Improved prediction of immune checkpoint blockade efficacy across multiple cancer types

Only a fraction of patients with cancer respond to immune checkpoint blockade (ICB) treatment, but current decision-making procedures have limited accuracy. In this study, we developed a machine learning model to predict ICB response by integrating genomic, molecular, demographic and clinical data f...

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Vydané v:Nature biotechnology Ročník 40; číslo 4; s. 499 - 506
Hlavní autori: Chowell, Diego, Yoo, Seong-Keun, Valero, Cristina, Pastore, Alessandro, Krishna, Chirag, Lee, Mark, Hoen, Douglas, Shi, Hongyu, Kelly, Daniel W., Patel, Neal, Makarov, Vladimir, Ma, Xiaoxiao, Vuong, Lynda, Sabio, Erich Y., Weiss, Kate, Kuo, Fengshen, Lenz, Tobias L., Samstein, Robert M., Riaz, Nadeem, Adusumilli, Prasad S., Balachandran, Vinod P., Plitas, George, Ari Hakimi, A., Abdel-Wahab, Omar, Shoushtari, Alexander N., Postow, Michael A., Motzer, Robert J., Ladanyi, Marc, Zehir, Ahmet, Berger, Michael F., Gönen, Mithat, Morris, Luc G. T., Weinhold, Nils, Chan, Timothy A.
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: New York Nature Publishing Group US 01.04.2022
Nature Publishing Group
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ISSN:1087-0156, 1546-1696, 1546-1696
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Popis
Shrnutí:Only a fraction of patients with cancer respond to immune checkpoint blockade (ICB) treatment, but current decision-making procedures have limited accuracy. In this study, we developed a machine learning model to predict ICB response by integrating genomic, molecular, demographic and clinical data from a comprehensively curated cohort (MSK-IMPACT) with 1,479 patients treated with ICB across 16 different cancer types. In a retrospective analysis, the model achieved high sensitivity and specificity in predicting clinical response to immunotherapy and predicted both overall survival and progression-free survival in the test data across different cancer types. Our model significantly outperformed predictions based on tumor mutational burden, which was recently approved by the U.S. Food and Drug Administration for this purpose 1 . Additionally, the model provides quantitative assessments of the model features that are most salient for the predictions. We anticipate that this approach will substantially improve clinical decision-making in immunotherapy and inform future interventions. A combination of genomic and clinical features improves predictions of response to immune checkpoint blockade.
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D.C., S.-K.Y., C.V., A.P., L.G.T.M., N.W. and T.A.C conceived and designed the study. D.C. and S.-K.Y. developed the machine learning model. D.C., S.-K.Y., C.V., A.P., C.K., M.L., D.H., H.S., D.W.K., N.P., V.M., K.W., T.L., R.M.S., N.R., P.S.A., V.P.B., G.P., A.A.H., A.N.S., M.A.P., R.J.M, M.L., A.Z., M.F.B., L.G.T.M. and N.W. acquired, analyzed or interpreted the data. M.G. provided statistical advice. All authors critically revised the manuscript for important intellectual content. L.G.T.M., N.W. and T.A.C. supervised the study.
Author contributions
ISSN:1087-0156
1546-1696
1546-1696
DOI:10.1038/s41587-021-01070-8