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Abstract P1-14-07: Randomized phase 3 study of anthracycline-containing regimens versus S-1 as first-line treatment for metastatic breast cancer (SELECT BC-CONFIRM)–A combined analysis of two randomized phase 3 studies (SELECT BC-CONFIRM and SELECT BC)–

Y Park, H Akabane, T Watanabe, M Takahashi, Y Sagara, R Nishimura, J Tsurutani, T Takashima, T Fujisawa, Y Hozumi, Y Uemura and H Mukai
Y Park
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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H Akabane
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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T Watanabe
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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M Takahashi
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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Y Sagara
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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R Nishimura
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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J Tsurutani
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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T Takashima
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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T Fujisawa
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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Y Hozumi
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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Y Uemura
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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H Mukai
Tohoku Medical and Pharmaceutical University, Faculty of Medicine, Sendai, Japan; Hokkaido P. W. F. A. C. Asahikawa-Kosei General Hospital, Asahikawa, Japan; National Hospital Organization, Sendai Medical Center, Sendai, Japan; National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan; Hakuaikai Medical Corp Sagara Hospital, Kagoshima, Japan; Kumamoto Shinto General Hospital, Kumamoto, Japan; Kindai University, Faculty of Medicine, Osakasayama, Japan; Osaka City University, Graduate School of Medicine, Osaka, Japan; Gunma Prefectural Cancer Center, Ota, Japan; University of Tsukuba Hospital /Ibaraki Prefectural Central Hospital, Kasama, Japan; The University of Tokyo Hospital, Tokyo, Japan; National Cancer Center Hospital East, Kashiwa, Japan
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DOI: 10.1158/1538-7445.SABCS18-P1-14-07 Published February 2019
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Abstracts: 2018 San Antonio Breast Cancer Symposium; December 4-8, 2018; San Antonio, Texas

Abstract

Background: Anthracycline-containing regimens and taxane have been standard as the first-line chemotherapy for metastatic breast cancer (MBC). We conducted SELECT BC (randomized phase 3 study of taxane versus S-1 as first-line treatment for MBC) for evaluating the efficacy of S-1 for patients with HER2-negative MBC from 2006 to 2010 in Japan. This study demonstrated non-inferiority of S-1 in overall survival (OS) (median OS was 37.2 months in taxes group and 35.0 months in S-1 group (HR 1.05, 95% CI 0.86–1.27, p=0.015)), and superiority in health-related quality of life (HRQOL) to taxanes. S-1 was also shown as less toxic than taxane (Lancet Oncol 2016; 17: 90-98). S-1 might provide clinical benefit as first-line treatment for patients with HER2-negative MBC. To confirm this suggestion, we have conducted further study (randomized phase 3 study of anthracycline-containing regimens versus S-1 as first-line treatment for HER2-negative MBC: SELECT BC-CONFIRM) from 2011 to present, and a combined analysis of two randomized studies (SELECT-BC CONFIRM and SELECT-BC).

Methods: In SELECT BC-CONFIRM, 230 patients receiving first-line treatment for MBC were randomly assigned to either anthracycline group (n=115) or S-1 group (n=115). Anthracycline group patients received anthracycline-containing regimens (AC, EC, FAC, FEC, q3w) at the discretion of the treating physician. S-1 group patients received S-1 40–60 mg twice daily based on the patient's body surface area for 28 days on, 14-day off. The primary endpoint was OS, and secondary endpoints were progression-free survival (PFS), time to treatment failure (TTF), adverse events, HRQOL, and cost-effectiveness. The results were combined with SELECT-BC, to confirm the hypothesis that S-1 treatment is not inferior to the standard therapy (taxanes / anthracycline) for HER2-negative MBC.

Results: A combined analysis of the two studies showed that HR was 1.06, 95%CI 0.90-1.253, and p=0.0071 between the standard therapy group and S-1 group. In addition, the Bayesian posterior probability for which HR would be less than 1.333 was about 99.6%.

Conclusions: A combined analysis of SELECT BC-CONFIRM and SELECT BC clearly demonstrated that OS with S-1 was not inferior to that with the standard therapy in patients receiving first-line treatment for HER2-negative MBC. S-1 could become a standard therapy for this patient population.

Citation Format: Park Y, Akabane H, Watanabe T, Takahashi M, Sagara Y, Nishimura R, Tsurutani J, Takashima T, Fujisawa T, Hozumi Y, Uemura Y, Mukai H. Randomized phase 3 study of anthracycline-containing regimens versus S-1 as first-line treatment for metastatic breast cancer (SELECT BC-CONFIRM)–A combined analysis of two randomized phase 3 studies (SELECT BC-CONFIRM and SELECT BC)– [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr P1-14-07.

  • ©2019 American Association for Cancer Research.
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Cancer Research: 79 (4 Supplement)
February 2019
Volume 79, Issue 4 Supplement
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Abstract P1-14-07: Randomized phase 3 study of anthracycline-containing regimens versus S-1 as first-line treatment for metastatic breast cancer (SELECT BC-CONFIRM)–A combined analysis of two randomized phase 3 studies (SELECT BC-CONFIRM and SELECT BC)–
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Abstract P1-14-07: Randomized phase 3 study of anthracycline-containing regimens versus S-1 as first-line treatment for metastatic breast cancer (SELECT BC-CONFIRM)–A combined analysis of two randomized phase 3 studies (SELECT BC-CONFIRM and SELECT BC)–
Y Park, H Akabane, T Watanabe, M Takahashi, Y Sagara, R Nishimura, J Tsurutani, T Takashima, T Fujisawa, Y Hozumi, Y Uemura and H Mukai
Cancer Res February 15 2019 (79) (4 Supplement) P1-14-07; DOI: 10.1158/1538-7445.SABCS18-P1-14-07

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Abstract P1-14-07: Randomized phase 3 study of anthracycline-containing regimens versus S-1 as first-line treatment for metastatic breast cancer (SELECT BC-CONFIRM)–A combined analysis of two randomized phase 3 studies (SELECT BC-CONFIRM and SELECT BC)–
Y Park, H Akabane, T Watanabe, M Takahashi, Y Sagara, R Nishimura, J Tsurutani, T Takashima, T Fujisawa, Y Hozumi, Y Uemura and H Mukai
Cancer Res February 15 2019 (79) (4 Supplement) P1-14-07; DOI: 10.1158/1538-7445.SABCS18-P1-14-07
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