Literature DB >> 14720348

Chemotherapy regimens in advanced non-small-cell lung cancer: recent randomized trials.

Chandra P Belani1.   

Abstract

Since the 1980s, cisplatin therapy for advanced non-small-cell lung cancer (NSCLC) has shown improvement in patient outcome with respect to overall survival. In the past decade, several new agents, such as the taxanes (paclitaxel and docetaxel), gemcitabine, vinorelbine, and irinotecan, have also shown promising single-agent efficacy in the treatment of advanced NSCLC. Superior efficacy was observed when these 5 agents were used in combination with cisplatin as compared to cisplatin alone for treatment of patients with NSCLC. The toxicity profiles of these 5 agents were found to be largely nonoverlapping with cisplatin. The results of recent randomized trials with different cisplatin-based chemotherapy regimens have shown that platinum-based therapy is still the mainstay for treatment of NSCLC; however, it appears that a chemotherapy efficacy plateau has been reached. Moreover, it has also been shown that for patients unable to tolerate cisplatin, nonplatinum doublets consisting of gemcitabine with either taxanes or vinorelbine are equivalent in efficacy and can be alternatives for first-line treatment of advanced NSCLC. Thus, the development of new and novel strategies is essential for treatment of NSCLC patients. Ongoing trials with vaccines, signal transduction modulators, antiangiogenic agents, and gene therapy in combination with chemotherapy

Entities:  

Year:  2002        PMID: 14720348     DOI: 10.3816/clc.2002.s.001

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  2 in total

1.  Hypoxia-induced autophagy mediates cisplatin resistance in lung cancer cells.

Authors:  Hui-Mei Wu; Zi-Feng Jiang; Pei-Shan Ding; Li-Jie Shao; Rong-Yu Liu
Journal:  Sci Rep       Date:  2015-07-23       Impact factor: 4.379

2.  Acetyl-11-keto-β-boswellic acid enhances the cisplatin sensitivity of non-small cell lung cancer cells through cell cycle arrest, apoptosis induction, and autophagy suppression via p21-dependent signaling pathway.

Authors:  Minghe Lv; Xibing Zhuang; Qi Zhang; Yunfeng Cheng; Duojiao Wu; Xiangdong Wang; Tiankui Qiao
Journal:  Cell Biol Toxicol       Date:  2020-06-20       Impact factor: 6.691

  2 in total

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