Literature DB >> 29214667

Effect of ribonucleotide reductase M1 expression on overall survival in patients with pancreatic cancer receiving gemcitabine chemotherapy: A literature-based meta-analysis.

Q L Han1, Y H Zhou1, Y Lyu1, H Yan1, G H Dai1.   

Abstract

WHAT IS KNOWN AND
OBJECTIVE: The prognostic value of ribonucleotide reductase M1 (RRM1) in patients with pancreatic cancer receiving gemcitabine chemotherapy has been evaluated in several studies. However, the conclusions remain controversial.
METHODS: By searching the PubMed and Embase databases, we conducted a meta-analysis to evaluate the prognostic significance of RRM1 expression in patients with pancreatic cancer receiving gemcitabine chemotherapy. Studies were pooled, and the hazard ratio (HR) and its corresponding 95% confidence interval (CI) were calculated.
RESULTS: Nine relevant articles were included for this meta-analysis study. Our results revealed that the high-RRM1 expression patients had significantly poorer overall survival (HR = 1.70, 95% CI = 1.33-2.16, Pheterogeneity  = .061, I2  = 44.8%) and disease-free survival (HR = 1.84, 95% CI = 1.56-2.18, Pheterogeneity  = .669, I2  = 0%) than the low-RRM1 expression patients. Furthermore, a statistically significant association between RRM1 expression and OS was found among both Japanese (HR = 1.80, 95% CI = 1.36-2.37, Pheterogeneity  = .843, I2  = 0%) and American patients (HR = 1.76, 95% CI = 1.60-1.94, Pheterogeneity  = .439, I2  = 0%). WHAT IS NEW AND
CONCLUSION: In conclusion, the expression of RRM1 can be considered a predictor of poor survival in patients with pancreatic cancer receiving gemcitabine chemotherapy. RRM1 expression assessment could provide more detailed information for patients with pancreatic cancer and could be used to optimize therapeutic schemes.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  gemcitabine; meta-analysis; pancreatic cancer; ribonucleotide reductase M1

Mesh:

Substances:

Year:  2017        PMID: 29214667     DOI: 10.1111/jcpt.12655

Source DB:  PubMed          Journal:  J Clin Pharm Ther        ISSN: 0269-4727            Impact factor:   2.512


  7 in total

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Journal:  Diagnostics (Basel)       Date:  2022-01-23

Review 2.  Resistance to Gemcitabine in Pancreatic Ductal Adenocarcinoma: A Physiopathologic and Pharmacologic Review.

Authors:  Tomas Koltai; Stephan Joel Reshkin; Tiago M A Carvalho; Daria Di Molfetta; Maria Raffaella Greco; Khalid Omer Alfarouk; Rosa Angela Cardone
Journal:  Cancers (Basel)       Date:  2022-05-18       Impact factor: 6.575

Review 3.  Chemoresistance in Pancreatic Cancer.

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Journal:  Int J Mol Sci       Date:  2019-09-11       Impact factor: 5.923

4.  RRM1 and ERCC1 as biomarkers in patients with locally advanced and metastatic malignant pleural mesothelioma treated with continuous infusion of low-dose gemcitabine plus cisplatin.

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Journal:  BMC Cancer       Date:  2021-08-05       Impact factor: 4.430

Review 5.  Cancer chemotherapy: insights into cellular and tumor microenvironmental mechanisms of action.

Authors:  Caitlin M Tilsed; Scott A Fisher; Anna K Nowak; Richard A Lake; W Joost Lesterhuis
Journal:  Front Oncol       Date:  2022-07-29       Impact factor: 5.738

6.  Glycogen synthase kinase-3β participates in acquired resistance to gemcitabine in pancreatic cancer.

Authors:  Masahiro Uehara; Takahiro Domoto; Satoshi Takenaka; Dilireba Bolidong; Osamu Takeuchi; Tomoharu Miyashita; Toshinari Minamoto
Journal:  Cancer Sci       Date:  2020-10-12       Impact factor: 6.716

Review 7.  The Current Treatment Paradigm for Pancreatic Ductal Adenocarcinoma and Barriers to Therapeutic Efficacy.

Authors:  Daniel R Principe; Patrick W Underwood; Murray Korc; Jose G Trevino; Hidayatullah G Munshi; Ajay Rana
Journal:  Front Oncol       Date:  2021-07-15       Impact factor: 6.244

  7 in total

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