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Intrathecal liposomal cytarabine plus systemic therapy versus systemic chemotherapy alone for newly diagnosed leptomeningeal metastasis from breast cancer.
Le Rhun, Emilie; Wallet, Jennifer; Mailliez, Audrey; Le Deley, Marie Cecile; Rodrigues, Isabelle; Boulanger, Thomas; Lorgis, Veronique; Barrière, Jerome; Robin, Yves Marie; Weller, Michael; Bonneterre, Jacques.
Afiliação
  • Le Rhun E; University of Lille, INSERM, Lille, France.
  • Wallet J; Neuro-oncology, General and Stereotaxic Neurosurgery service, University Hospital of Lille, Lille, France.
  • Mailliez A; Breast Cancer Department, Oscar Lambret Center, Lille, France.
  • Le Deley MC; Department of Neurology & Brain Tumor Center, University Hospital and University of Zurich, Zurich, Switzerland.
  • Rodrigues I; Biostatistics Unit, Oscar Lambret Center, Lille, France.
  • Boulanger T; Neuro-oncology, General and Stereotaxic Neurosurgery service, University Hospital of Lille, Lille, France.
  • Lorgis V; Biostatistics Unit, Oscar Lambret Center, Lille, France.
  • Barrière J; Center for Research in Epidemiology and Population Health (CESP, INSERM), Paris-Sud, Paris-Saclay University, Villejuif, France.
  • Robin YM; Neuro-oncology, General and Stereotaxic Neurosurgery service, University Hospital of Lille, Lille, France.
  • Weller M; Imaging Department, Oscar Lambret Center, Lille, France.
  • Bonneterre J; Department of Medical Oncology, Georges François Leclerc Center, Dijon, France.
Neuro Oncol ; 22(4): 524-538, 2020 04 15.
Article em En | MEDLINE | ID: mdl-31637444
BACKGROUND: DEPOSEIN (NCT01645839) was a randomized open-label phase III study to explore the role of intrathecal chemotherapy in patients with newly diagnosed leptomeningeal metastasis (LM), a common manifestation of breast cancer. METHODS: Patients with newly diagnosed LM defined by tumor cells in the cerebrospinal fluid or combination of clinical and neuroimaging signs of LM were randomized to receive systemic therapy alone (control group) or systemic therapy plus intrathecal liposomal cytarabine (experimental group). Progression-free survival related to LM (LM-PFS) was the primary endpoint. RESULTS: Thirty-seven and 36 patients were assigned to the control and the experimental groups. Median number of liposomal cytarabine injections in the experimental group was 5 (range 1-20). Focal radiotherapy was performed in 6 (16%) and 3 (8%) patients in the control and experimental groups. In the intent-to-treat population, median LM-PFS was 2.2 months (95% CI: 1.3-3.1) in the control versus 3.8 months (95% CI: 2.3-6.8) in the experimental group (hazard ratio 0.61, 95% CI: 0.38-0.98) (P = 0.04). Seventy-one patients have died. Median overall survival was 4.0 months (95% CI: 2.2-6.3) in the control versus 7.3 months (95% CI: 3.9-9.6) in the experimental group (hazard ratio 0.85, 95% CI: 0.53-1.36) (P = 0.51). Serious adverse events were reported in 22 and 30 patients, respectively. Quality of life until progression did not differ between groups. CONCLUSION: The addition of intrathecal liposomal cytarabine to systemic treatment improves LM-related PFS. Confirmatory trials with optimized patient selection criteria and more active drugs may be required to demonstrate a survival benefit from intrathecal pharmacotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Carcinomatose Meníngea Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Carcinomatose Meníngea Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article