Personalized medicine for mucositis: Bayesian networks identify unique gene clusters which predict the response to gamma-D-glutamyl-L-tryptophan (SCV-07) for the attenuation of chemoradiation-induced oral mucositis

被引:19
作者
Alterovitz, Gil [1 ]
Tuthill, Cynthia [2 ]
Rios, Israel [2 ]
Modelska, Katharina [2 ]
Sonis, Stephen [3 ]
机构
[1] MIT, Partners HealthCare Ctr Personalized Genet Med, Childrens Hosp Informat Program, Harvard MIT Hlth Sci & Technol Div,Dept Elect Eng, Cambridge, MA 02139 USA
[2] SciClone Pharmaceut, Foster City, CA USA
[3] Biomodels LLC, Watertown, MA USA
关键词
Mucositis; Personalized medicine; Genomics; Gamma-D-glutamyl-L-tryptophan; Radiation; EXPRESSION; THERAPY;
D O I
10.1016/j.oraloncology.2011.07.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Gamma-D-glutamyl-L-tryptophan (SCV-07) demonstrated an overall efficacy signal in ameliorating oral mucositis (OM) in a clinical trial of head and neck cancer patients. However, not all SCV-07-treated subjects responded positively. Here we determined if specific gene clusters could discriminate between subjects who responded to SCV-07 and those who did not. Microarrays were done using peripheral blood RNA obtained at screening and on the last day of radiation from 28 subjects enrolled in the SCV-07 trial. An analytical technique was applied that relied on learned Bayesian networks to identify gene clusters which discriminated between individuals who received SCV-07 and those who received placebo, and which differentiated subjects for whom SCV-07 was an effective OM intervention from those for whom it was not. We identified 107 genes that discriminated SCV-07 responders from non-responders using four models and applied Akaike Information Criteria (AIC) and Bayes Factor (BF) analysis to evaluate predictive accuracy. AIC were superior to BF: the accuracy of predicting placebo vs. treatment was 78% using BF, but 91% using the AIC score. Our ability to differentiate responders from non-responders using the AIC score was dramatic and ranged from 93% to 100% depending on the dataset that was evaluated. Predictive Bayesian networks were identified and functional cluster analyses were performed. A specific 10 gene cluster was a critical contributor to the predictability of the dataset. Our results demonstrate proof of concept in which the application of a genomics-based analytical paradigm was capable of discriminating responders and non-responders for an OM intervention. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:951 / 955
页数:5
相关论文
共 13 条
[1]
Adkins D, 2010, J CLIN ONCOL, V28
[2]
ADKINS D, 2010, INT SOC BIOL THER CA
[3]
How to infer gene networks from expression profiles [J].
Bansal, Mukesh ;
Belcastro, Vincenzo ;
Ambesi-Impiombato, Alberto ;
di Bernardo, Diego .
MOLECULAR SYSTEMS BIOLOGY, 2007, 3 (1)
[4]
JESSE M, 2008, EVIDENCE BASED EMERG
[5]
A REVIEW OF GOODNESS OF FIT STATISTICS FOR USE IN THE DEVELOPMENT OF LOGISTIC-REGRESSION MODELS [J].
LEMESHOW, S ;
HOSMER, DW .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1982, 115 (01) :92-106
[6]
Inferring cellular networks - a review [J].
Markowetz, Florian ;
Spang, Rainer .
BMC BIOINFORMATICS, 2007, 8 (Suppl 6)
[7]
From gene expression to gene regulatory networks in Arabidopsis thaliana [J].
Needham, Chris J. ;
Manfield, Iain W. ;
Bulpitt, Andrew J. ;
Gilmartin, Philip M. ;
Westhead, David R. .
BMC SYSTEMS BIOLOGY, 2009, 3 :85
[8]
Genetic markers for the efficacy of tumour necrosis factor blocking therapy in rheumatoid arthritis [J].
Padyukov, L ;
Lampa, J ;
Heimbürger, M ;
Ernestam, S ;
Cederholm, T ;
Lundkvist, I ;
Andersson, P ;
Hermansson, Y ;
Harju, A ;
Klareskog, L ;
Bratt, J .
ANNALS OF THE RHEUMATIC DISEASES, 2003, 62 (06) :526-529
[9]
Salonga D, 2000, CLIN CANCER RES, V6, P1322
[10]
Perspectives on cancer therapy-induced mucosal injury - Pathogenesis, measurement, epidemiology, and consequences for patients [J].
Sonis, ST ;
Elting, LS ;
Keefe, D ;
Peterson, DE ;
Schubert, M ;
Hauer-Jensen, M ;
Bekele, BN ;
Raber-Durlacher, J ;
Donnelly, JP ;
Rubenstein, EB .
CANCER, 2004, 100 (09) :1995-2025