Literature DB >> 20176443

Advanced gastric cancer--slow but steady progress.

Derek G Power1, David P Kelsen, Manish A Shah.   

Abstract

Progress in gastric cancer has been slow, but steady. Historically, patients commonly presented with significant disease related co-morbidity and received treatment of marginal benefit but unfortunately associated with significant toxicity. Today there is no universally accepted reference standard chemotherapy for this disease. However, there is reason for optimism. Meta-analyses of randomized trials have shown a benefit for first-line combination chemotherapy. Current three drug chemotherapy regimens remain toxic, though perhaps less so than previously, and can result in a small but significant survival advantage in carefully chosen patients. Incremental improvements have been observed in both treatment-related toxicity and survival after first-line therapy. More patients are candidates for chemotherapy beyond progression with first-line therapy and response rates with second-line regimens are similar to those seen in other solid tumor malignancies. Although there is no randomized data to support its use second-line treatment should be considered in appropriate patients. Even before the integration of targeted therapies in the treatment of gastric cancer, it was evident that survival for more than 2 years is possible in a subset of patients and large retrospective studies have highlighted clinicopathologic factors associated with improved survival. Presently, with the addition of targeted therapy, especially anti-angiogenic and anti-Her2 therapy, and a better understanding of the biology of the disease, perhaps a sense of optimism should indeed suppress the nihilism commonly associated with this disease. Copyright 2010. Published by Elsevier Ltd.

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Year:  2010        PMID: 20176443     DOI: 10.1016/j.ctrv.2010.01.005

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  76 in total

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8.  Epithelial cell-derived periostin functions as a tumor suppressor in gastric cancer through stabilizing p53 and E-cadherin proteins via the Rb/E2F1/p14ARF/Mdm2 signaling pathway.

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Journal:  Med Oncol       Date:  2013-03-27       Impact factor: 3.064

10.  Phase II study of oxaliplatin, irinotecan and S-1 therapy in patients with advanced gastric cancer: the Korean Cancer Study Group ST14-11.

Authors:  Hyeong Su Kim; Min-Hee Ryu; Dae Young Zang; Sook Ryun Park; Boram Han; Won Ki Kang; Sun Young Rha; Minkyu Jung; Jin-Soo Kim; Byung Woog Kang; Kyung-Hee Lee; Sang-Young Rho; Jung Han Kim; Kab Choong Kim; Ji Woong Cho; Dae Ro Choi; Hyun Lim; Ho Suk Kang; Jae Seung Soh; Min-Jeong Kim; Jinwon Seo; Yoon-Koo Kang
Journal:  Gastric Cancer       Date:  2018-01-25       Impact factor: 7.370

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