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

被引:0
|
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
来源
关键词
D O I
暂无
中图分类号
学科分类号
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.
引用
收藏
页码:535 / 542
页数:7
相关论文
共 50 条
  • [1] Germline polymorphisms as biomarkers of tumor response in colorectal cancer patients treated with anti-EGFR monoclonal antibodies: a systematic review and meta-analysis
    Morgen, E. K.
    Lenz, H-J
    Jonker, D. J.
    Tu, D.
    Milano, G.
    Graziano, F.
    Zalcberg, J.
    Karapetis, C. S.
    Dobrovic, A.
    O'Callaghan, C. J.
    Liu, G.
    PHARMACOGENOMICS JOURNAL, 2017, 17 (06): : 535 - 542
  • [2] Infectious complications in cancer patients treated with anti-EGFR monoclonal antibodies cetuximab and panitumumab: A systematic review and meta-analysis
    Funakoshi, Tomohiro
    Suzuki, Maya
    Tamura, Kazuo
    CANCER TREATMENT REVIEWS, 2014, 40 (10) : 1221 - 1229
  • [3] Optimal use of anti-EGFR monoclonal antibodies for patients with advanced colorectal cancer: a meta-analysis
    van Helden, E. J.
    van Oordt, C. W. Menke-van der Houven
    Heymans, M. W.
    Ket, J. C. F.
    van den Oord, R.
    Verheul, H. M. W.
    CANCER AND METASTASIS REVIEWS, 2017, 36 (02) : 395 - 406
  • [4] Optimal use of anti-EGFR monoclonal antibodies for patients with advanced colorectal cancer: a meta-analysis
    E. J. van Helden
    C. W. Menke-van der Houven van Oordt
    M. W. Heymans
    J. C. F. Ket
    R. van den Oord
    H. M. W. Verheul
    Cancer and Metastasis Reviews, 2017, 36 : 395 - 406
  • [5] Anti-EGFR Monoclonal Antibodies in Advanced Biliary Tract Cancer: A Systematic Review and Meta-analysis
    Rizzo, Alessandro
    Frega, Giorgio
    Ricci, Angela Dalia
    Palloni, Andrea
    Abbati, Francesca
    De Lorenzo, Stefania
    Deserti, Marzia
    Tavolari, Simona
    Brandi, Giovanni
    IN VIVO, 2020, 34 (02): : 479 - 488
  • [6] ANTI-EGFR MONOCLONAL ANTIBODIES AND RISK OF SEVERE HAEMATOLOGICAL ADVERSE EVENTS IN CANCER PATIENTS: A SYSTEMATIC REVIEW AND META-ANALYSIS
    Miroddi, M.
    Pellegrino, P.
    Sterrantino, C.
    Caridi, L.
    Rollo, A.
    Perrotta, C.
    Calapai, G.
    Radice, S.
    Clementi, E.
    CLINICAL THERAPEUTICS, 2015, 37 (08) : E83 - E83
  • [7] ANTI-EGFR MONOCLONAL ANTIBODIES INCREASE THE RISK OF PULMONARY EMBOLISM IN CANCER PATIENTS. A SYSTEMATIC REVIEW AND META-ANALYSIS
    Miroddi, M.
    Sterrantino, C.
    Conti, V.
    Rollo, A.
    Calapai, G.
    CLINICAL THERAPEUTICS, 2015, 37 (08) : E83 - E83
  • [8] ANTI-EGFR MONOCLONAL ANTIBODIES INCREASE THE RISK OF SEVERE GASTROINTESTINAL ADVERSE EVENTS IN CANCER PATIENTS: A SYSTEMATIC REVIEW AND META-ANALYSIS
    Sterrantino, C.
    Miroddi, M.
    Conti, V.
    Caridi, L.
    Venegoni, M.
    Calapai, G.
    CLINICAL THERAPEUTICS, 2015, 37 (08) : E83 - E84
  • [9] MicroRNA Signature in Metastatic Colorectal Cancer Patients Treated With Anti-EGFR Monoclonal Antibodies
    Cappuzzo, Federico
    Sacconi, Andrea
    Landi, Lorenza
    Ludovini, Vienna
    Biagioni, Francesca
    D'Incecco, Armida
    Capodanno, Alessandra
    Salvini, Jessica
    Corgna, Enrichetta
    Cupini, Samanta
    Barbara, Cecilia
    Fontanini, Gabriella
    Crino, Lucio
    Blandino, Giovanni
    CLINICAL COLORECTAL CANCER, 2014, 13 (01) : 37 - U62
  • [10] Hypomagnesemia and clinical benefits of anti-EGFR monoclonal antibodies in wild-type KRAS metastatic colorectal cancer: a systematic review and meta-analysis
    Hsieh, Meng-Chiao
    Wu, Chun-Feng
    Chen, Chun-Wei
    Shi, Chung-Sheng
    Huang, Wen-Shih
    Kuan, Feng-Che
    SCIENTIFIC REPORTS, 2018, 8