Prognostic value of EGFR and KRAS in resected non-small cell lung cancer: a systematic review and meta-analysis

被引:28
作者
Zhang, Shi-Ming [1 ]
Zhu, Qing-Ge [1 ]
Ding, Xiao-Xiao [1 ]
Lin, Song [1 ]
Zhao, Jing [1 ]
Guan, Lei [1 ]
Li, Ting [1 ]
He, Bing [1 ]
Zhang, Hu-Qin [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Key Lab Biomed Informat Engn, Minist Educ, 28 Xianning West Rd, Xian 710049, Shaanxi, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金; 中国博士后科学基金;
关键词
EGFR mutations; KRAS mutations; meta-analysis; non-small cell lung cancer; prognosis; resected; GROWTH-FACTOR RECEPTOR; POST-RECURRENCE SURVIVAL; MUTATION STATUS; GENE-MUTATIONS; ADJUVANT CHEMOTHERAPY; CLINICAL-FEATURES; JAPANESE PATIENTS; KI-67; EXPRESSION; ADENOCARCINOMA; IMPACT;
D O I
10.2147/CMAR.S167578
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The prognostic value of EGFR and KRAS mutations in resected non-small cell lung cancer (NSCLC) has been reported. However, conflicting results were reported in these studies. The effect of mutations in these two genes in resected NSCLC remains controversial. Methods: We searched Internet databases for studies reporting disease-free survival (DFS) and overall survival (OS) in resected NSCLC patients with EGFR or KRAS mutations. A meta-analysis calculating the pooled hazard ratio (HR) for DFS and OS was used to measure the association of EGFR or KRAS mutations with the prognosis of patients after surgery. Results: A total of 9,635 patients from 32 studies were included in this analysis. The combined HR for EGFR mutations on DFS was 0.77 (95% CI 0.66-0.90, p=0.001) and on OS was 0.72 (95% CI 0.66-0.80, p<0.00001). In addition, the combined HR for KRAS mutations on DFS was 1.5 (95% CI 1.15-1.96, p=0.002) and on OS was 1.49 (95% CI 1.28-1.73, p<0.00001). Sensitivity analysis, subgroup analysis, and bias analysis proved the stability of the results. Conclusion: The analysis showed that EGFR mutations were significantly associated with DFS and OS. These findings indicated that surgically treated NSCLC patients with EGFR mutations were inclined to exhibit a prolonged DFS and OS. In addition, the results indicated that KRAS mutations predicted worse DFS and OS in patients with resected NSCLC.
引用
收藏
页码:3393 / 3404
页数:12
相关论文
共 53 条
[1]   American Society of Clinical Oncology Provisional Clinical Opinion: Testing for KRAS Gene Mutations in Patients With Metastatic Colorectal Carcinoma to Predict Response to Anti-Epidermal Growth Factor Receptor Monoclonal Antibody Therapy [J].
Allegra, Carmen J. ;
Jessup, J. Milburn ;
Somerfield, Mark R. ;
Hamilton, Stanley R. ;
Hammond, Elizabeth H. ;
Hayes, Daniel F. ;
McAllister, Pamela K. ;
Morton, Roscoe F. ;
Schilsky, Richard L. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (12) :2091-2096
[2]   Assessment of MAGE-A Expression in Resected Non-Small Cell Lung Cancer in Relation to Clinicopathologic Features and Mutational Status of EGFR and KRAS [J].
Ayyoub, Maha ;
Memeo, Lorenzo ;
Alvarez-Fernandez, Emilio ;
Colarossi, Cristina ;
Costanzo, Rosario ;
Aiello, Eleonora ;
Martinetti, Daniela ;
Valmori, Danila .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (10) :943-948
[3]   Drug therapy: EGFR antagonists in cancer treatment [J].
Ciardiello, Fortunato ;
Tortora, Giampaolo .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (11) :1160-1174
[4]   Distinct Clinical Course of EGFR-Mutant Resected Lung Cancers Results of Testing of 1118 Surgical Specimens and Effects of Adjuvant Gefitinib and Erlotinib [J].
D'Angelo, Sandra P. ;
Janjigian, Yelena Y. ;
Ahye, Nicholas ;
Riely, Gregory J. ;
Chaft, Jamie E. ;
Sima, Camelia S. ;
Shen, Ronglai ;
Zheng, Junting ;
Dycoco, Joseph ;
Kris, Mark G. ;
Zakowski, Maureen F. ;
Ladanyi, Marc ;
Rusch, Valerie ;
Azzoli, Christopher G. .
JOURNAL OF THORACIC ONCOLOGY, 2012, 7 (12) :1815-1822
[5]   High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies [J].
Do, Hongdo ;
Krypuy, Michael ;
Mitchell, Paul L. ;
Fox, Stephen B. ;
Dobrovic, Alexander .
BMC CANCER, 2008, 8 (1)
[6]   Predictive and prognostic impact of epidermal growth factor receptor mutation in non-small-cell lung cancer patients treated with gefitinib [J].
Han, SW ;
Kim, TY ;
Hwang, PG ;
Jeong, S ;
Kim, J ;
Choi, IS ;
Oh, DY ;
Kim, LH ;
Kim, DW ;
Chung, DH ;
Im, SA ;
Kim, YT ;
Lee, JS ;
Heo, DS ;
Bang, YJ ;
Kim, NK .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2493-2501
[7]   Combination therapeutics in complex diseases [J].
He, Bing ;
Lu, Cheng ;
Zheng, Guang ;
He, Xiaojuan ;
Wang, Maolin ;
Chen, Gao ;
Zhang, Ge ;
Lu, Aiping .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2016, 20 (12) :2231-2240
[8]   A Comprehensive Analysis of the Dynamic Biological Networks in HCV Induced Hepatocarcinogenesis [J].
He, Bing ;
Zhang, Hao ;
Shi, Tieliu .
PLOS ONE, 2011, 6 (04)
[9]   HCCNet: an integrated network database of hepatocellular carcinoma [J].
He, Bing ;
Qiu, Xiaojie ;
Li, Peng ;
Wang, Lishan ;
Lv, Qi ;
Shi, Tieliu .
CELL RESEARCH, 2010, 20 (06) :732-734
[10]   Comprehensive analysis of EGFR signaling pathways in Japanese patients with non-small cell lung cancer [J].
Hosokawa, Shinobu ;
Toyooka, Shinichi ;
Fujiwara, Yoshiro ;
Tokumo, Masaki ;
Soh, Junichi ;
Takigawa, Nagio ;
Hotta, Katsuyuki ;
Yoshino, Tadashi ;
Date, Hiroshi ;
Tanimoto, Mitsune ;
Kiura, Katsuyuki .
LUNG CANCER, 2009, 66 (01) :107-113