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A phase II trial of prolonged, continuous infusion of low-dose gemcitabine plus cisplatin in patients with advanced malignant pleural mesothelioma
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  • 作者:Oscar Arrieta (1)
    Diego López-Macías (1)
    Víctor-Osvaldo Mendoza-García (1)
    Ludwing Bacon-Fonseca (1)
    Wendy Mu?oz-Monta?o (1)
    Eleazar-Omar Macedo-Pérez (1)
    Saé Mu?iz-Hernández (1)
    Monika Blake-Cerda (1)
    José-Francisco Corona-Cruz (1)
  • 关键词:Mesothelioma ; Prolonged infusion ; Gemcitabine ; Cisplatin
  • 刊名:Cancer Chemotherapy and Pharmacology
  • 出版年:2014
  • 出版时间:May 2014
  • 年:2014
  • 卷:73
  • 期:5
  • 页码:975-982
  • 全文大小:
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  • 作者单位:Oscar Arrieta (1)
    Diego López-Macías (1)
    Víctor-Osvaldo Mendoza-García (1)
    Ludwing Bacon-Fonseca (1)
    Wendy Mu?oz-Monta?o (1)
    Eleazar-Omar Macedo-Pérez (1)
    Saé Mu?iz-Hernández (1)
    Monika Blake-Cerda (1)
    José-Francisco Corona-Cruz (1)

    1. Thoracic Oncology Unit, Experimental Oncology Laboratory, Instituto Nacional de Cancerología (INCan), San Fernando # 22, Col. Sección XVI, Tlalpan, C.P. 14080, Mexico, D.F., Mexico
  • ISSN:1432-0843
文摘
Purpose Low-dose, prolonged infusion of gemcitabine has effects similar to standard doses in several cancers. We evaluated the toxicity and efficacy of low-dose gemcitabine in prolonged infusion plus cisplatin in patients with advanced pleural mesothelioma. Methods Patients with mesothelioma received gemcitabine (250?mg/m2) in a 6-h infusion plus cisplatin (35?mg/m2) on days 1 and 8 every three weeks. We used the modified response evaluation criteria in solid tumours. This study is registered in clinical trials (NCT01869023). Results We included 39 patients; 82.1?% were low risk according to the European Organisation for Research and Treatment of Cancer prognostic group. Partial response was observed in 53.8?% (21/39), stable disease in 33.3?% (13/39) and progression in 12.8?% (5/39). The median progression-free survival was 6.9?months (95?% CI 3.2-0.6?months), and the associated factors were the EORTC risk and histology. The median overall survival was 20.7?months (95?% CI 10.7-0.8?months). The functional, physical and emotional roles and dyspnoea, insomnia and pain symptom scales improved. The most commonly graded 3/4 side effects were neutropenia (24.4?%), lymphopenia (14.6?%), thrombocytopenia (14.7?%) and anaemia (12.2?%). Conclusions Low-dose, prolonged gemcitabine infusion plus cisplatin has acceptable toxicity and high efficacy with improved quality of life, representing an affordable regimen for the low-income population.

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