Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.

<h4>Background</h4>The response to cytotoxic chemotherapy varies greatly in patients with advanced non-small cell lung cancer (NSCLC), and molecular markers may be useful in determining a preferable therapeutic approach for individual patients. This retrospective study was performed to e...

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Autores principales: Xiaopeng Dong, Yingtao Hao, Yucheng Wei, Qiuwei Yin, Jiajun Du, Xiaogang Zhao
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Publicado: Public Library of Science (PLoS) 2014
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spelling oai:doaj.org-article:5191222fd2fd4354ac4b64cd904889922021-11-18T08:27:16ZResponse to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.1932-620310.1371/journal.pone.0092320https://doaj.org/article/5191222fd2fd4354ac4b64cd904889922014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24647522/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>The response to cytotoxic chemotherapy varies greatly in patients with advanced non-small cell lung cancer (NSCLC), and molecular markers may be useful in determining a preferable therapeutic approach for individual patients. This retrospective study was performed to evaluate the predictive value of ribonucleotide reductase regulatory subunit M1 (RRM1) on the therapeutic efficacy of platinum-based chemotherapy in patients with NSCLC.<h4>Methods</h4>Patients with advanced NSCLC who received platinum doublet chemotherapy (n = 229) were included in this retrospective study, and their clinical outcomes were analyzed according to RRM1 expression.<h4>Results</h4>In patients receiving gemcitabine-based therapy, the disease control rate (DCR) and progression-free survival (PFS) of patients with RRM1-negative tumors were significantly higher than in patients with RRMI-positive tumors (P = 0.041 and P = 0.01, respectively), and multivariate analysis showed that RRM1 expression was an independent prognostic factor (P = 0.013). No similar differences were found in patients receiving docetaxel- or vinorelbine-based therapy. In RRM1-positive patients, the DCRs for docetaxel and vinorelbine were higher than for gemcitabine (P = 0.047 and P = 0.047, respectively), and docetaxel and vinorelbine showed a longer PFS than gemcitabine-based chemotherapy (P = 0.012 and P = 0.007). No similar differences were found among patients with RRM1-negative tumors.<h4>Conclusions</h4>Negative RRM1 expression in advanced NSCLC is associated with a higher response rate to gemcitabine-based chemotherapy. In patients with RRM1-positive tumors, docetaxel and vinorelbine showed a higher therapeutic efficacy than gemcitabine-based therapy. Additional prospective studies are needed to investigate the predictive meaning of RRM1 in the response to chemotherapy.Xiaopeng DongYingtao HaoYucheng WeiQiuwei YinJiajun DuXiaogang ZhaoPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 3, p e92320 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xiaopeng Dong
Yingtao Hao
Yucheng Wei
Qiuwei Yin
Jiajun Du
Xiaogang Zhao
Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.
description <h4>Background</h4>The response to cytotoxic chemotherapy varies greatly in patients with advanced non-small cell lung cancer (NSCLC), and molecular markers may be useful in determining a preferable therapeutic approach for individual patients. This retrospective study was performed to evaluate the predictive value of ribonucleotide reductase regulatory subunit M1 (RRM1) on the therapeutic efficacy of platinum-based chemotherapy in patients with NSCLC.<h4>Methods</h4>Patients with advanced NSCLC who received platinum doublet chemotherapy (n = 229) were included in this retrospective study, and their clinical outcomes were analyzed according to RRM1 expression.<h4>Results</h4>In patients receiving gemcitabine-based therapy, the disease control rate (DCR) and progression-free survival (PFS) of patients with RRM1-negative tumors were significantly higher than in patients with RRMI-positive tumors (P = 0.041 and P = 0.01, respectively), and multivariate analysis showed that RRM1 expression was an independent prognostic factor (P = 0.013). No similar differences were found in patients receiving docetaxel- or vinorelbine-based therapy. In RRM1-positive patients, the DCRs for docetaxel and vinorelbine were higher than for gemcitabine (P = 0.047 and P = 0.047, respectively), and docetaxel and vinorelbine showed a longer PFS than gemcitabine-based chemotherapy (P = 0.012 and P = 0.007). No similar differences were found among patients with RRM1-negative tumors.<h4>Conclusions</h4>Negative RRM1 expression in advanced NSCLC is associated with a higher response rate to gemcitabine-based chemotherapy. In patients with RRM1-positive tumors, docetaxel and vinorelbine showed a higher therapeutic efficacy than gemcitabine-based therapy. Additional prospective studies are needed to investigate the predictive meaning of RRM1 in the response to chemotherapy.
format article
author Xiaopeng Dong
Yingtao Hao
Yucheng Wei
Qiuwei Yin
Jiajun Du
Xiaogang Zhao
author_facet Xiaopeng Dong
Yingtao Hao
Yucheng Wei
Qiuwei Yin
Jiajun Du
Xiaogang Zhao
author_sort Xiaopeng Dong
title Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.
title_short Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.
title_full Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.
title_fullStr Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.
title_full_unstemmed Response to first-line chemotherapy in patients with non-small cell lung cancer according to RRM1 expression.
title_sort response to first-line chemotherapy in patients with non-small cell lung cancer according to rrm1 expression.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/5191222fd2fd4354ac4b64cd90488992
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