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Explorative Analysis of Low-Dose Metronomic Chemotherapy with Cyclophosphamide and Methotrexate in a Cohort of Metastatic Breast Cancer Patients.
Krajnak, Slavomir; Battista, Marco; Brenner, Walburgis; Almstedt, Katrin; Elger, Tania; Heimes, Anne-Sophie; Hasenburg, Annette; Schmidt, Marcus.
Afiliação
  • Krajnak S; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Battista M; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Brenner W; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Almstedt K; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Elger T; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Heimes AS; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Hasenburg A; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
  • Schmidt M; Department of Gynecology and Obstetrics, University Medical Center Mainz, Mainz, Germany.
Breast Care (Basel) ; 13(4): 272-276, 2018 Aug.
Article em En | MEDLINE | ID: mdl-30319329
ABSTRACT

BACKGROUND:

Low-dose metronomic chemotherapy (LDMC) is increasingly used in metastatic breast cancer (MBC). In this retrospective analysis, we examined the therapeutic effects and side effects of LDMC in a cohort of MBC patients.

METHODS:

Patients with MBC were included when LDMC with oral cyclophosphamide (CTX) and methotrexate (MTX) was administered between 2009 and 2015. The primary endpoint was disease control rate (DCR) ≥ 24 weeks after the start of LDMC. Secondary endpoints were duration of progression-free survival (PFS), rates of discontinuation due to side effects, and DCR with regard to subgroups.

RESULTS:

Retrospective data of 35 patients were available for this analysis. 31% patients achieved DCR. The median PFS was 12 weeks. 9% of patients discontinued LDMC due to adverse events. DCR was 37% in the first 2 lines and 25% in further lines of therapy. 22% of patients with multiple metastases and 35% with ≤2 different metastatic sites achieved DCR. DCR was achieved in 33% of hormone receptor(HR)-positive patients and 27% of HR-negative patients.

CONCLUSION:

The DCR of 31% is in line with the results of previous phase II studies. LDMC was well tolerated. Subgroup analysis was not able to identify a group in which LDMC was more efficient.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Breast Care (Basel) Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Breast Care (Basel) Ano de publicação: 2018 Tipo de documento: Article