Robust prediction of response to immune checkpoint blockade therapy in metastatic melanoma

被引:514
作者
Auslander, Noam [1 ,2 ]
Zhang, Gao [3 ,4 ]
Lee, Joo Sang [1 ,2 ]
Frederick, Dennie T. [5 ]
Miao, Benchun [5 ]
Moll, Tabea [6 ]
Tian, Tian [7 ]
Wei, Zhi [7 ]
Madan, Sanna [1 ,2 ]
Sullivan, Ryan J. [5 ]
Boland, Genevieve [6 ]
Flaherty, Keith [5 ]
Herlyn, Meenhard [3 ,4 ]
Ruppin, Eytan [1 ,2 ]
机构
[1] Univ Maryland, Dept Comp Sci, Ctr Bioinformat & Computat Biol, College Pk, MD 20742 USA
[2] NCI, CDSL, NIH, Rockville, MD 20850 USA
[3] Wistar Inst Anat & Biol, Mol & Cellular Oncogenesis Program, 3601 Spruce St, Philadelphia, PA 19104 USA
[4] Wistar Inst Anat & Biol, Melanoma Res Ctr, 3601 Spruce St, Philadelphia, PA 19104 USA
[5] Massachusetts Gen Hosp, Canc Ctr, Boston, MA 02114 USA
[6] Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
[7] New Jersey Inst Technol, Dept Comp Sci, Newark, NJ 07102 USA
关键词
SPONTANEOUS REGRESSION; PD-1; BLOCKADE; MECHANISMS; NEUROBLASTOMA; RESISTANCE; PATHWAYS; CTLA-4;
D O I
10.1038/s41591-018-0157-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immune checkpoint blockade (ICB) therapy provides remarkable clinical gains and has been very successful in treatment of melanoma. However, only a subset of patients with advanced tumors currently benefit from ICB therapies, which at times incur considerable side effects and costs. Constructing predictors of patient response has remained a serious challenge because of the complexity of the immune response and the shortage of large cohorts of ICB-treated patients that include both 'omics' and response data. Here we build immuno-predictive score (IMPRES), a predictor of ICB response in melanoma which encompasses 15 pairwise transcriptomics relations between immune checkpoint genes. It is based on two key conjectures: (i) immune mechanisms underlying spontaneous regression in neuroblastoma can predict melanoma response to ICB, and (ii) key immune interactions can be captured via specific pairwise relations of the expression of immune checkpoint genes. IMPRES is validated on nine published datasets(1-6) and on a newly generated dataset with 31 patients treated with anti-PD-1 and 10 with anti-CTLA-4, spanning 297 samples in total. It achieves an overall accuracy of AUC = 0.83, outperforming existing predictors and capturing almost all true responders while misclassifying less than half of the nonresponders. Future studies are warranted to determine the value of the approach presented here in other cancer types.
引用
收藏
页码:1545 / +
页数:7
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