Annual report of the Japanese Breast Cancer Society registry for 2016
Annual report of the Japanese Breast Cancer Society registry for 2016
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DOI：
10.1007/s12282-020-01081-4
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发表时间：
2020-05-11
期刊：
影响因子：
4
通讯作者：
Jinno, Hiromitsu
中科院分区：
文献类型：
--
作者：
Kubo, Makoto;Kumamaru, Hiraku;Jinno, Hiromitsu
日本乳腺癌协会（JBCS）登记处于1975年开始收集数据，并于2012年整合到国家临床数据库中。截至2016年，JBCS登记处包含来自日本1400多家医院的656，896名乳腺癌患者的记录。在2016年的注册中，涉及的机构数量为1422个，患者总数为95，870人。我们在此总结了2016年收集的JBCS注册中心的年度数据。我们从不同角度分析登记的乳腺癌患者的人口统计学和临床病理学特征。特别是，我们检查了家族史，月经，发病年龄，根据年龄的体重指数，基于肿瘤大小和亚型的淋巴结状态，以及基于ER，PgR和HER2状态的比例。本报告基于JBCS登记研究，可为乳腺癌患者的临床管理和临床研究提供支持。
The Japanese Breast Cancer Society (JBCS) registry began data collection in 1975, and it was integrated into National Clinical Database in 2012. As of 2016, the JBCS registry contains records of 656,896 breast cancer patients from more than 1400 hospitals throughout Japan. In the 2016 registration, the number of institutes involved was 1422, and the total number of patients was 95,870. We herein present the summary of the annual data of the JBCS registry collected in 2016. We analyzed the demographic and clinicopathologic characteristics of registered breast cancer patients from various angles. Especially, we examined the registrations on family history, menstruation, onset age, body mass index according to age, nodal status based on tumor size and subtype, and proportion based on ER, PgR, and HER2 status. This report based on the JBCS registry would support clinical management for breast cancer patients and clinical study in the near future.