| Literature DB >> 26566626 |
Giandomenico Roviello1, Karol Polom2, Roberto Petrioli3, Luigi Marano4, Daniele Marrelli5, Giovanni Paganini6, Vinno Savelli7, Daniele Generali8, Lorenzo De Franco5, Andrea Ravelli9, Franco Roviello2.
Abstract
Gastric cancer (GC) is the second leading cause of cancer-related death, and despite having improved treatment modalities over the last decade, for most patients, only modest improvements have been seen in overall survival. Recent progress in understanding the molecular biology of GC and the related signaling pathways offers, from the clinical point of view, promising advances for selected groups of patients. In the past, targeted therapies have significantly impacted the treatment strategy of several common solid tumors such as breast, colorectal, and lung cancers. Unfortunately, translational and clinical research shows fewer encouraging targeted treatments with regards to the GC. To date, only two monoclonal antibodies (mAb), named trastuzumab and ramucirumab, are approved for the treatment of advanced GC, suggesting that in GC, maybe more than in other cancers, effective targeted therapy requires patient selection based on precise predictive molecular biomarkers. The aim of this review is to summarize the available data on the clinical advantages offered by the use of mAbs in the treatment of advanced/metastatic GC. Future perspective is also discussed.Entities:
Keywords: Bevacizumab; Gastric cancer; Ramucirumab; Target therapy; Trastuzumab
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Year: 2015 PMID: 26566626 DOI: 10.1007/s13277-015-4408-9
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283