with treatment outcome of advanced non-small cell lung cancer patients with cisplatin-based chemotherapy

被引:0
作者
Wu, Gun [1 ,2 ]
Jiang, Bin [2 ]
Liu, Xiaoqin [2 ]
Shen, Yi [1 ,2 ]
Yang, Shujuan [3 ]
机构
[1] Guangxi Med Univ, Grad Sch, Dept Thorac Surg, Nanning, Peoples R China
[2] Sichuan Canc Hosp, Dept Thorac Surg, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Sch Publ Hlth, Chengdu 610064, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2015年 / 8卷 / 10期
关键词
GSTM1; GSTT1; GSTP1; polymorphism; NSCLC; chemotherapy; GLUTATHIONE-S-TRANSFERASE; GENETIC-VARIABILITY; GST POLYMORPHISMS; BREAST-CANCER; PI EXPRESSION; ASSOCIATION; SURVIVAL; SMOKING;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We evaluated the association of GSTM1 null/present, GSTT1 null/present, and GSTPI Ile105Val polymorphisms with the clinical response to chemotherapy and treatment outcome of NSCLC. Between October 2009 and October 2012, a total of 282 patients with advanced NSCLC were enrolled into our study, and they were followed up until October 2014. The genotypes of GSTM1, GSTT1, and GSTP1 Ile105Val were performed by polymerase chain reaction (PCR) coupled with restriction fragment length polymorphism (RFLP). By logistic regression analysis, our study found that the Val/Val genotype of GSTP1 lIe105Val was associated with more CR+PR response to chemotherapy when compared with the Ile/Ile genotype, and the OR (95% CI) was 2.18 (1.16-4.12). By multivariate Cox proportional hazards regression analysis, we found the Val/Val genotype of GSTPI was correlated with lower risk of death in advanced NSCLC (HR, 0.48; 95% Cl, 0.25-0.93). However, no association was found between GSTT1 and GSTM1 polymorphisms and response to chemotherapy and overall survival of advanced NSCLC. Moreover, the Ile/ Val + Val/Val genotypes of GSTP1 were associated with lower risk of death in never smokers, and the adjusted HR (95% CI) was 0.34 (0.12-0.93). In conclusion, we found that the GSTP1 polymorphism was correlated with better response to chemotherapy and lower risk of death in advanced NSCLC patients.
引用
收藏
页码:13346 / 13352
页数:7
相关论文
共 22 条
  • [1] CYP and GST polymorphisms and survival in advanced non-small cell lung cancer patients
    Ada, A. O.
    Kunak, S. C.
    Hancer, F.
    Bilgen, S.
    Suzen, S. H.
    Alpar, S.
    Gulhan, M.
    Kurt, B.
    Iscan, M.
    [J]. NEOPLASMA, 2010, 57 (06) : 512 - 521
  • [2] Polymorphisms within glutathione S-transferase genes and initial response to glucocorticoids in childhood acute lymphoblastic leukaemia
    Anderer, G
    Schrappe, M
    Brechlin, AM
    Lauten, M
    Muti, P
    Welte, K
    Stanulla, M
    [J]. PHARMACOGENETICS, 2000, 10 (08): : 715 - 726
  • [3] Glutathione-S-Transferase-Pi Expression in Early Breast Cancer: Association With Outcome and Response to Chemotherapy
    Arun, Banu K.
    Granville, Laura A.
    Yin, Guosheng
    Middleton, Lavinia P.
    Dawood, Shaheenah
    Kau, Shu-Wan
    Kamal, Arif
    Hsu, Limin
    Hortobagyi, Gabriel N.
    Sahin, Aysegul A.
    [J]. CANCER INVESTIGATION, 2010, 28 (05) : 554 - 559
  • [4] The International Association for the Study of Lung Cancer Staging Project Prognostic Factors and Pathologic TNM Stage in Surgically Managed Non-small Cell Lung Cancer
    Chansky, Kari
    Sculier, Jean-Paul
    Crowley, John J.
    Giroux, Dori
    Van Meerbeeck, Jan
    Goldstraw, Peter
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (07) : 792 - 801
  • [5] Franco RL, 2012, J BUON, V17, P259
  • [6] Genetic variability of DNA repair mechanisms and glutathione- S- transferase genes influences treatment outcome in osteosarcoma
    Goricar, Katja
    Kovac, Viljem
    Jazbec, Janez
    Zakotnik, Branko
    Lamovec, Janez
    Dolzan, Vita
    [J]. CANCER EPIDEMIOLOGY, 2015, 39 (02) : 182 - 188
  • [7] Han B, 2015, INT J CLIN EXP PATHO, V8, P4113
  • [8] Germline polymorphisms in patients with advanced nonsmall cell lung cancer receiving first-line platinum-gemcitabine chemotherapy A Prospective Clinical Study
    Joerger, Markus
    Burgers, Sjaak A.
    Baas, Paul
    Smit, Egbert F.
    Haitjema, Tjeerd J.
    Bard, Martin P. L.
    Doodeman, Valerie D.
    Smits, Paul H. M.
    Vincent, Andrew
    Huitema, Alwin D. R.
    Beijnen, Jos H.
    Schellens, Jan H. M.
    [J]. CANCER, 2012, 118 (09) : 2466 - 2475
  • [9] Genetic variants in the glutathione S-transferase genes and survival in colorectal cancer patients after chemotherapy and differences according to treatment with oxaliplatin
    Kap, Elisabeth J.
    Richter, Swantje
    Rudolph, Anja
    Jansen, Lina
    Ulrich, Alexis
    Hoffmeister, Michael
    Ulrich, Cornelia M.
    Brenner, Hermann
    Chang-Claude, Jenny
    [J]. PHARMACOGENETICS AND GENOMICS, 2014, 24 (07) : 340 - 347
  • [10] Genetic polymorphisms and the efficacy and toxicity of cisplatin-based chemotherapy in ovarian cancer patients
    Khrunin, A. V.
    Moisseev, A.
    Gorbunova, V.
    Limborska, S.
    [J]. PHARMACOGENOMICS JOURNAL, 2010, 10 (01) : 54 - 61