Comprehensive prognostic report of the Japanese Breast Cancer Society Registry in 2004.
Comprehensive prognostic report of the Japanese Breast Cancer Society Registry in 2004.
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DOI：
10.1007/s12282-015-0644-5
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发表时间：
2016-01
期刊：
影响因子：
--
通讯作者：
Tokuda Y
中科院分区：
文献类型：
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作者：
Kinoshita T;Fukui N;Anan K;Iwamoto T;Niikura N;Kawai M;Hayashi N;Tsugawa K;Aogi K;Ishida T;Masuoka H;Masuda S;Iijima K;Nakamura S;Tokuda Y
1975年，乳腺癌研究小组（日本乳腺癌学会的前身）发起了乳腺癌登记，从1975年到2003年的29年间登记了188，265名乳腺癌患者。2004年，实施了新的登记制度，截至2009年，共登记了207 468名病人。2004年《个人信息保护法》生效后，以前的纸质登记系统被转换为基于网络的系统，其中包括匿名的疗效数据。与此同时，数据中心也从国立癌症中心转移到了非营利组织日本临床研究支援单位（J-CRSU）和公共卫生研究基金会。在此，我们很高兴地首次报告了在新系统下2004年登记的患者的5年预后结果（图1和2）。1、2、3、4、5、6、7、8、9;补充表1-9）。我们非常感谢医疗和管理人员以及合作参与本研究的患者。
In 1975, the Breast Cancer Study Group (the predecessor of the Japanese Breast Cancer Society) initiated the Breast Cancer Registry and had registered 188,265 breast cancer patients during the 29 years from 1975 to 2003. In 2004, a new registration system was implemented, which had registered a total of 207,468 patients up to 2009. When the Personal Information Protection Law came into effect in 2004, the previous paper-based registration system was converted to the web-based system, which includes anonymized efficacy data. At the same time, the data center was moved from the National Cancer Center to the Japan Clinical Research Support Unit (J-CRSU), a nonprofit organization, and the Public Health Research Foundation.Herein, we are pleased to report, for the first time under the new system, results on five-year prognosis of patients that were registered in 2004 (Figs. 1, 2, 3, 4, 5, 6, 7, 8, 9; Supplementary Tables 1–9). We are deeply grateful to the medical and administrative staff as well as the patients who co-operatively participated in this study.