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Association Between Proton Pump Inhibitors and Metronomic Capecitabine as Salvage Treatment for Patients With Advanced Gastrointestinal Tumors: A Randomized Phase II Trial.
Marchetti, Paolo; Milano, Annalisa; D'Antonio, Chiara; Romiti, Adriana; Falcone, Rosa; Roberto, Michela; Fais, Stefano.
Afiliação
  • Marchetti P; Department of Molecular and Clinical Medicine, Sapienza University of Rome, Rome, Italy.
  • Milano A; Department of Molecular and Clinical Medicine, Sapienza University of Rome, Rome, Italy.
  • D'Antonio C; Department of Molecular and Clinical Medicine, Sapienza University of Rome, Rome, Italy.
  • Romiti A; Department of Molecular and Clinical Medicine, Sapienza University of Rome, Rome, Italy.
  • Falcone R; Department of Molecular and Clinical Medicine, Sapienza University of Rome, Rome, Italy. Electronic address: rsfalcone@libero.it.
  • Roberto M; Department of Molecular and Clinical Medicine, Sapienza University of Rome, Rome, Italy.
  • Fais S; National Institute of Health, Rome, Italy.
Clin Colorectal Cancer ; 15(4): 377-380, 2016 12.
Article em En | MEDLINE | ID: mdl-27435761
ABSTRACT
The acidification of extracellular compartment represents a conceivable mechanism of drug resistance in malignant cells. In addition, it has been reported to drive proliferation and promote invasion and metastasis. Experimental evidence has shown that proton pump inhibitors can counteract tumor acidification and restore sensitivity to anticancer drugs. Moreover, early clinical data have supported the role of proton pump inhibitors in anticancer treatments. Metronomic capecitabine has demonstrated beneficial effects as salvage chemotherapy for heavily pretreated or frail patients with gastrointestinal cancer. The present study (EudraCT Number 2013-001096-20) was aimed at investigating the activity and safety of high-dose rabeprazole in combination with metronomic capecitabine in patients with advanced gastrointestinal cancer refractory to standard treatment. A total of 66 patients will be randomized 11 to receive capecitabine 1500 mg/daily, continuously with or without rabeprazole 1.5 mg/kg twice a day, 3 days a week until disease progression, undue toxicity, or withdrawal of informed consent. The primary endpoint is progression-free survival. The secondary endpoints are clinical benefit, which reflects the proportion of patients with complete response, partial response, and stable disease, and overall survival. Progression-free and overall survival will be evaluated using a log-rank test to determine the effect of rabeprazole independently at the 2-sided α-level of 0.05. Other assessments will include the frequency and severity of adverse events and changes in laboratory parameters to measure the safety, and the pharmacokinetics of capecitabine. The results are expected in 2016.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia de Salvação / Neoplasias Gastrointestinais Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia de Salvação / Neoplasias Gastrointestinais Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article