for children diagnosed in 1990-1994 for the remaining sites. The trend over time was statistically significant for ALL, ANLL, NHL, CNS tumors, NB, and osteosarcoma as well as for all malignancies together.\n\n\nCONCLUSIONS\nPopulation-based survival studies are useful complements to clinical studies. Survival results in the present study are similar to those presented for other European countries and the United States. For most types of neoplasm (except CNS) survival probability appears to stabilize 5-10 years after diagnosis.","PeriodicalId":18531,"journal":{"name":"Medical and pediatric oncology","volume":"284 1","pages":"481-8"},"PeriodicalIF":0.0000,"publicationDate":"2001-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":"{\"title\":\"Survival trends of childhood cancer diagnosed during 1970-1994 in Piedmont, Italy: a report from the Childhood Cancer Registry.\",\"authors\":\"G. Pastore, M. Mosso, F. Carnevale, L. C. Montezemolo, M. Forni, E. Madon, U. Ricardi, B. Terracini, C. Magnani\",\"doi\":\"10.1002/MPO.1113\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\nThe Childhood Cancer Registry of Piedmont (CCRP) started its activity in 1967. It is population based and covers the Piedmont Region (population 4,500,000; NW Italy). This article reports on time trends in survival after a childhood cancer diagnosed during 1970-1994.\\n\\n\\nPROCEDURE\\nDuring 1970-1994, 2,329 incident cases were registered at CCRP on the basis of histological and/or clinical information, excluding 30 cases reported only by death certificate. Histological or hematological diagnosis was available for 2,067 cases. Vital status was assessed through the offices of the town of residence. At the end of follow-up, 1,202 cases were alive, 1,084 dead and 43 were not traceable. Survival was measured for the major diagnostic groups using both univariate and multivariate statistics.\\n\\n\\nRESULTS\\nThe 5-yr survival rate for acute lymphoblastic leukemia (ALL) improved regularly from 24.7% in 1970-1974 to 81.1% in 1990-1994, for acute nonlymphoblastic leukemia (ANLL) from 0% to 38.1%, for non-Hodgkin lymphoma (NHL) from 25.2% to 67.7%, for tumors of the central nervous system (CNS) (all types) from 33.4% to 75.9% and for Ewing tumor from 0% to 90%. Focusing on survival by period of diagnosis, the highest 5-year survival rate was observed for children diagnosed during 1985-1989 for medulloblastoma, neuroblastoma (NB), retinoblastoma, Wilms tumor, osteosarcoma, and rhabdomyosarcoma and for children diagnosed in 1990-1994 for the remaining sites. The trend over time was statistically significant for ALL, ANLL, NHL, CNS tumors, NB, and osteosarcoma as well as for all malignancies together.\\n\\n\\nCONCLUSIONS\\nPopulation-based survival studies are useful complements to clinical studies. Survival results in the present study are similar to those presented for other European countries and the United States. For most types of neoplasm (except CNS) survival probability appears to stabilize 5-10 years after diagnosis.\",\"PeriodicalId\":18531,\"journal\":{\"name\":\"Medical and pediatric oncology\",\"volume\":\"284 1\",\"pages\":\"481-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"15\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical and pediatric oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/MPO.1113\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical and pediatric oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/MPO.1113","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15

摘要

皮埃蒙特儿童癌症登记处(CCRP)于1967年开始活动。它以人口为基础,覆盖皮埃蒙特地区(人口450万;意大利西北)。这篇文章报道了1970-1994年间诊断出儿童癌症后的生存率的时间趋势。在1970-1994年期间,CCRP根据组织学和/或临床信息登记了2,329例事件病例,不包括仅通过死亡证明报告的30例病例。2067例有组织学或血液学诊断。生命状况是通过居住城镇的办事处评估的。随访结束时,1202例存活,1084例死亡,43例无法追踪。使用单变量和多变量统计来测量主要诊断组的生存率。结果急性淋巴母细胞白血病(ALL)的5年生存率从1970-1974年的24.7%提高到1990-1994年的81.1%,急性非淋巴母细胞白血病(ANLL)的5年生存率从0%提高到38.1%,非霍奇金淋巴瘤(NHL)的5年生存率从25.2%提高到67.7%,中枢神经系统肿瘤(CNS)(所有类型)的5年生存率从33.4%提高到75.9%,尤因肿瘤的5年生存率从0%提高到90%。关注诊断期的生存率,观察到1985-1989年诊断为髓母细胞瘤、神经母细胞瘤(NB)、视网膜母细胞瘤、Wilms肿瘤、骨肉瘤和横纹肌肉瘤的儿童的5年生存率最高,而1990-1994年诊断为其余部位的儿童的5年生存率最高。随着时间的推移,ALL、ANLL、NHL、CNS肿瘤、NB和骨肉瘤以及所有恶性肿瘤的趋势都具有统计学意义。结论基于人群的生存研究是临床研究的有益补充。本研究的生存结果与其他欧洲国家和美国的研究结果相似。对于大多数类型的肿瘤(中枢神经系统除外),诊断后5-10年的生存率似乎稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Survival trends of childhood cancer diagnosed during 1970-1994 in Piedmont, Italy: a report from the Childhood Cancer Registry.
BACKGROUND The Childhood Cancer Registry of Piedmont (CCRP) started its activity in 1967. It is population based and covers the Piedmont Region (population 4,500,000; NW Italy). This article reports on time trends in survival after a childhood cancer diagnosed during 1970-1994. PROCEDURE During 1970-1994, 2,329 incident cases were registered at CCRP on the basis of histological and/or clinical information, excluding 30 cases reported only by death certificate. Histological or hematological diagnosis was available for 2,067 cases. Vital status was assessed through the offices of the town of residence. At the end of follow-up, 1,202 cases were alive, 1,084 dead and 43 were not traceable. Survival was measured for the major diagnostic groups using both univariate and multivariate statistics. RESULTS The 5-yr survival rate for acute lymphoblastic leukemia (ALL) improved regularly from 24.7% in 1970-1974 to 81.1% in 1990-1994, for acute nonlymphoblastic leukemia (ANLL) from 0% to 38.1%, for non-Hodgkin lymphoma (NHL) from 25.2% to 67.7%, for tumors of the central nervous system (CNS) (all types) from 33.4% to 75.9% and for Ewing tumor from 0% to 90%. Focusing on survival by period of diagnosis, the highest 5-year survival rate was observed for children diagnosed during 1985-1989 for medulloblastoma, neuroblastoma (NB), retinoblastoma, Wilms tumor, osteosarcoma, and rhabdomyosarcoma and for children diagnosed in 1990-1994 for the remaining sites. The trend over time was statistically significant for ALL, ANLL, NHL, CNS tumors, NB, and osteosarcoma as well as for all malignancies together. CONCLUSIONS Population-based survival studies are useful complements to clinical studies. Survival results in the present study are similar to those presented for other European countries and the United States. For most types of neoplasm (except CNS) survival probability appears to stabilize 5-10 years after diagnosis.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信