MDR1 and ERCC1 Expression Predict Outcome of Patients with Locally Advanced Bladder Cancer Receiving Adjuvant Chemotherapy

被引:151
作者
Hoffmann, Andreas-Claudius [1 ,2 ,3 ,4 ]
Wild, Peter [6 ]
Leicht, Christina [5 ]
Bertz, Simone [7 ]
Danenberg, Kathleen D. [4 ]
Danenberg, Peter V. [2 ,3 ]
Stoehr, Robert [7 ]
Stoeckle, Michael [8 ]
Lehmann, Jan [9 ]
Schuler, Martin [1 ]
Hartmann, Arndt [7 ]
机构
[1] Univ Duisburg Essen, Dept Med Canc Res, W German Canc Ctr, Essen, Germany
[2] Univ So Calif, Dept Biochem & Mol Biol, Los Angeles, CA USA
[3] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[4] Response Genet Inc, Los Angeles, CA USA
[5] Univ Hosp Regensburg, Dept Pathol, Regensburg, Germany
[6] ETH, Zurich, Switzerland
[7] Univ Hosp Erlangen, Dept Pathol, Erlangen, Germany
[8] Univ Saarland, Dept Urol, D-6650 Homburg, Germany
[9] Urol Practice Pruner Gang, Kiel, Germany
来源
NEOPLASIA | 2010年 / 12卷 / 08期
关键词
TRANSITIONAL-CELL-CARCINOMA; PHASE-III TRIAL; P-GLYCOPROTEIN; RADICAL CYSTECTOMY; RANDOMIZED-TRIAL; GENE-EXPRESSION; BREAST-CANCER; CISPLATIN; METHOTREXATE; VINBLASTINE;
D O I
10.1593/neo.10402
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
PURPOSE: The role of adjuvant chemotherapy in patients with locally advanced bladder cancer still remains to be defined. We hypothesized that assessing the gene expression of the chemotherapy response modifiers multidrug resistance gene 1 (MDR1) and excision repair cross-complementing 1 (ERCC1) may help identify the group of patients benefiting from cisplatin-based adjuvant chemotherapy. EXPERIMENTAL DESIGN: Formalin-fixed paraffin-embedded tumor samples from 108 patients with locally advanced bladder cancer, who had been enrolled inAUO-AB05/95, a phase 3 trial randomizing a maximum of three courses of adjuvant cisplatin and methotrexate (CM) versus methotrexate, vinblastine, epirubicin, and cisplatin (M-VEC), were included in the study. Tumor cells were retrieved by laser-captured microdissection and analyzed for MDR1 and ERCC1 expression using a quantitative real-time reverse transcription-polymerase chain reaction assay. Gene expression levels were correlated with clinical outcomes by multivariate Cox proportional hazards regression analysis. RESULTS: Expressions of MDR1 and ERCC1 were independently associated with overall progression-free survival (P = .001, relative risk = 2.9 and P = .01, relative risk = 2.24, respectively). The correlation of high MDR1 expression with inferior outcome was stronger in patients receiving M-VEC, whereas ERCC1 analysis performed equally in the CM and M-VEC groups. CONCLUSIONS: High MDR1 and ERCC1 gene expressions are associated with inferior outcome after cisplatin-based adjuvant chemotherapy for locally advanced bladder cancer. Prospective studies are warranted to define a role for MDR1 and ERCC1 analysis in individualizing multimodality treatment in locally advanced bladder cancer. Neoplasia (2010) 12, 628-636
引用
收藏
页码:628 / 636
页数:9
相关论文
共 36 条
[1]
Abolhoda A, 1999, CLIN CANCER RES, V5, P3352
[2]
[Anonymous], 1999, Lancet, V354, P533
[3]
Ashariati Ami, 2008, Acta Med Indones, V40, P187
[4]
EXPRESSION OF P-GLYCOPROTEIN IN HIGH-GRADE OSTEOSARCOMAS IN RELATION TO CLINICAL OUTCOME [J].
BALDINI, N ;
SCOTLANDI, K ;
BARBANTIBRODANO, G ;
MANARA, MC ;
MAURICI, D ;
BACCI, G ;
BERTONI, F ;
PICCI, P ;
SOTTILI, S ;
CAMPANACCI, M ;
SERRA, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (21) :1380-1385
[5]
Gene expression of ERCC1 as a novel prognostic marker in advanced bladder cancer patients receiving cisplatin-based chemotherapy [J].
Bellmunt, J. ;
Paz-Ares, L. ;
Cuello, M. ;
Cecere, F. L. ;
Albiol, S. ;
Guillem, V. ;
Gallardo, E. ;
Carles, J. ;
Mendez, P. ;
de la Cruz, J. J. ;
Taron, M. ;
Rosell, R. ;
Baselga, J. .
ANNALS OF ONCOLOGY, 2007, 18 (03) :522-528
[6]
MDR1 (C3435T) polymorphism: relation to the risk of breast cancer and therapeutic outcome [J].
Cizmarikova, M. ;
Wagnerova, M. ;
Schonova, L. ;
Habalova, V. ;
Kohut, A. ;
Linkova, A. ;
Sarissky, M. ;
Mojzis, J. ;
Mirossay, L. ;
Mirossay, A. .
PHARMACOGENOMICS JOURNAL, 2010, 10 (01) :62-69
[7]
Customizing cisplatin based on quantitative excision repair cross-complementing 1 mRNA expression:: A phase III trial in non-small-cell lung cancer [J].
Cobo, Manuel ;
Isla, Dolores ;
Massuti, Bartomeu ;
Montes, Ana ;
Miguel Sanchez, Jose ;
Provencio, Mariano ;
Vinolas, Nuria ;
Paz-Ares, Luis ;
Lopez-Vivanco, Guillermo ;
Angel Munoz, Miguel ;
Felip, Enriqueta ;
Alberola, Vicente ;
Camps, Carlos ;
Domine, Manuel ;
Sanchez, Jose Javier ;
Sanchez-Ronco, Maria ;
Danenberg, Kathleen ;
Taron, Miquel ;
Gandara, David ;
Rosell, Rafael .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (19) :2747-2754
[8]
P-glycoprotein confers methotrexate resistance in 3T6 cells with deficient carrier-mediated methotrexate uptake [J].
DeGraaf, D ;
Sharma, RC ;
Mechetner, EB ;
Schimke, RT ;
Roninson, IB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1238-1242
[9]
A randomized trial of radical cystectomy versus radical cystectomy plus cisplatin, vinblastine and methotrexate chemotherapy for muscle invasive bladder cancer [J].
Freiha, F ;
Reese, J ;
Torti, FM .
JOURNAL OF UROLOGY, 1996, 155 (02) :495-499
[10]
Goebell P J, 2009, Minerva Urol Nefrol, V61, P91