Literature DB >> 30042274

[Eribulin Administration Methods to Extend the Survival Time of Patients with Advanced or Recurrent Breast Cancer, Consideringthe Relative Dose Intensity, Time to Treatment Failure, Pretreatment Regimen Number, and Tumor Subtype].

Yuki Sunagawa1, Yutaka Mizuno.   

Abstract

Eribulin is evaluated as the only agent that can extend the survival time of patients with advanced or recurrent breast cancer, when used as or after third-line chemotherapy. We retrospectively analyzed the efficacy of eribulin for the treatment of advanced or recurrent breast cancer in our hospital, considering the relative dose intensity(RDI), time to treatment failure (TTF), pretreatment regimen number, and tumor subtype. Of the 36 patients who were treated with eribulin between December 2011 and August 2016, we studied 31 patients who received eribulin as a single agent. The median RDI was 0.75 (range: 0.44-1). The response rate was 22.5%, the disease control rate was 80.6%, and the clinical benefit rate was 45.2%. Overall survival(OS)was not associated with the RDI, previous regimen number, or tumor subtype; however, OS was affected by the TTF. Eribulin is a novel drug that has a different mechanism of action compared with those of conventional anticancer drugs. Therefore, prolonging the duration of eribulin administration may be more important than maintaining the RDI.

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Year:  2018        PMID: 30042274

Source DB:  PubMed          Journal:  Gan To Kagaku Ryoho        ISSN: 0385-0684


  2 in total

1.  Effect of renal function on neutrophil decreases following eribulin administration.

Authors:  Norifumi Suzuki; Hiroyuki Tanaka; Hirotoshi Murakami; Nobumoto Tomioka; Kenichi Watanabe; Masayuki Endo; Masato Takahashi
Journal:  Cancer Rep (Hoboken)       Date:  2020-06-17

2.  A systematic literature review of prognostic factors in patients with HR+/HER2- advanced breast cancer in Japan.

Authors:  Masaya Hattori; Diego Novick; Kana Takaura; Yoshinori Tanizawa; Tsutomu Kawaguchi; Josep Maria Haro; Anna Monistrol-Mula; Akira Onishi; Hiroji Iwata
Journal:  Jpn J Clin Oncol       Date:  2021-10-05       Impact factor: 3.019

  2 in total

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