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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.
Affiliation
  • 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 in 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Anthracyclines / Triple Negative Breast Neoplasms / Fluorouracil / Docetaxel Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Limits: Adult / Aged / Female / Humans / Middle aged Country/Region as subject: Asia Language: En Journal: Breast Journal subject: ENDOCRINOLOGIA / NEOPLASIAS Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Anthracyclines / Triple Negative Breast Neoplasms / Fluorouracil / Docetaxel Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Limits: Adult / Aged / Female / Humans / Middle aged Country/Region as subject: Asia Language: En Journal: Breast Journal subject: ENDOCRINOLOGIA / NEOPLASIAS Year: 2019 Document type: Article