Germline polymorphisms as biomarkers of tumor response in colorectal cancer patients treated with anti-EGFR monoclonal antibodies: a systematic review and meta-analysis

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作者
E K Morgen
H-J Lenz
D J Jonker
D Tu
G Milano
F Graziano
J Zalcberg
C S Karapetis
A Dobrovic
C J O’Callaghan
G Liu
机构
[1] Mount Sinai Hospital,Department of Pathology and Laboratory Medicine
[2] University of Toronto,Department of Pathobiology and Laboratory Medicine
[3] USC/Norris Comprehensive Cancer Center,Division of Medical Oncology
[4] The Ottawa Hospital Research Institute,Department of Pathology
[5] University of Ottawa,Departments of Medicine and Medical Biophysics
[6] Canadian Cancer Trials Group,undefined
[7] Queen’s University,undefined
[8] Laboratoire d'Oncopharmacologie EA 3836,undefined
[9] Centre Antoine Lacassagne,undefined
[10] Azienda “Ospedali Riuniti Marche Nord”,undefined
[11] Cancer Research Program,undefined
[12] School of Public Health and Preventive Medicine,undefined
[13] Faculty of Medicine,undefined
[14] Monash University,undefined
[15] Flinders University and Flinders Medical Centre,undefined
[16] Translational Genomics and Epigenomics Laboratory,undefined
[17] Olivia Newton-John Cancer Research Institute,undefined
[18] School of Cancer Medicine,undefined
[19] La Trobe University,undefined
[20] University of Melbourne,undefined
[21] Canadian Cancer Trials Group,undefined
[22] Queen’s University,undefined
[23] University of Toronto,undefined
[24] Dalla Lana School of Public Health,undefined
[25] University of Toronto,undefined
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摘要
Studies of germline polymorphisms as predictors of tumor response to anti-epidermal growth factor receptor (EGFR) monoclonal antibody agents in metastatic colorectal cancer have reported inconsistent results. We performed a systematic review of studies from 1990 to September 2015, followed by random-effects meta-analyses for polymorphisms examined in at least three studies. Of 87 studies, 40 passed the criteria for systematic review and 23 for meta-analysis. The polymorphisms suitable for meta-analysis were CCND1 (rs17852153), COX2 (rs20417), EGF (rs4444903), EGFR (rs712829, rs11543848, 3′UTR CA repeat), FCGR2A (rs1801274), FCGR3A (rs396991), IL8 (rs4073), KRAS (rs61764370) and VEGFA (rs3025039). Meta-analysis yielded nominal significance (at α=0.05) for rs4444903 and rs11543848, but showed no significant results after multiple testing correction; this was unchanged by sensitivity analyses to address subgroups, funnel-plot asymmetries, and study quality. This highlights a tendency for lack of replication in the face of initial positive results, and possibly the unsuitability of relying on tumor response as a surrogate marker in this setting.
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页码:535 / 542
页数:7
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