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Docetaxel increases the risk of severe infections in the treatment of non-small cell lung cancer: a meta-analysis.

作者信息

Du Qingcheng, Jiang Guanming, Li Silu, Liu Yong, Huang Zunnan

机构信息

School of Pharmacy, Guangdong Medical University, Dongguan, Guangdong 523808, China.

Department of Medical Oncology, Dongguan People's Hospital, Dongguan, Guangdong 523018, China.

出版信息

Oncoscience. 2018 Aug 22;5(7-8):220-238. doi: 10.18632/oncoscience.444. eCollection 2018 Jul.


DOI:10.18632/oncoscience.444
PMID:30234144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6142895/
Abstract

The purpose of this study was to determine whether docetaxel increases the risk of severe infections in patients with non-small cell lung cancer. A thorough literature search of the PubMed, EMBASE and Cochrane Central Register of Controlled Trials databases was performed (up to February 28, 2017) without any language restrictions. In addition, we searched the www.clinicaltrials.gov website and checked each reference listed in the included studies, relevant reviews and guidelines. We also included randomized controlled trials that reported severe infections in patients with non-small cell lung cancer who were administered docetaxel. A meta- analysis was conducted using relative risk and random effects models in Stata 14.0 software. Sensitivity analysis and meta-regression were performed using Stata 14.0 software. We identified 354 records from the initial search, and this systematic review ultimately included 43 trials with 12,447 participants. The results of our meta- analysis showed that docetaxel increased the risk of severe infections [relative risk: 2.10, 95% confidence interval: 1.51-2.93, = 69.6%, = 0.000]. Meta-regression analysis indicated that the type of intervention was a major source of heterogeneity. Our systematic review and meta-analysis suggest that docetaxel is associated with the risk of severe infections.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/5b96c9b2477a/oncoscience-05-220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/913a9b1a043e/oncoscience-05-220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/9e48deb16f35/oncoscience-05-220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/ae0abbb1414e/oncoscience-05-220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/5b96c9b2477a/oncoscience-05-220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/913a9b1a043e/oncoscience-05-220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/9e48deb16f35/oncoscience-05-220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/ae0abbb1414e/oncoscience-05-220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89c/6142895/5b96c9b2477a/oncoscience-05-220-g004.jpg

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Docetaxel increases the risk of severe infections in the treatment of non-small cell lung cancer: a meta-analysis.

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本文引用的文献

[1]
Non-Small Cell Lung Cancer, Version 5.2017, NCCN Clinical Practice Guidelines in Oncology.

J Natl Compr Canc Netw. 2017-4

[2]
Hyperprogressors after Immunotherapy: Analysis of Genomic Alterations Associated with Accelerated Growth Rate.

Clin Cancer Res. 2017-3-28

[3]
PD-1 inhibitors increase the incidence and risk of pneumonitis in cancer patients in a dose-independent manner: a meta-analysis.

Sci Rep. 2017-3-8

[4]
Randomized Phase III Study of Docetaxel Plus Cisplatin Versus Pemetrexed Plus Cisplatin as First-line Treatment of Nonsquamous Non-Small-cell Lung Cancer: A TRAIL Trial.

Clin Lung Cancer. 2017-7

[5]
Clinicians' Expectations of the Benefits and Harms of Treatments, Screening, and Tests: A Systematic Review.

JAMA Intern Med. 2017-3-1

[6]
Atezolizumab versus docetaxel in patients with previously treated non-small-cell lung cancer (OAK): a phase 3, open-label, multicentre randomised controlled trial.

Lancet. 2017-1-21

[7]
Second-line Erlotinib or Intermittent Erlotinib plus Docetaxel in Male Ex-smokers with Squamous NSCLC: The TALISMAN Randomized Trial.

Anticancer Res. 2016-12

[8]
Hyperprogressive Disease Is a New Pattern of Progression in Cancer Patients Treated by Anti-PD-1/PD-L1.

Clin Cancer Res. 2016-11-8

[9]
Economic sustainability of anti-PD-1 agents nivolumab and pembrolizumab in cancer patients: Recent insights and future challenges.

Cancer Treat Rev. 2016-6-7

[10]
Classification and Pathology of Lung Cancer.

Surg Oncol Clin N Am. 2016-7

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