Keisei Anan1, Naohito Fukui2, Takayuki Kinoshita3, Takayuki Iwamoto4, Naoki Niikura5, Masaaki Kawai6, Naoki Hayashi7, Kouichiro Tsugawa8, Kenjiro Aogi9, Takanori Ishida10, Hideji Masuoka11, Sinobu Masuda12, Kotaro Iijima13, Seigo Nakamura14, Yutaka Tokuda15. 1. Department of Surgery, Kitakyushu Municipal Medical Center, Kitakyushu, Japan. 2. The Japan Clinical Research Support Unit and the Public Health Research Foundation, Tokyo, Japan. 3. Department of Breast Surgery, National Cancer Center Hospital, Tokyo, Japan. 4. Department of Breast and Endocrine Surgery, Okayama University Hospital, Okayama, Japan. 5. Department of Breast and Endocrine Surgery, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan. 6. Department of Breast Surgery, Miyagi Cancer Center, Natori, Japan. 7. Department of Breast Surgery, St. Luke's International Hospital, Tokyo, Japan. 8. Division of Breast and Endocrine Surgery, Department of Surgery, St. Marianna University School of Medicine, Kawasaki, Japan. 9. Department of Breast Surgery, Shikoku Cancer Center, Matsuyama, Japan. 10. Department of Surgical Oncology, Graduate School of Medicine, Tohoku University, Sendai, Japan. 11. Sapporo-kotoni Breast Clinic, Sapporo, Japan. 12. Department of Pathology, Nihon University School of Medicine, Tokyo, Japan. 13. Department of Breast Oncology, Cancer Institute Hospital, Tokyo, Japan. 14. Division of Breast Surgical Oncology, Department of Surgery, Showa University, Tokyo, Japan. 15. Department of Breast and Endocrine Surgery, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan. tokuda@is.icc.u-tokai.ac.jp.
Abstract
Entities:
Keywords:
2005; Breast cancer; Japan; Prognosis; Registry; Report; The Japanese Breast Cancer Society
A population-based cancer registry has been used for the planning and evaluation of cancer control activities based on administration and the care of individual cancerpatients by those in the medical profession. The Japanese Breast Cancer Society (JBCS) registry was started in 1975. In 2004, the registry system was moved to a new system using web registration with the cooperation of the Non-Profit Organization Japan Clinical Research Support Unit and Public Health Research Foundation (Tokyo, Japan). Comprehensive individual patient data were recorded according to the Unio Internationalis Contra Cancrum (UICC) TNM classification [1] and the World Health Organization histological classification [2]. The details are described elsewhere [3]. Annual reports on this registry have since been published in Japanese and publicized through the JBCS web site to active members of the JBCS [4].a, b Kaplan–Meier curves for relapse-free and overall survival of all cases by tumor classification (cT-category). P values were calculated using the log rank test. Tis: Non-invasive ductal carcinoma, lobular carcinoma in situ, or Paget disease; T1a: ≤0.5 cm; T1b: 0.5< tumor ≤1.0 cm; T1c: 1.0< tumor ≤2.0 cm, T2: 2.0< tumor ≤5.0 cm; T3: >5.0 cm; T4: tumor of any size with direct extension to the chest wall and/or skin (ulceration or skin nodules) or inflammatory carcinomaa, b Kaplan–Meier curves for relapse-free and overall survival of all cases by regional lymph nodes status (cN-category). N0: no regional lymph node metastases; N1: metastases in movable ipsilateral level I, II axillary lymph node(s); N2: metastases in ipsilateral level I, II axillary lymph nodes that are clinically fixed or matted OR metastases in clinically detected ipsilateral internal mammary nodes in the absence of clinically evident axillary lymph node metastases; N3: metastases in ipsilateral infraclavicular (level III axillary) lymph node(s) with or without level I, II axillary lymph node involvement OR metastases in clinically detected ipsilateral internal mammary lymph node(s) with clinically evident level I, II axillary lymph node metastases OR metastases in ipsilateral supraclavicular lymph node(s) with or without axillary or internal mammary lymph node involvement. P values were calculated using the log rank testa, b Kaplan–Meier curves for relapse-free and overall survival of all cases by clinical stage (UICC). P values were calculated using the log rank testa, b Kaplan–Meier curves for relapse-free and overall survival of cases without neoadjuvant therapy by pathological tumor size (pT size). Tumor size is a marker of invasiveness. P values were calculated using the log rank testWe herein report the results of a 5-year prognostic analysis of cases registered in 2005 (Figs. 1, 2, 3, 4, 5, 6, 7, 8 and 9; Supplementary Tables 1–9). The number of facilities involved in the 2005 registration was 354 and the total number of cases was 20,786. The estimated incidence of breast cancer was reported to be 50,695 cases in 2005 by the National Cancer Center [5]. Therefore, approximately 41 % of newly diagnosed breast cancerpatients were included in the JBCS registry in 2005. In this prognostic study, we analyzed 9971 cases in which the survival data were available from 161 facilities. The background characteristics of the patients are summarized in Table 1. The median follow-up period was 60.0 months (range 0.1–60.0 months). Note that during the study period, not only the cutoff levels of estrogen receptor and progesterone receptor but also their corresponding test procedures were non-standardized and that trastuzumab was rarely used because it was not covered by the Japanese National Health Insurance program as an adjuvant therapy for humanepidermal growth factor receptor 2-positive breast cancer. On the whole, the survival data seem to be better than expected. However, it would be prudent to avoid commenting on any specific subject because the present study is part of an annual survival report. A data set spanning multiple years would be more suitable for addressing specific subjects, such as triple-negative type or HER2 type. This is planned for the next phase studies.
