Systemic high-dose intravenous methotrexate in patients with central nervous system metastatic breast cancer.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
01 Nov 2019
Historique:
received: 25 03 2019
accepted: 09 10 2019
entrez: 3 11 2019
pubmed: 5 11 2019
medline: 21 3 2020
Statut: epublish

Résumé

Infusion of high-dose intravenous methotrexate (MTX) has been demonstrating to penetrate the blood-brain barrier. The aim of this present study was to assess the efficacy and safety of high dose MTX in patients with central nervous system (CNS) metastases of breast cancer. Twenty-two patients with CNS metastases treated by MTX (3 g/m2) between April 2004 and October 2009 were enrolled. Clinical response rate, time to progression (TTP), overall survival (OS), and safety were assessed. In terms of brain metastases, 2 patients (9%) achieved a partial response, 10 patients (45%) had disease stabilization, and 10 patients (45%) had disease progression. In others metastatic sites, 7 patients (39%) achieved a disease stabilization, and 11 patients (61%) had disease progression. TTP and OS were 2.1 (95%CI 1.4-2.9) and 6.3 (95%CI 1.8-10) months, respectively. High-dose MTX demonstrated a moderate activity at 3 g/m

Sections du résumé

BACKGROUND BACKGROUND
Infusion of high-dose intravenous methotrexate (MTX) has been demonstrating to penetrate the blood-brain barrier. The aim of this present study was to assess the efficacy and safety of high dose MTX in patients with central nervous system (CNS) metastases of breast cancer.
METHODS METHODS
Twenty-two patients with CNS metastases treated by MTX (3 g/m2) between April 2004 and October 2009 were enrolled. Clinical response rate, time to progression (TTP), overall survival (OS), and safety were assessed.
RESULTS RESULTS
In terms of brain metastases, 2 patients (9%) achieved a partial response, 10 patients (45%) had disease stabilization, and 10 patients (45%) had disease progression. In others metastatic sites, 7 patients (39%) achieved a disease stabilization, and 11 patients (61%) had disease progression. TTP and OS were 2.1 (95%CI 1.4-2.9) and 6.3 (95%CI 1.8-10) months, respectively.
CONCLUSION CONCLUSIONS
High-dose MTX demonstrated a moderate activity at 3 g/m

Identifiants

pubmed: 31675937
doi: 10.1186/s12885-019-6228-6
pii: 10.1186/s12885-019-6228-6
pmc: PMC6823971
doi:

Substances chimiques

Antineoplastic Agents 0
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1029

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Auteurs

F Bazan (F)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

E Dobi (E)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

B Royer (B)

Department of Clinical Pharmacology and Toxicology, University Hospital of Besancon, Besancon, France.

E Curtit (E)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

L Mansi (L)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

N Menneveau (N)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

M J Paillard (MJ)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

G Meynard (G)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France.

C Villanueva (C)

Centre de Cancérologie du grand Montpellier, Montpellier, France.

X Pivot (X)

Centre Paul Strauss, Porte de l'Hopital Strasbourg, Strasbourg, France.

L Chaigneau (L)

Department of Medical Oncology, University Hospital of Besancon, Besancon, France. lchaigneau@chu-besancon.fr.
Department of Medical Oncology, University Hospital Jean Minjoz, Boulevard Alexandre Fleming, F-25000, Besancon, France. lchaigneau@chu-besancon.fr.

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Classifications MeSH