نتایج جستجو برای: regorafenib

تعداد نتایج: 831  

2017
Erika Martinelli Vincenzo Sforza Claudia Cardone Anna Capasso Anna Nappi Giulia Martini Stefania Napolitano Anna Maria Rachiglio Nicola Normanno Salvatore Cappabianca Alfonso Reginelli Maurizio Di Bisceglie Tiziana Pia Latiano Evaristo Maiello Michele Orditura Fernando De Vita Floriana Morgillo Fortunato Ciardiello Teresa Troiani

Background To investigate the potential predictors of response to regorafenib, in chemorefractory metastatic colorectal cancer (mCRC) patients with long-term efficacy from regorafenib treatment. Methods Retrospective, single institution analysis of patients with chemorefractory mCRC treated with regorafenib, in clinical practice setting. 123 patients were treated and stratified into two group...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2016
Jens Zierle Rosi Bissinger Ghada Bouguerra Salem Abbès Florian Lang

BACKGROUND/AIMS The multikinase inhibitor regorafenib is utilized for the treatment of malignancy. The substance is effective in part by triggering suicidal death or apoptosis of tumor cells. Side effects of regorafenib include anemia. At least in theory, regorafenib induced anemia could result from stimulated suicidal erythrocyte death or eryptosis, characterized by cell shrinkage and cell mem...

2017
Chun-Nan Yeh Yu-Chan Chang Yeu Su Dennis Shin-Shian Hsu Chi-Tung Cheng Ren-Chin Wu Yi-Hsiu Chung Kun-Chun Chiang Ta-Sen Yeh Meng-Lun Lu Chun-Yu Liu Peter Mu-Hsin Chang Ming-Han Chen Chi-Ying F. Huang Michael Hsiao Ming-Huang Chen

Intrahepatic cholangiocarcinoma (CCA) is an aggressive cancer that lacks an effective targeted therapy. Here, we assessed the therapeutic efficacy of regorafenib in CCA, as well as elucidated its underlying mechanism. We first demonstrated that regorafenib not only inhibited growth but also induced apoptosis in human CCA cells. Subsequently, we used in silico approaches to identify MALT1 (Mucos...

2016
Hironori Kitade Azusa Hiromasa-Yamasaki Kengo Hokkoku Mitsue Mori Michio Watanabe Masuo Nakai Seiji Yano

BACKGROUND Regorafenib and its metabolites may inhibit the activities of several CYP or UDP-glucuronosyltransferase isoforms, including that of CYP2C9. Therefore, pharmacological agents that are CYP2C9 substrates may show elevated circulating levels and enhanced drug efficacy when concurrently used with regorafenib. Previous studies showed that the area under the plasma concentration-time curve...

2015
Estelle Daudigeos-Dubus Ludivine Le Dret Claudia Lanvers-Kaminsky Olivia Bawa Paule Opolon Albane Vievard Irène Villa Mélanie Pagès Jacques Bosq Gilles Vassal Dieter Zopf Birgit Geoerger Joseph Najbauer

The multikinase inhibitor regorafenib (BAY 73-4506) exerts both anti-angiogenic and anti-tumorigenic activity in adult solid malignancies mainly advanced colorectal cancer and gastrointestinal stromal tumors. We intended to explore preclinically the potential of regorafenib against solid pediatric malignancies alone and in combination with anticancer agents to guide the pediatric development pl...

Journal: :American journal of hypertension 2012
Nilka de Jesus-Gonzalez Emily Robinson Radostin Penchev Margaret von Mehren Michael C Heinrich William Tap Qian Wang George Demetri Suzanne George Benjamin D Humphreys

BACKGROUND Hypertension is a toxicity of antiangiogenic therapies and a possible biomarker that identifies patients with superior cancer outcomes. Understanding its mechanism will aid in treatment and could lead to the development of other biomarkers for predicting toxicity and anticancer efficacy. Recent evidence implicates nitric oxide (NO) suppression and endothelin-1 (ET-1) stimulation as p...

Journal: :Experimental oncology 2014
B Yilmaz Y Kemal F Teker E Kut G Demirag I Yucel

Gastrointestinal stromal tumors (GISTs) are uncommon tumors of the gastrointestinal (GI) tract. Regorafenib is a new multikinase inhibitor and is approved for the treatment of GISTs in patients who develop resistance to imatinib and sunitinib. The most common drug-related adverse events with regorafenib are hypertension, hand-foot skin reactions, and diarrhea. Grade IV hypertensive side effect ...

2015
Hiroki Kitamoto Hironaga Satake Yukimasa Hatachi Tetsuro Inokuma Akihito Tsuji

Regorafenib, a multi-targeted tyrosine kinase inhibitor (TKI), is used in metastatic colorectal cancer (mCRC) and gastrointestinal stromal tumors (GIST) for salvageline therapy. From clinical trials, the most commonly reported adverse events of regorafenib are hand-foot skin reactions, fatigue, diarrhea and hypertension. We report two cases of hyperammonemic encephalopathy induced by regorafeni...

2016
Hao-Wei Teng Man-Hsin Hung Li-Ju Chen Mao-Ju Chang Feng-Shu Hsieh Ming-Hsien Tsai Jui-Wen Huang Chih-Lung Lin Hsiang-Wen Tseng Zong-Keng Kuo Jeng-Kai Jiang Shung-Haur Yang Chung-Wai Shiau Kuen-Feng Chen

Protein tyrosine phosphatase 1B (PTP1B) is known to promote the pathogenesis of diabetes and obesity by negatively regulating insulin and leptin pathways, but its role associated with colon carcinogenesis is still under debate. In this study, we demonstrated the oncogenic role of PTP1B in promoting colon carcinogenesis and predicting worse clinical outcomes in CRC patients. By co-immunoprecipit...

2016
Axel Grothey Gerald Prager Jean-Yves Blay

The European Society for Medical Oncology (ESMO) Congress was held in Copenhagen, Denmark from 7th–11th October 2016. The use of the promiscuous multikinase inhibitor regorafenib (Stivarga®, BAY 73-4506) in the treatment of cancers of the gastrointestinal (GI) tract was strongly featured at this meeting. Regorafenib targets multiple kinases involved in oncogenesis and angiogenesis, and is US Fo...

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