Validation of genomics-based prognostic tests in malignant pleura mesothelioma

被引:64
作者
Gordon, GJ
Rockwell, GN
Godfrey, PA
Jensen, RV
Glickman, JN
Yeap, BY
Richards, WG
Sugarbaker, DJ
Bueno, R
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Thorac Surg, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Thorac Surg Oncol Lab, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[4] Univ Massachusetts, Dept Phys, Boston, MA 02125 USA
[5] Massachusetts Gen Hosp, Dept Med, Hematol Oncol Unit, Boston, MA 02114 USA
[6] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Neurol, Cambridge, MA 02138 USA
关键词
D O I
10.1158/1078-0432.CCR-04-2181
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Malignant pleural mesothelioma (MPM) is a highly lethal neoplasm with limited pretreatment prognostication strategies. In this report, we examine the accuracy of a previously proposed prognostic test in an independent cohort of MPM patients. This test uses simple ratios of gene expression levels to provide a novel prognostication scheme. Experimental Design: Gene expression data using high-density oligonucleotide microarrays (similar to 22,000 genes) were obtained for a new cohort of human MPM tumors from patients undergoing similar treatments (n = 39). The relative expression levels for specific genes were also determined using real-time quantitative reverse transcription-PCR. We also used a subset of these tumors associated with widely divergent patient survival (n = 23) as a training set to identify new treatment-specific candidate prognostic molecular markers and gene ratio-based prognostic tests. The predictive nature of these newly discovered markers and gene ratio-based prognostic tests were then examined in an independent group of tumors (n = 52) using microarray data and quantitative reverse transcription-PCR. Results: Previously described MPM prognostic genes and gene ratio-based prognostic tests predicted clinical outcome in 39 independent MPM tumor specimens in a statistically significant manner. Newly discovered treatment-specific prognostic genes and gene ratio-based prognostic tests were highly accurate and statistically significant when examined in an independent group of 52 tumors from patients undergoing similar treatment. Conclusions: The data support the use of gene ratios in translating gene expression data into easily reproducible, statistically validated clinical tests for the prediction of outcome in MPM.
引用
收藏
页码:4406 / 4414
页数:9
相关论文
共 26 条
[1]  
Acebo E, 2001, HISTOL HISTOPATHOL, V16, P1031, DOI 10.14670/HH-16.1031
[2]  
AISNER J, 1996, COMPREHENSIVE TXB TH, P799
[3]  
Aisner J. M, 1996, COMPREHENSIVE TXB TH, P757
[4]   The epidemiology of mesothelioma [J].
Britton, M .
SEMINARS IN ONCOLOGY, 2002, 29 (01) :18-25
[5]   A diagnostic test for prostate cancer from gene expression profiling data [J].
Bueno, R ;
Loughlin, KR ;
Powell, MH ;
Gordon, GJ .
JOURNAL OF UROLOGY, 2004, 171 (02) :903-906
[6]   Expression of tetraspanins in human lung cancer cells: frequent downregulation of CD9 and its contribution to cell motility in small cell lung cancer [J].
Funakoshi, T ;
Tachibana, I ;
Hoshida, Y ;
Kimura, H ;
Takeda, Y ;
Kijima, T ;
Nishino, K ;
Goto, H ;
Yoneda, T ;
Kumagai, T ;
Osaki, T ;
Hayashi, S ;
Aozasa, K ;
Kawase, I .
ONCOGENE, 2003, 22 (05) :674-687
[7]  
Gordon GJ, 2002, CANCER RES, V62, P4963
[8]  
Gordon GJ, 2003, CANCER EPIDEM BIOMAR, V12, P905
[9]   Using gene expression ratios to predict outcome among patients with mesothelioma [J].
Gordon, GJ ;
Jensen, RV ;
Hsiao, LL ;
Gullans, SR ;
Blumenstock, JE ;
Richards, WG ;
Jaklitsch, MT ;
Sugarbaker, DJ ;
Bueno, R .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (08) :598-605
[10]   Of microarrays and meandering data points [J].
Gullans, SR .
NATURE GENETICS, 2000, 26 (01) :4-5