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Anthracycline could be essential for triple-negative breast cancer: A randomised phase II study by the Kanagawa Breast Oncology Group (KBOG) 1101.
Narui, Kazutaka; Ishikawa, Takashi; Shimizu, Daisuke; Yamada, Akimitsu; Tanabe, Mikiko; Sasaki, Takeshi; Oba, Mari S; Morita, Satoshi; Nawata, Shuichi; Kida, Kumiko; Mogaki, Masatoshi; Doi, Takako; Tsugawa, Koichiro; Ogata, Haruki; Ota, Tomohiko; Kosaka, Yoshimasa; Sengoku, Norihiko; Kuranami, Masaru; Niikura, Naoki; Saito, Yuki; Suzuki, Yasuhiro; Suto, Akihiko; Arioka, Hitoshi; Chishima, Takashi; Ichikawa, Yasushi; Endo, Itaru; Tokuda, Yutaka.
Afiliação
  • Narui K; Department of Breast and Thyroid Surgery, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: nr1@gc5.so-net.ne.jp.
  • Ishikawa T; Department of Breast and Thyroid Surgery, Yokohama City University Medical Center, Yokohama, Japan; Department of Breast Oncology and Surgery, Tokyo Medical University, Tokyo, Japan. Electronic address: tishik55@gmail.com.
  • Shimizu D; Department of Breast and Thyroid Surgery, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: d-shimizu.surg@yokohama.jrc.or.jp.
  • Yamada A; Department of Breast and Thyroid Surgery, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: yakimitsu@gmail.com.
  • Tanabe M; Division of Diagnostic Pathology, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: betana.m@gmail.com.
  • Sasaki T; Division of Diagnostic Pathology, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: takesasa@m.u-tokyo.ac.jp.
  • Oba MS; Department of Biostatistics and Epidemiology, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: mari.oba@med.toho-u.ac.jp.
  • Morita S; Department of Biostatistics and Epidemiology, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: smorita@kuhp.kyoto-u.ac.jp.
  • Nawata S; Pharmaceutical Department, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: nawa_shu@cmed.showa-u.ac.jp.
  • Kida K; Department of Breast and Thyroid Surgery, Yokohama City University Medical Center, Yokohama, Japan. Electronic address: kidakumiko117@gmail.com.
  • Mogaki M; Department of Surgery, Yokosuka Kyosai Hospital, Yokosuka, Japan. Electronic address: moga@yg.so-net.ne.jp.
  • Doi T; Kamakura Breast Cancer Center, Shonan Memorial Hospital, Kamakura, Japan. Electronic address: doi@syonankinenhp.or.jp.
  • Tsugawa K; Department of Breast and Endocrine Surgery, St. Marianna University School of Medicine, Kawasaki, Japan. Electronic address: koitsuga@marianna-u.ac.jp.
  • Ogata H; Department of Breast and Endocrine Surgery, St. Marianna University School of Medicine, Kawasaki, Japan. Electronic address: hogata@tth-japanpost.jp.
  • Ota T; Department of Translational Oncology, St. Marianna University School of Medicine, Kawasaki, Japan. Electronic address: to1@marianna-u.ac.jp.
  • Kosaka Y; Department of Breast and Endocrine Surgery, Kitasato University Hospital, Sagamihara, Japan. Electronic address: y-kosaka@med.kitasato-u.ac.jp.
  • Sengoku N; Department of Breast and Endocrine Surgery, Kitasato University Hospital, Sagamihara, Japan. Electronic address: sengoku@med.kitasato-u.ac.jp.
  • Kuranami M; Department of Breast and Endocrine Surgery, Kitasato University Hospital, Sagamihara, Japan. Electronic address: masaru.kuranami@yamatocity-hosp.jp.
  • Niikura N; Department of Breast and Endocrine Surgery, Tokai University School of Medicine, Isehara, Japan. Electronic address: niikura@is.icc.u-tokai.ac.jp.
  • Saito Y; Department of Breast and Endocrine Surgery, Tokai University School of Medicine, Isehara, Japan. Electronic address: yu-ki@is.icc.u-tokai.ac.jp.
  • Suzuki Y; Department of Breast and Endocrine Surgery, Tokai University School of Medicine, Isehara, Japan. Electronic address: luke-szk@is.icc.u-tokai.ac.jp.
  • Suto A; Department of Breast and Endocrine Surgery, St. Marianna University School of Medicine, Kawasaki, Japan. Electronic address: khksuto@marianna-u.ac.jp.
  • Arioka H; Department of Medical Oncology, Yokohama Rosai Hospital, Yokohama, Japan. Electronic address: arioka@yokohamah.rofuku.go.jp.
  • Chishima T; Department of Oncology, Yokohama City University, Yokohama, Japan. Electronic address: chissy@nifty.com.
  • Ichikawa Y; Department of Oncology, Yokohama City University, Yokohama, Japan. Electronic address: yasu0514@med.yokohama-rcu.ac.jp.
  • Endo I; Department of Gastroenterological Surgery, Yokohama City University, Yokohama, Japan. Electronic address: endoit@med.yokohama-cu.ac.jp.
  • Tokuda Y; Department of Translational Oncology, St. Marianna University School of Medicine, Kawasaki, Japan. Electronic address: tokuda@is.icc.u-tokai.ac.jp.
Breast ; 47: 1-9, 2019 Oct.
Article em En | MEDLINE | ID: mdl-31229857
ABSTRACT

BACKGROUND:

It is important to determine whether anthracycline-containing regimens or taxane-containing regimens are more effective in individual patients. The present study compared the efficacy of six cycles of docetaxel and cyclophosphamide (TC6) with that of three cycles of 5-fluorouracil, epirubicin and cyclophosphamide followed by docetaxel (FEC-D) in Japanese patients with hormone receptor (HR)-negative breast cancer (BC) to identify subtypes requiring anthracycline treatment.

METHODS:

The study included 103 patients with operable HR-negative BC. Of these patients 53 received FEC-D and 50 received TC6. The primary endpoint was pathological complete response (pCR). The secondary endpoints were safety, breast-conserving surgery, disease-free survival (DFS) and overall survival (OS). The predictive factors for each regimen were evaluated.

RESULTS:

Of the 103 patients, 97 completed the study (FEC-D, 50 patients; TC6, 47 patients). The pCR rate was higher with FEC-D (36%) than with TC6 (25.5%); however, the difference was not significant (P = 0.265). TC6 was safer than FEC-D, as the adverse events with docetaxel in the FEC-D regimen were similar to those with the TC6 regimen. Among patients with basal BC, the pCR rate was significantly higher with FEC-D (42.9%) than with TC6 (13.6%; P = 0.033). Among patients with triple-negative breast cancer (TNBC), the DFS and OS were significantly better with FEC-D than with TC6 (P = 0.016 and P = 0.034, respectively).

CONCLUSION:

TC6 was not as effective as FEC-D for treating HR-negative BC, as TC6 was not sufficient to treat TNBC, particularly the basal subtype. Our findings suggest that anthracyclines are better treatment options than taxanes for basal BC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Antraciclinas / Neoplasias de Mama Triplo Negativas / Fluoruracila / Docetaxel Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Antraciclinas / Neoplasias de Mama Triplo Negativas / Fluoruracila / Docetaxel Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article