Fig. 1
a, b Kaplan–Meier curves for relapse-free and overall survival of all cases by tumor classification (cT-category). P values were calculated using the log rank test. Tis: Non-invasive ductal carcinoma, lobular carcinoma in situ, or Paget disease; T1a: ≤0.5 cm; T1b: 0.5< tumor ≤1.0 cm; T1c: 1.0< tumor ≤2.0 cm, T2: 2.0< tumor ≤5.0 cm; T3: >5.0 cm; T4: tumor of any size with direct extension to the chest wall and/or skin (ulceration or skin nodules) or inflammatory carcinoma
Fig. 2
a, b Kaplan–Meier curves for relapse-free and overall survival of all cases by regional lymph nodes status (cN-category). N0: no regional lymph node metastases; N1: metastases in movable ipsilateral level I, II axillary lymph node(s); N2: metastases in ipsilateral level I, II axillary lymph nodes that are clinically fixed or matted OR metastases in clinically detected ipsilateral internal mammary nodes in the absence of clinically evident axillary lymph node metastases; N3: metastases in ipsilateral infraclavicular (level III axillary) lymph node(s) with or without level I, II axillary lymph node involvement OR metastases in clinically detected ipsilateral internal mammary lymph node(s) with clinically evident level I, II axillary lymph node metastases OR metastases in ipsilateral supraclavicular lymph node(s) with or without axillary or internal mammary lymph node involvement. P values were calculated using the log rank test
Fig. 3
a, b Kaplan–Meier curves for relapse-free and overall survival of all cases by clinical stage (UICC). P values were calculated using the log rank test
Fig. 4
a, b Kaplan–Meier curves for relapse-free and overall survival of cases without neoadjuvant therapy by pathological tumor size (pT size). Tumor size is a marker of invasiveness. P values were calculated using the log rank test
Fig. 5
a, b Kaplan–Meier curves for relapse-free and overall survival of cases without neoadjuvant therapy by the number of metastatic lymph nodes. P values were calculated using the log rank test
Fig. 6
a, b Kaplan–Meier curves for relapse-free and overall survival of all cases by age. P values were calculated using the log rank test
Fig. 7
a, b Kaplan–Meier curves for relapse-free and overall survival of T1–T4, any N and M0 cases with respect to estrogen receptor (ER) status and HER2 (human EGFR-related 2) amplification status. P values were calculated using the log rank test. Relapse-free survival and overall survival of patients with respect to combined ER and HER2 status
Fig. 8
a, b Kaplan–Meier curves for relapse-free and overall survival of ER-positive and M0 cases by progesterone receptor (PgR) status. P values were calculated using the log rank test
Fig. 9
a, b Kaplan–Meier curves for relapse-free and overall survival of ER-positive and M0 cases with respect to PgR and HER2 amplifications. P values were calculated using the log rank test
Table 1
Patient characteristics
Age
Mean
SD
57.36
12.81
Tumor size(cm)
Mean
SD
2.64
2.12
Tumor sizea
Count
(%)
T0
118
1.18
Tis
914
9.17
T1a
61
0.61
T1b
836
8.38
T1c
2923
29.32
T2
3346
33.56
T3
459
4.6
T4
550
5.52
Unknown
764
7.66
Na
N0
7616
76.38
N1
1791
17.96
N2
270
2.71
N3
121
1.21
Unknown
173
1.74
Ma
M0
9425
94.52
M1
257
2.58
Unknown
289
2.9
Stagea
0
841
8.43
I
3386
33.96
II
3635
36.46
III
752
7.54
IV
257
2.58
Unknown
1100
11.03
ER
Positive
7245
72.66
Negative
2325
23.32
Unknown
401
4.02
PgR
Positive
5945
59.62
Negative
3594
36.04
Unknown
432
4.33
HER2
Positive
1407
14.11
Negative
7351
73.72
Unknown
1213
12.17
ER estrogen receptor, PgR progesterone receptor, HER2 human epidermal growth factor receptor 2
a The TNM classification was identified by the UICC staging system
a, b Kaplan–Meier curves for relapse-free and overall survival of cases without neoadjuvant therapy by the number of metastatic lymph nodes. P values were calculated using the log rank testa, b Kaplan–Meier curves for relapse-free and overall survival of all cases by age. P values were calculated using the log rank testPatient characteristicsERestrogen receptor, PgRprogesterone receptor, HER2humanepidermal growth factor receptor 2a The TNM classification was identified by the UICC staging systema, b Kaplan–Meier curves for relapse-free and overall survival of T1–T4, any N and M0 cases with respect to estrogen receptor (ER) status and HER2 (human EGFR-related 2) amplification status. P values were calculated using the log rank test. Relapse-free survival and overall survival of patients with respect to combined ER and HER2 statusa, b Kaplan–Meier curves for relapse-free and overall survival of ER-positive and M0 cases by progesterone receptor (PgR) status. P values were calculated using the log rank testCancer control activities vary among nations and regional areas due to differences in population structures. The life expectancy for Japanese women, 87 years old in 2012, has been the longest worldwide for several years [6]. In addition, Japan is a super-aging society, with 25 % of citizens being 65 years of age or above as of October 2013, which is the highest number among all other nations [7]. We believe that the outcomes of our registry provide significant information for countries that are expected to have a similar population structure to that of Japan in the near future.a, b Kaplan–Meier curves for relapse-free and overall survival of ER-positive and M0 cases with respect to PgR and HER2 amplifications. P values were calculated using the log rank testSupplementary material 1 (XLSX 21 kb)